Literature DB >> 34669023

A phase I study of veliparib with cyclophosphamide and veliparib combined with doxorubicin and cyclophosphamide in advanced malignancies.

Antoinette R Tan1,2, Nancy Chan3, Brian F Kiesel4, Mark N Stein3,5, Rebecca A Moss3,6, Jyoti Malhotra3, Joseph Aisner3, Mansi Shah3, Murugesan Gounder3, Hongxia Lin3, Michael P Kane3, Yong Lin3, Jiuping Ji7, Alice Chen8, Jan H Beumer4, Janice M Mehnert3,9.   

Abstract

PURPOSE: Veliparib (V), an oral poly(ADP-ribose) polymerase (PARP) inhibitor, potentiates effects of alkylating agents and topoisomerase inhibitors in preclinical tumor models. We conducted a phase I trial of V with iv cyclophosphamide (C) and V plus iv doxorubicin (A) and C.
METHODS: Objectives were to establish the maximum tolerated dose (MTD) of the combinations, characterize V pharmacokinetics (PK) in the presence and absence of C, measure PAR in peripheral blood mononuclear cells (PBMCs) and γH2AX in circulating tumor cells (CTCs). In Group 1, dose escalations of V from 10 to 50 mg every 12 h Days 1-4 plus C 450 to 750 mg/m2 Day 3 in 21-day cycles were evaluated. In Group 2, V doses ranged from 50 to 150 mg every 12 h Days 1-4 with AC (60/600 mg/m2) Day 3 in 21-day cycles. In Group 3, patients received AC Day 1 plus V Days 1-7, and in Group 4, AC Day 1 plus V Days 1-14 was given in 21-day cycles to evaluate effects on γH2AX foci.
RESULTS: Eighty patients were enrolled. MTD was not reached for V and C. MTD for V and AC was V 100 mg every 12 h Days 1-4 with AC (60/600 mg/m2) Day 3 every 21 days. V PK appears to be dose-dependent and has no effect on the PK of C. Overall, neutropenia and anemia were the most common adverse events. Objective response in V and AC treated groups was 22% (11/49). Overall clinical benefit rate was 31% (25/80). PAR decreased in PBMCs. Percentage of γH2AX-positive CTCs increased after treatment with V and AC.
CONCLUSION: V and AC can be safely combined. Activity was observed in patients with metastatic breast cancer.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  PARP inhibitors; Pharmacokinetics; Phase I study; Veliparib

Mesh:

Substances:

Year:  2021        PMID: 34669023      PMCID: PMC8934569          DOI: 10.1007/s00280-021-04350-x

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


  22 in total

Review 1.  Drug interactions in oncology.

Authors:  Jos H Beijnen; Jan H M Schellens
Journal:  Lancet Oncol       Date:  2004-08       Impact factor: 41.316

2.  A phase I study of veliparib in combination with metronomic cyclophosphamide in adults with refractory solid tumors and lymphomas.

Authors:  Shivaani Kummar; Jiuping Ji; Robert Morgan; Heinz-Josef Lenz; Shannon L Puhalla; Chandra P Belani; David R Gandara; Deborah Allen; Brian Kiesel; Jan H Beumer; Edward M Newman; Larry Rubinstein; Alice Chen; Yiping Zhang; Lihua Wang; Robert J Kinders; Ralph E Parchment; Joseph E Tomaszewski; James H Doroshow
Journal:  Clin Cancer Res       Date:  2012-02-03       Impact factor: 12.531

3.  Pharmacodynamic and pharmacokinetic study of chronic low-dose metronomic cyclophosphamide therapy in mice.

Authors:  Urban Emmenegger; Yuval Shaked; Shan Man; Guido Bocci; Ivan Spasojevic; Giulio Francia; Andrew Kouri; Robert Coke; William Cruz-Munoz; Susan M Ludeman; O Michael Colvin; Robert S Kerbel
Journal:  Mol Cancer Ther       Date:  2007-08-01       Impact factor: 6.261

4.  Phase I Trial of Veliparib, a Poly ADP Ribose Polymerase Inhibitor, Plus Metronomic Cyclophosphamide in Metastatic HER2-negative Breast Cancer.

Authors:  Jesus Anampa; Alice Chen; John Wright; Margi Patel; Christine Pellegrino; Karen Fehn; Joseph A Sparano; Eleni Andreopoulou
Journal:  Clin Breast Cancer       Date:  2017-09-01       Impact factor: 3.225

5.  ABT-888, an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models.

Authors:  Cherrie K Donawho; Yan Luo; Yanping Luo; Thomas D Penning; Joy L Bauch; Jennifer J Bouska; Velitchka D Bontcheva-Diaz; Bryan F Cox; Theodore L DeWeese; Larry E Dillehay; Debra C Ferguson; Nayereh S Ghoreishi-Haack; David R Grimm; Ran Guan; Edward K Han; Rhonda R Holley-Shanks; Boris Hristov; Kenneth B Idler; Ken Jarvis; Eric F Johnson; Lawrence R Kleinberg; Vered Klinghofer; Loren M Lasko; Xuesong Liu; Kennan C Marsh; Thomas P McGonigal; Jonathan A Meulbroek; Amanda M Olson; Joann P Palma; Luis E Rodriguez; Yan Shi; Jason A Stavropoulos; Alan C Tsurutani; Gui-Dong Zhu; Saul H Rosenberg; Vincent L Giranda; David J Frost
Journal:  Clin Cancer Res       Date:  2007-05-01       Impact factor: 12.531

6.  Liquid chromatography-mass spectrometric assay for the quantitation in human plasma of ABT-888, an orally available, small molecule inhibitor of poly(ADP-ribose) polymerase.

Authors:  Robert A Parise; Mohammad Shawaqfeh; Merrill J Egorin; Jan H Beumer
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2008-07-31       Impact factor: 3.205

7.  New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1).

Authors:  E A Eisenhauer; P Therasse; J Bogaerts; L H Schwartz; D Sargent; R Ford; J Dancey; S Arbuck; S Gwyther; M Mooney; L Rubinstein; L Shankar; L Dodd; R Kaplan; D Lacombe; J Verweij
Journal:  Eur J Cancer       Date:  2009-01       Impact factor: 9.162

8.  Randomized phase II trial of cyclophosphamide and the oral poly (ADP-ribose) polymerase inhibitor veliparib in patients with recurrent, advanced triple-negative breast cancer.

Authors:  Shivaani Kummar; James L Wade; Amit M Oza; Daniel Sullivan; Alice P Chen; David R Gandara; Jiuping Ji; Robert J Kinders; Lihua Wang; Deborah Allen; Geraldine O'Sullivan Coyne; Seth M Steinberg; James H Doroshow
Journal:  Invest New Drugs       Date:  2016-03-21       Impact factor: 3.850

9.  Phase I Study of Veliparib (ABT-888) Combined with Cisplatin and Vinorelbine in Advanced Triple-Negative Breast Cancer and/or BRCA Mutation-Associated Breast Cancer.

Authors:  Eve T Rodler; Brenda F Kurland; Melissa Griffin; Julie R Gralow; Peggy Porter; Rosa F Yeh; Vijayakrishna K Gadi; Jamie Guenthoer; Jan H Beumer; Larissa Korde; Sandra Strychor; Brian F Kiesel; Hannah M Linden; John A Thompson; Elizabeth Swisher; Xiaoyu Chai; Stacie Shepherd; Vincent Giranda; Jennifer M Specht
Journal:  Clin Cancer Res       Date:  2016-01-22       Impact factor: 12.531

10.  Monitoring drug-induced gammaH2AX as a pharmacodynamic biomarker in individual circulating tumor cells.

Authors:  Lihua H Wang; Thomas D Pfister; Ralph E Parchment; Shivaani Kummar; Larry Rubinstein; Yvonne A Evrard; Martin E Gutierrez; Anthony J Murgo; Joseph E Tomaszewski; James H Doroshow; Robert J Kinders
Journal:  Clin Cancer Res       Date:  2010-01-26       Impact factor: 12.531

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  1 in total

1.  A phase 1 and pharmacodynamic study of chronically-dosed, single-agent veliparib (ABT-888) in patients with BRCA1- or BRCA2-mutated cancer or platinum-refractory ovarian or triple-negative breast cancer.

Authors:  Julia Manzo; Shannon Puhalla; Shalu Pahuja; Fei Ding; Yan Lin; Leonard Appleman; Hussein Tawbi; Ronald Stoller; James J Lee; Brenda Diergaarde; Brian F Kiesel; Jing Yu; Antoinette R Tan; Chandra P Belani; Helen Chew; Agustin A Garcia; Robert J Morgan; Andrea E Wahner Hendrickson; Daniel W Visscher; Rachel M Hurley; Scott H Kaufmann; Elizabeth M Swisher; Steffi Oesterreich; Tiffany Katz; Jiuping Ji; Yiping Zhang; Ralph E Parchment; Alice Chen; Wenrui Duan; Vincent Giranda; Stacie P Shepherd; S Percy Ivy; Edward Chu; Jan H Beumer
Journal:  Cancer Chemother Pharmacol       Date:  2022-04-18       Impact factor: 3.288

  1 in total

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