TY - JOUR
T1 - Lymph node regression and survival following neoadjuvant chemotherapy in oesophageal adenocarcinoma
AU - Davies, A. R.
AU - Myoteri, D.
AU - Zylstra, J.
AU - Baker, C. R.
AU - Wulaningsih, W.
AU - Van Hemelrijck, M.
AU - Maisey, N.
AU - Allum, W. H.
AU - Smyth, E.
AU - Gossage, J. A.
AU - Lagergren, J.
AU - Cunningham, D.
AU - Green, M.
AU - Kelly, M.
AU - Ngan, S.
AU - Qureshi, A.
AU - Gaya, A.
AU - Griffin, N.
AU - Jacques, A.
AU - Goh, V.
AU - Deere, H.
AU - Chang, F.
AU - Mahadeva, U.
AU - Gill-Barman, B.
AU - George, S.
AU - Dunn, J.
AU - Zeki, S.
AU - Meenan, J.
AU - Hynes, O.
AU - Tham, G.
AU - Iezzi, C.
AU - Dellaportas, D.
AU - Cowie, A.
AU - Knight, W.
AU - Valeri, N.
AU - the Guy's and St Thomas' Oesophago-Gastric Research Group and PROGRESS Study Group
PY - 2018/11/1
Y1 - 2018/11/1
N2 - Background: The aim was to define the pathological response in lymph nodes following neoadjuvant chemotherapy for oesophageal adenocarcinoma and to quantify any associated survival benefit. Methods: Lymph nodes retrieved at oesophagectomy were examined retrospectively by two pathologists for evidence of a response to chemotherapy. Patients were classified as lymph node-negative (either negative nodes with no evidence of previous tumour involvement or negative with evidence of complete regression) or positive (allocated a lymph node regression score based on the proportion of fibrosis to residual tumour). Lymph node responders (score 1, complete response; 2, less than 10 per cent remaining tumour; 3, 10–50 per cent remaining tumour) and non-responders (score 4, more than 50 per cent viable tumour; 5, no response) were compared in survival analyses using Kaplan–Meier and Cox regression analysis. Results: Among 377 patients, 256 had neoadjuvant chemotherapy. Overall, 68 of 256 patients (26·6 per cent) had a lymph node response and 115 (44·9 per cent) did not. The remaining 73 patients (28·5 per cent) had negative lymph nodes with no evidence of regression. Some patients had a lymph node response in the absence of a response in the primary tumour (27 of 99, 27 per cent). Lymph node responders had a significant survival benefit (P < 0·001), even when stratified by patients with or without a response in the primary tumour. On multivariable analysis, lymph node responders had decreased overall (hazard ratio 0·53, 95 per cent c.i. 0·36 to 0·78) and disease-specific (HR 0·42, 0·27 to 0·66) mortality, and experienced reduced local and systemic recurrence. Conclusion: Lymph node regression is a strong prognostic factor and may be more important than response in the primary tumour.
AB - Background: The aim was to define the pathological response in lymph nodes following neoadjuvant chemotherapy for oesophageal adenocarcinoma and to quantify any associated survival benefit. Methods: Lymph nodes retrieved at oesophagectomy were examined retrospectively by two pathologists for evidence of a response to chemotherapy. Patients were classified as lymph node-negative (either negative nodes with no evidence of previous tumour involvement or negative with evidence of complete regression) or positive (allocated a lymph node regression score based on the proportion of fibrosis to residual tumour). Lymph node responders (score 1, complete response; 2, less than 10 per cent remaining tumour; 3, 10–50 per cent remaining tumour) and non-responders (score 4, more than 50 per cent viable tumour; 5, no response) were compared in survival analyses using Kaplan–Meier and Cox regression analysis. Results: Among 377 patients, 256 had neoadjuvant chemotherapy. Overall, 68 of 256 patients (26·6 per cent) had a lymph node response and 115 (44·9 per cent) did not. The remaining 73 patients (28·5 per cent) had negative lymph nodes with no evidence of regression. Some patients had a lymph node response in the absence of a response in the primary tumour (27 of 99, 27 per cent). Lymph node responders had a significant survival benefit (P < 0·001), even when stratified by patients with or without a response in the primary tumour. On multivariable analysis, lymph node responders had decreased overall (hazard ratio 0·53, 95 per cent c.i. 0·36 to 0·78) and disease-specific (HR 0·42, 0·27 to 0·66) mortality, and experienced reduced local and systemic recurrence. Conclusion: Lymph node regression is a strong prognostic factor and may be more important than response in the primary tumour.
UR - http://www.scopus.com/inward/record.url?scp=85054604851&partnerID=8YFLogxK
U2 - 10.1002/bjs.10900
DO - 10.1002/bjs.10900
M3 - Article
C2 - 30047556
AN - SCOPUS:85054604851
SN - 0007-1323
VL - 105
SP - 1639
EP - 1649
JO - British Journal of Surgery
JF - British Journal of Surgery
IS - 12
ER -