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高剂量白细胞介素-2免疫疗法序贯靶向治疗对转移性肾细胞癌的影响:来自正在进行的白细胞介素-2临床试验(PROCLAIM)的转移性肾细胞癌患者结局与生存分析

Impact of Sequencing Targeted Therapies With High-dose Interleukin-2 Immunotherapy: An Analysis of Outcome and Survival of Patients With Metastatic Renal Cell Carcinoma From an On-going Observational IL-2 Clinical Trial: PROCLAIM.

作者信息

Clark Joseph I, Wong Michael K K, Kaufman Howard L, Daniels Gregory A, Morse Michael A, McDermott David F, Agarwala Sanjiv S, Lewis Lionel D, Stewart John H, Vaishampayan Ulka, Curti Brendan, Gonzalez René, Lutzky Jose, Rudraptna Venkatesh, Cranmer Lee D, Jeter Joanne M, Hauke Ralph J, Miletello Gerald, Milhem Mohammed M, Amin Asim, Richart John M, Fishman Mayer, Hallmeyer Sigrun, Patel Sapna P, Van Veldhuizen Peter, Agarwal Neeraj, Taback Bret, Treisman Jonathan S, Ernstoff Marc S, Perritt Jessica C, Hua Hong, Rao Tharak B, Dutcher Janice P, Aung Sandra

机构信息

Department of Medicine, Loyola University Medical Center, Maywood, IL.

Department of Medicine, University of Southern California, Los Angeles, CA.

出版信息

Clin Genitourin Cancer. 2017 Feb;15(1):31-41.e4. doi: 10.1016/j.clgc.2016.10.008. Epub 2016 Oct 29.

Abstract

BACKGROUND

This analysis describes the outcome for patients who received targeted therapy (TT) prior to or following high-dose interleukin-2 (HD IL-2).

PATIENTS AND METHODS

Patients with renal cell carcinoma (n = 352) receiving HD IL-2 were enrolled in Proleukin Observational Study to Evaluate the Treatment Patterns and Clinical Response in Malignancy (PROCLAIM) beginning in 2011. Statistical analyses were performed using datasets as of September 24, 2015.

RESULTS

Overall, there were 4% complete response (CR), 13% partial response (PR), 39% stable disease (SD), and 43% progressive disease (PD) with HD IL-2. The median overall survival (mOS) was not reached in patients with CR, PR, or SD, and was 15.5 months in patients with PD (median follow-up, 21 months). Sixty-one patients had prior TT before HD IL-2 with an overall response rate (ORR) to HD IL-2 of 19% (1 CR, 9 PR) and an mOS of 22.1 months. One hundred forty-nine patients received TT only after HD IL-2 with an mOS of 35.5 months. One hundred forty-two patients had no TT before or after HD IL-2, and mOS was not reached. The mOS was 8.5 months in PD patients who received HD IL-2 without follow-on TT and 29.7 months in PD patients who received follow-on TT after HD IL-2.

CONCLUSIONS

HD IL-2 as sole front-line therapy, in the absence of added TT, shows extended clinical benefit (CR, PR, and SD). Patients with PD after HD IL-2 appear to benefit from follow-on TT. Patients who progressed on TT and received follow-on HD IL-2 experienced major clinical benefit. HD IL-2 therapy should be considered in eligible patients.

摘要

背景

本分析描述了在接受大剂量白细胞介素-2(HD IL-2)之前或之后接受靶向治疗(TT)的患者的结局。

患者与方法

2011年起,将接受HD IL-2治疗的肾细胞癌患者(n = 352)纳入白细胞介素-2观察性研究以评估恶性肿瘤的治疗模式和临床反应(PROCLAIM)。使用截至2015年9月24日的数据集进行统计分析。

结果

总体而言,HD IL-2治疗的完全缓解(CR)率为4%,部分缓解(PR)率为13%,疾病稳定(SD)率为39%,疾病进展(PD)率为43%。CR、PR或SD患者的中位总生存期(mOS)未达到,PD患者的mOS为15.5个月(中位随访时间为21个月)。61例患者在HD IL-2之前接受过TT,其对HD IL-2的总缓解率(ORR)为19%(1例CR,9例PR),mOS为22.1个月。149例患者仅在HD IL-2之后接受TT,mOS为35.5个月。142例患者在HD IL-2之前和之后均未接受TT,mOS未达到。未接受后续TT的HD IL-2治疗的PD患者的mOS为8.5个月,HD IL-2之后接受后续TT的PD患者的mOS为29.7个月。

结论

HD IL-2作为唯一的一线治疗,在未添加TT的情况下,显示出延长的临床获益(CR、PR和SD)。HD IL-2治疗后发生PD的患者似乎从后续TT中获益。在TT治疗中进展并接受后续HD IL-2治疗的患者获得了显著的临床获益。符合条件的患者应考虑HD IL-2治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0928/6875755/63b26774693c/nihms-1058423-f0001.jpg

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