Asian race and origin have no clinically meaningful effects on polatuzumab vedotin pharmacokinetics in patients with relapsed/refractory B-cell non-Hodgkin lymphoma.
Antibodies, Monoclonal
/ administration & dosage
Asian People
/ statistics & numerical data
CD79 Antigens
/ immunology
Drug Resistance, Neoplasm
Follow-Up Studies
Humans
Immunoconjugates
/ administration & dosage
Lymphoma, Large B-Cell, Diffuse
/ drug therapy
Neoplasm Recurrence, Local
/ drug therapy
Prognosis
Salvage Therapy
Survival Rate
Treatment Outcome
Ethnic sensitivity assessment
NHL
Non-hodgkin lymphoma
PK
Polatuzumab vedotin
Journal
Cancer chemotherapy and pharmacology
ISSN: 1432-0843
Titre abrégé: Cancer Chemother Pharmacol
Pays: Germany
ID NLM: 7806519
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
20
03
2020
accepted:
19
07
2020
pubmed:
10
8
2020
medline:
18
2
2021
entrez:
10
8
2020
Statut:
ppublish
Résumé
The CD79b-targeted antibody-drug conjugate polatuzumab vedotin (pola), alone and with chemoimmunotherapy, has clinical efficacy and a tolerable safety profile in B-cell non-Hodgkin lymphoma (B-NHL). We assessed (a) whether exposure from global studies of pola is comparable to Asian patients, and (b) if the recommended pola dose is appropriate in Asian patients based on exposure. The pharmacokinetics (PK) of pola in Asian and global populations was characterized for three analytes (antibody-conjugated monomethyl auristatin E (MMAE) [acMMAE], total antibody, and unconjugated MMAE) in five phase 1b/2 single-agent and combination studies in B-NHL patients (JO29138 [JAPICCTI-142580], DCS4968g [NCT01290549], GO27834 [NCT01691898], GO29044 [NCT01992653], and GO29365 [NCT02257567]). PK data were compared between Japanese phase 1 JO29138 (JAPICCTI-142580) and global phase 1 DCS4968g (NCT01290549) studies and between Asian and non-Asian patients in the randomized relapsed/refractory B-NHL cohorts of the phase 1b/2 study GO29365 (NCT02257567). A population PK (popPK) model was used to assess the effects of Asian race and region on acMMAE and unconjugated MMAE exposure. PK non-compartmental analysis (NCA) parameters for the key analyte acMMAE in the Japanese JO29138 (JAPICCTI-142580) and global phase 1 DCS4968g (NCT01290549) studies were similar. In GO29365 (NCT02257567), the phase 1b/2 combination study, mean exposure to the analytes was generally lower in Asian patients (by ~ 9.9 to 17.5%), but not to a clinically meaningful extent. Overall, the popPK model further suggested comparable PK in Asian patients with B-NHL (race or region) versus non-Asian patients. Race has no clinically meaningful effect on pola PK. These results (and observations from efficacy/safety exposure-response analyses) support no pola dose adjustments are warranted for Asian patients with DLBCL.
Identifiants
pubmed: 32770353
doi: 10.1007/s00280-020-04119-8
pii: 10.1007/s00280-020-04119-8
pmc: PMC7478950
doi:
Substances chimiques
Antibodies, Monoclonal
0
CD79 Antigens
0
CD79B protein, human
0
Immunoconjugates
0
polatuzumab vedotin
KG6VO684Z6
Banques de données
ClinicalTrials.gov
['NCT01290549', 'NCT01691898', 'NCT01992653', 'NCT02257567']
Types de publication
Clinical Trial, Phase I
Clinical Trial, Phase II
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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