A Phase 1 Trial of Durvalumab in Combination with Bacillus Calmette-Guerin (BCG) or External Beam Radiation Therapy in Patients with BCG-unresponsive Non-muscle-Invasive Bladder Cancer: The Hoosier Cancer Research Network GU16-243 ADAPT-BLADDER Study.

Noah M Hahn, Michael A O'Donnell,Jason A Efstathiou, Marianna Zahurak,Gary L Rosner, Jeff Smith, Max R Kates,Trinity J Bivalacqua, Phuoc T Tran,Daniel Y Song, Alex S Baras,Andres Matoso, Woonyoung Choi,Kellie N Smith,Drew M Pardoll, Luigi Marchionni,Bridget McGuire, Mary Grace Phelan, Burles A Johnson, Tanya O'Neal,David J McConkey, Tracy L Rose,Marc Bjurlin, Emerson A Lim,Charles G Drake, James M McKiernan,Israel Deutsch, Christopher B Anderson,Donald L Lamm, Daniel M Geynisman,Elizabeth R Plimack, Mark A Hallman,Eric M Horwitz,Essel Al-Saleem, David Y T Chen,Richard E Greenberg, Alexander Kutikov, Gordon Guo,Timothy A Masterson, Nabil Adra,Hristos Z Kaimakliotis

European urology(2023)

引用 5|浏览70
暂无评分
摘要
BACKGROUND:Novel treatments and trial designs remain a high priority for bacillus Calmette-Guerin (BCG)-unresponsive non-muscle-invasive bladder cancer (NMIBC) patients. OBJECTIVE:To evaluate the safety and preliminary efficacy of anti-PD-L1 directed therapy with durvalumab (D), durvalumab plus BCG (D + BCG), and durvalumab plus external beam radiation therapy (D + EBRT). DESIGN, SETTING, AND PARTICIPANTS:A multicenter phase 1 trial was conducted at community and academic sites. INTERVENTION:Patients received 1120 mg of D intravenously every 3 wk for eight cycles. D + BCG patients also received full-dose intravesical BCG weekly for 6 wk with BCG maintenance recommended. D + EBRT patients received concurrent EBRT (6 Gy × 3 in cycle 1 only). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS:Post-treatment cystoscopy and urine cytology were performed at 3 and 6 -mo, with bladder biopsies required at the 6-mo evaluation. The recommended phase 2 dose (RP2D) for each regimen was the primary endpoint. Secondary endpoints included toxicity profiles and complete response (CR) rates. RESULTS AND LIMITATIONS:Twenty-eight patients were treated in the D (n = 3), D + BCG (n = 13), and D + EBRT (n = 12) cohorts. Full-dose D, full-dose BCG, and 6 Gy fractions × 3 were determined as the RP2Ds. One patient (4%) experienced a grade 3 dose limiting toxicity event of autoimmune hepatitis. The 3-mo CR occurred in 64% of all patients and in 33%, 85%, and 50% within the D, D + BCG, and D + EBRT cohorts, respectively. Twelve-month CRs were achieved in 46% of all patients and in 73% of D + BCG and 33% of D + EBRT patients. CONCLUSIONS:D combined with intravesical BCG or EBRT proved feasible and safe in BCG-unresponsive NMIBC patients. Encouraging preliminary efficacy justifies further study of combination therapy approaches. PATIENT SUMMARY:Durvalumab combination therapy can be safely administered to non-muscle-invasive bladder cancer patients with the goal of increasing durable response rates.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要