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Programmed death 1 (PD-1) and ligand (PD-L1) inhibitors in head and neck squamous cell carcinoma: A meta-analysis.
Levy, Dylan A; Patel, Jaimin J; Nguyen, Shaun A; Nicholas Jungbauer, W; Neskey, David M; Cohen, Ezra E W; Paulos, Chrystal M; Kaczmar, John A; Knochelmann, Hannah M; Day, Terry A.
Afiliação
  • Levy DA; Department of Otolaryngology-Head and Neck Surgery Medical University of South Carolina Charleston South Carolina USA.
  • Patel JJ; Department of Otolaryngology-Head and Neck Surgery Medical University of South Carolina Charleston South Carolina USA.
  • Nguyen SA; Department of Otolaryngology-Head and Neck Surgery Medical University of South Carolina Charleston South Carolina USA.
  • Nicholas Jungbauer W; Department of Otolaryngology-Head and Neck Surgery Medical University of South Carolina Charleston South Carolina USA.
  • Neskey DM; Department of Otolaryngology-Head and Neck Surgery Medical University of South Carolina Charleston South Carolina USA.
  • Cohen EEW; Department of Cell and Molecular Pharmacology and Developmental Therapeutics Medical University of South Carolina Charleston South Carolina USA.
  • Paulos CM; Department of Medicine, Division of Hematology-Oncology University of California, San Diego La Jolla California USA.
  • Kaczmar JA; Department of Microbiology and Immunology Medical University of South Carolina Charleston South Carolina USA.
  • Knochelmann HM; Department of Dermatology and Dermatologic Surgery Medical University of South Carolina Charleston South Carolina USA.
  • Day TA; Division of Hematology & Oncology Medical University of South Carolina Charleston South Carolina USA.
Article em En | MEDLINE | ID: mdl-36159902
ABSTRACT

Background:

PD-1 and PD-L1 inhibitors have emerged as promising treatments for patients with head and neck squamous cell carcinoma (HNSCC).

Methods:

Systematic review and meta-analysis of PD-1 and PD-L1 inhibitors in HNSCC.

Outcomes:

median overall survival (mOS), median progression-free survival (mPFS), Response Evaluation Criteria in Solid Tumors (RECIST) and treatment-related adverse events (TRAEs).

Results:

Eleven trials reported data on 1088 patients (mean age 59.9 years, range 18-90). The total mOS was 7.97 months (range 6.0-16.5). Mean mPFS for all studies was 2.84 months (range 1.9-6.5). PD-1 inhibitors had a lower rate of RECIST Progressive Disease than PD-L1 inhibitors (42.61%, 95% confidence interval [CI] 36.29-49.06 vs. 56.79%, 95% CI 49.18-64.19, P < 0.001). The rate of TRAEs of any grade (62.7%, 95% CI 59.8-65.6) did not differ.

Conclusions:

Meta-analysis shows the efficacy of PD-1 and PD-L1 inhibitors in HNSCC and suggests a possible difference in certain RECIST criterion between PD-1 and PD-L1 inhibitors. Future work to investigate the clinical significance of these findings is warranted.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article