Affiliation:
1. Department of Radiation Oncology Memorial Sloan Kettering Cancer Center New York New York USA
2. Department of Epidemiology and Biostatistics Memorial Sloan Kettering Cancer Center New York New York USA
3. Department of Medicine Memorial Sloan Kettering Cancer Center New York New York USA
4. Department of Medicine Weill Cornell Medicine New York New York USA
Abstract
AbstractBackgroundPrior work documented circadian rhythm impacts on efficacy and toxicity of cancer therapies.MethodsSecondary analysis of prospective, phase II trial of metastatic HNSCC randomized to nivolumab+/−SBRT. Used cutoffs of 1100 and 1630. Timing classified by first infusion or majority of SBRT (e.g., PM SBRT defined by two or three fractions after 1630).ResultsOf 62 patients, there was no significant difference in median PFS between AM nivolumab (n = 7, 175 days), PM nivolumab (n = 21, 58 days), or Mid‐Day nivolumab (n = 34, 67 days; p = 0.8). There was no significant difference in median PFS with AM SBRT (n = 4, 78 days), PM SBRT (n = 13, 111 days), or Mid‐Day SBRT (n = 15, 63 days; p = 0.8). There was no significant difference in Grade 3–4 toxicity or ORR. Sensitivity analyses with other timepoints were negative.ConclusionsFurther work may elucidate circadian impacts on select patients, tumors, and therapies; however, we found no significant effect in this study.
Funder
Memorial Sloan-Kettering Cancer Center
American Society of Clinical Oncology
National Cancer Institute