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- Lucas Goense, Pieter C van der Sluis, van RossumPeter S NPSNDepartment of Surgery, University Medical Center, Utrecht, The Netherlands.Department of Radiation Oncology, University Medical Center, Utrecht, The Netherlands., Sylvia van der Horst, Gert J Meijer, Nadia Haj Mohammad, Marco van Vulpen, Stella Mook, Jelle P Ruurda, and Richard van Hillegersberg.
- Department of Surgery, University Medical Center, Utrecht, The Netherlands.
- J Surg Oncol. 2017 Jun 1; 115 (7): 812-820.
ObjectivesTo evaluate toxicity, pathologic outcome, and survival after perioperative chemotherapy (pCT) compared to neoadjuvant chemoradiotherapy (nCRT) followed by surgery for patients with resectable esophageal or gastroesophageal junction (GEJ) adenocarcinoma.MethodsConsecutive patients with resectable esophageal or GEJ adenocarcinoma who underwent pCT (epirubicin, cisplatin, and capecitabine) or nCRT (paclitaxel, carboplatin, and 41.4 Gy) followed by surgery in a tertiary referral center in the Netherlands were compared. Propensity score matching was applied to create comparable groups.ResultsOf 193 eligible patients, 21 were discarded after propensity score matching; 86 and 86 patients who underwent pCT and nCRT, respectively, remained. Grade ≥3 thromboembolic events occurred only in the pCT group (19% vs. 0%, P < 0.001), whereas grade ≥3 leukopenia occurred more frequently in the nCRT group (14% vs. 4%, P = 0.015). No significant differences regarding postoperative morbidity and mortality were found. Pathologic complete response was more frequently observed with nCRT (18% vs. 11%, P < 0.001), without significantly improving radicality rates (95% vs. 89%, P = 0.149). Both strategies resulted in comparable 3-year progression-free survival (pCT vs. nCRT: 46% vs. 55%, P = 0.344) and overall survival rates (49% vs. 50%, P = 0.934). At 3-year follow-up, fewer locoregional disease progression occurred in the nCRT group (19% vs. 37%, P = 0.024).ConclusionsCompared to perioperative chemotherapy, neoadjuvant chemoradiotherapy achieves higher pathologic response rates and a lower risk of locoregional disease progression, without improving survival.© 2017 Wiley Periodicals, Inc.
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