| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Bhatia, Shailender |
| dc.contributor.author | Topalian, Suzanne |
| dc.contributor.author | Sharfman, William |
| dc.contributor.author | Meyer, Tim |
| dc.contributor.author | Steven, Neil |
| dc.contributor.author | Lao, Christopher D. |
| dc.contributor.author | Fariñas-Madrid, Lorena |
| dc.date.accessioned | 2025-03-21T09:17:05Z |
| dc.date.available | 2025-03-21T09:17:05Z |
| dc.date.issued | 2025-03-20 |
| dc.identifier.citation | Bhatia S, Topalian SL, Sharfman W, Meyer T, Steven N, Lao CD, et al. Nivolumab With or Without Ipilimumab in Patients With Recurrent or Metastatic Merkel Cell Carcinoma: A Nonrandomized, Open-Label, International, Multicenter Phase I/II Study. J Clin Oncol. 2025 Mar 20;43(9):1137–47. |
| dc.identifier.issn | 1527-7755 |
| dc.identifier.uri | http://hdl.handle.net/11351/12809 |
| dc.description | Nivolumab; Merkel cell carcinoma; Metastasis |
| dc.description.abstract | Purpose
Approximately 50% of patients with advanced Merkel cell carcinoma (MCC) have primary or acquired resistance to PD-(L)1 blockade, which may be overcome using combination immune checkpoint inhibition (ICI) with anti–cytotoxic T lymphocyte antigen-4 antibody. We present results from the recurrent/metastatic MCC cohort in CheckMate 358, a nonrandomized, multicohort, phase I/II study of nivolumab (NIVO) with or without ipilimumab (IPI) in virus-associated cancers (ClinicalTrials.gov identifier: NCT02488759).
Methods
ICI-naïve patients with recurrent/metastatic MCC and 0-2 previous systemic therapies were administered NIVO monotherapy at 240 mg once every 2 weeks or combination therapy with NIVO 3 mg/kg once every 2 weeks + IPI 1 mg/kg once every 6 weeks. The primary end point was objective response. Secondary end points included duration of response (DOR), progression-free survival (PFS), and overall survival (OS).
Results
Sixty-eight patients received NIVO (n = 25) or NIVO + IPI (n = 43). The objective response rate (95% CI) and median DOR (95% CI), respectively, were 60% (38.7 to 78.9) and 60.6 months (16.7 to not applicable [NA]) with NIVO and 58% (42.1 to 73) and 25.9 months (10.4 to NA) with NIVO + IPI. The median PFS (95% CI) and OS (95% CI), respectively, were 21.3 (9.2 to 62.5) and 80.7 (23.3 to NA) months with NIVO and 8.4 (3.7 to 24.3) and 29.8 (8.5 to 48.3) months with NIVO + IPI. The incidence of grade 3/4 treatment-related adverse events was 28% with NIVO and 47% with the combination.
Conclusion
This nonrandomized study showed frequent and durable responses with both NIVO and NIVO + IPI in patients with ICI-naïve advanced MCC. However, it did not show improvement in efficacy with the combination, thus contradicting previous study reports that had suggested clinical benefit with combination ICI. A randomized trial of NIVO + IPI versus NIVO monotherapy is warranted. |
| dc.language.iso | eng |
| dc.publisher | American Society of Clinical Oncology |
| dc.relation.ispartofseries | Journal of Clinical Oncology;43(9) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Pell - Càncer - Tractament |
| dc.subject | Medicaments antineoplàstics - Ús terapèutic - Efectes secundaris |
| dc.subject | Quimioteràpia combinada |
| dc.subject | Anticossos monoclonals - Ús terapèutic - Efectes secundaris |
| dc.subject | Pell - Càncer - Recaiguda |
| dc.subject | Avaluació de resultats (Assistència sanitària) |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Antineoplastic Agents, Immunological |
| dc.subject.mesh | /adverse effects |
| dc.subject.mesh | Neoplasm Recurrence, Local |
| dc.subject.mesh | Carcinoma, Merkel Cell |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Skin Neoplasms |
| dc.subject.mesh | Progression-Free Survival |
| dc.title | Nivolumab With or Without Ipilimumab in Patients With Recurrent or Metastatic Merkel Cell Carcinoma: A Nonrandomized, Open-Label, International, Multicenter Phase I/II Study |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1200/JCO-24-02138 |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | inmunoterapia antineoplásica |
| dc.subject.decs | /efectos adversos |
| dc.subject.decs | recurrencia neoplásica local |
| dc.subject.decs | carcinoma de células de Merkel |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | neoplasias cutáneas |
| dc.subject.decs | supervivencia libre de progresión |
| dc.relation.publishversion | https://doi.org/10.1200/JCO-24-02138 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Bhatia S] Division of Hematology-Oncology, University of Washington and Fred Hutchinson Cancer Center, Seattle, WA. [Topalian SL, Sharfman W] Division of Hematology-Oncology, University of Washington and Fred Hutchinson Cancer Center, Seattle, WA. Johns Hopkins Bloomberg-Kimmel Institute for Cancer Immunotherapy and Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD. [Meyer T] Department of Oncology, University College London Cancer Institute, London, United Kingdom. [Steven N] Institute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom. [Lao CD] Michigan Medicine, Rogel Cancer Center, Ann Arbor, MI. [Fariñas-Madrid L] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain |
| dc.identifier.pmid | 39889250 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |