Pembrolizumab with Chemoradiation as Treatment for Muscle-invasive Bladder Cancer: Analysis of Safety and Efficacy of the PCR-MIB Phase 2 Clinical Trial (ANZUP 1502)

医学 彭布罗利珠单抗 膀胱癌 临床终点 内科学 泌尿科 不利影响 实体瘤疗效评价标准 肿瘤科 临床研究阶段 外科 癌症 临床试验 免疫疗法
作者
Andrew Weickhardt,Farshad Foroudi,Nathan Lawrentschuk,Jing Xie,Mark Sidhom,Abhijit Pal,Peter Grimison,Alison Y. Zhang,Siobhan Ng,Colin Tang,Elizabeth Hovey,Colin Chen,George Hruby,Alexander Guminski,Margaret McJannett,Ciara Conduit,Ben Tran,Ian D. Davis,Dickon Hayne
出处
期刊:European Urology Oncology [Elsevier BV]
卷期号:7 (3): 469-477 被引量:18
标识
DOI:10.1016/j.euo.2023.09.011
摘要

Background Radiation may improve the efficacy of immune checkpoint inhibition. This study investigates the combination of pembrolizumab and chemoradiation (CRT) for muscle-invasive bladder cancer (MIBC). Objective To assess the feasibility and safety of pembrolizumab combined with CRT for MIBC. Design, setting, and participants A single-arm phase 2 trial was performed with 28 participants having cT2-T4aN0M0 MIBC (Eastern Cooperative Oncology Group performance status 0–1; estimated glomerular filtration rate ≥40 ml/min; no contraindications to pembrolizumab) suitable for CRT. Intervention Whole bladder radiation therapy (RT; 64 Gy in 32 daily fractions, over 6.5 wk, combined with cisplatin (35 mg/m2 intravenously [IV] weekly, six doses) and pembrolizumab (200 mg IV q3 weeks, seven doses), both starting with RT. Surveillance cystoscopy/biopsy and computerised tomography scans performed 12 and 24 wk after CRT. Outcome measurements and statistical analysis The primary endpoint was feasibility, determined by a prespecified satisfactory low rate of grade 3 or worse nonurinary toxicity or completion of planned CRT according to defined parameters. Secondary endpoints were complete cystoscopic response, locoregional progression-free survival (LRPFS), distant metastasis-free survival (DMFS), and overall survival (OS). Results and limitations Twenty-eight patients were enrolled with a 31-mo median follow-up. Six had Grade >3 nonurinary adverse events during/within 12 wk after treatment; three had more than one cisplatin dose reduction. The 24-wk post-CRT complete response (CR) rate was 88%. Eight patients developed metastatic disease, and three had nonmetastatic progression. The DMFS at 2 yr is 78% (95% confidence interval [CI] 54–90%), with LRPFS at 2 yr of 87% (95% CI 64–96%) and median OS of 39 mo (95% CI 17.1–not evaluable). Limitations are the single-arm design and sample size. Conclusions Combining pembrolizumab with CRT for MIBC was feasible, with manageable toxicity and promising CR rates. Patient summary Immunotherapy treats nonmetastatic/metastatic bladder cancer effectively. We combined pembrolizumab with chemotherapy and radiation to assess its safety and impact on treatment delivery. The combination was feasible with encouraging early activity. Further larger trials are warranted.
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