Ethnic sensitivity assessment: Polatuzumab vedotin pharmacokinetics in Asian and non-Asian patients with previously untreated diffuse large B-cell lymphoma in POLARIX.


Journal

Clinical and translational science
ISSN: 1752-8062
Titre abrégé: Clin Transl Sci
Pays: United States
ID NLM: 101474067

Informations de publication

Date de publication:
Dec 2023
Historique:
revised: 13 09 2023
received: 26 05 2023
accepted: 02 10 2023
pubmed: 21 10 2023
medline: 21 10 2023
entrez: 21 10 2023
Statut: ppublish

Résumé

This ethnic sensitivity analysis used data from the phase III POLARIX study (NCT03274492) to assess polatuzumab vedotin pharmacokinetics (PKs) in Asian versus non-Asian patients with previously untreated diffuse large B-cell lymphoma and examined the appropriateness of extrapolating global study findings to Asian patients. PK and population PK (PopPK) analyses assessed polatuzumab vedotin analyte exposures by ethnicity (Asian [n = 84] vs. non-Asian [n = 345] patients) and region (patients enrolled from Asia [n = 80] vs. outside Asia [n = 349]). In patients from Asia versus outside Asia, observed mean antibody-conjugated monomethyl auristatin E (acMMAE) concentrations were comparable (1.2% lower at cycle [C]1 postdose, 4.4% higher at C4 predose; and 6.8% lower at C4 postdose in patients from Asia). Observed mean unconjugated MMAE was lower in patients from Asia by 6.5% (C1 postdose), 20.0% (C4 predose), and 15.3% (C4 postdose). In the PopPK analysis, C6 area under the curve and peak plasma concentrations were also comparable for acMMAE (6.3% and 3.0% lower in Asian vs. non-Asian patients, respectively) and lower for unconjugated MMAE by 19.1% and 16.7%, respectively. By region, C6 mean acMMAE concentrations were similar, and C6 mean unconjugated MMAE concentrations were lower, in patients enrolled from Asia versus outside Asia, by 3.9%-7.0% and 17.3%-19.7%, respectively. In conclusion, polatuzumab vedotin PKs were similar between Asian and non-Asian patients by ethnicity and region, suggesting PKs are not sensitive to Asian ethnicity and dose adjustments are not required in Asian patients to maintain efficacy and safety.

Identifiants

pubmed: 37864313
doi: 10.1111/cts.13669
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2744-2755

Informations de copyright

© 2023 Genentech, Inc. and The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

Références

Shi R, Lu T, Ku G, et al. Asian race and origin have no clinically meaningful effects on polatuzumab vedotin pharmacokinetics in patients with relapsed/refractory B-cell non-Hodgkin lymphoma. Cancer Chemother Pharmacol. 2020;86:347-359.
Dornan D, Bennett F, Chen Y, et al. Therapeutic potential of an anti-CD79b antibody-drug conjugate, anti-CD79b-vc-MMAE, for the treatment of non-Hodgkin lymphoma. Blood. 2009;114:2721-2729.
Sehn LH, Herrera AF, Flowers CR, et al. Polatuzumab vedotin in relapsed or refractory diffuse large B-cell lymphoma. J Clin Oncol. 2020;38:155-165.
Tilly H, Morschhauser F, Sehn LH, et al. Polatuzumab Vedotin in previously untreated diffuse large B-cell lymphoma. N Engl J Med. 2022;386:351-363.
Genentech Inc. Genentech presents new and updated data for polivy in previously untreated diffuse large B-cell lymphoma at ASH 2022. 2022 Accessed August 2023. https://www.gene.com/media/press-releases/14976/2022-12-11/genentech-presents-new-and-updated-data
European Medicines Agency. POLIVY® summary of product characteristics. 2022. Accessed August 2023. https://www.ema.europa.eu/en/documents/product-information/polivy-epar-product-information_en.pdf
Genentech, Inc. FDA advisory committee votes in favor of the clinical benefit of genentech's polivy combination for people with previously untreated diffuse large B-cell lymphoma. 2023; Accessed August 2023 https://www.gene.com/media/press-releases/14984/2023-03-09/fda-advisory-committee-votes-in-favor-of
Chugai. Chugai obtains regulatory approval for POLIVY for additional indication of previously untreated diffuse large B-cell lymphoma. 2022. Accessed August 2023. https://www.chugai-pharm.co.jp/english/news/detail/20220824150000_944.html
Tyson RJ, Park CC, Powell JR, et al. Precision dosing priority criteria: drug, disease, and patient population variables. Front Pharmacol. 2020;11:420.
Gorovits B, Alley SC, Bilic S, et al. Bioanalysis of antibody-drug conjugates: American Association of Pharmaceutical Scientists antibody-drug conjugate working group position paper. Bioanalysis. 2013;5:997-1006.
Kaur S, Xu K, Saad OM, Dere RC, Carrasco-Triguero M. Bioanalytical assay strategies for the development of antibody-drug conjugate biotherapeutics. Bioanalysis. 2013;5:201-226.
Lu D, Lu T, Shi R, et al. Application of a two-analyte integrated population pharmacokinetic model to evaluate the impact of intrinsic and extrinsic factors on the pharmacokinetics of polatuzumab vedotin in patients with non-Hodgkin lymphoma. Pharm Res. 2020;37:252.
Deng R, Gibiansky L, Lu T, et al. Polatuzumab vedotin population pharmacokinetics (popPK) and exposure-response (ER) analyses from the POLARIX study in previously untreated diffuse large B-cell lymphoma (DLBCL). American Conference on Pharmacometrics. 2022.
Lu D, Lu T, Gibiansky L, et al. Integrated two-analyte population pharmacokinetic model of polatuzumab vedotin in patients with non-Hodgkin lymphoma. CPT Pharmacometrics Syst Pharmacol. 2020;9:48-59.
Palanca-Wessels MC, Czuczman M, Salles G, et al. Safety and activity of the anti-CD79B antibody-drug conjugate polatuzumab vedotin in relapsed or refractory B-cell non-Hodgkin lymphoma and chronic lymphocytic leukaemia: a phase 1 study. Lancet Oncol. 2015;16:704-715.
Hatake K, Kinoshita T, Terui Y, et al. A phase I pharmacokinetic and safety study of polatuzumab vedotin in Japanese patients with relapsed/refractory B-cell non-Hodgkin lymphoma: a comparison with non-Japanese DCS4968g study. Jpn J Clin Oncol. 2016;34:e19070.
Li C, Wang B, Lu D, et al. Ethnic sensitivity assessment of the antibody-drug conjugate trastuzumab emtansine (T-DM1) in patients with HER2-positive locally advanced or metastatic breast cancer. Cancer Chemother Pharmacol. 2016;78:547-558.
Suri A, Mould DR, Liu Y, Jang G, Venkatakrishnan K. Population PK and exposure-response relationships for the antibody-drug conjugate brentuximab Vedotin in CTCL patients in the phase III ALCANZA study. Clin Pharmacol Therapeut. 2018;104:989-999.
Song Y, Tilly H, Rai S, et al. Polatuzumab vedotin in previously untreated DLBCL: an Asia subpopulation analysis from the phase 3 POLARIX trial. Blood. 2023;141:1971-1981.
Li D, Lee D, Dere RC, et al. Evaluation and use of an anti-cynomolgus monkey CD79b surrogate antibody-drug conjugate to enable clinical development of polatuzumab vedotin. Br J Pharmacol. 2019;176:3805-3818.
Kadam RA, Borde SU, Madas SA, Salvi SS, Limaye SS. Challenges in recruitment and retention of clinical trial subjects. Perspect Clin Res. 2016;7:137-143.

Auteurs

Michael Z Liao (MZ)

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

Rong Deng (R)

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

Leonid Gibiansky (L)

QuantPharm LLC, North Potomac, Maryland, USA.

Tong Lu (T)

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

Priya Agarwal (P)

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

Randall Dere (R)

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

Calvin Lee (C)

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

Jamie Hirata (J)

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

Charles Herbaux (C)

CHU de Montpellier, Montpellier, France.

Gilles Salles (G)

Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Chunze Li (C)

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

Dale Miles (D)

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

Classifications MeSH