Randomized phase-III-trial of concurrent chemoradiation for locally advanced head and neck cancer comparing dose reduced radiotherapy with paclitaxel/cisplatin to standard radiotherapy with fluorouracil/cisplatin: The PacCis-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 2020
Historique:
received: 18 09 2019
revised: 13 01 2020
accepted: 16 01 2020
pubmed: 12 2 2020
medline: 15 4 2021
entrez: 12 2 2020
Statut: ppublish

Résumé

This multicenter, phase 3 trial investigates whether the incorporation of concurrent paclitaxel and cisplatin together with a reduced total dose of radiotherapy is superior to standard fluorouracil-cisplatin based CRT. Patients with SCCHN, stage III-IVB, were randomized to receive paclitaxel/cisplatin (PacCis)-CRT (arm A; paclitaxel 20 mg/m A total of 221 patients were enrolled between 2010 and 2015. With a median follow-up of 3.7 years, 3y-DFS in the CisFU arm and PacCis arm was 58.2% and 48.4%, respectively (HR 0.82, 95% CI 0.56-1.21, p = 0.52). The 3y-OS amounted to 64.6% in the CisFU arm, and to 59.2% in the PacCis arm (HR 0.82, 95% CI 0.54-1.24, p = 0.43). In the subgroup of p16-positive oropharyngeal carcinomas, 3y-DFS and 3y-OS was 84.6% vs 83.9% (p = 0.653), and 92.3% vs. 83.5% (p = 0.76) in arm A and B, respectively. Grade 3-4 hematological toxicities were significantly reduced in arm A (anemia, p = 0.01; leukocytopenia, p = 0.003), whereas grade 3 infections were reduced in arm B (p = 0.01). Paclitaxel/cisplatin-CRT with a reduced RT-dose is not superior to standard fluorouracil/cisplatin-CRT. Subgroup analyses indicate that a reduced radiation dose seems to be sufficient for p16+ oropharyngeal cancer or non-smokers. NCT01126216; EudraCT Number 2005-003484-23.

Sections du résumé

BACKGROUND AND PURPOSE
This multicenter, phase 3 trial investigates whether the incorporation of concurrent paclitaxel and cisplatin together with a reduced total dose of radiotherapy is superior to standard fluorouracil-cisplatin based CRT.
MATERIALS AND METHODS
Patients with SCCHN, stage III-IVB, were randomized to receive paclitaxel/cisplatin (PacCis)-CRT (arm A; paclitaxel 20 mg/m
RESULTS
A total of 221 patients were enrolled between 2010 and 2015. With a median follow-up of 3.7 years, 3y-DFS in the CisFU arm and PacCis arm was 58.2% and 48.4%, respectively (HR 0.82, 95% CI 0.56-1.21, p = 0.52). The 3y-OS amounted to 64.6% in the CisFU arm, and to 59.2% in the PacCis arm (HR 0.82, 95% CI 0.54-1.24, p = 0.43). In the subgroup of p16-positive oropharyngeal carcinomas, 3y-DFS and 3y-OS was 84.6% vs 83.9% (p = 0.653), and 92.3% vs. 83.5% (p = 0.76) in arm A and B, respectively. Grade 3-4 hematological toxicities were significantly reduced in arm A (anemia, p = 0.01; leukocytopenia, p = 0.003), whereas grade 3 infections were reduced in arm B (p = 0.01).
CONCLUSION
Paclitaxel/cisplatin-CRT with a reduced RT-dose is not superior to standard fluorouracil/cisplatin-CRT. Subgroup analyses indicate that a reduced radiation dose seems to be sufficient for p16+ oropharyngeal cancer or non-smokers.
CLINICAL TRIAL INFORMATION
NCT01126216; EudraCT Number 2005-003484-23.

Identifiants

pubmed: 32044419
pii: S0167-8140(20)30028-1
doi: 10.1016/j.radonc.2020.01.016
pii:
doi:

Substances chimiques

Paclitaxel P88XT4IS4D
Cisplatin Q20Q21Q62J
Fluorouracil U3P01618RT

Banques de données

ClinicalTrials.gov
['NCT01126216']

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

209-217

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Rainer Fietkau (R)

University Hospitals of Erlangen, Germany. Electronic address: Rainer.Fietkau@uk-erlangen.de.

Markus Hecht (M)

University Hospitals of Erlangen, Germany. Electronic address: Markus.Hecht@uk-erlangen.de.

Benjamin Hofner (B)

Institut für Medizininformatik, Biometrie und Epidemiologie, FAU Erlangen-Nürnberg, Germany. Electronic address: Benjamin.Hofner@pei.de.

Dorota Lubgan (D)

University Hospitals of Erlangen, Germany. Electronic address: dorota.lubgan@uk-erlangen.de.

Heinrich Iro (H)

University Hospitals of Erlangen, Germany. Electronic address: heinrich.iro@uk-erlangen.de.

Olaf Gefeller (O)

Institut für Medizininformatik, Biometrie und Epidemiologie, FAU Erlangen-Nürnberg, Germany. Electronic address: olaf.gefeller@imbe.med.uni-erlangen.de.

Claus Rödel (C)

J.W. Goethe University Hospital Frankfurt, Frankfurt am Main, Germany. Electronic address: claus.roedel@kgu.de.

Matthias G Hautmann (MG)

University Hospitals of Regensburg, Germany. Electronic address: matthias.hautmann@ukr.de.

Oliver Kölbl (O)

University Hospitals of Regensburg, Germany. Electronic address: oliver.koelbl@ukr.de.

Attila Salay (A)

Brüderkrankenhaus St. Josef, Paderborn, Germany. Electronic address: a.salay@bk-paderborn.de.

Christian Rübe (C)

University of Saarland, Homburg, Germany. Electronic address: radioonkologie@uks.eu.

Patrick Melchior (P)

University of Saarland, Homburg, Germany. Electronic address: patrick.melchior@uks.eu.

Peter Breinl (P)

Kliniken Pasing und Perlach, Munich, Germany. Electronic address: info@hno-arzt-gauting.de.

Waldemar Krings (W)

Krankenhaus Maria Hilf, Mönchengladbach, Germany. Electronic address: waldemar.krings@mariahilf.de.

Stephan Gripp (S)

University Hospitals of Düsseldorf, Germany. Electronic address: stephan.gripp@posteo.de.

Barbara Wollenberg (B)

University of Schleswig-Holstein, Lübeck, Germany. Electronic address: barbara.wollenberg@uksh.de.

Rainer Keerl (R)

Klinikum St. Elisabeth, Straubing, Germany. Electronic address: rainer.keerl@klinikum-straubing.de.

Ulrike Schreck (U)

Klinik am Eichert, Göppingen, Germany. Electronic address: ulrike.schreck@af-k.de.

Birgit Siekmeyer (B)

MVZ Mutterhaus der Borromäerinnen, Trier, Germany. Electronic address: birgit.siekmeyer@mutterhaus.de.

Gerhard G Grabenbauer (GG)

Coburg Cancer Center, Germany. Electronic address: gg@diacura.de.

Panagiotis Balermpas (P)

J.W. Goethe University Hospital Frankfurt, Frankfurt am Main, Germany; University Hospital of Zurich, Switzerland. Electronic address: panagiotis.balermpas@usz.ch.

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Classifications MeSH