Cancer Res Treat.  2021 Jul;53(3):671-677. 10.4143/crt.2020.824.

Outcomes and Biomarkers of Immune Checkpoint Inhibitor Therapy in Patients with Refractory Head and Neck Squamous Cell Carcinoma: KCSG HN18-12

Affiliations
  • 1Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea
  • 2Department of Internal Medicine, International St. Mary’s Hospital, Catholic Kwandong University College of Medicine, Incheon, Korea
  • 3Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
  • 4Department of Internal Medicine, Bucheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Korea
  • 5Department of Internal Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea
  • 6Department of Hemato-Oncology, Keimyung University Dongsan Medical Center, Daegu, Korea
  • 7Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan, Korea
  • 8Department of Internal Medicine, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
  • 9Department of Hematology and Oncology, Ewha Womans University Hospital, Seoul, Korea
  • 10Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea
  • 11Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea
  • 12Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • 13Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
  • 14Department of Internal Medicine, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea

Abstract

Purpose
This study was conducted to determine the effectiveness of immune checkpoint inhibitors (ICIs) in recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) after platinum-containing chemotherapy. We also identified clinical biomarkers which may be predictive of patient prognosis.
Materials and Methods
We analyzed 125 patients with R/M HNSCC who received ICIs, retrospectively. Overall response rate (ORR) was the primary study outcome. Overall survival (OS) and progression-free survival (PFS) were the secondary study outcomes.
Results
The patients received anti–programmed cell death protein-1 (PD-1) (n=73, 58%), anti–programmed death-ligand 1 (PD-L1) (n=24, 19%), or a combination of anti–PD-1/PD-L1 and anti–cytotoxic T-lymphocyte antigen 4 (n=28, 22%). The median age was 57 years (range, 37 to 87). The location of the primary tumor was in the oral cavity in 28% of the cases, followed by oropharynx (27%), hypopharynx (20%), and larynx (12%). The ORR was 15% (19/125). With 12.3 months of median follow-up, median PFS was 2.7 months. Median OS was 10.8 months. A neutrophil-to-lymphocyte ratio (NLR) > 4 was significantly associated with poor response to ICIs (odds ratio, 0.30; p=0.022). A sum of the target lesions > 40 mm (hazard ratio [HR], 1.53; p=0.046] and a NLR > 4 (HR, 1.75; p=0.009) were considered to be predictive markers of short PFS. A poor performance status (HR, 4.79; p < 0.001), a sum of target lesions > 40 mm (HR, 1.93; p=0.025), and an NLR > 4 (HR, 3.36; p < 0.001) were the significant predictors for poor survival.
Conclusion
ICIs exhibited favorable antitumor activity in R/M HNSCC. Clinically, our findings can be used to recognize patients benefit from receiving ICI.

Keyword

Head and neck neoplasms; Biomarkers; Immune check point; Platinum refractory; Sum of target lesions

Figure

  • Fig. 1 Efficacy of immune checkpoint inhibitors based on Response Evaluation Criteria in Solid Tumors ver. 1.1 by investigator assessment. The data shown represents the maximum percentage change from baseline in the sum of the longest diameter of the largest lesions (n=110). CR, complete response; PD, progressive disease; PR, partial response; SD, stable disease.

  • Fig. 2 Progression-free survival and overall survival in 123 evaluable patients. (A) Median progression-free survival: 2.7 months (95% confidence interval [CI], 2.2 to 3.5). (B) Median overall survival: 10.8 months (95% CI, 7.5 to 18.7). (C) Overall survival by primary tumor location. (D) Overall survival by oropharynx vs. non-oropharynx (hazards ratio, 0.46; 95% CI, 0.24 to 0.86; p=0.016).


Reference

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