Pathologic Lymph Node Regression After Neoadjuvant Chemotherapy Predicts Recurrence and Survival in Esophageal Adenocarcinoma: A Multicenter Study in the United Kingdom

Author:

Moore Jonathan L.12ORCID,Green Michael3,Santaolalla Aida2,Deere Harriet3,Evans Richard P.T.4,Elshafie Mona5,Lavery Anita6ORCID,McManus Damian T.7,McGuigan Andrew6ORCID,Douglas Rosalie6ORCID,Horne Joanne8,Walker Robert9ORCID,Mir Hira10,Terlizzo Monica10,Kamarajah Sivesh K.5ORCID,Van Hemelrijck Mieke2,Maisey Nick11,Sita-Lumsden Ailsa11,Ngan Sarah11,Kelly Mark12ORCID,Baker Cara R.12,Kumar Sacheen12ORCID,Lagergren Jesper1213ORCID,Allum William H.12,Gossage James A.12,Griffiths Ewen A.5ORCID,Grabsch Heike I.1415ORCID,Turkington Richard C.6ORCID,Underwood Tim J.9ORCID,Smyth Elizabeth C.16,Fitzgerald Rebecca C.1718ORCID,Cunningham David19ORCID,Davies Andrew R.12,Puig S.,Chaudry A.,Jacques A.,Griffin N.,Goh V.,Owczarczyk K.,Qureshi A,Subesinghe M.,Chang F.,Mahadeva U.,Gill-Barman B.,George S.,Ong M.,Waters J.,Cominos M.,Sevitt T.,Hill M.,Hynes O.,Tham G.,Knight W R C,Dunn J. M.,Zeki S. S.,

Affiliation:

1. Department of Upper Gastrointestinal and General Surgery, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom

2. School of Cancer and Pharmaceutical Sciences, King's College London, United Kingdom

3. Department of Histopathology, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom

4. Department of Upper Gastrointestinal Surgery, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom

5. Department of Pathology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom

6. Patrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom

7. Department of Pathology, Royal Victoria Hospital, Belfast Health and Social Care Trust, Belfast, United Kingdom

8. Department of Histopathology, University Hospitals Southampton NHS Foundation Trust, Southampton, United Kingdom

9. School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom

10. Department of Histopathology, The Royal Marsden NHS Foundation Trust, London, United Kingdom

11. Department of Medical Oncology, St Thomas' Hospital, London, United Kingdom

12. Department of Upper Gastrointestinal Surgery, The Royal Marsden NHS Foundation Trust, London, United Kingdom

13. Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden

14. Department of Pathology, GROW School for Oncology and Reproduction, Maastricht University Medical Center+, Maastricht, the Netherlands

15. Division of Pathology and Data Analytics, Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, United Kingdom

16. Department of Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom

17. Early Cancer Institute, University of Cambridge and Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom

18. Department of Gastroenterology, Addenbrooke's Hospital, Cambridge University NHS Foundation Trust, Cambridge, United Kingdom

19. Department of Medical Oncology, The Royal Marsden Hospital, London, United Kingdom

Abstract

PURPOSE There is limited evidence regarding the prognostic effects of pathologic lymph node (LN) regression after neoadjuvant chemotherapy for esophageal adenocarcinoma, and a definition of LN response is lacking. This study aimed to evaluate how LN regression influences survival after surgery for esophageal adenocarcinoma. METHODS Multicenter cohort study of patients with esophageal adenocarcinoma treated with neoadjuvant chemotherapy followed by surgical resection at five high-volume centers in the United Kingdom. LNs retrieved at esophagectomy were examined for chemotherapy response and given a LN regression score (LNRS)—LNRS 1, complete response; 2, <10% residual tumor; 3, 10%-50% residual tumor; 4, >50% residual tumor; and 5, no response. Survival analysis was performed using Cox regression adjusting for confounders including primary tumor regression. The discriminatory ability of different LN response classifications to predict survival was evaluated using Akaike information criterion and Harrell C-index. RESULTS In total, 17,930 LNs from 763 patients were examined. LN response classified as complete LN response (LNRS 1 ≥1 LN, no residual tumor in any LN; n = 62, 8.1%), partial LN response (LNRS 1-3 ≥1 LN, residual tumor ≥1 LN; n = 155, 20.3%), poor/no LN response (LNRS 4-5; n = 303, 39.7%), or LN negative (no tumor/regression; n = 243, 31.8%) demonstrated superior discriminatory ability. Mortality was reduced in patients with complete LN response (hazard ratio [HR], 0.35; 95% CI, 0.22 to 0.56), partial LN response (HR, 0.72; 95% CI, 0.57 to 0.93) or negative LNs (HR, 0.32; 95% CI, 0.25 to 0.42) compared with those with poor/no LN response. Primary tumor regression and LN regression were discordant in 165 patients (21.9%). CONCLUSION Pathologic LN regression after neoadjuvant chemotherapy was a strong prognostic factor and provides important information beyond pathologic TNM staging and primary tumor regression grading. LN regression should be included as standard in the pathologic reporting of esophagectomy specimens.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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