Einhorn Lawrence H, Brames Mary J, Juliar Beth, Williams Stephen D
Division of Hematology-Oncology, Indiana University School of Medicine, Walther Cancer Institute, Indianapolis, IN, USA.
J Clin Oncol. 2007 Feb 10;25(5):513-6. doi: 10.1200/JCO.2006.07.7271.
To determine long-term survival and potential cure with salvage chemotherapy with paclitaxel plus gemcitabine after progression after both cisplatin combination chemotherapy and subsequent high-dose chemotherapy with tandem transplantation.
One hundred eighty-four patients received salvage high-dose chemotherapy at Indiana University (Indianapolis, IN) from February 1996 to December 2004. After further evidence of progressive disease, 32 patients were subsequently treated with paclitaxel 100 mg/n2 over 1 hour plus gemcitabine 1,000 mg/m2 over 30 minutes, days 1, 8, and 15 every 4 weeks for a maximum of six courses. This is a retrospective review of this patient population. Patients were evaluated for response, duration of response, and survival. Patients were ineligible if they received prior paclitaxel or gemcitabine.
Ten (31%) of 32 patients achieved objective response, including four partial remissions (2- to 6-month duration) and six complete responses (CRs). Four of these six CRs (12.5% of total patient population) are continuously disease free (NED) with paclitaxel plus gemcitabine alone (no postchemotherapy surgery) at more than 20, 40, 44, and 57 months from start of paclitaxel plus gemcitabine, respectively. One additional CR is currently NED more than 63 months after paclitaxel plus gemcitabine with two subsequent resections of carcinoma.
Long-term disease-free survival is possible with paclitaxel plus gemcitabine in this patient population that progressed after high-dose chemotherapy, and had not received prior paclitaxel or gemcitabine.
确定在顺铂联合化疗及随后的大剂量串联移植化疗进展后,使用紫杉醇联合吉西他滨进行挽救性化疗的长期生存率及潜在治愈率。
1996年2月至2004年12月期间,184例患者在印第安纳大学(印第安纳波利斯,印第安纳州)接受了挽救性大剂量化疗。在出现进一步疾病进展证据后,32例患者随后接受紫杉醇100mg/m²静脉滴注1小时联合吉西他滨1000mg/m²静脉滴注30分钟,于第1、8和15天给药,每4周重复,最多6个疗程。这是对该患者群体的回顾性研究。评估患者的反应、反应持续时间及生存率。若患者之前接受过紫杉醇或吉西他滨治疗,则不符合入组标准。
32例患者中有10例(31%)达到客观反应,包括4例部分缓解(持续2至6个月)和6例完全缓解(CR)。这6例CR中有4例(占总患者群体的12.5%)仅使用紫杉醇联合吉西他滨(化疗后未行手术),分别在开始使用紫杉醇联合吉西他滨后的20、40、44和57个月时持续无疾病证据(NED)。另有1例CR目前在接受紫杉醇联合吉西他滨治疗63个月后仍为NED,随后进行了两次癌切除术。
对于在大剂量化疗后进展且之前未接受过紫杉醇或吉西他滨治疗的该患者群体,使用紫杉醇联合吉西他滨有可能实现长期无病生存。