Shin Sang Joon, Ahn Joong Bae, Choi Hye Jin, Cho Byoung Chul, Jeung Hei-Cheul, Rha Sun Young, Chung Hyun Cheol, Roh Jae Kyung
Department of Internal Medicine, Cancer Metastasis Research Center, Yonsei Cancer Center, Yonsei University College of Medicine, 134, Shinchon-Dong, Seodaemun-Ku, Seoul, 120-752, South Korea.
Cancer Chemother Pharmacol. 2008 Jan;61(1):75-81. doi: 10.1007/s00280-007-0447-2. Epub 2007 Mar 21.
Since the combination of capecitabine and irinotecan has successfully been used as a first-line treatment in metastatic colorectal cancer (MCRC), we expected promising results when given as a second-line treatment to metastatic colorectal patients who had been pretreated with 5-Fluorouracil and Oxaliplatin.
Thirty-three MCRC patients participated in this study and received an oral dose of 1,000 mg/m(2 )capecitabine twice daily on days 1-14 and a dose of 100 mg/m(2) irinotecan infused over 90 min on days 1 and 8, every 3 weeks.
The overall response rate in intent-to-treat was 33.3% (95% CI, 21.5-58.3%), including one complete response (3.0%) and ten partial responses (30.3%); 12 patients (36.4%) had disease stabilization and only 9 (27.3%) progressed. The median time to progression was 6.7 months (95% CI, 4.8-8.6 months). After a median follow-up time of 12 months, nine patients (27.3%) were still alive with metastatic disease. The median response duration for all patients was 6.7 months (95% CI, 3.9-9.5 months) and the median overall survival was 13.4 months (95% CI, 11.0-15.8 months) with a 1-year survival rate of 55.4%. Myelosuppression was commonly observed; NCI-CTC (v 2.0) grade 3/4 neutropenia, however, occurred in eight (24%) patients and grade 3 anemia was seen in one patient (3%). The most common (grade 3/4) non-hematological toxicity was diarrhea (15%) and the other severe grade 3/4 toxicities included nausea/vomiting in one patient (3%), stomatitis in one patient (3%), hand-foot syndrome in one patient (3%).
The combination of capecitabine and irinotecan is an effective and well-tolerated regimen for second-line treatment of metastatic colorectal cancer. However, further phase III trials are required to clarify its use in the treatment of metastastic colorectal cancer patients who have been pretreated with 5-fluorouracil and oxaliplatin.
鉴于卡培他滨与伊立替康联合用药已成功用于转移性结直肠癌(MCRC)的一线治疗,我们预期将其用于经5-氟尿嘧啶和奥沙利铂预处理的转移性结直肠癌患者的二线治疗时会取得良好效果。
33例MCRC患者参与本研究,在第1 - 14天每天口服2次卡培他滨,剂量为1000mg/m²,在第1天和第8天静脉输注伊立替康100mg/m²,持续90分钟,每3周重复一次。
意向性治疗的总缓解率为33.3%(95%CI,21.5 - 58.3%),包括1例完全缓解(3.0%)和10例部分缓解(30.3%);12例患者(36.4%)病情稳定,仅9例(27.3%)进展。中位疾病进展时间为6.7个月(95%CI,4.8 - 8.6个月)。中位随访12个月后,9例患者(27.3%)仍有转移性疾病存活。所有患者的中位缓解持续时间为6.7个月(95%CI,3.9 - 9.5个月),中位总生存期为13.4个月(95%CI,11.0 - 15.8个月),1年生存率为55.4%。常见骨髓抑制;然而,美国国立癌症研究所常见毒性标准(v2.0)3/4级中性粒细胞减少症发生在8例(24%)患者中,1例患者(3%)出现3级贫血。最常见的(3/4级)非血液学毒性是腹泻(15%),其他严重的3/4级毒性包括1例患者出现恶心/呕吐(3%)、1例患者出现口腔炎(3%)、1例患者出现手足综合征(3%)。
卡培他滨与伊立替康联合用药是转移性结直肠癌二线治疗的有效且耐受性良好的方案。然而,需要进一步的III期试验来明确其在经5-氟尿嘧啶和奥沙利铂预处理的转移性结直肠癌患者治疗中的应用。