دورية أكاديمية

Pyrexia in patients treated with dabrafenib plus trametinib across clinical trials in BRAF-mutant cancers

التفاصيل البيبلوغرافية
العنوان: Pyrexia in patients treated with dabrafenib plus trametinib across clinical trials in BRAF-mutant cancers
المؤلفون: Schadendorf, Dirk, Robert, Caroline, Dummer, Reinhard, Flaherty, Keith T, Tawbi, Hussein A, Menzies, Alexander M, Banerjee, Hiya, Lau, Mike, Long, Georgina V
المصدر: Schadendorf, Dirk; Robert, Caroline; Dummer, Reinhard; Flaherty, Keith T; Tawbi, Hussein A; Menzies, Alexander M; Banerjee, Hiya; Lau, Mike; Long, Georgina V (2021). Pyrexia in patients treated with dabrafenib plus trametinib across clinical trials in BRAF-mutant cancers. European Journal of Cancer, 153:234-241.
بيانات النشر: Elsevier
سنة النشر: 2021
المجموعة: University of Zurich (UZH): ZORA (Zurich Open Repository and Archive
مصطلحات موضوعية: Dermatology Clinic, 610 Medicine & health, Cancer Research, Oncology
الوصف: Background: Dabrafenib plus trametinib has demonstrated clinical benefit across multiple BRAF-mutant tumours, leading to approval for resected stage III and metastatic melanoma, non-small-cell lung cancer (NSCLC) and anaplastic thyroid cancer. Pyrexia is a common adverse event in patients treated with dabrafenib plus trametinib. Here, we characterise the incidence, patterns and management of pyrexia in patients receiving dabrafenib plus trametinib in clinical trials. Methods: Patients (N = 1076) included in the analysis received dabrafenib plus trametinib in the following clinical trials: phase II registration trial in advanced NSCLC (N = 82), phase III COMBI-AD study in resectable stage III melanoma (N = 435) and phase III COMBI-d and COMBI-v studies in unresectable or metastatic melanoma (N = 209 and N = 350, respectively). Results: Among the 1076 patients enrolled in the clinical trials, 61.3% developed pyrexia, 5.7% developed grade 3/4 pyrexia and 15.6% developed a protocol-defined serious pyrexia event. Among the 660 patients with pyrexia, 33.0% had 1 occurrence, 19.8% had 2 occurrences and 47.1% had ≥3 occurrences. The incidence of pyrexia was highest early in treatment and decreased with time on treatment. Temporary dose interruption of dabrafenib or trametinib was the most common and effective management strategy. Conclusions: Pyrexia is the most common adverse event associated with dabrafenib plus trametinib but is manageable with dose interruption. Trial registration: ClinicalTrials.gov (Phase II NSCLC, NCT01336634; COMBI-AD, NCT01682083; COMBI-d, NCT01584648; COMBI-v, NCT01597908). Keywords: Adverse event; BRAF V600–mutant melanoma; BRAF inhibitor; MEK inhibitor; Pyrexia.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 0959-8049
العلاقة: https://www.zora.uzh.ch/id/eprint/206022/1/903_Schadendorf_D._et_al._Pyrexia_in_patients_treated_with_dabrafenib_plus_trametinib_across_clinical_trials_in_BRAF-mutant_cancers_EJC_2021.pdfTest; info:pmid/34225229; urn:issn:0959-8049
DOI: 10.5167/uzh-206022
DOI: 10.1016/j.ejca.2021.05.005
الإتاحة: https://doi.org/10.5167/uzh-20602210.1016/j.ejca.2021.05.005Test
https://www.zora.uzh.ch/id/eprint/206022Test/
https://www.zora.uzh.ch/id/eprint/206022/1/903_Schadendorf_D._et_al._Pyrexia_in_patients_treated_with_dabrafenib_plus_trametinib_across_clinical_trials_in_BRAF-mutant_cancers_EJC_2021.pdfTest
حقوق: info:eu-repo/semantics/openAccess ; Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) ; http://creativecommons.org/licenses/by-nc-nd/4.0Test/
رقم الانضمام: edsbas.851E9AC8
قاعدة البيانات: BASE
الوصف
تدمد:09598049
DOI:10.5167/uzh-206022