Blum Murphy Mariela, Xiao Lianchum, Patel Viren R, Maru Dipen M, Correa Arlene M, G Amlashi Fatemeh, Liao Zhongxing, Komaki Ritsuko, Lin Steven H, Skinner Heath D, Vaporciyan Ara, Walsh Garrett L, Swisher Stephen G, Sepesi Boris, Lee Jeffrey H, Bhutani Manoop S, Weston Brian, Hofstetter Wayne L, Ajani Jaffer A
Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2017 Nov 1;123(21):4106-4113. doi: 10.1002/cncr.30953. Epub 2017 Sep 8.
Reports are limited regarding clinical and pretreatment features that might predict a pathological complete response (pathCR) after treatment in patients with esophageal cancer (EC). This might allow patient selection for different strategies. This study examines the association of a pathCR with pretreatment variables, overall survival (OS), recurrence-free survival (RFS), and patterns of recurrence in a large cohort from a single institution.
The baseline clinical features of 911 consecutive patients with EC who were treated with trimodality therapy from January 2000 to November 2013 were analyzed. A pathCR was defined as a surgical specimen with no residual carcinoma (primary or nodes). Logistic regressions were used to identify independent baseline features associated with a pathCR. We applied log-rank testing and Cox models to determine the association between a pathCR and the time-to-event outcomes (OS and RFS).
Of 911 patients, 218 (23.9%) achieved a pathCR. The pathCR rate was 23.1% for adenocarcinoma and 32.2% for squamous cell carcinoma. A lower pathCR rate was observed for 1) older patients (>60 years), 2) patients with poorly differentiated tumors, 3) patients with signet ring cells (SRCs), and 4) patients with a higher T stage. Patients with a pathCR had longer OS and RFS than those without a pathCR (P = .0021 and P = .0011, respectively). Recurrences occurred more in non-pathCR patients. Distant metastases were the most common type of recurrence. PathCR patients developed brain metastases at a marginally higher rate than non-pathCR patients (P = .051).
In this large cohort study, a pathCR is confirmed to be associated with better OS and RFS. The presence of a poorly differentiated tumor or SRCs reduces the likelihood of a pathCR. Future research should focus on molecular classifiers. Cancer 2017;123:4106-4113. © 2017 American Cancer Society.
关于食管癌(EC)患者治疗后可能预测病理完全缓解(pathCR)的临床和治疗前特征的报道有限。这可能有助于为不同治疗策略选择合适的患者。本研究在一个来自单一机构的大型队列中,考察了pathCR与治疗前变量、总生存期(OS)、无复发生存期(RFS)以及复发模式之间的关联。
分析了2000年1月至2013年11月期间连续接受三联疗法治疗的911例EC患者的基线临床特征。pathCR定义为手术标本中无残留癌(原发灶或淋巴结)。采用逻辑回归分析来确定与pathCR相关的独立基线特征。我们应用对数秩检验和Cox模型来确定pathCR与事件发生时间结局(OS和RFS)之间的关联。
911例患者中,218例(23.9%)达到pathCR。腺癌的pathCR率为23.1%,鳞状细胞癌为32.2%。在以下患者中观察到较低的pathCR率:1)老年患者(>60岁);2)肿瘤分化差的患者;3)印戒细胞(SRC)患者;4)T分期较高的患者。达到pathCR的患者比未达到pathCR的患者具有更长的OS和RFS(分别为P = 0.0021和P = 0.0011)。非pathCR患者的复发更多。远处转移是最常见的复发类型。pathCR患者发生脑转移的比例略高于非pathCR患者(P = 0.051)。
在这项大型队列研究中,证实pathCR与更好的OS和RFS相关。肿瘤分化差或存在SRC会降低pathCR的可能性。未来的研究应聚焦于分子分类器。《癌症》2017年;123:4106 - 4113。©2017美国癌症协会