From Vanderbilt University Medical Center (L. Horn) and Sarah Cannon Research Institute-Tennessee Oncology (M.L.J.), Nashville; Mayo Clinic, Rochester, MN (A.S.M.); Mazowieckie Centrum Leczenia Chorób Płuc i Gruźlicy, Otwock (A. Szczęsna), and Centrum Onkologii-Instytut im. Marii Skłodowskiej-Curie w Warszawie, Warsaw (M.K.) - both in Poland; Thomayerova Nemocnice, Pneumologická Klinika 1.LF UK, Prague, Czech Republic (L. Havel); the Department of Respiratory and Critical Care Medicine (M.J.H.) and the 2nd Department of Respiratory and Critical Care Medicine (F.H.), Ludwig Boltzmann Institute for COPD and Respiratory Epidemiology-Sozialmedizinisches Zentrum Baumgartner Höhe, Otto-Wagner-Spital, Vienna; Semmelweis Egyetem ÁOK, Pulmonológiai Klinika, Budapest, Hungary (G.L.); the Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo (M.N.); LungenClinic Grosshansdorf, Airway Research Center North, German Center for Lung Research, Grosshansdorf, Germany (M.R.); State Key Laboratory of South China, Chinese University of Hong Kong, Hong Kong (T.M.), and F. Hoffmann-La Roche, Shanghai (J.L.) - both in China; Genentech, South San Francisco, CA (S.L., D.S.S., B.D., A.L.-C., F.K., W.L., A. Sandler); and Georgetown University, Washington DC (S.V.L.).
N Engl J Med. 2018 Dec 6;379(23):2220-2229. doi: 10.1056/NEJMoa1809064. Epub 2018 Sep 25.
Enhancing tumor-specific T-cell immunity by inhibiting programmed death ligand 1 (PD-L1)-programmed death 1 (PD-1) signaling has shown promise in the treatment of extensive-stage small-cell lung cancer. Combining checkpoint inhibition with cytotoxic chemotherapy may have a synergistic effect and improve efficacy.
We conducted this double-blind, placebo-controlled, phase 3 trial to evaluate atezolizumab plus carboplatin and etoposide in patients with extensive-stage small-cell lung cancer who had not previously received treatment. Patients were randomly assigned in a 1:1 ratio to receive carboplatin and etoposide with either atezolizumab or placebo for four 21-day cycles (induction phase), followed by a maintenance phase during which they received either atezolizumab or placebo (according to the previous random assignment) until they had unacceptable toxic effects, disease progression according to Response Evaluation Criteria in Solid Tumors, version 1.1, or no additional clinical benefit. The two primary end points were investigator-assessed progression-free survival and overall survival in the intention-to-treat population.
A total of 201 patients were randomly assigned to the atezolizumab group, and 202 patients to the placebo group. At a median follow-up of 13.9 months, the median overall survival was 12.3 months in the atezolizumab group and 10.3 months in the placebo group (hazard ratio for death, 0.70; 95% confidence interval [CI], 0.54 to 0.91; P=0.007). The median progression-free survival was 5.2 months and 4.3 months, respectively (hazard ratio for disease progression or death, 0.77; 95% CI, 0.62 to 0.96; P=0.02). The safety profile of atezolizumab plus carboplatin and etoposide was consistent with the previously reported safety profile of the individual agents, with no new findings observed.
The addition of atezolizumab to chemotherapy in the first-line treatment of extensive-stage small-cell lung cancer resulted in significantly longer overall survival and progression-free survival than chemotherapy alone. (Funded by F. Hoffmann-La Roche/Genentech; IMpower133 ClinicalTrials.gov number, NCT02763579 .).
通过抑制程序性死亡配体 1(PD-L1)-程序性死亡 1(PD-1)信号来增强肿瘤特异性 T 细胞免疫在广泛期小细胞肺癌的治疗中显示出了前景。联合检查点抑制与细胞毒性化疗可能具有协同作用并提高疗效。
我们进行了这项双盲、安慰剂对照、3 期临床试验,以评估在未经治疗的广泛期小细胞肺癌患者中,阿特珠单抗联合卡铂和依托泊苷的疗效。患者以 1:1 的比例随机分配,接受卡铂和依托泊苷联合阿特珠单抗或安慰剂治疗,共 4 个 21 天周期(诱导期),随后进入维持期,在此期间他们接受阿特珠单抗或安慰剂(根据之前的随机分组),直到出现不可接受的毒性作用、根据实体瘤反应评估标准 1.1 进展为疾病进展或无额外临床获益。主要终点是在意向治疗人群中研究者评估的无进展生存期和总生存期。
共有 201 名患者被随机分配至阿特珠单抗组,202 名患者被随机分配至安慰剂组。中位随访 13.9 个月时,阿特珠单抗组的中位总生存期为 12.3 个月,安慰剂组为 10.3 个月(死亡风险比,0.70;95%置信区间 [CI],0.54 至 0.91;P=0.007)。中位无进展生存期分别为 5.2 个月和 4.3 个月(疾病进展或死亡风险比,0.77;95%CI,0.62 至 0.96;P=0.02)。阿特珠单抗联合卡铂和依托泊苷的安全性与之前报道的各单药的安全性一致,未观察到新的发现。
在广泛期小细胞肺癌的一线治疗中,阿特珠单抗联合化疗与单纯化疗相比,显著延长了总生存期和无进展生存期。(由 F. Hoffmann-La Roche/Genentech 资助;IMpower133 ClinicalTrials.gov 编号,NCT02763579)。