阿替唑单抗
转移性尿路上皮癌
医学
肿瘤科
内科学
临床研究阶段
耐火材料(行星科学)
癌
尿路上皮癌
泌尿科
化疗
癌症
免疫疗法
膀胱癌
无容量
生物
天体生物学
作者
Alexandra Drakaki,Thomas Powles,Aristotelis Bamias,Juan Martín-Liberal,Sang Joon Shin,Terence W. Friedlander,Diego Tosi,Chandler Park,Carlos Gomez‐Roca,Florence Joly,Daniel Castellano,Rafael Morales‐Barrera,Irene Moreno,Aude Fléchon,Kobe Yuen,Deepali Rishipathak,Kelly DuPree,Fiona Young,Francesca Michielin,Colby S. Shemesh,Elizabeth E. Steinberg,Patrick Williams,Jae‐Lyun Lee
标识
DOI:10.1158/1078-0432.ccr-23-0798
摘要
The MORPHEUS platform was designed to identify early efficacy signals and evaluate the safety of novel immunotherapy combinations across cancer types. The phase Ib/II MORPHEUS-UC trial (NCT03869190) is evaluating atezolizumab plus magrolimab, niraparib, or tocilizumab in platinum-refractory locally advanced or metastatic urothelial carcinoma (mUC). Additional treatment combinations were evaluated and will be reported separately.Patients had locally advanced or mUC that progressed during or following treatment with a platinum-containing regimen. The primary efficacy endpoint was investigator-assessed objective response rate (ORR). Key secondary endpoints included investigator-assessed progression-free survival (PFS) and overall survival (OS). Safety and exploratory biomarker analyses were also conducted.Seventy-six patients were randomized to receive either atezolizumab plus magrolimab (n = 16), atezolizumab plus niraparib (n = 15), atezolizumab plus tocilizumab (n = 15), or atezolizumab monotherapy (control; n = 30). No additive benefit in ORR, PFS, or OS was seen in the treatment arms versus the control. The best confirmed ORR was 26.7% with atezolizumab plus magrolimab, 6.7% with atezolizumab plus niraparib, 20.0% with atezolizumab plus tocilizumab, and 27.6% with atezolizumab monotherapy. Overall, the treatment combinations were tolerable, and adverse events were consistent with each agent's known safety profile. Trends were observed for shrinkage of programmed death-ligand 1-positive tumors (atezolizumab, atezolizumab plus magrolimab, atezolizumab plus tocilizumab), inflamed tumors, or tumors with high mutational burden (atezolizumab), and immune excluded tumors (atezolizumab plus magrolimab).The evaluated regimens in MORPHEUS-UC were tolerable. However, response rates for the combinations did not meet the criteria for further development in platinum-experienced locally advanced or mUC.
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