Assessing toxicities of curative radiotherapy combined with concomitant non anti-cancer drugs: A sub-analysis of the prospective epidemiological RIT 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:
03 2022
Historique:
received: 28 06 2021
revised: 10 01 2022
accepted: 10 01 2022
pubmed: 24 1 2022
medline: 8 4 2022
entrez: 23 1 2022
Statut: ppublish

Résumé

Limited data are available about non-anticancer treatment (NACTs)/radiation combinations. MORSE 02-17 was the first study to report on the interaction resulting from such combinations in a heterogeneous population. Therefore, the aim of this study was to describe acute and late toxicities in a homogenous cohort of cancer patients receiving NACTs and undergoing radiation therapy. An analysis of the RIT (Radiation Impact on Thromboembolic events) prospective trial was carried-out. Patients with non-metastatic solid tumors and treated with radiotherapy and/or brachytherapy in a curative intent between 2016 and 2019 were included. Data about NACTs and toxicities were then collected. Out of 382 patients, 293 were prescribed NACTs (76.7%) with a median number of 3.6 (range: 1-14) NACTs per patient. Among1006 NACTs, the most prescribed drugs were anti-hypertensive, in 153 patients (52.2%). In accordance with MORSE 02-17 data, four of the main side effects of radiotherapy were analysed: genitourinary, gastrointestinal, dermatitis/mucositis and fatigue. Regarding acute and late toxicities -whatever the grade- no statistical difference was found between NACTs classes and these toxicities. When we compared the rates of toxicities with literature data, NACTs did not seem to have a worsening effect. One could conclude that NACTs concomitantly given with RT do not influence toxicity outcome. We then advocate a development of new platform for toxicity profile investigation of drugs-RT combination.

Sections du résumé

BACKGROUND AND PURPOSE
Limited data are available about non-anticancer treatment (NACTs)/radiation combinations. MORSE 02-17 was the first study to report on the interaction resulting from such combinations in a heterogeneous population. Therefore, the aim of this study was to describe acute and late toxicities in a homogenous cohort of cancer patients receiving NACTs and undergoing radiation therapy.
MATERIAL AND METHODS
An analysis of the RIT (Radiation Impact on Thromboembolic events) prospective trial was carried-out. Patients with non-metastatic solid tumors and treated with radiotherapy and/or brachytherapy in a curative intent between 2016 and 2019 were included. Data about NACTs and toxicities were then collected.
RESULTS
Out of 382 patients, 293 were prescribed NACTs (76.7%) with a median number of 3.6 (range: 1-14) NACTs per patient. Among1006 NACTs, the most prescribed drugs were anti-hypertensive, in 153 patients (52.2%). In accordance with MORSE 02-17 data, four of the main side effects of radiotherapy were analysed: genitourinary, gastrointestinal, dermatitis/mucositis and fatigue. Regarding acute and late toxicities -whatever the grade- no statistical difference was found between NACTs classes and these toxicities.
CONCLUSION
When we compared the rates of toxicities with literature data, NACTs did not seem to have a worsening effect. One could conclude that NACTs concomitantly given with RT do not influence toxicity outcome. We then advocate a development of new platform for toxicity profile investigation of drugs-RT combination.

Identifiants

pubmed: 35065997
pii: S0167-8140(22)00016-0
doi: 10.1016/j.radonc.2022.01.012
pii:
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

23-27

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Nicolas Magné (N)

Department of Radiation Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France; Department of Research and Teaching in Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France; Molecular and Cellular Radiobiology Lab, CNRS UMR 5822, Institut de Physique Nucléaire de Lyon, IPNL, 69622 Lyon Medicine University, Lyon, France. Electronic address: nicolas.magne@icloire.fr.

Wafa Bouleftour (W)

Department of Research and Teaching in Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

Elisabeth Daguenet (E)

Department of Research and Teaching in Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

Emilie Natier (E)

Department of Radiation Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

Mathilde Maison (M)

Department of Research and Teaching in Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

Fabien Tinquaut (F)

Department of Research and Teaching in Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

Jean-Philippe Suchaud (JP)

Department of Radiotherapy, Public General Hospital, Roanne, France.

Chloé Rancoule (C)

Department of Radiation Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France; Department of Research and Teaching in Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

Jean-Baptiste Guy (JB)

Department of Radiation Oncology, Lucien Neuwirth Cancer Centre, Saint Priest en Jarez, France.

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