Update of a prognostic survival model in head and neck squamous cell carcinoma patients treated with immune checkpoint inhibitors using an expansion cohort
Majd Issa,
Brett G. Klamer,
Nikol Mladkova,
Georgios I. Laliotis,
Vidhya Karivedu,
Priyanka Bhateja,
Chase Byington,
Khaled Dibs,
Xueliang Pan,
Arnab Chakravarti,
John Grecula,
Sachin R. Jhawar,
Darrion Mitchell,
Sujith Baliga,
Matthew Old,
Ricardo L. Carrau,
James W. Rocco,
Dukagjin M. Blakaj,
Marcelo Bonomi
Affiliations
Majd Issa
Department of Internal Medicine, Division of Medical Oncology, The Ohio State University Wexner Medical Center
Brett G. Klamer
Center for Biostatistics, Department of Biomedical Informatics, The Ohio State University
Nikol Mladkova
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Georgios I. Laliotis
Sidney Kimmel Comprehensive Cancer Center and Department of Oncology, Johns Hopkins University
Vidhya Karivedu
Department of Internal Medicine, Division of Medical Oncology, The Ohio State University Wexner Medical Center
Priyanka Bhateja
Department of Internal Medicine, Division of Medical Oncology, The Ohio State University Wexner Medical Center
Chase Byington
Department of Internal Medicine, Division of Medical Oncology, The Ohio State University Wexner Medical Center
Khaled Dibs
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Xueliang Pan
Center for Biostatistics, Department of Biomedical Informatics, The Ohio State University
Arnab Chakravarti
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
John Grecula
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Sachin R. Jhawar
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Darrion Mitchell
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Sujith Baliga
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Matthew Old
Department of Otolaryngology - Head and Neck Surgery, The Ohio State University Wexner Medical Center
Ricardo L. Carrau
Department of Otolaryngology - Head and Neck Surgery, The Ohio State University Wexner Medical Center
James W. Rocco
Department of Otolaryngology - Head and Neck Surgery, The Ohio State University Wexner Medical Center
Dukagjin M. Blakaj
Division of Radiation Oncology, The Ohio State University Wexner Medical Center
Marcelo Bonomi
Department of Internal Medicine, Division of Medical Oncology, The Ohio State University Wexner Medical Center
Abstract Background Immune checkpoint inhibitors (ICI) treatment in recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) offers new therapeutic venues. We have previously developed a predictive survival model in this patient population based on clinical parameters, and the purpose of this study was to expand the study cohort and internally validate the model. Methods A single institutional retrospective analysis of R/M HNSCC patients treated with ICI. Clinical parameters collected included p-16 status, hemoglobin (Hb), albumin (Alb), lactate dehydrogenase (LDH), neutrophil, lymphocyte and platelet counts. Cox proportional hazard regression was used to assess the impact of patient characteristics and clinical variables on survival. A nomogram was created using the rms package to generate individualized survival prediction. Results 201 patients were included, 47 females (23%), 154 males (77%). Median age was 61 years (IQR: 55-68). P-16 negative (66%). Median OS was 12 months (95% CI: 9.4, 14.9). Updated OS model included age, sex, absolute neutrophil count, absolute lymphocyte count, albumin, hemoglobin, LDH, and p-16 status. We stratified patients into three risk groups based on this model at the 0.33 and 0.66 quantiles. Median OS in the optimal risk group reached 23.7 months (CI: 18.5, NR), 13.8 months (CI: 11.1, 20.3) in the average risk group, and 2.3 months (CI: 1.7, 4.4) in the high-risk group. Following internal validation, the discriminatory power of the model reached a c-index of 0.72 and calibration slope of 0.79. Conclusions Our updated nomogram could assist in the precise selection of patients for which ICI could be beneficial and cost-effective.