Induction chemotherapy in nonlaryngeal human papilloma virus-negative high-risk head and neck cancer: a real-world experience.


Journal

Anti-cancer drugs
ISSN: 1473-5741
Titre abrégé: Anticancer Drugs
Pays: England
ID NLM: 9100823

Informations de publication

Date de publication:
11 2020
Historique:
pubmed: 16 9 2020
medline: 1 9 2021
entrez: 15 9 2020
Statut: ppublish

Résumé

The role of induction chemotherapy in the multidisciplinary treatment of locally advanced, nonlaryngeal high-risk human papilloma virus (HPV)-negative head and neck squamous cells carcinoma (HNSCC) is uncertain in terms of overall survival (OS). The primary objective of this study was to identify possible predictive factors of survival and outcome in patients with HNSCC who were treated with induction chemotherapy. Fifty-nine patients with stage IVa/b HPV-negative non-laryngeal HNSCC (mostly originating from the oral cavity) who underwent induction chemotherapy at Policlinico Umberto I were reviewed. Treatment outcomes in term of objective response rate (ORR), progression-free survival (PFS), OS and toxicities were analyzed. A significant association between nodal status, ORR, ongoing smoking use, toxicities and OS was demonstrated. ORR (obtained in 61% of patients) was associated with a reduction in mortality of 80% (P< 0.0001). Early discontinuation after just one cycle of induction chemotherapy was associated to a significantly shorter OS. In oral cavity radical surgery with negative margins was obtained in 15/16 patients. In 42% of patients G3-G4 toxicity occurred. Toxicity requiring hospitalization occurred in 42% and 21% of patients with oropharyngeal and oral cavity carcinoma, respectively. Five patients died of treatment-related causes. No treatment-related mortality occurred in oral cavity patients. G5 toxicities were different according to the sub-sites of disease (P = 0.05). Induction chemotherapy in non-laryngeal high-risk HNSCC is an active strategy, most importantly in oral cavity cancer, even though burdened with a high (G ≥ 3) toxicity and early discontinuation rate. These data will however need to be confirmed in further and larger studies.

Identifiants

pubmed: 32932276
doi: 10.1097/CAD.0000000000000977
pii: 00001813-202011000-00011
doi:

Substances chimiques

Docetaxel 15H5577CQD
Cisplatin Q20Q21Q62J
Fluorouracil U3P01618RT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1074-1083

Références

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Auteurs

Silvia Mezi (S)

Departments of Radiological, Oncological and Pathological Science.

Giulia Pomati (G)

Departments of Radiological, Oncological and Pathological Science.

Andrea Botticelli (A)

Clinical and Molecular Medicine.

Michela Roberto (M)

Clinical and Molecular Medicine.

Bruna Cerbelli (B)

Departments of Radiological, Oncological and Pathological Science.

Alessio Cirillo (A)

Departments of Radiological, Oncological and Pathological Science.

Cira Di Gioia (C)

Departments of Radiological, Oncological and Pathological Science.

Alessandro Corsi (A)

Molecular Medicine.

Francesco Vullo (F)

Departments of Radiological, Oncological and Pathological Science.

Marco De Vincentiis (M)

Odontostomatological and Maxillo-Facial Science, 'Sapienza' University of Rome, Italy.

Antonella Polimeni (A)

Odontostomatological and Maxillo-Facial Science, 'Sapienza' University of Rome, Italy.

Vincenzo Tombolini (V)

Departments of Radiological, Oncological and Pathological Science.

Valentino Valentini (V)

Odontostomatological and Maxillo-Facial Science, 'Sapienza' University of Rome, Italy.

Paolo Marchetti (P)

Clinical and Molecular Medicine.

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