Department of Hematology & Medical Oncology, Taussig Cancer Institute Cleveland Clinic, Cleveland, OH, USA.
Department of Hospital Medicine, Cleveland Clinic, Cleveland, OH, USA.
Target Oncol. 2018 Jun;13(3):353-361. doi: 10.1007/s11523-018-0561-6.
Little is known about the outcomes, safety, and response to subsequent therapies of patients with metastatic urothelial carcinoma (mUC) treated with atezolizumab outside clinical trials.
The objectives of the study include to report the clinical efficacy and safety of atezolizumab, and the response to future therapies in clinical practice outside clinical trials.
This is a retrospective, single-center study including consecutive patients with confirmed mUC who received at least one dose of atezolizumab 1200 mg every 3 weeks between May 2016 and April 2017.
Seventy-nine patients, median age 72 years (range 29-93), 71% men and 76% ECOG PS 0-1, were identified. Most patients (79%) had primary cancer in the bladder, 62% had prior surgery, and 75% received at least one prior line of treatment (34 patients had prior cisplatin-based chemotherapy). Best response included 18% partial response, 29% stable disease, and 53% progressive disease. Patients were on atezolizumab for a median of 2.7 months (95%CI, 1.8-3.6) and median PFS was 3.2 months (95%CI, 1.6-4.8). A total of 33 (42%) patients had significant (any cause) AEs, including grade 4 hyperbilirubinemia in two patients; no toxic deaths were reported. At time of data analysis, only 18% of patients received at least one subsequent line of treatment for a median of 1.8 months (95%CI, 0.0-5.0) while 42% were referred to palliative care/hospice or died.
Patients with mUC who progressed on atezolizumab were unlikely to receive subsequent systemic treatments and the benefit of those treatments appeared limited in our cohort. The findings may impact timing and designs of clinical trials in mUC.
在临床试验之外,接受阿替利珠单抗治疗的转移性尿路上皮癌(mUC)患者的结局、安全性以及对后续治疗的反应鲜为人知。
本研究旨在报告阿替利珠单抗的临床疗效和安全性,以及在临床试验之外的临床实践中对后续治疗的反应。
这是一项回顾性、单中心研究,纳入了 2016 年 5 月至 2017 年 4 月期间至少接受过一次阿替利珠单抗 1200mg、每 3 周 1 次治疗的确诊 mUC 连续患者。
共确定了 79 例患者,中位年龄 72 岁(范围 29-93 岁),71%为男性,76%为 ECOG PS 0-1。大多数患者(79%)原发肿瘤位于膀胱,62%接受过手术,75%接受过至少一线治疗(34 例接受过顺铂类化疗)。最佳缓解包括 18%的部分缓解、29%的疾病稳定和 53%的疾病进展。患者接受阿替利珠单抗治疗的中位时间为 2.7 个月(95%CI,1.8-3.6),中位无进展生存期(PFS)为 3.2 个月(95%CI,1.6-4.8)。共有 33 例(42%)患者发生了有意义的(任何原因)不良事件(AE),包括 2 例患者出现 4 级高胆红素血症;未报告毒性死亡。在数据分析时,只有 18%的患者接受了至少一线后续治疗,中位时间为 1.8 个月(95%CI,0.0-5.0),而 42%的患者被转介姑息治疗/临终关怀或死亡。
阿替利珠单抗治疗后进展的 mUC 患者不太可能接受后续系统性治疗,且这些治疗的获益在本队列中似乎有限。这些发现可能会影响 mUC 临床试验的时间安排和设计。