Literature DB >> 28341300

A phase I pharmacokinetic study of intraperitoneal bortezomib and carboplatin in patients with persistent or recurrent ovarian cancer: An NRG Oncology/Gynecologic Oncology Group study.

Danielle A Jandial1, William E Brady2, Stephen B Howell3, Heather A Lankes4, Russell J Schilder5, Jan H Beumer6, Susan M Christner7, Sandra Strychor8, Matthew A Powell9, Andrea R Hagemann10, Kathleen N Moore11, Joan L Walker12, Paul A DiSilvestro13, Linda R Duska14, Paula M Fracasso15, Don S Dizon16.   

Abstract

PURPOSE: Intraperitoneal (IP) therapy improves survival compared to intravenous (IV) treatment for women with newly diagnosed, optimally cytoreduced, ovarian cancer. However, the role of IP therapy in recurrent disease is unknown. Preclinical data demonstrated IP administration of the proteasome inhibitor, bortezomib prior to IP carboplatin increased tumor platinum accumulation resulting in synergistic cytotoxicity. We conducted this phase I trial of IP bortezomib and carboplatin in women with recurrent disease.
METHODS: Women with recurrent ovarian cancer were treated with escalating doses of IP bortezomib - in combination with IP carboplatin (AUC 4 or 5) every 21days for 6cycles. Pharmacokinetics of both agents were evaluated in cycle 1.
RESULTS: Thirty-three women participated; 32 were evaluable for safety. Two patients experienced dose-limiting toxicity (DLT) at the first dose level (carboplatin AUC 5, bortezomib 0.5mg/m2), prompting carboplatin reduction to AUC 4 for subsequent dose levels. With carboplatin dose fixed at AUC 4, bortezomib was escalated from 0.5 to 2.5mg/m2 without DLT. Grade 3/4 related toxicities included abdominal pain, nausea, vomiting, and diarrhea which were infrequent. The overall response rate in patients with measurable disease (n=21) was 19% (1 complete, 3 partial). Cmax and AUC in peritoneal fluid and plasma increased linearly with dose, with a favorable exposure ratio of the peritoneal cavity relative to peripheral blood plasma.
CONCLUSION: IP administration of this novel combination was feasible and showed promising activity in this phase I trial of heavily pre-treated women with ovarian cancer. Further evaluation of this IP combination should be conducted.
Copyright © 2017. Published by Elsevier Inc.

Entities:  

Keywords:  Intraperitoneal; Ovarian cancer; Platinum; Proteasome inhibition

Mesh:

Substances:

Year:  2017        PMID: 28341300      PMCID: PMC5706109          DOI: 10.1016/j.ygyno.2017.03.013

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  26 in total

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Authors:  K Jaaback; N Johnson
Journal:  Cochrane Database Syst Rev       Date:  2006-01-25

4.  Phase I trial of bortezomib and carboplatin in recurrent ovarian or primary peritoneal cancer.

Authors:  C Aghajanian; D S Dizon; P Sabbatini; J J Raizer; J Dupont; D R Spriggs
Journal:  J Clin Oncol       Date:  2005-09-01       Impact factor: 44.544

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Authors:  Danielle D Jandial; Salman Farshchi-Heydari; Christopher A Larson; Gregory I Elliott; Wolfgang J Wrasidlo; Stephen B Howell
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Journal:  Cancer Invest       Date:  2004       Impact factor: 2.176

9.  Phase I trial of the proteasome inhibitor bortezomib in combination with carboplatin in patients with platinum- and taxane-resistant ovarian cancer.

Authors:  Pedro T Ramirez; Charles N Landen; Robert L Coleman; Michael R Milam; Charles Levenback; Taren A Johnston; David M Gershenson
Journal:  Gynecol Oncol       Date:  2007-10-01       Impact factor: 5.482

10.  Use and Effectiveness of Intraperitoneal Chemotherapy for Treatment of Ovarian Cancer.

Authors:  Alexi A Wright; Angel Cronin; Dana E Milne; Michael A Bookman; Robert A Burger; David E Cohn; Mihaela C Cristea; Jennifer J Griggs; Nancy L Keating; Charles F Levenback; Gina Mantia-Smaldone; Ursula A Matulonis; Larissa A Meyer; Joyce C Niland; Jane C Weeks; David M O'Malley
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4.  Pharmacokinetics and toxicity of carboplatin used for hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment of epithelial ovarian cancer.

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6.  Chirality and asymmetry increase the potency of candidate ADRM1/RPN13 inhibitors.

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