braf突变黑色素瘤患者完全缓解后应该继续进行靶向治疗吗?

Dermatology (Basel, Switzerland) Pub Date : 2022-01-01 Epub Date: 2021-10-27 DOI:10.1159/000518718
Eve Bédouelle, Jean Michel Nguyen, Emilie Varey, Amir Khammari, Brigitte Dreno
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引用次数: 4

摘要

背景:靶向治疗用于治疗braf突变的转移性黑色素瘤患者,并持续治疗直至疾病进展或出现严重毒性。没有关于实现完全缓解(CR)的患者管理的可靠数据。主要目的:确定cr患者停止靶向治疗后第一年的复发率。次要目的:确定整个随访期间的复发率,并确定1年复发的预后因素。方法:对纳入RIC-Mel数据库的晚期黑色素瘤患者进行回顾性、单中心观察性研究,这些患者在CT扫描和PET/CT扫描证实CR后停止靶向治疗。结果:纳入29例患者。17例(58.6%)患者单独使用BRAF抑制剂(BRAFi), 12例(41.4%)患者使用BRAFi联合MEK抑制剂(BRAFi + MEKi)。中位治疗时间为9.7个月。停药后12个月复发率为69% (BRAFi: 70.6%;BRAFi + MEKi: 66.7%)和36个月时的76% (BRAFi: 76.5%;BRAFi + MEKi: 75%)。女性复发风险增加的趋势不显著(p = 0.1;RR 3.36;95% CI 0.77-17.07),在LDH水平高于正常上限的患者中(p = 0.58;RR 2.43;95% CI 0.10-56.71),当涉及两个以上转移部位时(p = 0.19;RR 4.6;95% ci 0.46-46.51)。复发后,17例患者恢复靶向治疗(BRAFi 7例;10例BRAFi + MEKi),有效率为53%。结论:这项现实生活中的研究为CR后停止靶向治疗的患者提供了长期数据,大多数患者在停止靶向治疗后的第一年复发,其中50%在前3个月复发。恢复靶向治疗后,53%的复发患者达到客观缓解。患者应在停药后的第一年接受随访。此外,转移部位少于3个、基线LDH水平正常、男性和对治疗反应迅速的患者在停药后更有可能维持CR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Should Targeted Therapy Be Continued in BRAF-Mutant Melanoma Patients after Complete Remission?

Background: Targeted therapy is used to treat patients with a BRAF-mutated metastatic melanoma and is continued until disease progression or severe toxicity. No robust data on the management of patients achieving a complete remission (CR) are available.

Main objective: To determine the relapse rate in the first year after targeted therapy discontinuation in patients in CR.

Secondary objectives: To determine the relapse rates throughout the follow-up and to identify prognostic factors for relapse at 1 year.

Methods: A retrospective, monocentric observational study was conducted in patients with advanced melanoma included in the RIC-Mel database who discontinued targeted therapy after achieving a CR confirmed by CT scan and PET/CT scan.

Results: Twenty-nine patients were included. Seventeen (58.6%) patients were treated with BRAF inhibitor (BRAFi) alone and 12 (41.4%) with a BRAFi combined with a MEK inhibitor (BRAFi + MEKi). The median treatment duration was 9.7 months. The relapse rates after discontinuation were 69% at 12 months (BRAFi: 70.6%; BRAFi + MEKi: 66.7%) and 76% at 36 months (BRAFi: 76.5%; BRAFi + MEKi: 75%). A non-significant trend towards a higher risk of relapse was found in women (p = 0.1; RR 3.36; 95% CI 0.77-17.07), in patients with an LDH level greater than the upper limits of normal (p = 0.58; RR 2.43; 95% CI 0.10-56.71), and when more than two metastatic sites were involved (p = 0.19; RR 4.6; 95% CI 0.46-46.51). After relapse, targeted therapy was resumed in 17 patients (7 with BRAFi; 10 with BRAFi + MEKi) with a response rate of 53%.

Conclusions: This real-life study provided long-term data in patients who discontinued targeted therapy after CR. Most patients experienced a relapse in the first year after targeted therapy discontinuation, of whom 50% were in the first 3 months. After targeted therapy resumption, 53% of relapsing patients achieved an objective response. Patients should be followed during the first year after treatment discontinuation. In addition, patients with less than 3 metastatic sites, a baseline LDH level with normal ranges, men, and patients responding rapidly to treatment would be more likely to maintain a CR after treatment discontinuation.

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