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BRAF 突变型黑色素瘤的治疗:对接受序贯治疗患者的单中心回顾性分析

BRAF-mutant melanoma management: a single center retrospective analysis of patients treated with sequential therapy.

作者信息

Proietti Ilaria, De Falco Elena, Pacini Luca, Spagnoli Alessandra, Melone Velia, Petrozza Vincenzo, Di Cristofano Claudio, Mangino Giorgio, Romeo Giovanna, Rosa Paolo, Calogero Antonella, Potenza Concetta

机构信息

Department of Medical-Surgical Sciences and Biotechnologies, Dermatology Unit "Daniele Innocenzi", Sapienza University of Rome, Latina, Italy.

Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.

出版信息

Melanoma Manag. 2024 Dec;11(1):2432826. doi: 10.1080/20450885.2024.2432826. Epub 2024 Nov 29.

Abstract

AIMS

In treating patients with melanoma, the order in which therapy is administered, choosing between targeted therapy and immune checkpoint inhibition, has garnered growing interest.

PATIENTS AND METHODS

We conducted a retrospective, real-world analysis of patients with advanced melanoma undergoing immunotherapy or targeted therapy as first-line at a single center.

RESULTS

A total of 88 patients diagnosed with melanoma were identified. At 7 years, in this cohort, 68.4% (95% CI: 55.9%-83.6%) of patients were alive. In all, 47 tumors harbored BRAF mutations; 10 patients who did not receive therapy were excluded from this subgroup. Of the 37 patients with a BRAF mutation, 29 received first-line targeted therapy and 8 received first-line immunotherapy. At 2 years, 28 (76%) patients were alive and 9 (24%) had died. Of the 28 survivors, 22 received first-line targeted therapy and 6 received first-line immunotherapy. In addition, 29 patients were administered a MEK inhibitor in first line. Of these, 66.4% (95% CI: 48.3-91.2) of patients were alive at 7 years.

CONCLUSIONS

There was no significant difference between survival and first-line immunotherapy or first-line targeted therapy. Additional studies are required to establish whether front-line immunotherapy is linked to more effective long-term disease control compared to first-line targeted therapy.

摘要

目的

在治疗黑色素瘤患者时,治疗的给药顺序,即在靶向治疗和免疫检查点抑制之间进行选择,已引起越来越多的关注。

患者与方法

我们对在单一中心接受免疫治疗或靶向治疗作为一线治疗的晚期黑色素瘤患者进行了一项回顾性的真实世界分析。

结果

共确定了88例诊断为黑色素瘤的患者。在该队列中,7年后,68.4%(95%置信区间:55.9%-83.6%)的患者存活。总共有47个肿瘤携带BRAF突变;10例未接受治疗的患者被排除在该亚组之外。在37例BRAF突变患者中,29例接受一线靶向治疗,8例接受一线免疫治疗。2年后,28例(76%)患者存活,9例(24%)死亡。在28名幸存者中,22例接受一线靶向治疗,6例接受一线免疫治疗。此外,29例患者一线使用MEK抑制剂。其中,66.4%(95%置信区间:48.3-91.2)的患者在7年后存活。

结论

一线免疫治疗和一线靶向治疗在生存率方面无显著差异。需要进一步研究以确定与一线靶向治疗相比,一线免疫治疗是否与更有效的长期疾病控制相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82fa/11974465/f92186dcd268/IMMT_A_2432826_F0001_B.jpg

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