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西妥昔单抗用于免疫疗法难治性/不适用的皮肤鳞状细胞癌

Cetuximab for Immunotherapy-Refractory/Ineligible Cutaneous Squamous Cell Carcinoma.

作者信息

Marin-Acevedo Julian A, Withycombe Bethany M, Kim Youngchul, Brohl Andrew S, Eroglu Zeynep, Markowitz Joseph, Tarhini Ahmad A, Tsai Kenneth Y, Khushalani Nikhil I

机构信息

Medical Oncology, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN 46202, USA.

Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL 33612, USA.

出版信息

Cancers (Basel). 2023 Jun 14;15(12):3180. doi: 10.3390/cancers15123180.

Abstract

Anti-PD1 therapy demonstrated impressive, prolonged responses in advanced cutaneous squamous cell carcinoma (CSCC). Therapy for ICI-refractory/ineligible disease remains unclear. We performed a retrospective analysis in locally-advanced/metastatic CSCC using cetuximab across three cohorts: immediately after ICI failure (A), not immediately following ICI failure (B), or without prior ICI (C). The primary endpoint was the overall response rate (ORR). Secondary endpoints included disease-control rate (DCR), progression-free survival (PFS), overall survival (OS), time-to-response (TTR) and toxicity. Twenty-three patients were included. In cohort A (n = 11), the ORR was 64% and DCR was 91%, with six ongoing responses at data cutoff. In cohort B (n = 2), all patients had progression as the best response. At a median follow-up of 21 months for A and B, TTR and PFS were 2.0 and 17.3 months, respectively. The median OS was not reached. In cohort C (n = 10), the ORR and DCR were 80%, including five ongoing responses at the data cutoff. At a median follow-up of 22.4 months, the TTR, PFS and OS were 2.5, 7.3 and 23.1 months, respectively. Cetuximab was well tolerated in all cohorts. In summary, cetuximab is effective in patients with failure/contraindications to ICI. Cetuximab immediately after ICI failure yielded particularly fast, durable responses. If confirmed, this could be the preferred therapy following ICI failure.

摘要

抗程序性死亡蛋白1(PD1)疗法在晚期皮肤鳞状细胞癌(CSCC)中显示出令人印象深刻的、持久的反应。对于免疫检查点抑制剂(ICI)难治/不适用的疾病,其治疗方法仍不明确。我们对局部晚期/转移性CSCC患者进行了一项回顾性分析,在三个队列中使用西妥昔单抗:ICI治疗失败后立即用药(A组)、ICI治疗失败后未立即用药(B组)或未接受过ICI治疗(C组)。主要终点是总缓解率(ORR)。次要终点包括疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)、缓解时间(TTR)和毒性。共纳入23例患者。在A组(n = 11)中,ORR为64%,DCR为91%,在数据截止时仍有6例患者持续缓解。在B组(n = 2)中,所有患者的最佳反应均为疾病进展。A组和B组的中位随访时间为21个月,TTR和PFS分别为2.0个月和17.3个月。中位OS未达到。在C组(n = 10)中,ORR和DCR均为80%,在数据截止时仍有5例患者持续缓解。中位随访时间为22.4个月,TTR、PFS和OS分别为2.5个月、7.3个月和23.1个月。所有队列中西妥昔单抗的耐受性均良好。总之,西妥昔单抗对ICI治疗失败/禁忌的患者有效。ICI治疗失败后立即使用西妥昔单抗可产生特别快速、持久的反应。如果得到证实,这可能是ICI治疗失败后的首选治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0619/10295991/b5beba65e92d/cancers-15-03180-g001.jpg

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