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经过≥1 年随访后,阿维鲁单抗治疗既往治疗转移性 Merkel 细胞癌患者的疗效更新:JAVELIN Merkel 200,一项 2 期临床试验。

Updated efficacy of avelumab in patients with previously treated metastatic Merkel cell carcinoma after ≥1 year of follow-up: JAVELIN Merkel 200, a phase 2 clinical trial.

机构信息

Rutgers Cancer Institute of New Jersey, 195 Little Albany Street, Room 2007, New Brunswick, NJ, 08901, USA.

Present Address: Replimune Inc, Woburn, MA, USA.

出版信息

J Immunother Cancer. 2018 Jan 19;6(1):7. doi: 10.1186/s40425-017-0310-x.

Abstract

BACKGROUND

Merkel cell carcinoma (MCC) is a rare, aggressive skin cancer associated with poor survival outcomes in patients with distant metastatic disease (mMCC). In an initial analysis from JAVELIN Merkel 200, a phase 2, prospective, open-label, single-arm trial in mMCC, avelumab-a human anti-programmed death-ligand 1 (PD-L1) monoclonal antibody-showed promising efficacy and a safety profile that was generally manageable and tolerable. Here, we report the efficacy of avelumab after ≥1 year of follow-up in patients with distant mMCC that had progressed following prior chemotherapy for metastatic disease.

PATIENTS AND METHODS

Patients received avelumab 10 mg/kg by 1-h intravenous infusion every 2 weeks until confirmed disease progression, unacceptable toxicity, or withdrawal. The primary endpoint was best overall response. Secondary endpoints included duration of response (DOR), progression-free survival (PFS), and overall survival (OS).

RESULTS

Patients (N = 88) were followed for a minimum of 12 months. The confirmed objective response rate was 33.0% (95% CI, 23.3%-43.8%; complete response: 11.4%). An estimated 74% of responses lasted ≥1 year, and 72.4% of responses were ongoing at data cutoff. Responses were durable, with the median DOR not yet reached (95% CI, 18.0 months-not estimable), and PFS was prolonged; 1-year PFS and OS rates were 30% (95% CI, 21%-41%) and 52% (95% CI, 41%-62%), respectively. Median OS was 12.9 months (95% CI, 7.5-not estimable). Subgroup analyses suggested a higher probability of response in patients receiving fewer prior lines of systemic therapy, with a lower baseline disease burden, and with PD-L1-positive tumors; however, durable responses occurred irrespective of baseline factors, including tumor Merkel cell polyomavirus status.

CONCLUSIONS

With longer follow-up, avelumab continues to show durable responses and promising survival outcomes in patients with distant mMCC whose disease had progressed after chemotherapy.

TRIAL REGISTRATION

Clinicaltrials.gov identifier: NCT02155647.

摘要

背景

默克尔细胞癌(MCC)是一种罕见的侵袭性皮肤癌,患有远处转移性疾病(mMCC)的患者生存结局较差。在 JAVELIN Merkel 200 的初步分析中,这是一项在 mMCC 中进行的 II 期、前瞻性、开放标签、单臂试验中,avelumab-一种人抗程序性死亡配体 1(PD-L1)单克隆抗体-显示出有希望的疗效和总体上可管理和耐受的安全性。在这里,我们报告了在先前接受转移性疾病化疗后进展的远处 mMCC 患者中,avelumab 的疗效,这些患者的随访时间≥1 年。

方法

患者每 2 周接受 1 小时静脉输注 10mg/kg 的avelumab,直到确认疾病进展、无法耐受的毒性或停药。主要终点是最佳总体缓解。次要终点包括缓解持续时间(DOR)、无进展生存期(PFS)和总生存期(OS)。

结果

患者(N=88)至少随访 12 个月。确认的客观缓解率为 33.0%(95%CI,23.3%-43.8%;完全缓解:11.4%)。估计有 74%的缓解持续时间≥1 年,且数据截止时 72.4%的缓解仍在持续。缓解持久,中位 DOR 尚未达到(95%CI,18.0 个月-无法估计),且 PFS 延长;1 年 PFS 和 OS 率分别为 30%(95%CI,21%-41%)和 52%(95%CI,41%-62%)。中位 OS 为 12.9 个月(95%CI,7.5-无法估计)。亚组分析表明,在接受较少线数的系统治疗、疾病基线负担较低且 PD-L1 阳性肿瘤的患者中,应答的可能性更高;然而,无论基线因素如何,包括肿瘤 Merkel 细胞多瘤病毒状态,都可发生持久缓解。

结论

随着随访时间的延长,avelumab 在化疗后疾病进展的远处 mMCC 患者中继续显示出持久的缓解和有希望的生存结局。

试验注册

Clinicaltrials.gov 标识符:NCT02155647。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51d5/5774167/82c364072b95/40425_2017_310_Fig1_HTML.jpg

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