Fields Abbie L, Einstein Mark H, Novetsky Akiva P, Gebb Juliana, Goldberg Gary L
Virginia Gynecologic Oncology, 7603 Forest Avenue, Suite 207, Richmond, VA 23229, USA.
Gynecol Oncol. 2008 Jan;108(1):201-6. doi: 10.1016/j.ygyno.2007.09.025. Epub 2007 Nov 8.
To evaluate disease-free survival (DFS) and overall survival (OS) in patients treated with pelvic radiation "sandwiched" between six cycles of paclitaxel(T)/platinum(P) chemotherapy with optimally reduced uterine papillary serous carcinoma (UPSC).
Surgically staged patients with UPSC and no visible residual disease were enrolled. Treatment involved T (175 mg/m2) and either cisplatin (75 mg/m2) or carboplatin (AUC=6.0, 6.5, 7.5) every 21 days x 3 doses, followed by pelvic RT (45 Gy). Fields were extended for >2 positive pelvic or confirmed para-aortic node disease. Three additional cycles of T/P were administered after RT. Toxicity was graded by NCI CTC Version 3.0. Kaplan-Meier survival statistics were used for DFS/OS.
30 women were enrolled between 1999 and 2004. Median age was 69 years (45-82 years). 60% (18/30) of patients had disease confined to the uterus (Stage I/II) and 40% (12/30) had extra-uterine disease (Stage III/IV). 29 patients completed protocol treatment. One patient was discontinued due to non-compliance and recurred at 7 months. All 30 patients are included in survival analysis. Three-year DFS and OS with Stage I/II disease was 69% and 75% and Stage III/IV disease was 54% and 52%, respectively. Of 177 chemotherapy cycles administered, grade 3 or 4 neutropenia, thrombocytopenia or anemia occurred in 42%, 1% and 3% of cycles, respectively. Six cycles were delayed 1 week for neutropenia. 43% of all neutropenic episodes occurred after RT.
Radiation "sandwiched" between T/P chemotherapy is a well-tolerated and efficacious regimen for patients with completely resected UPSC. A larger multi-institutional clinical trial should be considered to confirm these pilot data.
评估接受盆腔放疗“夹在”六个周期紫杉醇(T)/铂类(P)化疗之间治疗的子宫浆液性乳头状癌(UPSC)患者的无病生存期(DFS)和总生存期(OS),化疗方案为优化减量方案。
纳入手术分期为UPSC且无可见残留病灶的患者。治疗方案为每21天给予T(175mg/m²)和顺铂(75mg/m²)或卡铂(AUC = 6.0、6.5、7.5),共3剂,随后进行盆腔放疗(45Gy)。对于盆腔淋巴结阳性>2个或证实有腹主动脉旁淋巴结转移的患者,放疗野扩大。放疗后再给予3个周期的T/P化疗。毒性反应按照美国国立癌症研究所(NCI)不良事件通用术语标准(CTC)第3.0版进行分级。采用Kaplan-Meier生存统计方法计算DFS/OS。
1999年至2004年间共纳入了30名女性患者。中位年龄为69岁(45 - 82岁)。60%(18/30)的患者疾病局限于子宫(I/II期),40%(12/30)的患者有子宫外疾病(III/IV期)。29名患者完成了方案治疗。1名患者因不依从治疗而中断治疗,7个月后复发。所有30名患者均纳入生存分析。I/II期疾病的三年DFS和OS分别为69%和75%,III/IV期疾病的三年DFS和OS分别为54%和52%。在总共177个化疗周期中,3/4级中性粒细胞减少、血小板减少或贫血分别发生在42%、1%和3%的周期中。6个周期因中性粒细胞减少而推迟1周。所有中性粒细胞减少事件的43%发生在放疗后。
对于完全切除的UPSC患者,T/P化疗“夹着”放疗是一种耐受性良好且有效的治疗方案。应考虑开展更大规模的多机构临床试验以证实这些初步数据。