4.7 Article

A randomized clinical trial of neoadjuvant chemotherapy versus neoadjuvant chemoradiotherapy for cancer of the oesophagus or gastro-oesophageal junction

期刊

ANNALS OF ONCOLOGY
卷 27, 期 4, 页码 660-667

出版社

OXFORD UNIV PRESS
DOI: 10.1093/annonc/mdw010

关键词

oesophageal carcinoma; neoadjuvant treatment; chemotherapy; chemoradiotherapy

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资金

  1. Swedish Society of Medicine
  2. Swedish Cancer Society
  3. Cancer Research Foundations of Radiumhemmet
  4. Stockholm County Council

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Neoadjuvant chemoradiotherapy gives increased local tumour control compared with neoadjuvant chemotherapy, without significantly affecting survival in oesophageal cancer.Neoadjuvant therapy improves long-term survival after oesophagectomy, treating oesophageal cancer, but the evidence to date is insufficient to determine which of the two main neoadjuvant therapy types, chemotherapy (nCT) or chemoradiotherapy (nCRT), is more beneficial. We aimed to compare the effects of nCT with those of nCRT. This multicentre trial, which was conducted in Sweden and Norway, recruited 181 patients with carcinoma of the oesophagus or the gastro-oesophageal junction who were candidates for curative-intended treatment. The primary end point was histological complete response after neoadjuvant treatment, which has been shown to be correlated with increased long-term survival. Study participants were randomized to nCT or nCRT, followed by surgery with two-field lymphadenectomy. Three cycles of platin/5-fluorouracil were administered in both arms, whereas 40 Gy of concomitant radiotherapy was added in the nCRT arm. The trial met the primary end point, histological complete response being achieved in 28% after nCRT versus 9% after nCT (P = 0.002). Lymph-node metastases were observed in 62% in the nCT group versus 35% in the nCRT group (P = 0.001). The R0 resection rate was 87% after nCRT and 74% after nCT (P = 0.04). There was no difference in overall survival between the treatment arms. The addition of radiotherapy to neoadjuvant chemotherapy results in higher histological complete response rate, higher R0 resection rate, and a lower frequency of lymph-node metastases, without significantly affecting survival. NCT01362127 (; The full study protocol was registered in the Clinical Trials Database).

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