Lymph node regression and survival following neoadjuvant chemotherapy in oesophageal adenocarcinoma

Author:

Davies A R123ORCID,Myoteri D4,Zylstra J123,Baker C R12,Wulaningsih W5,Van Hemelrijck M5ORCID,Maisey N6,Allum W H7,Smyth E7,Gossage J A123,Lagergren J123,Cunningham D78,Green M4,Kelly M9,Ngan S10,Qureshi A10,Gaya A10,Griffin N11,Jacques A11,Goh V11,Deere H9,Chang F9,Mahadeva U9,Gill-Barman B9,George S9,Dunn J11,Zeki S11,Meenan J11,Hynes O9,Tham G9,Iezzi C9,Dellaportas D9,Cowie A9,Knight W12,Valeri N13

Affiliation:

1. Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK

2. Gastrointestinal Cancer, King's College London, London, UK

3. Upper Gastrointestinal Surgery, Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden

4. Department of Cellular Pathology, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK

5. Translational Oncology and Urology Research, School of Cancer Sciences, King's College London, London, UK

6. Department of Oncology, Guy's Cancer Centre, Guy's Hospital, London, UK

7. Department of Oncology, Royal Marsden Hospital, London, UK

8. Institute of Cancer Research, London, UK

9. Guy's and St Thomas’ Oesophago-Gastric Centre, London, UK

10. Guy's Cancer Centre, Guy's Hospital, London, UK

11. Guy's and St Thomas’ NHS Foundation Trust, London, UK

12. Guy's and St Thomas’ Oesophago-Gastric Centre, and School of Cancer Sciences, King's College London, London, UK

13. Royal Marsden Hospital and Institute of Cancer Research, London, UK

Abstract

Abstract 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.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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