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

机译:假定为转移性黑色素瘤的患者认为采用免疫检查点抑制剂和靶向治疗的治疗和BRAF检测方式

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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.
机译:患有BRAF V600(BRAF)突变的转移性黑色素瘤的患者有资格接受免疫检查点抑制剂和靶向疗法的治疗,这使治疗选择成为一个复杂的决定。本研究旨在描述在新一代免疫检查点抑制剂和靶向疗法获得批准后的几年中,假定患有BRAF突变(BRAF +)的转移性黑色素瘤患者的免疫疗法和靶向疗法以及BRAF检测的治疗方式(2014年– 2016)。使用了两个大型的美国商业索赔数据库[Truven Health Analytics MarketScan和IQVIA现实世界数据裁决索赔–美国(IQVIA RWD裁决索赔–美国)]。如果患者接受了至少2种治疗,其中至少1种包括靶向治疗,则被认为是BRAF +。描述了第一(1L),第二(2L)和第三(3L)中使用的治疗路线和方案的顺序,以及按治疗顺序进行BRAF测试的时间。在Truven样本(n = 162)中,有针对性的疗法在1L中使用了66%,在2L中使用了54%,并且62%进行了BRAF测试;在IQVIA RWD裁决的权利要求–美国样本(n = 247)中,靶向治疗的1L使用率是62%,2L使用的是50%,BRAF测试率为68%。在声称在1L之前进行BRAF测试的患者中,超过三分之二的患者开始了靶向治疗。这些发现表明,在针对转移性疾病的BRAF靶向治疗方案获得批准后的几年中,BRAF检测率仍然较低。鉴于最近批准的用于III期黑色素瘤的辅助治疗选择,提高BRAF检测率变得越来越重要。

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