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The influence of Circumferential Resection Margin Status on Loco-Regional Recurrence in Esophageal Squamous Cell Carcinoma

Authors
Park, Hae JinKim, Hak JaeChie, Eui KyuKang, Chang HyunKim, Young Tae
Issue Date
Jun-2013
Publisher
WILEY-BLACKWELL
Keywords
circumferential resection margin; esophageal squamous cell carcinoma; radiotherapy
Citation
JOURNAL OF SURGICAL ONCOLOGY, v.107, no.7, pp.762 - 766
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF SURGICAL ONCOLOGY
Volume
107
Number
7
Start Page
762
End Page
766
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/162521
DOI
10.1002/jso.23313
ISSN
0022-4790
Abstract
Background To analyze treatment outcomes and patterns of recurrence, and to examine the impact of adjuvant postoperative radiotherapy (PORT) after esophagectomy in esophageal squamous cell carcinoma (SqCC) regarding the status of circumferential resection margin (CRM). Patients and Methods We performed a retrospective review of esophageal cancer patients operated in Seoul National University Hospital between 2003 and 2010. Pathologically proven T3 SqCC patients with written reports mentioning the status of CRM were selected. Fifty-nine out of 71 patients (83.1%) had CRM+. Twenty-eight patients had radiotherapy in CRM+ and CRM, respectively. The median follow-up period was 17.1 months (range: 5.263.1). Results Median survival and 2-year overall survival were 13.8 months and 41.9% in CRM+, and 27.3 months and 74.1% in CRM, respectively. Loco-regional relapse-free survival (LRRFS) rate at 2 years was 33.6% and 74.1% in each groups (P=0.029). Loco-regional recurrence was the major pattern of failure in CRM+. PORT did not improve LRRFS. Conclusion The esophageal SqCC patients with CRM+ after resection showed worse LRRFS. This finding validated the prognostic value of CRM status. Nevertheless, we failed to demonstrate the benefits of adjuvant PORT in CRM+. This might suggest the necessity of neoadjuvant therapy to decrease the CRM+ rate after esophagectomy.
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COLLEGE OF MEDICINE (DEPARTMENT OF RADIATION ONCOLOGY)
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