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肿瘤类型患者接受 PD1/PDL1 抗体治疗后的假性进展证据。

Evidence of pseudoprogression in patients treated with PD1/PDL1 antibodies across tumor types.

机构信息

Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.

Oncology Department, Clínica Universidad de Navarra, Madrid, Spain.

出版信息

Cancer Med. 2020 Apr;9(8):2643-2652. doi: 10.1002/cam4.2797. Epub 2020 Feb 19.

Abstract

BACKGROUND

PD(L)1 antibodies (anti-PD(L)-1) have been a major breakthrough in several types of cancer. Novel patterns of response and progression have been described with anti-PD(L)-1. We aimed at characterizing pseudoprogression (PSPD) among patients with various solid tumor types treated by anti-PD(L)-1.

METHODS

All consecutive patients (pts) enrolled in phase 1 trials with advanced solid tumors and lymphomas treated in phase I clinical trials evaluating monotherapy by anti-PD(L)-1 at Gustave Roussy were analyzed. We aimed to assess prevalence and outcome of PSPD across tumor types. We also intended to describe potential clinical and pathological factors associated with PSPD.

RESULTS

A total of 169 patients treated with anti-PD(L)-1 were included in the study. Most frequent tumor types included melanoma (n = 57) and non-small cell lung cancer (n = 19). At first tumor evaluation 77 patients (46%) presented with immune unconfirmed progressive disease. Six patients (8%) experienced PSPD: 2 patients with partial response; 4 patients with stable disease. Increase in target lesions in the first CT-scan was more frequently associated to PSPD (67% vs 33%; P = .04). Patients with a PSPD had a superior survival when compared to patients progressing (median OS: 10.7 months vs 8.7 months; P = .07).

CONCLUSIONS

A small subset of PSPD patients may experience response after an initial progression. Assessment of the current strategy for immune-related response evaluations may require further attention.

摘要

背景

PD(L)1 抗体(抗 PD(L)-1)在多种癌症中取得了重大突破。已有研究描述了抗 PD(L)-1 治疗时新的反应和进展模式。我们旨在描述各种实体瘤类型的患者接受抗 PD(L)-1 治疗时出现的假性进展(PSPD)。

方法

所有连续入组的晚期实体瘤和淋巴瘤患者,均接受了 Gustave Roussy 进行的 I 期临床试验中评估的抗 PD(L)-1 单药治疗。我们旨在评估不同肿瘤类型中 PSPD 的发生率和结局。我们还打算描述与 PSPD 相关的潜在临床和病理因素。

结果

共有 169 例接受抗 PD(L)-1 治疗的患者纳入了本研究。最常见的肿瘤类型包括黑色素瘤(n=57)和非小细胞肺癌(n=19)。在首次肿瘤评估时,77 例患者(46%)表现为免疫未确认的进展性疾病。6 例患者(8%)发生了 PSPD:2 例部分缓解,4 例病情稳定。首次 CT 扫描中靶病灶增加更常与 PSPD 相关(67% vs 33%;P=0.04)。与进展患者相比,PSPD 患者的生存时间更优(中位 OS:10.7 个月 vs 8.7 个月;P=0.07)。

结论

一小部分 PSPD 患者在初始进展后可能会出现缓解。可能需要进一步关注目前免疫相关反应评估策略的评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7163099/c9b599b850c2/CAM4-9-2643-g001.jpg

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