Programmed Death Ligand-1 and Tumor Burden Score Dictate Treatment Responses in Patients with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Author:

Lien Ming-Yu12,Wang Chih-Chun34,Hwang Tzer-Zen34,Hsieh Ching-Yun12,Yang Chuan-Chien34,Wang Chien-Chung34,Lien Ching-Feng34,Shih Yu-Chen45,Yeh Shyh-An46,Hsieh Meng-Che47

Affiliation:

1. Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, Taichung 40201, Taiwan

2. School and Medicine, China Medical University, Taichung 40201, Taiwan

3. Department of Otolaryngology, E-Da Hospital, Kaohsiung 82445, Taiwan

4. College of Medicine, I-Shou University, Kaohsiung 82445, Taiwan

5. Department of Otolaryngology, E-Da Cancer Hospital, Kaohsiung 82445, Taiwan

6. Department of Radiation Oncology, E-Da Hospital, Kaohsiung 82445, Taiwan

7. Department of Hematology-Oncology, E-Da Cancer Hospital, Kaohsiung 82445, Taiwan

Abstract

Background: The significance of tumor burden for survival is unknown for patients with recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC). The purpose of our study was to evaluate the prognostic impact of programmed death ligand-1 (PD-L1) and tumor burden score (TBS) in patients with R/M HNSCC. Patients and Methods: R/M HNSCC patients who were treated with cisplatin, 5-fluorouracil plus cetuximab (EPF) or pembrolizumab (PPF) as first-line treatment were included in our study. PD-L1 and TBS were estimated and correlated with treatment responses. Kaplan–Meier curves were plotted for outcomes estimation. Results: A total of 252 R/M HNSCC patients were included, with 126 high tumor burden (HTB) and 126 low tumor burden (LTB) patients. Median progression-free survival (PFS) was 7.1 months in LTB and 3.9 months in HTB (p < 0.001) and median overall survival (OS) was 14.2 months in LTB and 9.2 months in HTB (p = 0.001). Patients with LTB had better PFS and OS than those with HTB independent of PD-L1 status. Subgroup analysis showed HTB patients treated with EPF had better survival than those treated with PPF, regardless of PD-L1 expression. For LTB PD-L1 positive patients, there was a longer survival with PPF than EPF, while for LTB PD-L1 negative patients, survival was similar between PPF and EPF. Multivariate analysis exhibited that tumor burden was significantly correlated with OS. Conclusions: Tumor burden is significantly correlated with survival in patients with R/M HNSCC. PD-L1 and TBS should be taken into consideration to determine first-line treatment.

Funder

E-Da Hospital

Publisher

MDPI AG

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