Cary Clint, Pedrosa Jose A, Jacob Joseph, Beck Stephen D W, Rice Kevin R, Einhorn Lawrence H, Foster Richard S
Department of Urology, Indiana University School of Medicine, Indianapolis, Indiana.
Melvin and Bren Simon Cancer Center, Indiana University, Indianapolis, Indiana.
Cancer. 2015 Dec 15;121(24):4369-75. doi: 10.1002/cncr.29678. Epub 2015 Sep 15.
Characterizing the role of postchemotherapy retroperitoneal lymph node dissection (PC-RPLND) after high-dose chemotherapy (HDCT) has been limited by small sample sizes. This study reports on survival after HDCT with stem cell support and PC-RPLND as well as histologic findings in the retroperitoneum.
The prospectively maintained testicular cancer database of Indiana University was queried for patients receiving HDCT with stem cell transplantation before PC-RPLND. The cause and date of death were obtained through patient chart review and contact with referring physicians. The Kaplan-Meier method was used to evaluate overall survival (OS). The log-rank test was used for tests of significance. A multivariate, backward, stepwise Cox regression model was built to evaluate predictors of overall mortality.
A total of 92 patients were included in the study. In the entire cohort, the retroperitoneal (RP) histology findings at the time of PC-RPLND were necrosis (26%), teratoma (34%), and cancer (38%). Sixty-six patients (72%) harbored either a teratoma or active cancer in the RP specimen at PC-RPLND. The median follow-up for the entire cohort was 80.6 months. A total of 28 patients (30%) died during follow-up. The 5-year OS rate of the entire cohort was 70%. The most significant predictor of death was PC-RPLND performed in the desperation setting with elevated markers.
Despite these patients being heavily pretreated with multiple cycles of chemotherapy, including HDCT, approximately three-fourths were found to have a teratoma and/or active cancer in the retroperitoneum. This underscores the importance of PC-RPLND for rendering patients free of disease and providing a potential for cure.
大剂量化疗(HDCT)后进行化疗后腹膜后淋巴结清扫术(PC-RPLND)的作用,因样本量小而受到限制。本研究报告了接受HDCT联合干细胞支持及PC-RPLND后的生存率,以及腹膜后的组织学发现。
查询印第安纳大学前瞻性维护的睾丸癌数据库,以获取在PC-RPLND前接受HDCT联合干细胞移植的患者。通过查阅患者病历并与转诊医生联系,获取死亡原因和日期。采用Kaplan-Meier方法评估总生存率(OS)。使用对数秩检验进行显著性检验。构建多变量、向后逐步Cox回归模型,以评估总死亡率的预测因素。
共有92例患者纳入本研究。在整个队列中,PC-RPLND时腹膜后(RP)组织学发现为坏死(26%)、畸胎瘤(34%)和癌(38%)。66例患者(72%)在PC-RPLND时RP标本中存在畸胎瘤或活动性癌。整个队列的中位随访时间为80.6个月。共有28例患者(30%)在随访期间死亡。整个队列的5年OS率为70%。死亡的最显著预测因素是在绝望情况下且标志物升高时进行的PC-RPLND。
尽管这些患者接受了包括HDCT在内的多个周期的强烈预处理,但约四分之三的患者在腹膜后发现有畸胎瘤和/或活动性癌。这突出了PC-RPLND对于使患者无病生存并提供治愈可能性的重要性。