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Chemotherapy and radiotherapy in locally advanced head and neck cancer: an individual patient data network meta-analysis

  • Claire Petit
  • , Benjamin Lacas
  • , Jean Pierre Pignon
  • , Quynh Thu Le
  • , Vincent Grégoire
  • , Cai Grau
  • , Allan Hackshaw
  • , Björn Zackrisson
  • , Mahesh K.B. Parmar
  • , Ju Whei Lee
  • , Maria Grazia Ghi
  • , Giuseppe Sanguineti
  • , Stéphane Temam
  • , Maurice Cheugoua-Zanetsie
  • , Brian O'Sullivan
  • , Marshall R. Posner
  • , Everett E. Vokes
  • , Juan J. Cruz Hernandez
  • , Zbigniew Szutkowski
  • , Eric Lartigau
  • Volker Budach, Rafal Suwiński, Michael Poulsen, Shaleen Kumar, Sarbani Ghosh Laskar, Jean Jacques Mazeron, Branislav Jeremic, John Simes, Lai Ping Zhong, Jens Overgaard, Catherine Fortpied, Pedro Torres-Saavedra, J. Bourhis, A. Aupérin, Pierre Blanchard*, MACH-NC and MARCH Collaborative Groups, J. Johansen (Medlem af forfattergruppering)
*Kontaktforfatter
  • University of Paris-Saclay
  • Institut Gustave Roussy
  • Groupe d'Oncologie Radiothérapie Tête Et Cou
  • Stanford University
  • The Léon Bérard Cancer Center
  • Aarhus Universitetshospital
  • Cancer Research UK
  • Umeå University
  • Institute for Global Health
  • Dana–Farber Cancer Institute
  • Veneto Institute of Oncology–IRCCS
  • Regina Elena National Cancer Institute
  • University of Toronto
  • Icahn School of Medicine at Mount Sinai
  • University of Chicago
  • University of Salamanca
  • Maria Sklodowska-Curie National Research Institute of Oncology
  • Centre Oscar Lambret
  • Berlin Institute of Health
  • Mater Centre
  • Sanjay Gandhi Postgraduate Institute of Medical Sciences Lucknow
  • Tata Memorial Hospital
  • Public Hospital System of Paris
  • BioIRC Center for Biomedical Research
  • NHMRC Clinical Trials Center
  • Shanghai Jiao Tong University
  • EORTC Headquarters
  • American College of Radiology, Reston
  • Lausanne University Hospital

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Abstract

Background: Randomised, controlled trials and meta-analyses have shown the survival benefit of concomitant chemoradiotherapy or hyperfractionated radiotherapy in the treatment of locally advanced head and neck cancer. However, the relative efficacy of these treatments is unknown. We aimed to determine whether one treatment was superior to the other. Methods: We did a frequentist network meta-analysis based on individual patient data of meta-analyses evaluating the role of chemotherapy (Meta-Analysis of Chemotherapy in Head and Neck Cancer [MACH-NC]) and of altered fractionation radiotherapy (Meta-Analysis of Radiotherapy in Carcinomas of Head and Neck [MARCH]). Randomised, controlled trials that enrolled patients with non-metastatic head and neck squamous cell cancer between Jan 1, 1980, and Dec 31, 2016, were included. We used a two-step random-effects approach, and the log-rank test, stratified by trial to compare treatments, with locoregional therapy as the reference. Overall survival was the primary endpoint. The global Cochran Q statistic was used to assess homogeneity and consistency and P score to rank treatments (higher scores indicate more effective therapies). Findings: 115 randomised, controlled trials, which enrolled patients between Jan 1, 1980, and April 30, 2012, yielded 154 comparisons (28 978 patients with 19 253 deaths and 20 579 progression events). Treatments were grouped into 16 modalities, for which 35 types of direct comparisons were available. Median follow-up based on all trials was 6·6 years (IQR 5·0–9·4). Hyperfractionated radiotherapy with concomitant chemotherapy (HFCRT) was ranked as the best treatment for overall survival (P score 97%; hazard ratio 0·63 [95% CI 0·51–0·77] compared with locoregional therapy). The hazard ratio of HFCRT compared with locoregional therapy with concomitant chemoradiotherapy with platinum-based chemotherapy (CLRTP) was 0·82 (95% CI 0·66–1·01) for overall survival. The superiority of HFCRT was robust to sensitivity analyses. Three other modalities of treatment had a better P score, but not a significantly better HR, for overall survival than CLRTP (P score 78%): induction chemotherapy with taxane, cisplatin, and fluorouracil followed by locoregional therapy (ICTaxPF-LRT; 89%), accelerated radiotherapy with concomitant chemotherapy (82%), and ICTaxPF followed by CLRT (80%). Interpretation: The results of this network meta-analysis suggest that further intensifying chemoradiotherapy, using HFCRT or ICTaxPF-CLRT, could improve outcomes over chemoradiotherapy for the treatment of locally advanced head and neck cancer. Fundings: French Institut National du Cancer, French Ligue Nationale Contre le Cancer, and Fondation ARC.

OriginalsprogEngelsk
TidsskriftThe Lancet Oncology
Vol/bind22
Udgave nummer5
Sider (fra-til)727-736
ISSN1470-2045
DOI
StatusUdgivet - maj 2021

Bibliografisk note

Publisher Copyright:
© 2021 Elsevier Ltd

Finansiering

CP reports a grant from Fondation ARC during the conduct of the study. J-PP reports grants from Ligue National Contre le Cancer, during the conduct of the study. AA reports grants from Ligue Contre le Cancer and Programme Hospitalier de Recherche Clinique en Cancérologie–Institut National du Cancer, during the conduct of the study; grants from F Hoffmann-La Roche, and from the French Radiation and Oncology Group for Head and Neck (GORTEC), outside the submitted work. EEV and QTL report personal fees AbbVie, Amgen, AstraZeneca, Biolumina, BMS, Celgene, Eli Lilly, EMD Serono, Genentech, Merck, Regeneron, Novartis for EEV, and Grail for QTL outside the submitted work. J-WL reports grants from the US National Institutes of Health, during the conduct of the study. JJCH reports other payment from Sanofi Aventis during the conduct of the study; payment for an advisory role and conferences from Merck, Bristol Myers Squibb, Merck Sharp & Dohme España, Novartis, and Roche Pharma outside the submitted work. All other authors declare no competing interests. This research was funded by grants from Institut National du Cancer (Programme Hospitalier de Recherche Clinique), Ligue Nationale Contre le Cancer, and Fondation ARC pour la recherche contre le cancer. We thank the trialists and the MARCH and MACH-NC collaborative groups who agreed to share their data. The contents of this publication and methods used are solely the responsibility of the authors and do not necessarily represent the official views of the ECOG-ACRIN Cancer Research Group, and NRG Oncology.

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