دورية أكاديمية

Atypical (non-V600E) BRAF mutations in metastatic colorectal cancer in population and real-world cohorts

التفاصيل البيبلوغرافية
العنوان: Atypical (non-V600E) BRAF mutations in metastatic colorectal cancer in population and real-world cohorts
المؤلفون: Osterlund, Emerik, Ristimäki, Ari, Mäkinen, Markus J., Kytölä, Soili, Kononen, Juha, Pfeiffer, Per, Soveri, Leena‐Maija, Keinänen, Mauri, Sorbye, Halfdan, Nunes, Luís, Salminen, Tapio, Nieminen, Lasse, Uutela, Aki, Halonen, Päivi, Ålgars, Annika, Sundström, Jari, Kallio, Raija, Ristamäki, Raija, Lamminmäki, Annamarja, Stedt, Hanna, Heervä, Eetu, Kuopio, Teijo, Sjöblom, Tobias, Isoniemi, Helena, Glimelius, Bengt, Osterlund, Pia
بيانات النشر: John Wiley & Sons
سنة النشر: 2024
المجموعة: JYX - Jyväskylä University Digital Archive / Jyväskylän yliopiston julkaisuarkisto
مصطلحات موضوعية: aBRAF, BRAFmutation, colorectal cancer, metastatic, non-V600E, paksusuolisyöpä, etäpesäkkeet, kohorttitutkimus, syöpägeenit, biomarkkerit, mutaatiot, väestötutkimus
الوصف: BRAF-V600E mutation (mt) is a strong negative prognostic and predictive biomarker in metastatic colorectal cancer (mCRC). Non-V600Emt, designated atypical BRAFmt (aBRAFmt) are rare, and little is known about their frequency, co-mutations and prognostic and predictive role. These were compared between mutational groups of mCRC patients collected from three Nordic population-based or real-world cohorts. Pathology of aBRAFmt was studied. The study included 1449 mCRC patients with 51 (3%) aBRAFmt, 182 (13%) BRAF-V600Emt, 456 (31%) RAS&BRAF wild-type (wt) and 760 (52%) RASmt tumours. aBRAFmt were seen in 2% of real-world and 4% of population-based cohorts. Twenty-six different aBRAFmt were detected, 11 (22%) class 2 (serrated adenocarcinoma in 2/9 tested), 32 (64%) class 3 (serrated in 15/25) and 4 (8%) unclassified. aBRAFmt patients were predominantly male, had more rectal primaries, less peritoneal metastases, deficient mismatch repair in one (2%), and better survival after metastasectomy (89% 5-year overall survival [OS]-rate) compared with BRAF-V600Emt. aBRAFmt and BRAF-V600Emt had poorer performance status and received fewer treatment lines than RAS&BRAFwt and RASmt. OS among aBRAFmt (median 14.4 months) was longer than for BRAF-V600Emt (11.2 months), but shorter than for RAS&BRAFwt (30.5 months) and RASmt (23.4 months). Addition of bevacizumab trended for better OS for the aBRAFmt. Nine patients with aBRAFmt received cetuximab/panitumumab without response. aBRAFmt represents a distinct subgroup differing from other RAS/BRAF groups, with serrated adenocarcinoma in only half. OS for patients with aBRAFmt tumours was slightly better than for BRAF-V600Emt, but worse than for RASmt and RAS&BRAFwt. aBRAFmt should not be a contraindication for metastasectomy. ; peerReviewed
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf; 488-503; fulltext
اللغة: English
تدمد: 0020-7136
العلاقة: International Journal of Cancer; 154; Osterlund, E., Ristimäki, A., Mäkinen, M. J., Kytölä, S., Kononen, J., Pfeiffer, P., Soveri, L., Keinänen, M., Sorbye, H., Nunes, L., Salminen, T., Nieminen, L., Uutela, A., Halonen, P., Ålgars, A., Sundström, J., Kallio, R., Ristamäki, R., Lamminmäki, A., . . . Osterlund, P. (2024). Atypical (non-V600E) BRAF mutations in metastatic colorectal cancer in population and real-world cohorts. International Journal of Cancer , 154 (3), 488-503. https://doi.org/10.1002/ijc.34733Test; CONVID_184976535; URN:NBN:fi:jyu-202309215229; http://urn.fi/URN:NBN:fi:jyu-202309215229Test
الإتاحة: https://doi.org/10.1002/ijc.34733Test
http://urn.fi/URN:NBN:fi:jyu-202309215229Test
حقوق: CC BY-NC 4.0 ; © 2023 the Authors ; openAccess ; https://creativecommons.org/licenses/by-nc/4.0Test/
رقم الانضمام: edsbas.2C66C82C
قاعدة البيانات: BASE