Immunotherapy around the Clock: Impact of Infusion Timing on Stage IV Melanoma Outcomes

Author:

Gonçalves Lisa1ORCID,Gonçalves Duarte2ORCID,Esteban-Casanelles Teresa3ORCID,Barroso Tiago1ORCID,Soares de Pinho Inês1ORCID,Lopes-Brás Raquel1ORCID,Esperança-Martins Miguel14ORCID,Patel Vanessa1,Torres Sofia1,Teixeira de Sousa Rita1,Mansinho André5ORCID,Costa Luís14ORCID

Affiliation:

1. Department of Oncology, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, 1649-035 Lisboa, Portugal

2. Department of Economics, University College London, London WC1H 0AX, UK

3. Department of Political Economy, King’s College London, London WC2B 4BG, UK

4. Instituto de Medicina Molecular-João Lobo Antunes, Faculdade de Medicina de Lisboa, 1649-028 Lisboa, Portugal

5. START Lisbon, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, 1649-035 Lisboa, Portugal

Abstract

Although the impact of circadian timing on immunotherapy has yet to be integrated into clinical practice, chronoimmunotherapy is an emerging and promising field as circadian oscillations are observed in immune cell numbers as well as the expression of immunotherapy targets, e.g., programmed cell death protein-1 and its ligand programmed death ligand 1. Concurrent retrospective studies suggest that morning infusions may lead to higher effectiveness of immune checkpoint inhibitors in melanoma, non-small cell lung cancer, and kidney cancer. This paper discusses the results of a retrospective study (2016–2022) exploring the impact of infusion timing on the outcomes of all 73 patients with stage IV melanoma receiving immunotherapy at a particular medical center. While the median overall survival (OS) was 24.2 months (95% confidence interval [CI] 9.04–39.8), for a median follow-up of 15.3 months, our results show that having more than 75% of infusions in the afternoon results in shorter median OS (14.9 vs. 38.1 months; hazard ratio 0.45 [CI 0.23–0.86]; p < 0.01) with more expressive impacts on particular subgroups: women, older patients, and patients with a lower tumor burden at the outset of immunotherapy. Our findings highlight the potential benefits of follow-up validation in prospective and translational randomized studies.

Publisher

MDPI AG

Subject

General Medicine

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