Kudoh S, Fujiwara Y, Takada Y, Yamamoto H, Kinoshita A, Ariyoshi Y, Furuse K, Fukuoka M
First Department of Internal Medicine, Osaka City University Medical School, Osaka, Japan.
J Clin Oncol. 1998 Mar;16(3):1068-74. doi: 10.1200/JCO.1998.16.3.1068.
Irinotecan (CPT-11) is effective against small-cell lung cancer (SCLC) as monotherapy. Cisplatin is also a key drug against SCLC. We conducted a phase II study of CPT-11 combined with cisplatin to evaluate the efficacy and toxicity of this regimen in patients with previously untreated SCLC.
Seventy-five patients with previously untreated SCLC were enrolled onto the study. CPT-11 60 mg/m2 was administered intravenously on days 1, 8, and 15 in combination with cisplatin 60 mg/m2 on day 1 every 28 days. Four courses of chemotherapy followed by thoracic irradiation were given to patients with limited disease (LD) and six courses to patients with extensive disease (ED).
The overall response rate was 84%, with a complete response (CR) rate of 29%. Forty patients with LD achieved an overall response rate of 83% and a CR rate of 30% and 35 patients with ED achieved an overall response rate of 86% and a CR rate of 29%. The median response duration was 8.0 months for LD patients and 6.6 months for ED patients. The median survival was 14.3 months for LD patients and 13.0 months for ED patients. The major grade 3 or 4 toxicities were neutropenia (77%), leukopenia (45%), diarrhea (19%), and anemia (39%). Two patients died with concomitant neutropenia and diarrhea.
This is a new active regimen for SCLC, especially ED-SCLC, with acceptable toxicity. A phase III study that compares CPT-11/cisplatin with etoposide/cisplatin for ED-SCLC is now being conducted.
伊立替康(CPT - 11)作为单一疗法对小细胞肺癌(SCLC)有效。顺铂也是治疗SCLC的关键药物。我们开展了一项CPT - 11联合顺铂的II期研究,以评估该方案对既往未接受治疗的SCLC患者的疗效和毒性。
75例既往未接受治疗的SCLC患者入组本研究。每28天为一周期,第1、8和15天静脉给予CPT - 11 60 mg/m²,同时第1天给予顺铂60 mg/m²。局限期(LD)患者接受4个周期化疗后进行胸部放疗,广泛期(ED)患者接受6个周期化疗。
总缓解率为84%,完全缓解(CR)率为29%。40例LD患者的总缓解率为83%,CR率为30%;35例ED患者的总缓解率为86%,CR率为29%。LD患者的中位缓解持续时间为8.0个月,ED患者为6.6个月。LD患者的中位生存期为14.3个月,ED患者为13.0个月。主要的3级或4级毒性反应为中性粒细胞减少(77%)、白细胞减少(45%)、腹泻(19%)和贫血(39%)。2例患者死于合并的中性粒细胞减少和腹泻。
这是一种治疗SCLC尤其是ED - SCLC的新的有效方案,毒性可接受。目前正在进行一项III期研究,比较CPT - 11/顺铂与依托泊苷/顺铂治疗ED - SCLC的疗效。