Asian race and origin have no clinically meaningful effects on polatuzumab vedotin pharmacokinetics in patients with relapsed/refractory B-cell non-Hodgkin lymphoma.


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
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

347-359

Références

Blood. 2017 Oct 19;130(16):1800-1808
pubmed: 28774879
Leuk Lymphoma. 2013 Feb;54(2):268-76
pubmed: 22800091
Leuk Lymphoma. 2020 Jul 24;:1-10
pubmed: 32705923
J Clin Pharmacol. 2013 Aug;53(8):866-77
pubmed: 23754575
CPT Pharmacometrics Syst Pharmacol. 2020 Jan;9(1):48-59
pubmed: 31749251
Leuk Res. 2013 Apr;37(4):386-91
pubmed: 23352640
Cancer Chemother Pharmacol. 2016 Sep;78(3):547-58
pubmed: 27423671
Lancet Oncol. 2019 Jul;20(7):998-1010
pubmed: 31101489
Blood. 2010 Sep 23;116(12):2040-5
pubmed: 20548096
Pharmacogenet Genomics. 2008 Jul;18(7):621-31
pubmed: 18551042
Best Pract Res Clin Haematol. 2018 Sep;31(3):293-298
pubmed: 30213399
Ann Acad Med Singap. 2011 Aug;40(8):356-61
pubmed: 22065001
Blood. 2007 Jul 15;110(2):616-23
pubmed: 17374736
Clin Pharmacol Ther. 2018 Nov;104(5):989-999
pubmed: 29377077
J Clin Pharmacol. 2014 May;54(5):483-94
pubmed: 24242979
Lancet Oncol. 2015 Jun;16(6):704-15
pubmed: 25925619
Hematology Am Soc Hematol Educ Program. 2011;2011:498-505
pubmed: 22160081
Ann Oncol. 2015 Sep;26 Suppl 5:v116-25
pubmed: 26314773
Lancet Haematol. 2019 May;6(5):e254-e265
pubmed: 30935953
J Clin Oncol. 2020 Jan 10;38(2):155-165
pubmed: 31693429
J Clin Oncol. 2017 Nov 1;35(31):3529-3537
pubmed: 28796588

Auteurs

Rong Shi (R)

Genentech Inc., South San Francisco, CA, USA. rongshi@gmail.com.

Tong Lu (T)

Genentech Inc., South San Francisco, CA, USA.

Grace Ku (G)

Genentech Inc., South San Francisco, CA, USA.

Hao Ding (H)

Genentech Inc., South San Francisco, CA, USA.

Tomohisa Saito (T)

Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

Leonid Gibiansky (L)

QuantPharm LLC, North Potomac, MD, USA.

Priya Agarwal (P)

Genentech Inc., South San Francisco, CA, USA.

Xiaobin Li (X)

Genentech Inc., South San Francisco, CA, USA.

Jin Yan Jin (JY)

Genentech Inc., South San Francisco, CA, USA.

Sandhya Girish (S)

Genentech Inc., South San Francisco, CA, USA.

Dale Miles (D)

Genentech Inc., South San Francisco, CA, USA.

Chunze Li (C)

Genentech Inc., South San Francisco, CA, USA.

Dan Lu (D)

Genentech Inc., South San Francisco, CA, USA. Lu.Dan@gene.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH