Nivolumab exposure-response analysis for adjuvant treatment of melanoma supporting a change in posology.


Journal

CPT: pharmacometrics & systems pharmacology
ISSN: 2163-8306
Titre abrégé: CPT Pharmacometrics Syst Pharmacol
Pays: United States
ID NLM: 101580011

Informations de publication

Date de publication:
07 2021
Historique:
revised: 11 03 2021
received: 11 03 2021
accepted: 01 04 2021
pubmed: 7 5 2021
medline: 27 1 2022
entrez: 6 5 2021
Statut: ppublish

Résumé

Nivolumab monotherapy is approved as adjuvant treatment for melanoma based on results from the pivotal CheckMate 238 trial. We present a model-based, benefit-risk assessment of nivolumab in adjuvant melanoma supporting a posology change from a weight-based to a less frequent, flat-dosing regimen. The exposure-response (E-R) relationship for efficacy was evaluated using recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) end points from the CheckMate 238 trial. The E-R for safety was evaluated using data from 14 studies across a broad range of doses in several tumor types using grade 3+ adverse event (AE) and grade 2+ immune-mediated AE (IMAE) end points. Nivolumab trough exposures were not significant predictors of RFS or DMFS. Covariates significantly associated with increased risk of disease recurrence or death were programmed death ligand 1 (PD-L1; less than 5% cutoff), lower baseline lactate dehydrogenase, and higher age. Covariates associated with increased risk of distant metastasis or death were PD-L1 (less than 5% cutoff) and higher age. Higher nivolumab maximum concentration after first dose (Cmax1) was significantly associated with grade 2+ IMAEs, but not grade 3+ AEs. The risk of grade 3+ AEs was significantly lower in adjuvant versus advanced melanoma. Eastern Cooperative Oncology Group Performance Status higher than zero was associated with higher incidences of grade 2+ IMAEs and grade 3+ AEs. Female patients had significantly higher incidences of grade 2+ IMAEs than male patients. Nivolumab monotherapy in adjuvant melanoma demonstrated a relatively flat E-R relationship over the range of exposures produced by 3 mg/kg every 2 weeks and predicted a comparable benefit-risk profile to flat-dosing regimens.

Identifiants

pubmed: 33955714
doi: 10.1002/psp4.12642
pmc: PMC8302247
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Nivolumab 31YO63LBSN

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

748-759

Subventions

Organisme : Bristol Myers Squibb

Informations de copyright

© 2021 Bristol Myers Squibb Co. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Kinjal Sanghavi (K)

Bristol Myers Squibb, Princeton, New Jersey, USA.

Pradeep Vuppala (P)

Bristol Myers Squibb, Princeton, New Jersey, USA.

Vijay Ivaturi (V)

University of Maryland, Baltimore, Maryland, USA.

Lora Hamuro (L)

Bristol Myers Squibb, Princeton, New Jersey, USA.

Amit Roy (A)

Bristol Myers Squibb, Princeton, New Jersey, USA.

Satyendra Suryawanshi (S)

Bristol Myers Squibb, Princeton, New Jersey, USA.

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Classifications MeSH