Saif M W, Hashmi Shahrukh, Zelterman Daniel, Almhanna Khaldoun, Kim Richard
Section of Medical Oncology, Yale University School of Medicine, 333 Cedar Street, FMP 116, New Haven, CT 06520, USA.
Int J Colorectal Dis. 2008 Feb;23(2):139-45. doi: 10.1007/s00384-007-0382-z. Epub 2007 Oct 2.
Standard therapy for locally advanced rectal cancer (LARC) is concurrent neo-adjuvant chemo-radiation using infusional 5-fluorouracil (CIV-5-FU). Capecitabine (CAP) offers a convenient oral replacement for CIV-5-FU. There is no randomized trial comparing infusional 5-FU to capecitabine. We retrospectively compared the safety and efficacy of CAP-based regimens with well-established CIV-5-FU-based regimens in LARC.
We collected published data on 542 patients treated on either CIV-5-FU (197) or CAP (345) with concurrent radiation (external radiation treatment, XRT) for LARC. This included Phase I or II studies published or available from Pubmed. Safety was assessed by determining proportion of patients who experienced grade III/IV adverse effects. Efficacy was assessed by determining pathological complete response (pCR). Chi-square tests were used to compare the two regimens. A P value less than 0.05 was considered statistically significant. Statistical tests were further corrected for multiplicity using the method of Benjamini and Yekutieli (Ann Stat, 29(4):1165-1188, 2001).
pCR was significantly higher in patients getting CAP vs CIV-5-FU (25 vs 13%; P = 0.008,.P adj = 0.034). Both regimens were generally well tolerated. There was no grade IV toxicity reported. Grade III hand foot syndrome was more common in the CAP group, and grade III diarrhea was more common in the CIV group.
CAP when compared to CIV seems to have superior efficacy with reasonable toxicities. It is reasonable to treat LARC with CAP + XRT.
局部晚期直肠癌(LARC)的标准治疗是使用持续静脉输注5-氟尿嘧啶(CIV-5-FU)进行同步新辅助放化疗。卡培他滨(CAP)为CIV-5-FU提供了一种方便的口服替代药物。尚无比较持续静脉输注5-氟尿嘧啶与卡培他滨的随机试验。我们回顾性比较了基于CAP的方案与已确立的基于CIV-5-FU的方案在LARC中的安全性和疗效。
我们收集了已发表的关于542例接受CIV-5-FU(197例)或CAP(345例)同步放疗(外照射治疗,XRT)治疗LARC患者的数据。这包括在Pubmed上发表或可获取的I期或II期研究。通过确定发生III/IV级不良反应的患者比例来评估安全性。通过确定病理完全缓解(pCR)来评估疗效。采用卡方检验比较两种方案。P值小于0.05被认为具有统计学意义。使用Benjamini和Yekutieli方法(《统计学年鉴》,29(4):1165 - 1188,2001年)对统计检验进行多重性校正。
接受CAP治疗的患者pCR显著高于接受CIV-5-FU治疗的患者(25%对13%;P = 0.008,P校正 = 0.034)。两种方案总体耐受性良好。未报告IV级毒性反应。III级手足综合征在CAP组更常见,III级腹泻在CIV组更常见。
与CIV相比,CAP似乎具有更好的疗效且毒性合理。用CAP + XRT治疗LARC是合理的。