晚期默克尔细胞癌患者抗pd -(L)1治疗进展性疾病的临床结果和治疗

IF 7.9 1区 医学 Q1 ONCOLOGY European Journal of Cancer Pub Date : 2025-02-25 Epub Date: 2025-01-27 DOI:10.1016/j.ejca.2025.115254
Jeremy Mo , Anne Zaremba , Andrisha-Jade Inderjeeth , Perla El Zeinaty , Ao Li , Alexandre Wicky , Nicholas Della Marta , Caroline Gaudy Marqueste , Ann-Sophie Bohne , Margarida Matias , Nicholas McNamee , Lucia Festino , Charley Chen , Sydney Ch’ng , Alexander C.J. van Akkooi , Laetitia Da Meda , John J. Park , Paolo A. Ascierto , Axel Hauschild , Jenny H. Lee , Ines Pires da Silva
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引用次数: 0

摘要

目的:默克尔细胞癌(MCC)是一种罕见的皮肤癌,在世界范围内发病率呈上升趋势。抗程序性死亡-1/配体-1 (anti-PD-(L)1)疗法对晚期MCC的治疗是有效的。本研究探讨了晚期MCC对抗pd -(L)1治疗的反应/进展模式,并描述了随后的管理。方法:这是一项多中心国际回顾性队列研究,数据收集截至2023年5月,来自6个国家的17个中心。结果包括抗pd -(L)1和后续治疗的客观缓解率(ORR)、缓解持续时间(DOR)、无进展生存期(PFS)和总生存期(OS)。结果:185例晚期MCC患者接受了抗pd -(L)1治疗。中位随访28.7个月(95 % CI: 21.4-38.3), ORR为57.3% %,中位DOR为42.8个月(95 % CI, 25.8 -未达到(NR)),中位PFS为14个月(95 % CI, 8.1- 19.8),中位OS为42.8个月(95 % CI, 30.3 - NR)。108例患者(59 %)出现进展性疾病;50 % (n = 54/108)为初级电阻,26 % (n = 28/108)为次级电阻。50例(27 %;N = 50/185)接受了随后的全身治疗(+/-局部治疗),并有应答数据;18(36 %;n = 18/50)接受双铂化疗(ORR 67 %,DOR 5.0个月[95 % CI;3.7 - NR])和16(32 %;n = 16/50)再次接受抗pd -(L)1 (ORR为56 %,DOR为20.2个月[95 % CI;8.3 - nr])。结论:原发性耐药患者最常见的后续治疗是化疗,而继发性耐药患者最常见的是进一步的抗pd -(L)1治疗联合其他治疗。尽管两种疗法都显示出有希望的ORR,但与抗pd -(L)1再挑战相比,双重铂化疗的DOR更差。
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Clinical outcomes and management following progressive disease with anti-PD-(L)1 therapy in patients with advanced Merkel Cell Carcinoma

Aim

Merkel Cell Carcinoma (MCC) is a rare skin cancer with a rising incidence worldwide. Anti-programmed death-1/ligand-1 (anti-PD-(L)1) therapies are effective for the treatment of advanced MCC. This study examines patterns of response / progression of advanced MCC to anti-PD-(L)1 therapies and describes subsequent management.

Method

This is a multi-centre international retrospective cohort study with data collected up to May 2023 from 17 centres across 6 countries. Outcomes included objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS) for anti-PD-(L)1 and subsequent therapy.

Results

One-hundred and eighty-five advanced MCC patients received anti-PD-(L)1 therapy. At median follow-up of 28.7 months (95 % CI: 21.4–38.3), ORR was 57.3 %, median DOR was 42.8 months (95 % CI, 25.8 – not reached (NR)), median PFS was 14 months (95 % CI, 8.1– 19.8), and median OS was 42.8 months (95 % CI, 30.3 – NR). One-hundred and eight patients (59 %) experienced progressive disease; 50 % (n = 54/108) with primary resistance and 26 % (n = 28/108) with secondary resistance. Fifty patients (27 %; n = 50/185) received subsequent systemic therapies (+/- local therapy) with response data; 18 (36 %; n = 18/50) received doublet platinum chemotherapy (ORR 67 %, DOR 5.0 months [95 % CI; 3.7 - NR]) and 16 (32 %; n = 16/50) were rechallenged with anti-PD-(L)1 (ORR 56 %, DOR 20.2 months [95 % CI; 8.3 - NR]).

Conclusion

The most common subsequent treatment for patients with primary resistance was chemotherapy, while those with secondary resistance most frequently underwent further anti-PD-(L)1 therapy in combination with other therapies. Despite both therapies demonstrating promising ORR, doublet platinum chemotherapy had a poorer DOR compared to anti-PD-(L)1 rechallenge.
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来源期刊
European Journal of Cancer
European Journal of Cancer 医学-肿瘤学
CiteScore
11.50
自引率
4.80%
发文量
953
审稿时长
23 days
期刊介绍: The European Journal of Cancer (EJC) serves as a comprehensive platform integrating preclinical, digital, translational, and clinical research across the spectrum of cancer. From epidemiology, carcinogenesis, and biology to groundbreaking innovations in cancer treatment and patient care, the journal covers a wide array of topics. We publish original research, reviews, previews, editorial comments, and correspondence, fostering dialogue and advancement in the fight against cancer. Join us in our mission to drive progress and improve outcomes in cancer research and patient care.
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