Shiozawa Toshihiro, Sekine Ikuo, Aida Yuka, Watanabe Hiroko, Nakazawa Kensuke, Kurishima Koichi, Satoh Hiroaki, Hizawa Nobuyuki
Department of Respiratory Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Department of Medical Oncology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Case Rep Oncol. 2018 Sep 7;11(3):622-632. doi: 10.1159/000492780. eCollection 2018 Sep-Dec.
Sensitive-relapsed small-cell lung cancer (SCLC) is thought to be sensitive to chemotherapy; therefore, second-line chemotherapy is recommended. Although platinum rechallenge is performed in the second-line chemotherapy for sensitive-relapsed SCLC, it remains unclear whether such a strategy is effective.
We retrospectively analyzed the outcome of rechallenge chemotherapy for sensitive-relapsed SCLC. The endpoints of this study were progression-free survival from the time of relapse (PFS-Re) and overall survival from the time of relapse (OS-Re). We also compared the toxicity profile of rechallenge chemotherapy to that of first-line chemotherapy.
Of the 133 SCLC patients who received first-line treatment, 20 patients satisfied the definition of sensitive relapse and received rechallenge chemotherapy. Combined carboplatin and etoposide was the most commonly used rechallenge regimen, and 17 (85%) received it at a reduced dose due to hematological toxicity during the first-line treatment. Median PFS-Re and OS-Re were 4.5 months (95% CI: 3.5-5.4) and 10.5 months (95% CI: 7.9-13.0), respectively. There was no association between dose adjustment and survival. The frequency of hematologic toxicity tended to be lower with rechallenge than first-line treatment. The incidence of grade 3 febrile neutropenia decreased from 40% in first-line treatment to 15% in rechallenge.
Platinum rechallenge could be a useful second-line option for sensitive-relapsed SCLC, having favorable efficacy and safety. Dose adjustment at rechallenge based on the toxicity profile during the first-line chemotherapy could reduce toxicity without weakening efficacy.
敏感复发的小细胞肺癌(SCLC)被认为对化疗敏感;因此,推荐进行二线化疗。尽管在敏感复发SCLC的二线化疗中会进行铂类再挑战,但这种策略是否有效仍不清楚。
我们回顾性分析了敏感复发SCLC再挑战化疗的结果。本研究的终点是从复发时间开始的无进展生存期(PFS-Re)和从复发时间开始的总生存期(OS-Re)。我们还比较了再挑战化疗与一线化疗的毒性特征。
在接受一线治疗的133例SCLC患者中,20例符合敏感复发的定义并接受了再挑战化疗。卡铂联合依托泊苷是最常用的再挑战方案,17例(85%)因一线治疗期间的血液学毒性而接受了减量治疗。PFS-Re和OS-Re的中位数分别为4.5个月(95%CI:3.5-5.4)和10.5个月(95%CI:7.9-13.0)。剂量调整与生存之间无关联。再挑战时血液学毒性的发生率往往低于一线治疗。3级发热性中性粒细胞减少的发生率从一线治疗时的40%降至再挑战时的15%。
铂类再挑战可能是敏感复发SCLC有用的二线选择,具有良好的疗效和安全性。根据一线化疗期间的毒性特征在再挑战时进行剂量调整可降低毒性而不削弱疗效。