المؤلفون: Menon Usha, Gentry-Maharaj Aleksandra, Burnell Matthew, Apostolidou Sophia, Ryan Andy, Kalsi Jatinderpal K, Singh Naveena, Fallowfield Lesley, McGuire Alistair J, Campbell Stuart, Skates Steven J, Dawnay Anne, Parmar Mahesh, Jacobs Ian J

المصدر: Health Technology Assessment (2023)

مصطلحات موضوعية: screening, randomised controlled trial, conduct, design, ovarian cancer, Medical technology, R855-855.5

الوصف: Randomised controlled trials are challenging to deliver. There is a constant need to review and refine recruitment and implementation strategies if they are to be completed on time and within budget. We present the strategies adopted in the United Kingdom Collaborative Trial of Ovarian Cancer Screening, one of the largest individually randomised controlled trials in the world. The trial recruited over 202,000 women (2001–5) and delivered over 670,000 annual screens (2001–11) and over 3 million women-years of follow-up (2001–20). Key to the successful completion were the involvement of senior investigators in the day-to-day running of the trial, proactive trial management and willingness to innovate and use technology. Our underlying ethos was that trial participants should always be at the centre of all our processes. We ensured that they were able to contact either the site or the coordinating centre teams for clarifications about their results, for follow-up and for rescheduling of appointments. To facilitate this, we shared personal identifiers (with consent) with both teams and had dedicated reception staff at both site and coordinating centre. Key aspects were a comprehensive online trial management system which included an electronic data capture system (resulting in an almost paperless trial), biobanking, monitoring and project management modules. The automation of algorithms (to ascertain eligibility and classify results and ensuing actions) and processes (scheduling of appointments, printing of letters, etc.) ensured the protocol was closely followed and timelines were met. Significant engagement with participants ensured retention and low rates of complaints. Our solutions to the design, conduct and analyses issues we faced are highly relevant, given the renewed focus on trials for early detection of cancer. Future work There is a pressing need to increase the evidence base to support decision making about all aspects of trial methodology. Trial registration ISRCTN-22488978; ClinicalTrials.gov-NCT00058032. Funding This article presents independent research funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme as award number 16/46/01. The long-term follow-up UKCTOCS (2015 20) was supported by National Institute for Health and Care Research (NIHR HTA grant 16/46/01), Cancer Research UK, and The Eve Appeal. UKCTOCS (2001–14) was funded by the MRC (G9901012 and G0801228), Cancer Research UK (C1479/A2884), and the UK Department of Health, with additional support from The Eve Appeal. Researchers at UCL were supported by the NIHR UCL Hospitals Biomedical Research Centre and by the MRC Clinical Trials Unit at UCL core funding (MC_UU_00004/09, MC_UU_00004/08, MC_UU_00004/07). The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, or the UK Department of Health and Social Care. Plain language summary Randomised controlled trials help us decide whether new health-care approaches are better than those in current use. To successfully complete these on time and within budget, there is a constant need to review and revise the procedures used for delivering various aspects such as invitation, enrolment, follow-up of participants, delivery of the new test, data collection, and analysis. We report on the processes used in the United Kingdom Collaborative Trial of Ovarian Cancer Screening, one of the largest such trials. The United Kingdom Collaborative Trial of Ovarian Cancer Screening enrolled over 202,000 women (2001–5), delivered over 670,000 yearly screens (2001–11) and followed all participants until 2020. Key to our successful completion were the involvement of senior investigators in day-to-day running of the trial, a pre-emptive approach to issues, a willingness to innovate, and the use of technology. Our underlying ethos was that trial participants should always be at the centre of all our processes. We ensured that they were able to always contact either their local or the central team for clarifications and rescheduling of appointments. To facilitate this, we shared participant contact details (with consent) with both teams. We built a comprehensive electronic system to manage all aspects of the trial. This included online forms that the teams completed in real time (resulting in an almost paperless trial) and systems to check and manage trial processes and track blood samples. We automated key steps such as checking whether participants were eligible, assigning correct action based on results of screening tests, scheduling appointments and printing letters. As a result, all participants were treated as set out in the trial plan. Our engagement with participants ensured that they continued participating and we had a low rate of complaints. We faced issues with regard to our initial trial design and the way we planned to analyse the data. We feel that our solutions are highly relevant, especially as there is a renewed focus on trials for early detection of cancer.

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1366-5278Test; https://doaj.org/toc/2046-4924Test

الوصول الحر: https://doaj.org/article/cadca67484d4477f9481760a388b2e8cTest

المؤلفون: Menon Usha, Gentry-Maharaj Aleksandra, Burnell Matthew, Ryan Andy, Kalsi Jatinderpal K, Singh Naveena, Dawnay Anne, Fallowfield Lesley, McGuire Alistair J, Campbell Stuart, Skates Steven J, Parmar Mahesh, Jacobs Ian J

المصدر: Health Technology Assessment (2023)

مصطلحات موضوعية: ovarian cancer, ovarian epithelial carcinoma, ovarian neoplasms, cancer screening, early detection of cancer, ukctocs, randomised controlled trial, rct, ca-125 antigen, transvaginal ultrasound, ultrasonography, general population, Medical technology, R855-855.5

الوصف: Background Ovarian and tubal cancers are lethal gynaecological cancers, with over 50% of the patients diagnosed at advanced stage. Trial design Randomised controlled trial involving 27 primary care trusts adjacent to 13 trial centres based at NHS Trusts in England, Wales and Northern Ireland. Methods Participants Postmenopausal average-risk women, aged 50–74, with intact ovaries and no previous ovarian or current non-ovarian cancer. Interventions One of two annual screening strategies: (1) multimodal screening (MMS) using a longitudinal CA125 algorithm with repeat CA125 testing and transvaginal scan (TVS) as second line test (2) ultrasound screening (USS) using TVS alone with repeat scan to confirm any abnormality. The control (C) group had no screening. Follow-up was through linkage to national registries, postal follow-up questionnaires and direct communication with trial centres and participants. Objective To assess comprehensively risks and benefits of ovarian cancer screening in the general population. Outcome Primary outcome was death due to ovarian or tubal cancer as assigned by an independent outcomes review committee. Secondary outcomes included incidence and stage at diagnosis of ovarian and tubal cancer, compliance, performance characteristics, harms and cost-effectiveness of the two screening strategies and a bioresource for future research. Randomisation The trial management system confirmed eligibility and randomly allocated participants using computer-generated random numbers to MMS, USS and C groups in a 1:1:2 ratio. Blinding Investigators and participants were unblinded and outcomes review committee was masked to randomisation group. Analyses Primary analyses were by intention to screen, comparing separately MMS and USS with C using the Versatile test. Results Recruitment 1,243,282 women were invited and 205,090 attended for recruitment between April 2001 and September 2005. Randomised 202,638 women: 50,640 MMS, 50,639 USS and 101,359 C group. Numbers analysed for primary outcome 202,562 (>99.9%): 50,625 (>99.9%) MMS, 50,623 (>99.9%) USS, and 101,314 (>99.9%) C group. Outcome Women in MMS and USS groups underwent 345,570 and 327,775 annual screens between randomisation and 31 December 2011. At median follow-up of 16.3 (IQR 15.1–17.3) years, 2055 women developed ovarian or tubal cancer: 522 (1.0% of 50,625) MMS, 517 (1.0% of 50,623) USS, and 1016 (1.0% of 101314) in C group. Compared to the C group, in the MMS group, the incidence of Stage I/II disease was 39.2% (95% CI 16.1 to 66.9) higher and stage III/IV 10.2% (95% CI –21.3 to 2.4) lower. There was no difference in stage in the USS group. 1206 women died of the disease: 296 (0.6%) MMS, 291 (0.6%) USS, and 619 (0.6%) C group. There was no significant reduction in ovarian and tubal cancer deaths in either MMS (p = 0.580) or USS (p = 0.360) groups compared to the C group. Overall compliance with annual screening episode was 80.8% (345,570/420,047) in the MMS and 78.0% (327,775/420,047) in the USS group. For ovarian and tubal cancers diagnosed within one year of the last test in a screening episode, in the MMS group, the sensitivity, specificity and positive predictive values were 83.8% (95% CI 78.7 to 88.1), 99.8% (95% CI 99.8 to 99.9), and 28.8% (95% CI 25.5 to 32.2) and in the USS group, 72.2% (95% CI 65.9 to 78.0), 99.5% (95% CI 99.5 to 99.5), and 9.1% (95% CI 7.8 to 10.5) respectively. The final within-trial cost-effectiveness analysis was not undertaken as there was no mortality reduction. A bioresource (UKCTOCS Longitudinal Women’s Cohort) of longitudinal outcome data and over 0.5 million serum samples including serial annual samples in women in the MMS group was established and to date has been used in many new studies, mainly focused on early detection of cancer. Harms Both screening tests (venepuncture and TVS) were associated with minor complications with low (8.6/100,000 screens MMS; 18.6/100,000 screens USS) complication rates. Screening itself did not cause anxiety unless more intense repeat testing was required following abnormal screens. In the MMS group, for each screen-detected ovarian or tubal cancer, an additional 2.3 (489 false positives; 212 cancers) women in the MMS group had unnecessary false-positive (benign adnexal pathology or normal adnexa) surgery. Overall, 14 (489/345,572 annual screens) underwent unnecessary surgery per 10,000 screens. In the USS group, for each screen-detected ovarian or tubal cancer, an additional 10 (1630 false positives; 164 cancers) underwent unnecessary false-positive surgery. Overall, 50 (1630/327,775 annual screens) women underwent unnecessary surgery per 10,000 screens. Conclusions Population screening for ovarian and tubal cancer for average-risk women using these strategies should not be undertaken. Decreased incidence of Stage III/IV cancers during multimodal screening did not translate to mortality reduction. Researchers should be cautious about using early stage as a surrogate outcome in screening trials. Meanwhile the bioresource provides a unique opportunity to evaluate early cancer detection tests. Funding Long-term follow-up UKCTOCS (2015–2020) – National Institute for Health and Care Research (NIHR HTA grant 16/46/01), Cancer Research UK, and The Eve Appeal. UKCTOCS (2001–2014) – Medical Research Council (MRC) (G9901012/G0801228), Cancer Research UK (C1479/A2884), and the UK Department of Health, with additional support from The Eve Appeal. Researchers at UCL were supported by the NIHR UCL Hospitals Biomedical Research Centre and by MRC Clinical Trials Unit at UCL core funding (MR_UU_12023). Plain language summary What was the question? Most women with ovarian cancer are diagnosed after the disease has spread widely (advanced stage – III and IV) and more than half die within 5 years. We wanted to find out if testing women without symptoms could pick up ovarian cancer at an earlier stage before it has spread beyond the ovaries and tubes and reduce deaths. We also wanted to assess the risks and benefits of such screening. What did we do? We invited over 1.2 million women living near 13 centres in England, Wales and Northern Ireland. Of them, 202,638 joined the trial. All women were between 50 and 74 and were no longer having periods. They had never been diagnosed with ovarian cancer or were not having treatment for any other cancer. They did not have many relatives with ovarian or breast cancer. The volunteers were placed into one of three groups at random: The blood test group contained 50,640 women who had yearly CA125 blood tests. If these showed a moderate or high chance of ovarian cancer, they had repeat CA125 tests and a scan. The scan group contained 50,639 women who had yearly internal scans of their ovaries and tubes which were repeated if they showed an abnormality. The no-screening group contained 101,359 women. Those in the blood and scan groups had screening every year until December 2011. We sent all women health questionnaires and also, with their permission, received information about them from the national cancer and death registries till mid-2020. What did we find? Women in the screened groups had an average of eight years of screening. We followed them for approximately 16 years after they had joined the trial. During this period, 2055 women were diagnosed with ovarian and tubal cancer. It was about 1 in 100 women (1%) in all three groups: 522 of 50,625 in the blood group 517 of 50,623 in the scan group 1016 of 101,314 in the no-screening group More women were diagnosed with early-stage cancer and fewer were diagnosed with advanced cancer in the blood group compared to the no-screening group. There was no difference in the number diagnosed with early or advanced disease between the scan and no-screening group. Despite this difference, the number of women in each group who died from ovarian and tubal cancer was similar in all three groups: 296 of 50,625 (0.6%) in the blood group, 291 of 50,623 (0.6%) in the scan group and 619 of 101,314 (0.6%) in the no-screening group. Other results showed: Overall, 81% women in the blood group and 78% in the scan group attended all of their annual screening appointments. In the blood group, screening detected 84% of ovarian and tubal cancers diagnosed within one year of the test and correctly classified as normal 99.8% of women who did not have ovarian and tubal cancer. In the scan group, screening detected 72% of ovarian and tubal cancers diagnosed within one year of the last test and correctly classified 99.5% of those who did not have ovarian and tubal cancer. Both screening tests were associated with minor complications. While screening did not increase anxiety, there was slightly increased worry in women who were asked to return for more intense repeat testing. Both screening methods picked up changes that were in fact not ovarian cancer. This meant that women had unnecessary surgery together with the worry and risk of complications that go with it. ◦In the blood group 14 women had unnecessary surgery for every 10,000 women screened annually. This means that for each woman found to have ovarian cancer, an additional 2 women had unnecessary surgery. ◦In the scan group 50 women had unnecessary surgery for every 10,000 women screened annually. This means that for each woman found to have ovarian cancer, an additional 10 women had unnecessary surgery. A biobank with all the donated data and over 0.5 million serum samples, including yearly samples from women in the blood group, was built and continues to be used in many new studies, mainly focused on early detection of cancer. What does this mean? Screening using the CA125 blood test or transvaginal ultrasound scan to test for ovarian cancer did not save lives. Additionally, it was associated with some harm. Therefore, an ovarian cancer screening programme for most women cannot be currently recommended. The trial also showed for the first time that ovarian cancer can be detected earlier through screening. However, for screening to save lives, the test needs to pick up many more women earlier in the course of the disease so that available treatments are effective. The biobank provides an opportunity for scientists to see if newer tests for cancer can detect the disease earlier.

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1366-5278Test; https://doaj.org/toc/2046-4924Test

الوصول الحر: https://doaj.org/article/b38b3c1cc47244c5afd068e650ac4ac7Test

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المساهمون: Tumasyan, A., Adam, W., Andrejkovic, J. W., Bergauer, T., Chatterjee, S., Damanakis, K., Dragicevic, M., Del Valle, A. Escalante, Fruhwirth, R., Jeitler, M., Krammer, N., Lechner, L., Liko, D., Mikulec, I, Paulitsch, P., Pitters, F. M., Schieck, J., Schofbeck, R., Schwarz, D., Templ, S., Waltenberger, W., Wulz, C-E, Chekhovsky, V, Litomin, A., Makarenko, V, Darwish, M. R., De Wolf, E. A., Janssen, T., Kello, T., Lelek, A., Sfar, H. Rejeb, Van Mechelen, P., Van Putte, S., Van Remortel, N., Blekman, F., Bols, E. S., D'Hondt, J., Delcourt, M., El Faham, H., Lowette, S., Moortgat, S., Morton, A., Mueller, D., Sahasransu, A. R., Tavernier, S., Van Doninck, W., Beghin, D., Bilin, B., Clerbaux, B., De Lentdecker, G., Favart, L., Kalsi, A. K., Lee, K., Mahdavikhorrami, M., Makarenko, I, Moureaux, L., Petre, L., Popov, A., Postiau, N., Starling, E., Thomas, L., Vanden Bemden, M., Vander Velde, C., Vanlaer, P., Cornelis, T., Dobur, D., Knolle, J., Lambrecht, L., Mestdach, G., Niedziela, M., Rendon, C., Roskas, C., Samalan, A., Skovpen, K., Tytgat, M., Vermassen, B., Wezenbeek, L., Benecke, A., Bethani, A., Bruno, G., Bury, F., Caputo, C., David, P., Delaere, C., Donertas, I. S., Giammanco, A., Jaffel, K., Jain, Sa, Lemaitre, V, Mondal, K., Prisciandaro, J., Taliercio, A., Teklishyn, M., Tran, T. T., Vischia, P., Wertz, S., Alves, G. A., Hensel, C., Moraes, A., Rebello Teles, P.

مصطلحات موضوعية: DOUBLE PARTON INTERACTIONS, P(P)OVER-BAR COLLISIONS, MATRIX-ELEMENT, JET, EVENTS, HELAC-ONIA, SCATTERINGS, GENERATOR, PP

الوصف: Protons consist of three valence quarks, two up-quarks and one down-quark, held together by gluons and a sea of quark-antiquark pairs. Collectively, quarks and gluons are referred to as partons. In a proton-proton collision, typically only one parton of each proton undergoes a hard scattering - referred to as single-parton scattering - leaving the remainder of each proton only slightly disturbed. Here, we report the study of double- and triple-parton scatterings through the simultaneous production of three J/psi mesons, which consist of a charm quark-antiquark pair, in proton-proton collisions recorded with the CMS experiment at the Large Hadron Collider. We observed this process - reconstructed through the decays of J/psi mesons into pairs of oppositely charged muons - with a statistical significance above five standard deviations. We measured the inclusive fiducial cross-section to be 272(-104)(+141) (stat) +/- 17 (syst) fb, and compared it to theoretical expectations for triple-J/psi meson production in single-, double- and triple-parton scattering scenarios. Assuming factorization of multiple hard-scattering probabilities in terms of single-parton scattering cross-sections, double- and triple-parton scattering are the dominant contributions for the measured process.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000927936700008; volume:19; issue:3; firstpage:338; lastpage:350; numberofpages:13; journal:NATURE PHYSICS; https://hdl.handle.net/11568/1223914Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85162051065; https://www.nature.com/articles/s41567-022-01838-yTest

الإتاحة: https://doi.org/10.1038/s41567-022-01838-yTest
https://hdl.handle.net/11568/1223914Test
https://www.nature.com/articles/s41567-022-01838-yTest

المؤلفون: Tumasyan, A., Adam, W., Bergauer, T., Dragicevic, M., Del Valle, A. Escalante, Fruehwirth, R., Jeitler, M., Krammer, N., Lechner, L., Liko, D., Mikulec, I., Pitters, F. M., Rad, N., Schieck, J., Schoefbeck, R., Spanring, M., Templ, S., Waltenberger, W., Wulz, C. -E., Zarucki, M., Darwish, M. R., De Wolf, E. A., Janssen, T., Kello, T., Lelek, A., Pieters, M., Sfar, H. Rejeb, Van Mechelen, P., Van Putte, S., Van Remortel, N., Blekman, F., Bols, E. S., Chhibra, S. S., D'Hondt, J., De Clercq, J., Lontkovskyi, D., Lowette, S., Marchesini, I., Moortgat, S., Morton, A., Mueller, D., Python, Q., Tavernier, S., Van Doninck, W., Van Mulders, P., Beghin, D., Bilin, B., Clerbaux, B., De Lentdecker, G., Dorney, B., Favart, L., Grebenyuk, A., Kalsi, A. K., Makarenko, I., Moureaux, L., Petre, L., Popov, A., Postiau, N., Starling, E., Thomas, L., Vander Velde, C., Vanlaer, P., Vannerom, D., Wezenbeek, L., Cornelis, T., Dobur, D., Gruchala, M., Khvastunov, I., Mestdach, G., Niedziela, M., Roskas, C., Skovpen, K., Tytgat, M., Verbeke, W., Vermassen, B., Vit, M., Bethani, A., Bruno, G., Bury, F., Caputo, C., David, P., Delaere, C., Delcourt, M., Donertas, I. S., Giammanco, A., Lemaitre, V., Mondal, K., Prisciandaro, J., Taliercio, A., Teklishyn, M., Vischia, P., Wertz, S., Wuyckens, S., Alves, G. A., Hensel, C., Moraes, A., Alda Junior, W. L., Belchior Batista Das Chagas, E., Brandao Malbouisson, H., Carvalho, W., Chinellato, J., Coelho, E., Da Costa, E. M., Da Silveira, G. G., De Jesus Damiao, D., Fonseca De Souza, S., Martins, J., Matos Figueiredo, D., Medina Jaime, M., Mora Herrera, C., Mundim, L., Nogima, H., Rebello Teles, P., Sanchez Rosas, L. J., Santoro, A., Silva Do Amaral, S. 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المساهمون: Tumasyan, A., Adam, W., Bergauer, T., Dragicevic, M., Del Valle, A. Escalante, Fruehwirth, R., Jeitler, M., Krammer, N., Lechner, L., Liko, D., Mikulec, I., Pitters, F. M., Rad, N., Schieck, J., Schoefbeck, R., Spanring, M., Templ, S., Waltenberger, W., Wulz, C. -E., Zarucki, M., Darwish, M. R., De Wolf, E. A., Janssen, T., Kello, T., Lelek, A., Pieters, M., Sfar, H. Rejeb, Van Mechelen, P., Van Putte, S., Van Remortel, N., Blekman, F., Bols, E. S., Chhibra, S. S., D'Hondt, J., De Clercq, J., Lontkovskyi, D., Lowette, S., Marchesini, I., Moortgat, S., Morton, A., Mueller, D., Python, Q., Tavernier, S., Van Doninck, W., Van Mulders, P., Beghin, D., Bilin, B., Clerbaux, B., De Lentdecker, G., Dorney, B., Favart, L., Grebenyuk, A., Kalsi, A. K., Makarenko, I., Moureaux, L., Petre, L., Popov, A., Postiau, N., Starling, E., Thomas, L., Vander Velde, C., Vanlaer, P., Vannerom, D., Wezenbeek, L., Cornelis, T., Dobur, D., Gruchala, M., Khvastunov, I., Mestdach, G., Niedziela, M., Roskas, C., Skovpen, K., Tytgat, M., Verbeke, W., Vermassen, B., Vit, M., Bethani, A., Bruno, G., Bury, F., Caputo, C., David, P., Delaere, C., Delcourt, M., Donertas, I. S., Giammanco, A., Lemaitre, V., Mondal, K., Prisciandaro, J., Taliercio, A., Teklishyn, M., Vischia, P., Wertz, S., Wuyckens, S., Alves, G. A., Hensel, C., Moraes, A., Alda Junior, W. L., Belchior Batista Das Chagas, E., Brandao Malbouisson, H., Carvalho, W.

مصطلحات موضوعية: CMS, Photon-proton, Collectivity, PROTON-LEAD COLLISIONS, PLUS AU COLLISIONS, ANGULAR-CORRELATIONS, FLOW, PARTICLES, SIGNATURE, PHYSICS, SIDE

الوصف: The first measurements of the Fourier coefficients (V-n Delta) of the azimuthal distributions of charged hadrons emitted from photon-proton (gamma p) interactions are presented. The data are extracted from 68.8nb(-1) of ultra-peripheral proton-lead (pPb) collisions at root s(NN)= 8.16 TeV using the CMS detector. The high energy lead ions produce a flux of photons that can interact with the oncoming proton. This gamma p system provides a set of unique initial conditions with multiplicity lower than in photon-lead collisions but comparable to recent electron-positron and electron-proton data. The V-n Delta coefficients are presented in ranges of event multiplicity and transverse momentum (p(T)) and are compared to corresponding hadronic minimum bias pPb results. For a given multiplicity range, the mean p(T) of charged particles is smaller in gamma p than in pPb collisions. For both the gamma p and pPb samples, V-1 Delta is negative, V-2 Delta is positive, and V-3 Delta consistent with 0. For each multiplicity and p(T) range, V-2 Delta is larger for gamma p events. The gamma p data are consistent with model predictions that have no collective effects. (c) 2023 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0Test/). Funded by SCOAP(3).

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:001060187600001; volume:844; journal:PHYSICS LETTERS. SECTION B; https://hdl.handle.net/11568/1223969Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85168004410; https://www.sciencedirect.com/science/article/pii/S0370269323002393Test

الإتاحة: https://doi.org/10.1016/j.physletb.2023.137905Test
https://hdl.handle.net/11568/1223969Test
https://www.sciencedirect.com/science/article/pii/S0370269323002393Test

المؤلفون: null, null, Tumasyan, A., Adam, W., Bergauer, T., Dragicevic, M., Escalante Del Valle, A., Frühwirth, R., Jeitler, M., Krammer, N., Lechner, L., Liko, D., Mikulec, I., Pitters, F. M., Schieck, J., Schöfbeck, R., Spanring, M., Templ, S., Waltenberger, W., Wulz, C. -E., Zarucki, M., Darwish, M. R., De Wolf, E. A., Janssen, T., Kello, T., Lelek, A., Pieters, M., Rejeb Sfar, H., Van Mechelen, P., Van Putte, S., Van Remortel, N., Blekman, F., Bols, E. S., D’Hondt, J., De Clercq, J., Lontkovskyi, D., Lowette, S., Marchesini, I., Moortgat, S., Morton, A., Müller, D., Sahasransu, A. R., Tavernier, S., Van Doninck, W., Van Mulders, P., Beghin, D., Bilin, B., Clerbaux, B., De Lentdecker, G., Dorney, B., Favart, L., Grebenyuk, A., Kalsi, A. K., Lee, K., Makarenko, I., Moureaux, L., Pétré, L., Popov, A., Postiau, N., Starling, E., Thomas, L., Vander Velde, C., Vanlaer, P., Vannerom, D., Wezenbeek, L., Cornelis, T., Dobur, D., Gruchala, M., Khvastunov, I., Mestdach, G., Niedziela, M., Roskas, C., Skovpen, K., Tytgat, M., Verbeke, W., Vermassen, B., Vit, M., Bethani, A., Bruno, G., Bury, F., Caputo, C., David, P., Delaere, C., Delcourt, M., Donertas, I. S., Giammanco, A., Lemaitre, V., Mondal, K., Prisciandaro, J., Taliercio, A., Teklishyn, M., Vischia, P., Wertz, S., Wuyckens, S., Alves, G. A., Hensel, C., Moraes, A., Aldá Júnior, W. L., Belchior Batista Das Chagas, E., BRANDAO MALBOUISSON, H., Carvalho, W., Chinellato, J., Coelho, E., Da Costa, E. M., Da Silveira, G. G., De Jesus Damiao, D., Fonseca De Souza, S., Martins, J., Matos Figueiredo, D., Mora Herrera, C., Mundim, L., Nogima, H., Rebello Teles, P., Sanchez Rosas, L. J., Santoro, A., Silva Do Amaral, S. M., Sznajder, A., Thiel, M., Torres Da Silva De Araujo, F., Vilela Pereira, A., Bernardes, C. A., Calligaris, L., Fernandez Perez Tomei, T. R., Gregores, E. M., Lemos, D. S., Mercadante, P. G., Novaes, S. F., Padula, Sandra S., Aleksandrov, A., Antchev, G., Atanassov, I., Hadjiiska, R., Iaydjiev, P., Misheva, M., Rodozov, M., Shopova, M., Sultanov, G., Dimitrov, A., Ivanov, T., Litov, L., Pavlov, B., Petkov, P., Petrov, A., Cheng, T., Fang, W., Guo, Q., Mittal, M., Wang, H., Yuan, L., Ahmad, M., Bauer, G., Hu, Z., Wang, Y., Yi, K., Chapon, E., Chen, G. M., Chen, H. S., Chen, M., Javaid, T., Kapoor, A., Leggat, D., Liao, H., Liu, Z. -A., Sharma, R., Spiezia, A., Tao, J., Thomas-Wilsker, J., Wang, J., Zhang, H., Zhang, S., Zhao, J., Agapitos, A., Ban, Y., Chen, C., Huang, Q., Levin, A., Li, Q., Lu, M., Lyu, X., Mao, Y., Qian, S. J., Wang, D., Wang, Q., Xiao, J., You, Z., Gao, X., Okawa, H., Xiao, M., Avila, C., Cabrera, A., Florez, C., Fraga, J., Sarkar, A., Segura Delgado, M. 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A., Cakir, A., Cankocak, K., Komurcu, Y., Sen, S., Aydogmus Sen, F., Cerci, S., Kaynak, B., Ozkorucuklu, S., Sunar Cerci, D., Grynyov, B., Levchuk, L., Bhal, E., Bologna, S., Brooke, J. J., Bundock, A., Clement, E., Cussans, D., Flacher, H., Goldstein, J., Heath, G. P., Heath, H. F., Kreczko, L., Krikler, B., Paramesvaran, S., Sakuma, T., Seif El Nasr-Storey, S., Smith, V. J., Stylianou, N., Taylor, J., Titterton, A., Bell, K. W., Belyaev, A., Brew, C., Brown, R. M., Cockerill, D. J. A., Ellis, K. V., Harder, K., Harper, S., Linacre, J., Manolopoulos, K., Newbold, D. M., Olaiya, E., Petyt, D., Reis, T., Schuh, T., Shepherd-Themistocleous, C. H., Thea, A., Tomalin, I. R., Williams, T., Bainbridge, R., Bloch, P., Bonomally, S., Borg, J., Breeze, S., Buchmuller, O., Cepaitis, V., Chahal, G. S., Colling, D., Dauncey, P., Davies, G., Della Negra, M., Fedi, G., Hall, G., Iles, G., Langford, J., Lyons, L., Magnan, A. -M., Malik, S., Martelli, A., Milosevic, V., Nash, J., Palladino, V., Pesaresi, M., Raymond, D. M., Richards, A., Rose, A., Scott, E., Seez, C., Shtipliyski, A., Tapper, A., Uchida, K., Virdee, T., Wardle, N., Webb, S. N., Winterbottom, D., Zecchinelli, A. G., Cole, J. E., Khan, A., Kyberd, P., Mackay, C. K., Reid, I. D., Teodorescu, L., Zahid, S., Abdullin, S., Brinkerhoff, A., Call, K., Caraway, B., Dittmann, J., Hatakeyama, K., Kanuganti, A. R., Madrid, C., McMaster, B., Pastika, N., Sawant, S., Smith, C., Wilson, J., Bartek, R., Dominguez, A., Uniyal, R., Vargas Hernandez, A. M., Buccilli, A., Charaf, O., Cooper, S. I., Di Croce, D., Gleyzer, S. V., Henderson, C., Perez, C. U., Rumerio, P., West, C., Akpinar, A., Albert, A., Arcaro, D., Cosby, C., Demiragli, Z., Gastler, D., Rohlf, J., Salyer, K., Sperka, D., Spitzbart, D., Suarez, I., Yuan, S., Zou, D., Benelli, G., Burkle, B., Coubez, X., Cutts, D., Duh, Y. t., Hadley, M., Heintz, U., Hogan, J. M., Kwok, K. H. M., Laird, E., Landsberg, G., Lau, K. T., Luo, J., Narain, M., Sagir, S., Usai, E., Wong, W. Y., Yan, X., Yu, D., Zhang, W., Band, R., Brainerd, C., Breedon, R., Calderon De La Barca Sanchez, M., Chertok, M., Conway, J., Conway, R., Cox, P. T., Erbacher, R., Flores, C., Jensen, F., Kukral, O., Lander, R., Mulhearn, M., Pellett, D., Shi, M., Taylor, D., Tripathi, M., Yao, Y., Zhang, F., Bachtis, M., Cousins, R., Dasgupta, A., Datta, A., Hamilton, D., Hauser, J., Ignatenko, M., Iqbal, M. A., Lam, T., Mccoll, N., Nash, W. A., Regnard, S., Saltzberg, D., Schnaible, C., Stone, B., Valuev, V., Burt, K., Chen, Y., Clare, R., Gary, J. W., Hanson, G., Karapostoli, G., Long, O. R., Manganelli, N., Olmedo Negrete, M., Si, W., Wimpenny, S., Zhang, Y., Branson, J. G., Cittolin, S., Cooperstein, S., Deelen, N., Duarte, J., Gerosa, R., Giannini, L., Gilbert, D., Krutelyov, V., Letts, J., Masciovecchio, M., May, S., Padhi, S., Pieri, M., Sharma, V., Tadel, M., Vartak, A., Würthwein, F., Yagil, A., Amin, N., Campagnari, C., Citron, M., Dorsett, A., Dutta, V., Incandela, J., Kilpatrick, M., Marsh, B., Mei, H., Ovcharova, A., Qu, H., Quinnan, M., Richman, J., Sarica, U., Stuart, D., Wang, S., Bornheim, A., Cerri, O., Dutta, I., Lawhorn, J. M., Lu, N., Mao, J., Newman, H. B., Ngadiuba, J., Nguyen, T. Q., Spiropulu, M., Vlimant, J. R., Wang, C., Xie, S., Zhang, Z., Zhu, R. Y., Alison, J., Andrews, M. B., Ferguson, T., Mudholkar, T., Paulini, M., Vorobiev, I., Cumalat, J. P., Ford, W. T., MacDonald, E., Patel, R., Perloff, A., Stenson, K., Ulmer, K. A., Wagner, S. R., Alexander, J., Cheng, Y., Chu, J., Cranshaw, D. J., Mcdermott, K., Monroy, J., Patterson, J. R., Quach, D., Ryd, A., Sun, W., Tan, S. M., Tao, Z., Thom, J., Wittich, P., Zientek, M., Albrow, M., Alyari, M., Apollinari, G., Apresyan, A., Apyan, A., Bauerdick, L. A. T., Beretvas, A., Berry, D., Berryhill, J., Bhat, P. C., Burkett, K., Butler, J. N., Canepa, A., Cerati, G. B., Cheung, H. W. K., Chlebana, F., Cremonesi, M., Di Petrillo, K. F., Elvira, V. D., Freeman, J., Gecse, Z., Gray, L., Green, D., Grünendahl, S., Gutsche, O., Harris, R. M., Heller, R., Herwig, T. C., Hirschauer, J., Jayatilaka, B., Jindariani, S., Johnson, M., Joshi, U., Klabbers, P., Klijnsma, T., Klima, B., Kortelainen, M. J., Lammel, S., Lincoln, D., Lipton, R., Liu, T., Lykken, J., Maeshima, K., Mason, D., McBride, P., Merkel, P., Mrenna, S., Nahn, S., O’Dell, V., Papadimitriou, V., Pedro, K., Pena, C., Prokofyev, O., Ravera, F., Reinsvold Hall, A., Ristori, L., Schneider, B., Sexton-Kennedy, E., Smith, N., Soha, A., Spiegel, L., Strait, J., Taylor, L., Tkaczyk, S., Tran, N. V., Uplegger, L., Vaandering, E. W., Weber, H. A., Acosta, D., Avery, P., Bourilkov, D., Cadamuro, L., Cherepanov, V., Errico, F., Field, R. D., Guerrero, D., Joshi, B. M., Kim, M., Konigsberg, J., Korytov, A., Lo, K. H., Matchev, K., Menendez, N., Mitselmakher, G., Rosenzweig, D., Shi, K., Sturdy, J., Zuo, X., Adams, T., Askew, A., Diaz, D., Habibullah, R., Hagopian, S., Hagopian, V., Johnson, K. F., Khurana, R., Kolberg, T., Martinez, G., Prosper, H., Schiber, C., Yohay, R., Zhang, J., Baarmand, M. M., Butalla, S., Elkafrawy, T., Hohlmann, M., Kumar Verma, R., Noonan, D., Rahmani, M., Saunders, M., Yumiceva, F., Adams, M. R., Apanasevich, L., Becerril Gonzalez, H., Cavanaugh, R., Chen, X., Dittmer, S., Evdokimov, O., Gerber, C. E., Hangal, D. A., Hofman, D. J., Mills, C., Oh, G., Roy, T., Tonjes, M. B., Varelas, N., Viinikainen, J., Wang, X., Wu, Z., Ye, Z., Alhusseini, M., Dilsiz, K., Durgut, S., Gandrajula, R. P., Haytmyradov, M., Khristenko, V., Köseyan, O. K., Merlo, J. -P., Mestvirishvili, A., Moeller, A., Nachtman, J., Ogul, H., Onel, Y., Ozok, F., Penzo, A., Snyder, C., Tiras, E., Wetzel, J., Amram, O., Blumenfeld, B., Corcodilos, L., Eminizer, M., Gritsan, A. V., Kyriacou, S., Maksimovic, P., Mantilla, C., Roskes, J., Swartz, M., Vámi, T. Á., Baldenegro Barrera, C., Baringer, P., Bean, A., Bylinkin, A., Isidori, T., Khalil, S., King, J., Krintiras, G., Kropivnitskaya, A., Lindsey, C., Minafra, N., Murray, M., Rogan, C., Royon, C., Sanders, S., Schmitz, E., Tapia Takaki, J. D., Williams, J., Wilson, G., Duric, S., Ivanov, A., Kaadze, K., Kim, D., Maravin, Y., Mitchell, T., Modak, A., Rebassoo, F., Wright, D., Adams, E., Baden, A., Baron, O., Belloni, A., Eno, S. C., Feng, Y., Hadley, N. J., Jabeen, S., Kellogg, R. G., Koeth, T., Mignerey, A. C., Nabili, S., Seidel, M., Skuja, A., Tonwar, S. C., Wang, L., Wong, K., Abercrombie, D., Bi, R., Brandt, S., Busza, W., Cali, I. A., D’Alfonso, M., Gomez-Ceballos, G., Goncharov, M., Harris, P., Hu, M., Klute, M., Kovalskyi, D., Krupa, J., Lee, Y. -J., Luckey, P. D., Maier, B., Marini, A. C., Mironov, C., Niu, X., Paus, C., Rankin, D., Roland, C., Roland, G., Shi, Z., Stephans, G. S. F., Tatar, K., Velicanu, D., Wang, T. W., Wang, Z., Wyslouch, B., Chatterjee, R. M., Evans, A., Hansen, P., Hiltbrand, J., Jain, Sh., Krohn, M., Kubota, Y., Lesko, Z., Mans, J., Revering, M., Rusack, R., Saradhy, R., Schroeder, N., Strobbe, N., Wadud, M. A., Acosta, J. G., Oliveros, S., Bloom, K., Bryson, M., Claes, D. R., Fangmeier, C., Finco, L., Golf, F., González Fernández, J. R., Joo, C., Kravchenko, I., Siado, J. E., Snow, G. R., Tabb, W., Yan, F., Agarwal, G., Bandyopadhyay, H., Hay, L., Iashvili, I., Kharchilava, A., McLean, C., Nguyen, D., Pekkanen, J., Rappoccio, S., Alverson, G., Barberis, E., Freer, C., Haddad, Y., Hortiangtham, A., Li, J., Madigan, G., Marzocchi, B., Morse, D. M., Nguyen, V., Orimoto, T., Parker, A., Skinnari, L., Tishelman-Charny, A., Wamorkar, T., Wang, B., Wisecarver, A., Wood, D., Bueghly, J., Chen, Z., Gilbert, A., Gunter, T., Hahn, K. A., Odell, N., Schmitt, M. H., Sung, K., Velasco, M., Bucci, R., Dev, N., Goldouzian, R., Hildreth, M., Hurtado Anampa, K., Jessop, C., Lannon, K., Loukas, N., Marinelli, N., Mcalister, I., Meng, F., Mohrman, K., Musienko, Y., Ruchti, R., Siddireddy, P., Wayne, M., Wightman, A., Wolf, M., Zygala, L., Alimena, J., Bylsma, B., Cardwell, B., Durkin, L. S., Francis, B., Hill, C., Lefeld, A., Winer, B. L., Yates, B. R., Addesa, F. M., Bonham, B., Das, P., Dezoort, G., Elmer, P., Frankenthal, A., Greenberg, B., Haubrich, N., Higginbotham, S., Kalogeropoulos, A., Kopp, G., Kwan, S., Lange, D., Lucchini, M. T., Marlow, D., Mei, K., Ojalvo, I., Olsen, J., Palmer, C., Piroué, P., Stickland, D., Tully, C., Norberg, S., Bakshi, A. S., Barnes, V. E., Chawla, R., Das, S., Gutay, L., Jones, M., Jung, A. W., Karmarkar, S., Liu, M., Negro, G., Neumeister, N., Peng, C. C., Piperov, S., Purohit, A., Schulte, J. F., Stojanovic, M., Wang, F., Wildridge, A., Xiao, R., Xie, W., Dolen, J., Parashar, N., Baty, A., Dildick, S., Ecklund, K. M., Freed, S., Geurts, F. J. M., Li, W., Padley, B. P., Redjimi, R., Roberts, J., Shi, W., Stahl Leiton, A. G., Bodek, A., de Barbaro, P., Demina, R., Dulemba, J. L., Fallon, C., Ferbel, T., Galanti, M., Garcia-Bellido, A., Hindrichs, O., Khukhunaishvili, A., Ranken, E., Taus, R., Chiarito, B., Chou, J. P., Gandrakota, A., Gershtein, Y., Halkiadakis, E., Hart, A., Heindl, M., Hughes, E., Kaplan, S., Karacheban, O., Laflotte, I., Lath, A., Montalvo, R., Nash, K., Osherson, M., Salur, S., Schnetzer, S., Somalwar, S., Stone, R., Thayil, S. A., Thomas, S., Acharya, H., Delannoy, A. G., Spanier, S., Bouhali, O., Dalchenko, M., Delgado, A., Eusebi, R., Gilmore, J., Huang, T., Kamon, T., Luo, S., Malhotra, S., Mueller, R., Overton, D., Rathjens, D., Safonov, A., Akchurin, N., Damgov, J., Hegde, V., Kunori, S., Lamichhane, K., Mengke, T., Muthumuni, S., Peltola, T., Undleeb, S., Volobouev, I., Whitbeck, A., Appelt, E., Greene, S., Gurrola, A., Johns, W., Maguire, C., Melo, A., Ni, H., Padeken, K., Romeo, F., Sheldon, P., Tuo, S., Velkovska, J., Arenton, M. W., Cox, B., Cummings, G., Hakala, J., Hirosky, R., Joyce, M., Ledovskoy, A., Li, A., Neu, C., Tannenwald, B., Wolfe, E., Karchin, P. E., Poudyal, N., Thapa, P., Black, K., Bose, T., Buchanan, J., Caillol, C., Dasu, S., De Bruyn, I., Everaerts, P., Galloni, C., He, H., Herndon, M., Hervé, A., Hussain, U., Lanaro, A., Loeliger, A., Loveless, R., Madhusudanan Sreekala, J., Mallampalli, A., Mohammadi, A., Pinna, D., Savin, A., Shang, V., Smith, W. H., Teague, D., Trembath-Reichert, S., Vetens, W., Afanasiev, S., Andreev, V., Andreev, Yu., Aushev, T., Azarkin, M., Babaev, A., Blinov, V., Boos, E., Borchsh, V., Budkouski, D., Bunichev, V., Bunin, P., Bychkova, O., Chadeeva, M., Chekhovsky, V., Dermenev, A., Dimova, T., Dremin, I., Dubinin, M., Dudko, L., Epshteyn, V., Ershov, A., Gavrilenko, M., Gavrilov, G., Gavrilov, V., Gninenko, S., Golovtcov, V., Golubev, N., Golutvin, I., Gorbunov, I., Iuzhakov, A., Ivanchenko, V., Ivanov, Y., Kachanov, V., Kalinin, A., Kamenev, A., Kardapoltsev, L., Karjavine, V., Karneyeu, A., Kim, V., Kirakosyan, M., Kirsanov, M., Klyukhin, V., Konstantinov, D., Korneeva, N., Krasnikov, N., Kuznetsova, E., Lanev, A., Litomin, A., Lychkovskaya, N., Makarenko, V., Malakhov, A., Matveev, V., Murzin, V., Nikitenko, A., Obraztsov, S., Okhotnikov, V., Oreshkin, V., Ovtin, I., Palichik, V., Pashenkov, A., Perelygin, V., Perfilov, M., Philippov, D., Pivovarov, G., Popov, V., Popova, E., Rusinov, V., Safronov, G., Savina, M., Savrin, V., Seitova, D., Shalaev, V., Shmatov, S., Shulha, S., Skovpen, Y., Smirnov, I., Smirnov, V., Sosnov, D., Spiridonov, A., Stepennov, A., Sukhikh, L., Sulimov, V., Tcherniaev, E., Terkulov, A., Teryaev, O., Tlisov, D., Toms, M., Toropin, A., Uvarov, L., Uzunian, A., Vlasov, E., Volkov, P., Volkov, S., Vorobyev, A., Voytishin, N., Zarubin, A., Zhizhin, I., Zhokin, A.

المساهمون: Null, Null, Tumasyan, A., Adam, W., Bergauer, T., Dragicevic, M., Escalante Del Valle, A., Frühwirth, R., Jeitler, M., Krammer, N., Lechner, L., Liko, D., Mikulec, I., Pitters, F. M., Schieck, J., Schöfbeck, R., Spanring, M., Templ, S., Waltenberger, W., Wulz, C. -E., Zarucki, M., Darwish, M. R., De Wolf, E. A., Janssen, T., Kello, T., Lelek, A., Pieters, M., Rejeb Sfar, H., Van Mechelen, P., Van Putte, S., Van Remortel, N., Blekman, F., Bols, E. S., D’Hondt, J., De Clercq, J., Lontkovskyi, D., Lowette, S., Marchesini, I., Moortgat, S., Morton, A., Müller, D., Sahasransu, A. R., Tavernier, S., Van Doninck, W., Van Mulders, P., Beghin, D., Bilin, B., Clerbaux, B., De Lentdecker, G., Dorney, B., Favart, L., Grebenyuk, A., Kalsi, A. K., Lee, K., Makarenko, I., Moureaux, L., Pétré, L., Popov, A., Postiau, N., Starling, E., Thomas, L., Vander Velde, C., Vanlaer, P., Vannerom, D., Wezenbeek, L., Cornelis, T., Dobur, D., Gruchala, M., Khvastunov, I., Mestdach, G., Niedziela, M., Roskas, C., Skovpen, K., Tytgat, M., Verbeke, W., Vermassen, B., Vit, M., Bethani, A., Bruno, G., Bury, F., Caputo, C., David, P., Delaere, C., Delcourt, M., Donertas, I. S., Giammanco, A., Lemaitre, V., Mondal, K., Prisciandaro, J., Taliercio, A., Teklishyn, M., Vischia, P., Wertz, S., Wuyckens, S., Alves, G. A., Hensel, C., Moraes, A., Aldá Júnior, W. L., Belchior Batista Das Chagas, E., BRANDAO MALBOUISSON, H., Carvalho, W.

مصطلحات موضوعية: CP Violation, Hadron-Hadron Scattering, Top Physics

الوصف: Results are presented from a search for CP violation in top quark pair production, using proton-proton collisions at a center-of-mass energy of 13TeV. The data used for this analysis consist of final states with two charged leptons collected by the CMS experiment, and correspond to an integrated luminosity of 35.9 fb(-1). The search uses two observables, O-1 and O-3, which are Lorentz scalars. The observable O-1 is constructed from the four-momenta of the charged leptons and the reconstructed top quarks, while O-3 consists of the four-momenta of the charged leptons and the b quarks originating from the top quarks. Asymmetries in these observables are sensitive to CP violation, and their measurement is used to determine the chromoelectric dipole moment of the top quark. The results are consistent with the expectation from the standard model.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:001062403500001; volume:2023; issue:7; numberofpages:45; journal:JOURNAL OF HIGH ENERGY PHYSICS; https://hdl.handle.net/11568/1223991Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85166271575; https://link.springer.com/article/10.1007/JHEP07Test(2023)023

الإتاحة: https://doi.org/10.1007/jhep07Test(2023)023
https://hdl.handle.net/11568/1223991Test

المؤلفون: Tumasyan, A., Adam, W., Andrejkovic, J. W., Bergauer, T., Chatterjee, S., Dragicevic, M., Del Valle, A. Escalante, Fruehwirth, R., Jeitler, M., Krammer, N., Lechner, L., Liko, D., Mikulec, I., Paulitsch, P., Pitters, F. M., Schieck, J., Schoefbeck, R., Schwarz, D., Templ, S., Waltenberger, W., Wulz, C. -E., Darwish, M. R., De Wolf, E. A., Janssen, T., Kello, T., Lelek, A., Sfar, H. Rejeb, Van Mechelen, P., Van Putte, S., Van Remortel, N., Blekman, F., Bols, E. S., D'Hondt, J., Delcourt, M., El Faham, H., Lowette, S., Moortgat, S., Morton, A., Mueller, D., Sahasransu, A. R., Tavernier, S., Van Doninck, W., Van Mulders, P., Beghin, D., Bilin, B., Clerbaux, B., De Lentdecker, G., Favart, L., Grebenyuk, A., Kalsi, A. K., Lee, K., Mahdavikhorrami, M., Makarenko, I., Moureaux, L., Petre, L., Popov, A., Postiau, N., Starling, E., Thomas, L., Vanden Bemden, M., Vander Velde, C., Vanlaer, P., Cornelis, T., Dobur, D., Knolle, J., Lambrecht, L., Mestdach, G., Niedziela, M., Roskas, C., Samalan, A., Skovpen, K., Tytgat, M., Vermassen, B., Vit, M., Wezenbeek, L., Benecke, A., Bethani, A., Bruno, G., Bury, F., Caputo, C., David, P., Delaere, C., Donertas, I. S., Giammanco, A., Jaffel, K., Jain, Sa., Lemaitre, V., Mondal, K., Prisciandaro, J., Taliercio, A., Teklishyn, M., Tran, T. T., Vischia, P., Wertz, S., Alves, G. A., Hensel, C., Moraes, A., Alda Junior, W. L., Alves Gallo Pereira, M., Barroso Ferreira Filho, M., Brandao Malbouisson, H., Carvalho, W., Chinellato, J., Da Costa, E. M., Da Silveira, G. G., De Jesus Damiao, D., Fonseca De Souza, S., Mora Herrera, C., Mota Amarilo, K., Mundim, L., Nogima, H., Rebello Teles, P., Santoro, A., Silva Do Amaral, S. M., Sznajder, A., Thiel, M., Torres Da Silva De Araujo, F., Vilela Pereira, A., Bernardes, C. A., Calligaris, L., Fernandez Perez Tomei, T. R., Gregores, E. M., Lemos, D. S., Mercadante, P. G., Novaes, S. F., Padula, Sandra S., Aleksandrov, A., Antchev, G., Hadjiiska, R., Iaydjiev, P., Misheva, M., Rodozov, M., Shopova, M., Sultanov, G., Dimitrov, A., Ivanov, T., Litov, L., Pavlov, B., Petkov, P., Petrov, A., Cheng, T., Javaid, T., Mittal, M., Yuan, L., Ahmad, M., Bauer, G., Dozen, C., Hu, Z., Martins, J., Wang, Y., Yi, K., Chapon, E., Chen, G. M., Chen, H. S., Chen, M., Iemmi, F., Kapoor, A., Leggat, D., Liao, H., Liu, Z. -A., Milosevic, V., Monti, F., Sharma, R., Tao, J., Thomas-Wilsker, J., Wang, J., Zhang, H., Zhao, J., Agapitos, A., An, Y., Ban, Y., Chen, C., Levin, A., Li, Q., Lyu, X., Mao, Y., Qian, S. J., Wang, D., Wang, Q., Xiao, J., Lu, M., You, Z., Gao, X., Okawa, H., Zhang, Y., Lin, Z., Xiao, M., Avila, C., Cabrera, A., Florez, C., Fraga, J., Mejia Guisao, J., Ramirez, F., Ruiz Alvarez, J. D., Salazar Gonzalez, C. A., Giljanovic, D., Godinovic, N., Lelas, D., Puljak, I., Antunovic, Z., Kovac, M., Sculac, T., Brigljevic, V., Ferencek, D., Majumder, D., Roguljic, M., Starodumov, A., Susa, T., Attikis, A., Christoforou, K., Erodotou, E., Ioannou, A., Kole, G., Kolosova, M., Konstantinou, S., Mousa, J., Nicolaou, C., Ptochos, F., Razis, P. A., Rykaczewski, H., Saka, H., Finger, M., Finger M., Jr., Kveton, A., Ayala, E., Carrera Jarrin, E., Abu Zeid, S., Assran, Y., Mahmoud, M. A., Mohammed, Y., Bhowmik, S., Dewanjee, R. K., Ehataht, K., Kadastik, M., Nandan, S., Nielsen, C., Pata, J., Raidal, M., Tani, L., Veelken, C., Eerola, P., Forthomme, L., Kirschenmann, H., Osterberg, K., Voutilainen, M., Bharthuar, S., Brucken, E., Garcia, F., Havukainen, J., Kim, M. S., Kinnunen, R., Lampen, T., Lassila-Perini, K., Lehti, S., Linden, T., Lotti, M., Martikainen, L., Myllymaki, M., Ott, J., Siikonen, H., Tuominen, E., Tuominiemi, J., Luukka, P., Petrow, H., Tuuva, T., Amendola, C., Besancon, M., Couderc, F., Dejardin, M., Denegri, D., Faure, J. L., Ferri, F., Ganjour, S., Givernaud, A., Gras, P., Hamel de Monchenault, G., Jarry, P., Lenzi, B., Locci, E., Malcles, J., Rander, J., Rosowsky, A., Sahin, M. O., Savoy-Navarro, A., Titov, M., Yu, G. B., Ahuja, S., Beaudette, F., Bonanomi, M., Buchot Perraguin, A., Busson, P., Cappati, A., Charlot, C., Davignon, O., Diab, B., Falmagne, G., Ghosh, S., Granier de Cassagnac, R., Hakimi, A., Kucher, I., Motta, J., Nguyen, M., Ochando, C., Paganini, P., Rembser, J., Salerno, R., Sarkar, U., Sauvan, J. B., Sirois, Y., Tarabini, A., Zabi, A., Zghiche, A., Agram, J. -L., Andrea, J., Apparu, D., Bloch, D., Bourgatte, G., Brom, J. -M., Chabert, E. 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