Zhang Xiang-Ru, Zhu Yun-Zhong, Xiu Qing-Yu, Han Fu-Cai, Liu Duan-Qi, Chu Da-Tong
Department of Medical Oncology, Cancer Hospital (Institute), Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100021, China.
Zhonghua Zhong Liu Za Zhi. 2006 Oct;28(10):777-9.
To evaluate the efficacy and adverse events of irinotecan (CPT-11) combined with cisplatin (DDP) in the treatment of patients with advanced non-small cell lung cancer (NSCLC).
Of 36 NSCLC patients consisting of 23 males and 13 females with a medium age of 52 years included, there were 26 adenocarcinomas, 7 squamous cell carcinomas, 1 adeno-squamous cell carcinoma and 2 unclassified types; 13 stage III B and 23 stage IV; 24 chemonaive and 12 previously treated by chemotherapy with a medium Karnofsky status of 90. All patients had measurable or evaluable parameters. The regimen was administered as following: CPT-11 60 mg/m2, IV, D1, 8 and 15; DDP 80 mg/m2, IV, D1; every 28 days as a cycle.
Totally, 97 cycles were carried out in these 36 patients with a medium cycles of 3. Of 35 evaluable patients, 22.9% (8/35) achieved partial response, 60.0% (21/35) had stable disease and 17.1% (6/35) progressive disease. The response rate was 29.2% (7/24) for chemonaive patients and 9.1% (1/11) for these previously treated. The 1-year survival rate was 45.4% with a medium time to tumor progression (TTP) of 199 days for the responders. The incidence rate of grade III/IV adverse events were: 16.7% for neutropenia, 13.9% alopecia, 5.6% diarrhea, 2.8% nausea and vomiting, respectively.
Irinotecan plus cisplatin is effective with tolerable adverse events in treating patients with advanced non-small cell lung cancer, but further investigation trials are needed.
评估伊立替康(CPT-11)联合顺铂(DDP)治疗晚期非小细胞肺癌(NSCLC)患者的疗效及不良事件。
纳入36例NSCLC患者,其中男性23例,女性13例,中位年龄52岁。腺癌26例,鳞癌7例,腺鳞癌1例,未分类2例;ⅢB期13例,Ⅳ期23例;初治24例,曾接受化疗12例,中位卡氏评分90分。所有患者均有可测量或可评估指标。治疗方案如下:CPT-11 60 mg/m²,静脉滴注,第1、8和15天;DDP 80 mg/m²,静脉滴注,第1天;每28天为1个周期。
36例患者共进行97个周期化疗,中位周期数为3个。35例可评估患者中,部分缓解率为22.9%(8/35),疾病稳定率为60.0%(21/35),疾病进展率为17.1%(6/35)。初治患者缓解率为29.2%(7/24),曾接受化疗患者缓解率为9.1%(1/11)。缓解者1年生存率为45.4%,中位肿瘤进展时间(TTP)为199天。Ⅲ/Ⅳ级不良事件发生率分别为:中性粒细胞减少16.7%,脱发13.9%,腹泻5.6%,恶心呕吐2.8%。
伊立替康联合顺铂治疗晚期非小细胞肺癌有效,不良事件可耐受,但仍需进一步研究试验。