Neoadjuvant and Definitive Radiochemotherapeutic Approaches in Esophageal Cancer: A Retrospective Evaluation of 122 Cases in Daily Clinical Routine.


Journal

Oncology research and treatment
ISSN: 2296-5262
Titre abrégé: Oncol Res Treat
Pays: Switzerland
ID NLM: 101627692

Informations de publication

Date de publication:
2020
Historique:
received: 01 10 2019
accepted: 04 04 2020
pubmed: 3 6 2020
medline: 25 9 2020
entrez: 3 6 2020
Statut: ppublish

Résumé

Esophageal cancer (EC) is a common malignant tumor entity with increasing occurrence. The incidence of esophageal adenocarcinoma (AC), particularly, is constantly rising in the Western world. The mainstays of therapy with curative intent for EC in advanced stages are neoadjuvant radiochemotherapy (neoRCT) with surgery and definitive radiochemotherapy (defRCT). We examined our internal files to identify patients suffering from EC. Palliative cases were excluded. Statistical testing was performed by χ2 test, Student's t test, Kaplan-Meier analyses, and the Mann-Whitney U test. One hundred and twenty-two cases were included. Histology revealed squamous cell carcinoma in 92 cases and AC in 23 cases. Ninety-five patients underwent defRCT, 27 underwent neoRCT, and 114 (in both therapy regimes) received simultaneous chemotherapy. There was no difference in the overall survival (OS) (p = 0.654; HR 1.145; 95% CI 0.629-2.086) or and progression-free survival (PFS) (p = 0.912) of patients who underwent neoRCT or defRCT. Median OS was 13.5 (2-197) months for defRCT patients and 19.5 (2-134) months for neoRCT patients (p = 0.751). Karnofsky index (KI) with a cut-off of 70% was strongest, but not a significant parameter for OS (p = 0.608) or PFS (p = 0.137). defRCT is a valid and an equal alternative to neoRCT for patients suffering from EC. Selection of patients for therapy is of crucial relevance. Further studies and improvements in follow-up are needed when neoRCT has been completed before surgery, in order to spare the patient undergoing operative treatment if there is complete remission. The identification of valid markers urgently needed to limit treatment side effects.

Identifiants

pubmed: 32485721
pii: 000507737
doi: 10.1159/000507737
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

372-379

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Patrick Mayr (P)

Department of Radio-Oncology, University Hospital of Augsburg, Augsburg, Germany, patrick.mayr@uk-augsburg.de.
Department of Hematology and Oncology, University Hospital of Augsburg, Augsburg, Germany, patrick.mayr@uk-augsburg.de.

Benedikt Martin (B)

Department of Pathology, University Hospital of Augsburg, Augsburg, Germany.

Verena Fries (V)

Department of Radio-Oncology, University Hospital of Augsburg, Augsburg, Germany.

Rainer Claus (R)

Department of Hematology and Oncology, University Hospital of Augsburg, Augsburg, Germany.

Matthias Anthuber (M)

Department of Surgery, University Hospital of Augsburg, Augsburg, Germany.

Helmut Messmann (H)

Department of Gastroenterology, University Hospital of Augsburg, Augsburg, Germany.

Gerhard Schenkirsch (G)

Department of Tumor Data Management, University Hospital of Augsburg, Augsburg, Germany.

Vera Blodow (V)

Department of Nuclear Medicine, University Hospital of Augsburg, Augsburg, Germany.

Klaus Henning Kahl (KH)

Department of Radio-Oncology, University Hospital of Augsburg, Augsburg, Germany.

Georg Stüben (G)

Department of Radio-Oncology, University Hospital of Augsburg, Augsburg, Germany.

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Classifications MeSH