Open Access
CC BY-NC-ND 4.0 · South Asian J Cancer 2022; 11(01): 058-061
DOI: 10.1055/s-0041-1733317
Original Article
Head and Neck Cancer

Nivolumab in Recurrent/Metastatic Squamous Cell Carcinoma of Head and Neck: A Tertiary Cancer Center Experience

Ananya Pareek
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Apurva A. Patel
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Mukesh Kumar
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Philip G. Kuttikat
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Harshavardhan Annadanam
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Shantanu Pendse
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Naseer Mohammed
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
,
Harsha P. Panchal
1   Department of Medical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, Gujarat, India
› Institutsangaben

Funding Nil.
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Abstract

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Apurva A. Patel
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Ananya Pareek

Background Immunotherapy is a proven therapeutic option in recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) after platinum therapy. At present, there are no published Indian data regarding administration of nivolumab in this setting.

Aim The aim of this study is to retrospectively evaluate the efficacy and toxicity of nivolumab in R/M HNSCC among Indian patients who progressed after one or more lines of chemotherapy, including platinum agents.

Methods All patients of R/M HNSCC who received nivolumab between 2/6/2018 to 31/3/2020 were assessed retrospectively for the efficacy and toxicity of nivolumab therapy.

Statistical Analysis All the data analysis was performed using IBM SPSS Statistics for Windows, version 25 (IBM Corp., Armonk, N.Y., USA). Descriptive analysis was performed to obtain baseline characteristic of the study sample. Survival analysis was done using the Kaplan–Meier method.

Results Nivolumab therapy was tolerated well, with no new safety concerns, except one (8.3%) patient experienced grade ¾ toxicity (gastrointestinal). The clinical benefit rate (CBR) was found to be 66.7%. The median progression-free survival (PFS) was 3 months (95% CI; 2.093–3.907), and median overall survival (OS) was 8 months (95% CI; 3.731–12.269) from the date of first dose of nivolumab.

Conclusions In our study, efficacy and toxicity were comparable with international data with no new safety concerns. Nivolumab emerged as an astonishing treatment option with tolerable toxicity profile in patients with R/M HNSCC postplatinum therapy, although limited treatment options are available at present.



Publikationsverlauf

Artikel online veröffentlicht:
31. Dezember 2021

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