Investigation of Relation of Radiation Therapy Quality With Toxicity and Survival in LAP07 Phase 3 Trial for Locally Advanced Pancreatic Carcinoma.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
15 07 2021
Historique:
received: 21 10 2020
revised: 22 01 2021
accepted: 30 01 2021
pubmed: 10 2 2021
medline: 25 9 2021
entrez: 9 2 2021
Statut: ppublish

Résumé

The LAP07 multicenter randomized study assessed whether chemoradiation therapy increases overall survival versus continuation chemotherapy in patients whose locally advanced pancreatic cancer was controlled after 4 months of induction chemotherapy. This analysis investigated whether failure to adhere to radiation therapy (RT) guidelines influenced survival and toxicity. This is a planned analysis of secondary objectives in the framework of a randomized international phase 3 trial. The protocol included detailed written RT guidelines. All participating institutions undertook an initial benchmark case to check adherence to protocol guidelines. Centers with major deviation were not allowed to include patients until they achieved a significant improvement and rigorously followed the guidelines. On-trial RT quality assurance consisted of a central review of treatment plan with dose-volume histograms for each patient. Adherence to guidelines was graded as per protocol (PP), minor deviation (MiD), or major deviation (MaD). Fifty-seven benchmark cases were evaluated, 26% were classified as PP, 60% were MiD, and 14% were MaD. Among the 442 included patients, 133 patients were randomized in the chemoradiation therapy arm, and 117 patients were assessable for RT quality analysis. RT quality was graded as PP in 38.5% of patients, MiD in 43.6% of patients, and MaD in 17.9% of patients. The most frequent protocol violations were dose distribution heterogeneities. Median overall survival was 17 months with PP and MiD versus 13.4 months with MaD (hazard ratio [HR], 1.63; 95% confidence interval [CI], 0.99-2.71; P = .055). There was no difference in terms of progression-free survival (HR, 1.09; 95% CI, 0.66-1.8; P = .72). Patients with MaD had more nausea than patients treated PP or with MiD (P = .0045). MaD was associated with a trend for worst survival. There was no difference in terms of progression-free survival. Because of the low rate of major deviations, their effects on the LAP07 trial results may be negligeable.

Identifiants

pubmed: 33561507
pii: S0360-3016(21)00164-4
doi: 10.1016/j.ijrobp.2021.01.055
pii:
doi:

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

993-1002

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Paul Giraud (P)

Department of Radiation Oncology, Tenon Hospital, Institut Universitaire du Cancer, AP-HP, Sorbonne Université, Paris, France.

Séverine Racadot (S)

Department of Radiation Oncology, Centre Léon Bérard, Lyon, France.

Dewi Vernerey (D)

Methodology and Quality of Life in Oncology Unit (EA 3181) and Quality of Life and Cancer Clinical Research Platform, CHU de Besançon, Besançon, France.

David Goldstein (D)

Department of Medical Oncology, Prince of Wales Hospital, Randwick, Australia.

Bengt Glimelius (B)

Department of Immunology, Genetics and Pathology, Uppsala University, Sweden.

Paul Van Houtte (P)

Department of Radiation Oncology, Institut Jules-Bordet, Brussels, Belgium.

Michael Gubanski (M)

Department of Oncology, Karolinska University Hospital, Stockholm, Sweden.

Nigel Spry (N)

Department of Radiation Oncology, Sir Charles Gairdner Hospital, Nedlands, Australia.

Jean Luc Van Laethem (JL)

Department of Gastroenterology and Gastrointestinal cancer Unit, Erasme Hospital, Université Libre Bruxelles, Brussels, Belgium.

Pascal Hammel (P)

Service de Gastroentérologie-Pancréatologie, Beaujon Hospital, AP-HP, Clichy, France.

Florence Huguet (F)

Department of Radiation Oncology, Tenon Hospital, Institut Universitaire du Cancer, AP-HP, Sorbonne Université, Paris, France. Electronic address: florence.huguet@aphp.fr.

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