Literature DB >> 32222808

Pharmacokinetics of polatuzumab vedotin in combination with R/G-CHP in patients with B-cell non-Hodgkin lymphoma.

Colby S Shemesh1, Priya Agarwal2, Tong Lu2, Calvin Lee3, Randall C Dere4, Xiaobin Li2, Chunze Li2, Jin Y Jin2, Sandhya Girish2, Dale Miles2, Dan Lu5.   

Abstract

PURPOSE: The phase Ib/II open-label study (NCT01992653) evaluated the antibody-drug conjugate polatuzumab vedotin (pola) plus rituximab/obinutuzumab, cyclophosphamide, doxorubicin, and prednisone (R/G-CHP) as first-line therapy for B-cell non-Hodgkin lymphoma (B-NHL). We report the pharmacokinetics (PK) and drug-drug interaction (DDI) for pola.
METHODS: Six or eight cycles of pola 1.0-1.8 mg/kg were administered intravenously every 3 weeks (q3w) with R/G-CHP. Exposures of pola [including antibody-conjugated monomethyl auristatin E (acMMAE) and unconjugated MMAE] and R/G-CHP were assessed by non-compartmental analysis and/or descriptive statistics with cross-cycle comparisons to cycle 1 and/or after multiple cycles. Pola was evaluated as a potential victim and perpetrator of a PK drug-drug interaction with R/G-CHP. Population PK (popPK) analysis assessed the impact of prior treatment status (naïve vs. relapsed/refractory) on pola PK.
RESULTS: Pola PK was similar between treatment arms and independent of line of therapy. Pola PK was dose proportional from 1.0 to 1.8 mg/kg with R/G-CHP. Geometric mean volume of distribution and clearance of acMMAE ranged from 57.3 to 95.6 mL/kg and 12.7 to 18.2 mL/kg/day, respectively. acMMAE exhibited multi-exponential decay (elimination half-life ~ 1 week). Unconjugated MMAE exhibited formation rate-limited kinetics. Exposures of pola with R/G-CHP were similar to those in the absence of CHP; exposures of R/G-CHP in the presence of pola were comparable to those in the absence of pola.
CONCLUSIONS: Pola PK was well characterized with no clinically meaningful DDIs with R/G-CHP. Findings are consistent with previous studies of pola + R/G, and support pola + R/G-CHP use in previously untreated diffuse large B-cell lymphoma.

Entities:  

Keywords:  B-cell non-Hodgkin lymphoma; Combination therapy; Drug interactions; Pharmacokinetics; Phase Ib/II; Polatuzumab vedotin

Year:  2020        PMID: 32222808     DOI: 10.1007/s00280-020-04054-8

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  3 in total

1.  A phase 2 study of polatuzumab vedotin + bendamustine + rituximab in relapsed/refractory diffuse large B-cell lymphoma.

Authors:  Yasuhito Terui; Shinya Rai; Koji Izutsu; Motoko Yamaguchi; Jun Takizawa; Junya Kuroda; Takayuki Ishikawa; Koji Kato; Youko Suehiro; Noriko Fukuhara; Ken Ohmine; Hideki Goto; Kazuhito Yamamoto; Nobuhiro Kanemura; Yasunori Ueda; Kenichi Ishizawa; Kyoya Kumagai; Atsuko Kawasaki; Tomohisa Saito; Misato Hashizume; Hirohiko Shibayama
Journal:  Cancer Sci       Date:  2021-06-04       Impact factor: 6.716

2.  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.

Authors:  Dan Lu; Tong Lu; Rong Shi; Leonid Gibiansky; Priya Agarwal; Colby S Shemesh; Randall C Dere; Uzor Ogbu; Jamie Hirata; Pascal Chanu; Sandhya Girish; Jin Yan Jin; Chunze Li; Dale Miles
Journal:  Pharm Res       Date:  2020-12-01       Impact factor: 4.200

Review 3.  Clinical Pharmacology of Antibody-Drug Conjugates.

Authors:  Iftekhar Mahmood
Journal:  Antibodies (Basel)       Date:  2021-05-21
  3 in total

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