Inflammatory side effects of BRAF and MEK inhibitors

被引:17
|
作者
Mackin, Anna G. [1 ]
Pecen, Paula E. [1 ]
Dinsmore, Amanda L. [3 ]
Patnaik, Jennifer L. [1 ]
Gonzalez, Rene [2 ]
Robinson, William A. [2 ]
Palestine, Alan G. [1 ]
机构
[1] Univ Colorado, Sch Med, Dept Ophthalmol, Aurora, CO USA
[2] Univ Colorado, Sch Med, Cutaneous Oncol Clin, Dept Med,Div Med Oncol, Aurora, CO USA
[3] Birmingham VA Med Ctr, Dept Ophthalmol, Birmingham, AL USA
关键词
BRAF inhibitor; inflammation; malignant melanoma; MEK inhibitor; safety; METASTATIC MELANOMA; IMPROVED SURVIVAL; OPEN-LABEL; DABRAFENIB; MUTATIONS; VEMURAFENIB; MULTICENTER; COMBINATION; TRAMETINIB; MANAGEMENT;
D O I
10.1097/CMR.0000000000000599
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to describe inflammatory side effects in patients treated with BRAF and MEK inhibitors at a single tertiary care institution. This was a retrospective chart review of patients prescribed single-agent or combination BRAF and MEK inhibitors from January 2010 until May 2015. The primary outcome was the presence of inflammatory side effects. Among 124 patients, 56.4% were male, the median age was 59 years, and most (91.1%) were treated for metastatic melanoma. Most patients (74.2%) developed inflammatory side effects, some with multiple occurrences, for a total of 211 occurrences. The overall prevalence of inflammatory side effects did not differ across therapies. In a subanalysis, patients treated with both single-agent and combination therapies were more likely to experience an inflammatory side effect on single-agent therapy (P = 0.0126 for BRAF inhibitor, P = 0.0833 for MEK inhibitor). The most common inflammatory side effects for the entire cohort included arthralgias/myalgias (32.9%), nonacneiform rash (28.0%), pyrexia (25.5%), and erythema nodosum (11.2%), although side effects differed across the class of therapy. Corticosteroids were initiated in 73 side effect instances among 47 patients. Drug interruption or dose reduction was reported in 78 side effect instances in 50 patients. Fifteen side effect instances led to treatment termination. There is a high prevalence of inflammatory side effects encompassing all organ systems in patients treated with BRAF and MEK inhibitors. There is no significant difference in the prevalence of inflammatory side effects in patients treated with single-agent versus combination therapies, however, side effect profile differs across agents.
引用
收藏
页码:522 / 526
页数:5
相关论文
共 50 条
  • [21] Initial experience with combined BRAF and MEK inhibition with stereotactic radiosurgery for BRAF mutant melanoma brain metastases
    Patel, Bindiya G.
    Ahmed, Kamran A.
    Johnstone, Peter A. S.
    Yu, Hsiang-Hsuan Michael
    Etame, Arnold B.
    MELANOMA RESEARCH, 2016, 26 (04) : 382 - 386
  • [22] Cardiotoxicity mechanisms of the combination of BRAF-inhibitors and MEK-inhibitors
    Bronte, Enrico
    Bronte, Giuseppe
    Novo, Giuseppina
    Rinaldi, Gaetana
    Bronte, Fabrizio
    Passiglia, Francesco
    Russo, Antonio
    PHARMACOLOGY & THERAPEUTICS, 2018, 192 : 65 - 73
  • [23] Severe gastrointestinal toxicity of MEK inhibitors
    Mourad, Nadim
    Lourenco, Nelson
    Delyon, Julie
    Eftekhari, Pirayeh
    Bertheau, Philippe
    Allayous, Clara
    Ballon, Alice
    Pages, Cecile
    Allez, Matthieu
    Lebbe, Celeste
    Baroudjian, Barouyr
    MELANOMA RESEARCH, 2019, 29 (05) : 556 - 559
  • [24] Efficacy and Safety of BRAF Inhibitors With or Without MEK Inhibitors in BRAF-Mutant Advanced Non-Small-Cell Lung Cancer: Findings From a Real-Life Cohort
    Dudnik, Elizabeth
    Bar, Jair
    Peled, Nir
    Bshara, Llias
    Kuznetsov, Teodor
    Cohen, Aharon Yonathan
    Shochat, Tzippy
    Nechushtan, Hovav
    Onn, Amir
    Agbarya, Abed
    Moskovitz, Mor
    Keren, Shoshana
    Popovits-Hadar, Noa
    Urban, Damien
    Mishaeli, Moshe
    Rabinovich, Natalie Maimon
    Brenner, Ronen
    Zer, Mona
    Rotem, Ofer
    Roisman, Laila C.
    Wollner, Mira
    CLINICAL LUNG CANCER, 2019, 20 (04) : 278 - +
  • [25] Antitumor effects of immunotherapy combined with BRAF and MEK inhibitors in BRAF V600E metastatic colorectal cancer
    Tak, Eunyoung
    An, Hye-In
    Lee, Amy Sinyoung
    Han, Kyuyoung
    Choi, Jiwan
    Kim, Hyung-don
    Hong, Yong Sang
    Kim, Sun Young
    Choi, Eun Kyung
    Kim, Jeong Eun
    Kim, Tae Won
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 2025, 74 (05)
  • [26] Clinical and radiological response of BRAF inhibition and MEK inhibition in patients with brain metastases from BRAF-mutated melanoma
    Foppen, Marnix H. Geukes
    Boogerd, Willem
    Blank, Christian U.
    van Thienen, Johannes V.
    Haanen, John B.
    Brandsma, Dieta
    MELANOMA RESEARCH, 2018, 28 (02) : 126 - 133
  • [27] The Nature and Management of Metastatic Melanoma After Progression on BRAF Inhibitors: Effects of Extended BRAF Inhibition
    Chan, Matthew M. K.
    Haydu, Lauren E.
    Menzies, Alexander M.
    Azer, Mary W. F.
    Klein, Oliver
    Lyle, Megan
    Clements, Arthur
    Guminski, Alexander
    Kefford, Richard F.
    Long, Georgina V.
    CANCER, 2014, 120 (20) : 3142 - 3153
  • [28] Characterization and Outcomes of Disease Progression in 52 Patients Treated with BRAF-V600+MEK Inhibitors for Advanced Melanoma
    Lucas, Philippine
    Boulinguez, Serge
    Sibaud, Vincent
    Mourey, Loic
    Lamant, Laurence
    Paul, Carle
    Meyer, Nicolas
    DERMATOLOGY, 2018, 234 (3-4) : 92 - 98
  • [29] Incidence and relative risk of cutaneous squamous cell carcinoma with single-agent BRAF inhibitor and dual BRAF/MEK inhibitors in cancer patients: a meta-analysis
    Peng, Ling
    Wang, Yina
    Hong, Yun
    Ye, Xianghua
    Shi, Peng
    Zhang, Junyan
    Zhao, Qiong
    ONCOTARGET, 2017, 8 (47) : 83280 - 83291
  • [30] BRAF and MEK inhibition for the treatment of advanced BRAF mutant melanoma
    Richman, Juliet
    Martin-Liberal, Juan
    Diem, Stefan
    Larkin, James
    EXPERT OPINION ON PHARMACOTHERAPY, 2015, 16 (09) : 1285 - 1297