The role of surgery after prolonged primary chemotherapy for advanced oesophageal adenocarcinoma.


Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
Dec 2021
Historique:
revised: 01 08 2021
received: 01 05 2021
accepted: 02 08 2021
pubmed: 18 8 2021
medline: 24 11 2021
entrez: 17 8 2021
Statut: ppublish

Résumé

Most patients presenting with oesophageal cancer do so with advanced disease not suitable for surgery. However, there are examples of encouraging survival following surgery in highly selected patients who respond well to chemotherapy. This was a retrospective cohort study of patients who presented with advanced but nonvisceral metastatic oesophageal cancer. Consecutive patients on a prolonged primary chemotherapy pathway who underwent surgical resection following a favourable response to chemotherapy were included. Survival and recurrence rates were analysed using Cox regression, providing hazard ratios (HRs) with 95% confidence intervals (CIs). A total of 57 patients included in the cohort operated between 2007 and 2015, the overall median survival was 44 months and the 5-year survival was 42%. Prechemotherapy cN0/cN1 (HR: 0.27, 95% CI: 0.12-0.62) conferred an independent survival advantage compared to cN2 and cN3 disease. Poor differentiation (HR: 2.46, 95% CI: 1.11-5.42), R1 resection (HR: 2.43, 95% CI: 1.14-5.19) and advanced nodal status (HR: 3.28, 95% CI: 1.44-7.47) predicted worse survival on univariable analysis. Poor differentiation (HR: 3.93, 95% CI: 1.62-9.56) was independently associated with poor survival when adjusted for other variables. Patients who present with advanced inoperable oesophageal cancer who have a favourable response to chemotherapy represent a limited group of patients who may benefit from surgery.

Sections du résumé

BACKGROUND BACKGROUND
Most patients presenting with oesophageal cancer do so with advanced disease not suitable for surgery. However, there are examples of encouraging survival following surgery in highly selected patients who respond well to chemotherapy.
METHODS METHODS
This was a retrospective cohort study of patients who presented with advanced but nonvisceral metastatic oesophageal cancer. Consecutive patients on a prolonged primary chemotherapy pathway who underwent surgical resection following a favourable response to chemotherapy were included. Survival and recurrence rates were analysed using Cox regression, providing hazard ratios (HRs) with 95% confidence intervals (CIs).
RESULTS RESULTS
A total of 57 patients included in the cohort operated between 2007 and 2015, the overall median survival was 44 months and the 5-year survival was 42%. Prechemotherapy cN0/cN1 (HR: 0.27, 95% CI: 0.12-0.62) conferred an independent survival advantage compared to cN2 and cN3 disease. Poor differentiation (HR: 2.46, 95% CI: 1.11-5.42), R1 resection (HR: 2.43, 95% CI: 1.14-5.19) and advanced nodal status (HR: 3.28, 95% CI: 1.44-7.47) predicted worse survival on univariable analysis. Poor differentiation (HR: 3.93, 95% CI: 1.62-9.56) was independently associated with poor survival when adjusted for other variables.
CONCLUSION CONCLUSIONS
Patients who present with advanced inoperable oesophageal cancer who have a favourable response to chemotherapy represent a limited group of patients who may benefit from surgery.

Identifiants

pubmed: 34403501
doi: 10.1002/jso.26648
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1296-1305

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Mohamed S Aboul-Enein (MS)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
General Surgery Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

William Knight (W)

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

Wahyu Wulaningsih (W)

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

Daniel M Foley (DM)

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

Dionysios Dellaportas (D)

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

Janine Zylstra (J)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
General Surgery Department, Faculty of Medicine, Tanta University, Tanta, Egypt.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.

Cara R Baker (CR)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Mark Kelly (M)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Elizabeth Smyth (E)

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

Jesper Lagergren (J)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Nick Maisey (N)

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

William H Allum (WH)

Department of Surgery, Royal Marsden Hospital, London, UK.

James A Gossage (JA)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
General Surgery Department, Faculty of Medicine, Tanta University, Tanta, Egypt.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.

David Cunningham (D)

Department of Oncology, Royal Marsden Hospital, London, UK.
Biomedical Research Centre, Institute of Cancer Research, London, UK.

Andrew R Davies (AR)

Department of Surgery, Guy's and St Thomas' Oesophago-Gastric Centre, London, UK.
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

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