Deep regional hyperthermia with preoperative radiochemotherapy in locally advanced rectal cancer, a prospective phase II trial.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
06 2021
Historique:
received: 29 12 2020
revised: 07 03 2021
accepted: 08 03 2021
pubmed: 21 3 2021
medline: 29 6 2021
entrez: 20 3 2021
Statut: ppublish

Résumé

The goal of the present study was to investigate the effect of deep regional hyperthermia on early and long-term oncological outcomes in the context of preoperative radiochemotherapy in rectal cancer. In this prospective phase II trial, patients with locally advanced rectal cancer were treated with 5-fluorouracil based preoperative radiochemotherapy with 50.4 Gy in 28 fractions. Deep regional hyperthermia was scheduled twice weekly. Pathological tumor regression was scored according to the Dworak regression system. The primary endpoint was pathological complete response (pCR). Further endpoints were local control (LC), distant control (DC), disease-free survival (DFS) and overall survival (OS). Hyperthermia was defined as feasible if 70% of patients received at least eight treatments. Quality of life was assessed at follow-up by the EORTC-QLQ-C30 and QLQ-CR29 questionnaires. Time to event data was analyzed according to Kaplan-Meier based on first-events. The study was registered on clinicaltrials.gov (NCT02353858). From 2012 until 2017, 78 patients were recruited. Median follow-up was 54 months. Based on magnetic resonance imaging, the mesorectal fascia was involved or threatened in 60% of the patients. Compliance with radiotherapy was 99%, 91% received both cycles of chemotherapy and 77% had eight or more hyperthermia treatments. Median time from the end of radiotherapy to surgery was 6.7 weeks. A pathological complete response was reported in 14% of the patients, 50% had either Dworak 4 (complete regression) or Dworak 3 regression (scattered tumor cells only). Three year estimates for OS, DFS, LC and DC were 94%, 81%, 96% and 87%. Patients with higher hyperthermia related cumulative temperatures showed stronger tumor regression. Global health status based on EORTC-QLQ-C30 was comparable with data from the general population. Deep regional hyperthermia was feasible, did not compromise standard treatments and resulted in promising long-term oncological outcomes and QoL.

Identifiants

pubmed: 33741467
pii: S0167-8140(21)06137-5
doi: 10.1016/j.radonc.2021.03.011
pii:
doi:

Substances chimiques

Fluorouracil U3P01618RT

Banques de données

ClinicalTrials.gov
['NCT02353858']

Types de publication

Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-160

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The Department of Radiation Oncology Tübingen receives within the frame of research agreements financial and technical support as well as sponsoring for travels and scientific symposia from: Elekta AB (Stockholm, Sweden), Dr. Sennewald GmbH, Philips GmbH, Siemens, PTW Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH.

Auteurs

Cihan Gani (C)

University Hospital Tübingen, Department of Radiation Oncology, Germany; German Cancer Research Center (DKFZ) Heidelberg and German Consortium for Translational Cancer Research (DKTK), Partner Site Tübingen, Germany. Electronic address: cihan.gani@med.uni-tuebingen.de.

Ulf Lamprecht (U)

University Hospital Tübingen, Department of Radiation Oncology, Germany.

Alexander Ziegler (A)

Department of Internal Medicine, Oncology/Hematology, Gastroenterology, Hospital Esslingen GmbH, Germany.

Matthias Moll (M)

Department of Radiation Oncology, Medical University of Vienna, Wien, Austria.

Johanna Gellermann (J)

Praxis/Zentrum für Strahlentherapie und Radioonkologie, Berlin, Germany.

Vanessa Heinrich (V)

University Hospital Tübingen, Department of Radiation Oncology, Germany.

Svetlana Wenz (S)

Institute of Pathology and Neuropathology, Eberhard-Karls University, Tuebingen, Germany.

Falko Fend (F)

German Cancer Research Center (DKFZ) Heidelberg and German Consortium for Translational Cancer Research (DKTK), Partner Site Tübingen, Germany; Institute of Pathology and Neuropathology, Eberhard-Karls University, Tuebingen, Germany.

Alfred Königsrainer (A)

University Hospital Tübingen, Department of General, Visceral and Transplant Surgery, Germany.

Michael Bitzer (M)

University Hospital Tübingen, Department of Internal Medicine I, Germany.

Daniel Zips (D)

University Hospital Tübingen, Department of Radiation Oncology, Germany; German Cancer Research Center (DKFZ) Heidelberg and German Consortium for Translational Cancer Research (DKTK), Partner Site Tübingen, Germany.

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Classifications MeSH