Patterns of treatment and BRAF testing with immune checkpoint inhibitors and targeted therapy in patients with metastatic melanoma presumed to be BRAF positive

被引:5
|
作者
Ghate, Sameer [1 ]
Ionescu-Ittu, Raluca [3 ]
Burne, Rebecca [3 ]
Ndife, Briana [1 ]
Laliberte, Francois [3 ]
Nakasato, Antonio [1 ]
Duh, Mei Sheng [2 ]
机构
[1] Novartis Pharmaceut, E Hanover, NJ USA
[2] Anal Grp Inc, 111 Huntington Ave,14th Floor, Boston, MA 02199 USA
[3] Grp Anal Ltee, Montreal, PQ, Canada
关键词
BRAF testing; immune checkpoint inhibitors; metastatic melanoma; targeted therapy; OPEN-LABEL; SYSTEMIC THERAPY; COMBINED NIVOLUMAB; IMPROVED SURVIVAL; POOLED ANALYSIS; IPILIMUMAB; DABRAFENIB; MULTICENTER; VEMURAFENIB; MUTATION;
D O I
10.1097/CMR.0000000000000504
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with BRAF V600 (BRAF) mutated metastatic melanoma are eligible for therapy with both immune checkpoint inhibitors and targeted therapies, making treatment choice a complex decision. The present study aimed to describe patterns of treatment with immunotherapy and targeted therapy and BRAF testing in patients with metastatic melanoma presumed to have BRAF mutations (BRAF+) in the years following the approval of the newer generation of immune checkpoint inhibitors and targeted therapies (2014-2016). Two large US commercial claims databases [Truven Health Analytics MarketScan and IQVIA Real-World Data Adjudicated Claims - USA (IQVIA RWD Adjudicated Claims - USA)] were used. Patients were presumed BRAF+ if they received at least 2 lines of therapy of which at least 1 included targeted therapy. Sequence of lines of therapy and regimens used in first (1L), second (2L), and third (3L), as well as timing of BRAF testing by sequence of therapy were described. In the Truven sample (n= 162), targeted therapy was used by 66% in 1L and by 54% in 2L, and 62% had a BRAF test; in the IQVIA RWD Adjudicated Claims - USA sample (n= 247), targeted therapy was used by 62% in 1L and by 50% in 2L, and 68% had a BRAF test. Among those with a claim for a BRAF test prior to 1L, over two-thirds were initiated on targeted therapy. These findings suggest that the rate of BRAF testing remained low in the years following the approval of BRAF-targeted regimens for metastatic disease. Given the recently approved adjuvant treatment options for stage III melanoma, improving the rates of BRAF testing becomes increasingly important. Copyright (c) 2018 The Author(s). Published by Wolters Kluwer Health, Inc.
引用
收藏
页码:301 / 310
页数:10
相关论文
共 50 条
  • [21] Clinicopathologic features associated with efficacy and long-term survival in metastatic melanoma patients treated with BRAF or combined BRAF and MEK inhibitors
    Menzies, Alexander M.
    Wilmott, James S.
    Drummond, Martin
    Lo, Serigne
    Lyle, Megan
    Chan, Matthew M. K.
    Thompson, John F.
    Guminski, Alex
    Carlino, Matteo S.
    Scolyer, Richard A.
    Kefford, Richard F.
    Long, Georgina V.
    CANCER, 2015, 121 (21) : 3826 - 3835
  • [22] Potential clinical and immunotherapeutic utility of talimogene laherparepvec for patients with melanoma after disease progression on immune checkpoint inhibitors and BRAF inhibitors
    Chesney, Jason
    Imbert-Fernandez, Yoannis
    Telang, Sucheta
    Baum, Mary
    Ranjan, Smita
    Fraig, Mostafa
    Batty, Nicolas
    MELANOMA RESEARCH, 2018, 28 (03) : 250 - 255
  • [23] Combined BRAF-Targeted Therapy with Immunotherapy in BRAF-Mutated Advanced Melanoma Patients
    Ferrucci, Pier Francesco
    Lens, Marko
    Cocorocchio, Emilia
    CURRENT ONCOLOGY REPORTS, 2021, 23 (12)
  • [24] Utilization of Reactive Oxygen Species Targeted Therapy to Prolong the Efficacy of BRAF Inhibitors in Melanoma
    Yuan, Long
    Mishra, Rosalie
    Patel, Hima
    Abdulsalam, Safnas
    Greis, Kenneth D.
    Kadekaro, Ana Luisa
    Merino, Edward J.
    Garrett, Joan T.
    JOURNAL OF CANCER, 2018, 9 (24): : 4665 - 4676
  • [25] Efficacy of BRAF Inhibitors in Asian Metastatic Melanoma Patients: Potential Implications of Genomic Sequencing in BRAF-Mutated Melanoma
    Kim, Hee Kyung
    Lee, Sunyoung
    Kim, Kyung
    Heo, Mi Hwa
    Lee, Hansang
    Cho, Jinhyun
    Kim, Nayoung K. D.
    Park, Woongyang
    Lee, Su Jin
    Kim, Jung Han
    Jang, Kee-Taek
    Choi, Sang-Hee
    Lee, Jeeyun
    TRANSLATIONAL ONCOLOGY, 2016, 9 (06): : 557 - 564
  • [26] Real-world effectiveness of immune checkpoint inhibitors and BRAF/ MEK inhibitors among veteran patients with cutaneous melanoma
    Kim, Daniel Y.
    Swetter, Susan M.
    Huhmann, Linden
    Dizon, Matthew P.
    Ferguson, Jacqueline M.
    Osborne, Thomas F.
    Spence, Allyson C.
    Ziad, Amina
    Fillmore, Nathanael
    Hartman, Rebecca I.
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2024, 90 (03) : 620 - 623
  • [27] Targeted agents or immuno-oncology therapies as first-line therapy for BRAF-mutated metastatic melanoma: a real-world study
    Luke, Jason J.
    Ghate, Sameer R.
    Kish, Jonathan
    Lee, Choo Hyung
    McAllister, Lindsay
    Mehta, Sonam
    Ndife, Briana
    Feinberg, Bruce A.
    FUTURE ONCOLOGY, 2019, 15 (25) : 2933 - 2942
  • [28] BRAF-targeted therapy and immune responses to melanoma
    Ngiow, Shin Foong
    Knight, Deborah A.
    Ribas, Antoni
    McArthur, Grant A.
    Smyth, Mark J.
    ONCOIMMUNOLOGY, 2013, 2 (06)
  • [29] The association between immune checkpoint or BRAF/MEK inhibitor therapy and uveitis in patients with advanced cutaneous melanoma
    Dimitriou, Florentia
    Urner-Bloch, Ursula
    Eggenschwiler, Corinne
    Mitsakakis, Nicholas
    Mangana, Joanna
    Dummer, Reinhard
    Urner, Martin
    EUROPEAN JOURNAL OF CANCER, 2021, 144 : 215 - 223
  • [30] Empiric Therapy with BRAF and MEK Inhibitors in Metastatic Melanoma
    Cann, Christopher G.
    Tillman, Benjamin F.
    Davis, Elizabeth J.
    Johnson, Douglas B.
    ONCOLOGIST, 2019, 24 (11): : 1495 - 1496