Association between clinical complete response and pathological complete response after preoperative chemoradiation in patients with gastroesophageal cancer: analysis in a large cohort

被引:89
作者
Cheedella, N. K. S. [1 ]
Suzuki, A. [1 ]
Xiao, L. [2 ]
Hofstetter, W. L. [3 ]
Maru, D. M. [4 ]
Taketa, T. [1 ]
Sudo, K. [1 ]
Blum, M. A. [1 ]
Lin, S. H. [5 ]
Welch, J. [5 ]
Lee, J. H. [6 ]
Bhutani, M. S. [6 ]
Rice, D. C. [3 ]
Vaporciyan, A. A. [3 ]
Swisher, S. G. [3 ]
Ajani, J. A. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Cardiovasc Surg, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Gastroenterol Hepatol & Nutr, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
clinical complete response; esophageal cancer; multimodality therapy; pathologic complete response; prediction; POSITRON-EMISSION-TOMOGRAPHY; PHASE-III TRIAL; ESOPHAGEAL CANCER; SURGERY; RADIOTHERAPY; CARCINOMA; CHEMORADIOTHERAPY; ADENOCARCINOMA; CHEMOTHERAPY; CISPLATIN;
D O I
10.1093/annonc/mds617
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Chemoradiation followed by surgery is the preferred treatment of localized gastroesophageal cancer (GEC). Surgery causes considerable life-altering consequences and achievement of clinical complete response (clinCR; defined as postchemoradiation [but presurgery] endoscopic biopsy negative for cancer and positron emission tomographic (PET) scan showing physiologic uptake) is an enticement to avoid/delay surgery. We examined the association between clinCR and pathologic complete response (pathCR). Patients and methods: Two hundred eighty-four patients with GEC underwent chemoradiation and esophagectomy. The chi-square test, Fisher exact test, t-test, Kaplan-Meier method, and log-rank test were used. Results: Of 284 patients, 218 (77%) achieved clinCR. However, only 67 (31%) of the 218 achieved pathCR. The sensitivity of clinCR for pathCR was 97.1% (67/69), but the specificity was low (29.8%; 64/215). Of the 66 patients who had less than a clinCR, only 2 (3%) had a pathCR. Thus, the rate of pathCR was significantly different in patients with clinCR than in those with less than a clinCR (P < 0.001). Conclusions: clinCR is not highly associated with pathCR; the specificity of clinCR for pathCR is too low to be used for clinical decision making on delaying/avoiding surgery. Surgery-eligible GEC patients should be encouraged to undergo surgery following chemoradiation despite achieving a clinCR.
引用
收藏
页码:1262 / 1266
页数:5
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