Comparative effectiveness of second-line ipilimumab vs. nivolumab in combination with ipilimumab in patients with advanced melanoma who received frontline anti-PD-1 antibodies.


Journal

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372

Informations de publication

Date de publication:
Apr 2021
Historique:
pubmed: 20 5 2020
medline: 5 5 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Anti-PD-1 antibodies are commonly used as frontline therapy for patients with metastatic melanoma. Although these medications can cause long term responses, a significant number of patients will not respond or will lose response. Optimal second-line therapy after losing response to anti-PD-1 antibodies is not well established. Therefore, we retrospectively compared the overall survival of patients who lost response to anti-PD1 antibodies between patients treated with single agent ipilimumab or ipilimumab and nivolumab. A de-identified U.S. nationwide electronic health record-derived database was reviewed for patients with advanced melanoma treated with single agent anti-PD1 antibodies in the frontline setting and who subsequently received second-line ipilimumab or combination ipilimumab and nivolumab. Overall survival from initiation of second-line therapy was compared using Kaplan Meier curves and log-rank analysis. Other known prognostic markers for melanoma were analyzed for correlation with survival in a similar fashion. Disease characteristics between the two groups were compared using chi-square analysis. A total of 842 patients with advanced melanoma who received frontline anti-PD-1 antibodies were included for analysis. Of these, 57 received either ipilimumab ( In this small, retrospective analysis, for patients who lost response to frontline anti-PD-1 therapy, patients treated with ipilimumab had similar survival to those who received ipilimumab in combination with anti-PD-1 antibodies.

Identifiants

pubmed: 32423325
doi: 10.1177/1078155220924719
doi:

Substances chimiques

Ipilimumab 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0
Nivolumab 31YO63LBSN

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

555-559

Auteurs

Kelsey Baron (K)

Department of Internal Medicine, Intermountain Medical Center, Murray, USA.

Justin C Moser (JC)

HonorHealth Research Institute, Scottsdale, USA.

Shiven Patel (S)

Division of Medical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.

Kenneth F Grossmann (KF)

Division of Medical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.

Sarah V Colonna (SV)

Division of Medical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.

John R Hyngstrom (JR)

Division of Surgical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.
Division of General Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.

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Classifications MeSH