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Efficacy of second-line chemotherapy or immune checkpoint inhibitors for patients with a prolonged objective response (≥ 6 months) after first-line therapy for recurrent or metastatic head and neck squamous cell carcinoma: a retrospective study.
Vienne, Agathe; Collet, Laetitia; Chevalier, Thomas; Borel, Christian; Tardy, Magalie; Huguet, Florence; Richard, Sandrine; Salas, Sebastien; Saada-Bouzid, Esma; Fayette, Jerome; Daste, Amaury.
Affiliation
  • Vienne A; Department of Medical Oncology, Hôpital Saint-André, CHU Bordeaux-University of Bordeaux, 1 Rue Jean Burguet, Bordeaux, 33000, France.
  • Collet L; Department of Medical Oncology, Léon Bérard Center, University of Lyon, Lyon, France.
  • Chevalier T; Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Bruxelles, Belgium.
  • Borel C; Department of Medical Oncology, CHU la Timone, AP-HM, Marseille, France.
  • Tardy M; Department of Medical Oncology, Institut de Cancérologie Strasbourg Europe, Strasbourg, France.
  • Huguet F; Department of Medical Oncology, Centre Antoine Lacassagne, Université Côte d'Azur, Nice, France.
  • Richard S; Department of Radiation Oncology, AP-HP, Tenon Hospital, Sorbonne University, Paris, France.
  • Salas S; Department of Medical Oncology, Tenon Hospital, AP-HP Sorbonne University, Paris, France.
  • Saada-Bouzid E; Department of Medical Oncology, CHU la Timone, AP-HM, Marseille, France.
  • Fayette J; Department of Medical Oncology, Centre Antoine Lacassagne, Université Côte d'Azur, Nice, France.
  • Daste A; Department of Medical Oncology, Léon Bérard Center, University of Lyon, Lyon, France.
BMC Cancer ; 23(1): 663, 2023 Jul 14.
Article in En | MEDLINE | ID: mdl-37452287
ABSTRACT

BACKGROUND:

Patients with recurrent or metastatic head and neck squamous cell carcinoma (R/M-HNSCC) have a poor prognosis and limited therapeutic options. Immune checkpoint inhibitors (ICIs) are effective in patients with tumor progression < 6 months following first-line, platinum-based chemotherapy (PBC), but data are missing for patients with progression ≥ 6 months after the last platinum dose.

METHODS:

Retrospective analysis (six French centers, 2008-2019) of all consecutive R/M-HNSCC patients. treated first-line with PBC and tumor progression ≥ 6 months after the last platinum dose. PRIMARY ENDPOINT progression-free survival after second-line therapy (PFS2). Additional endpoints overall survival from Day 1 of first-line (OS1) and second-line (OS2) therapy.

RESULTS:

R/M-HNSCC patients (n = 144) received cisplatinum (n = 67, 47%) or carboplatinum (n = 77, 53%) first-line. Response after first-line complete response (CR; n = 16, 11%); partial response (PR; n = 77, 53%); stable disease (n = 22, 15%). Second-line therapy PBC (n = 95, 66%); platinum-free regimen (PFR) (n = 25, 17%); ICI (n = 24, 17%). Median [95% confidence interval] PFS (months) PBC 5.0 [3.8-6.2]; PFR 4.0 [1-7.0]; ICI 2.0 [0.4-3.6] (p = 0.16). For PBC, PFR, and ICI, respectively OS1 30, 23, and 29 months (p = 1.02); OS2 14, 10, and 16 months (p = 0.25); PR, 26%, 16%, and 21% patients; CR, 0%, 8%, and 4% patients. For subsequent lines, ICIs were administered for PBC (n = 11, 12%) and PFR (n = 2, 8%). No predictive factor for efficacy (PFS, OS) was identified.

CONCLUSIONS:

Our retrospective study suggests similar efficacy regarding OS2 for second-line chemotherapy or ICI in R/M-HNSCC patients with progression ≥ 6 months after the last first-line platinum dose.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Immune Checkpoint Inhibitors / Head and Neck Neoplasms Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Immune Checkpoint Inhibitors / Head and Neck Neoplasms Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Year: 2023 Type: Article