Dept. of Reproductive Medicine, Moores Cancer Center, University of California, San Diego School of Medicine, La Jolla, CA 92093, USA.
Gynecol Oncol. 2013 Apr;129(1):22-7. doi: 10.1016/j.ygyno.2012.12.022. Epub 2012 Dec 20.
This two-stage phase II study was designed to assess the activity of the combination of temsirolimus and bevacizumab in patients with recurrent or persistent endometrial carcinoma (EMC).
Eligible patients had persistent or recurrent EMC after receiving 1-2 prior cytotoxic regimens, measurable disease, and Gynecologic Oncology Group performance status ≤ 2. Treatment consisted of bevacizumab 10 mg/kg every other week and temsirolimus 25 mg IV weekly until disease progression or prohibitory toxicity. Primary end points were progression-free survival (PFS) at six months and overall response rate using RECIST criteria.
Fifty-three patients were enrolled. Forty-nine patients were eligible and evaluable. Median age was 63 years, and prior treatment consisted of one or two regimens in 40 (82%) and 9 (18%), respectively. Twenty (41%) received prior radiation. Adverse events were consistent with those expected with bevacizumab and temsirolimus treatment. Two gastrointestinal-vaginal fistulas, one grade 3 epistaxis, two intestinal perforations and 1 grade 4 thrombosis/embolism were seen. Three patient deaths were possibly treatment related. Twelve patients (24.5%) experienced clinical responses (one complete and 11 partial responses), and 23 patients (46.9%) survived progression free for at least six months. Median progression-free survival (PFS) and overall survival (OS) were 5.6 and 16.9 months, respectively.
Combination of temsirolimus and bevacizumab is deemed active based on both objective tumor response and PFS at six months in recurrent or persistent EMC. However, this treatment regimen was associated with significant toxicity in this pretreated group. Future study will be guided by strategies to decrease toxicity and increase response rates.
这项两阶段二期研究旨在评估替西罗莫司联合贝伐珠单抗治疗复发性或持续性子宫内膜癌(EMC)患者的疗效。
符合条件的患者在接受 1-2 种先前的细胞毒性治疗方案后出现持续性或复发性 EMC,有可测量的疾病,且妇科肿瘤学组体能状态 ≤ 2。治疗包括贝伐珠单抗 10 mg/kg,每两周一次,替西罗莫司 25 mg,静脉注射,每周一次,直到疾病进展或出现不可耐受的毒性。主要终点是 6 个月时的无进展生存期(PFS)和根据 RECIST 标准的总缓解率。
共招募了 53 名患者。49 名患者符合入组条件并可进行评估。中位年龄为 63 岁,之前的治疗方案分别为 1 个或 2 个方案,占 40%和 18%。20 名患者(41%)接受过放疗。不良事件与贝伐珠单抗和替西罗莫司治疗相关的预期事件一致。发生了 2 例胃肠道-阴道瘘、1 例 3 级鼻出血、2 例肠穿孔和 1 例 4 级血栓/栓塞事件。3 例患者死亡可能与治疗有关。12 名患者(24.5%)出现临床缓解(1 例完全缓解,11 例部分缓解),23 名患者(46.9%)无进展生存期至少为 6 个月。中位无进展生存期(PFS)和总生存期(OS)分别为 5.6 个月和 16.9 个月。
替西罗莫司联合贝伐珠单抗在复发性或持续性 EMC 患者中,基于客观肿瘤反应和 6 个月时的 PFS,被认为具有活性。然而,在这种预处理的患者群体中,这种治疗方案与显著的毒性相关。未来的研究将以降低毒性和提高反应率的策略为指导。