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Randomized trial comparing two methods of re-irradiation after salvage surgery in head and neck squamous cell carcinoma: Once daily split-course radiotherapy with concomitant chemotherapy or twice daily radiotherapy with cetuximab.
Tao, Yungan; Faivre, Laura; Laprie, Anne; Boisselier, Pierre; Ferron, Christophe; Jung, Guy Michel; Racadot, Séverine; Gery, Bernard; Even, Caroline; Breuskin, Ingrid; Bourhis, Jean; Janot, François.
Afiliación
  • Tao Y; Gustave Roussy Cancer Campus, Villejuif, France.
  • Faivre L; Gustave Roussy Cancer Campus, Villejuif, France.
  • Laprie A; Institut Claudius Regaud, Toulouse, France.
  • Boisselier P; Institut du Cancer Val d'Aurelle, Montpellier, France.
  • Ferron C; Centre Hospitalier Universitaire de Nantes, France.
  • Jung GM; Centre Paul Strauss, Strasbourg, France.
  • Racadot S; Centre Léon Berard, Lyon, France.
  • Gery B; Centre François Baclesse, Caen, France.
  • Even C; Gustave Roussy Cancer Campus, Villejuif, France.
  • Breuskin I; Gustave Roussy Cancer Campus, Villejuif, France.
  • Bourhis J; Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
  • Janot F; Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: Francois.JANOT@gustaveroussy.fr.
Radiother Oncol ; 128(3): 467-471, 2018 09.
Article en En | MEDLINE | ID: mdl-29784451
ABSTRACT

BACKGROUND:

A previous randomized trial in recurrent Head and Neck squamous-cell carcinoma (HNSCC) has shown re-irradiation combined with chemotherapy after salvage surgery significantly improved disease-free survival (DFS). The objective of this randomized trial was to compare two methods of re-irradiation in terms of toxicity and survival. PATIENTS AND

METHODS:

Patients with recurrence/second primary in previously irradiated area were randomly allocated to receive either 60 Gy over 11 weeks with concomitant 5FU - hydroxyurea (VP-arm), or 60 Gy (1.2 Gy twice daily) over 5 weeks with cetuximab (HFR-arm). Primary endpoint was treatment interruption >15 days (acute toxicity).

RESULTS:

Twenty-six patients were included in VP-arm and 27 in HFR-arm. One patient in VP-arm experienced >15 days interruption due to toxicity, and none in HFR-arm. In both arms, all patients received at least 60 Gy. In VP-arm, 8/26 patients had chemotherapy delay and/or dose reduction. In HFR-arm, 4/27 patients had <6 cycles cetuximab. There was no significant difference in overall survival (Median OS 37.4 months vs 21.9 months, p = 0.12). Toxicities and DFS were not different between 2 arms.

CONCLUSIONS:

Twice daily schedule of re-irradiation of 60 Gy/5 weeks with cetuximab was tolerable and no significant difference in treatment delays occurred between two arms.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Quimioradioterapia / Reirradiación / Neoplasias de Cabeza y Cuello Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Radiother Oncol Año: 2018 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Quimioradioterapia / Reirradiación / Neoplasias de Cabeza y Cuello Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Radiother Oncol Año: 2018 Tipo del documento: Article País de afiliación: Francia
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