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Safety and Preliminary Efficacy of Vorinostat With R-EPOCH in High-risk HIV-associated Non-Hodgkin's Lymphoma (AMC-075).
- Source :
-
Clinical lymphoma, myeloma & leukemia [Clin Lymphoma Myeloma Leuk] 2018 Mar; Vol. 18 (3), pp. 180-190.e2. Date of Electronic Publication: 2018 Feb 02. - Publication Year :
- 2018
-
Abstract
- Introduction: Vorinostat (VOR), a histone deacetylase inhibitor, enhances the anti-tumor effects of rituximab (R) and cytotoxic chemotherapy, induces viral lytic expression and cell killing in Epstein-Barr virus-positive (EBV <superscript>+</superscript> ) or human herpesvirus-8-positive (HHV-8 <superscript>+</superscript> ) tumors, and reactivates latent human immunodeficiency virus (HIV) for possible eradication by combination antiretroviral therapy (cART).<br />Patients and Methods: We performed a phase I trial of VOR given with R-based infusional EPOCH (etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin hydrochloride) (n = 12) and cART in aggressive HIV-associated B-cell non-Hodgkin lymphoma (NHL) in order to identify safe dosing and schedule. VOR (300 or 400 mg) was given orally on days 1 to 5 with each cycle of R-EPOCH for 10 high-risk patients with diffuse large B-cell lymphoma (1 EBV <superscript>+</superscript> ), 1 EBV <superscript>+</superscript> /HHV-8 <superscript>+</superscript> primary effusion lymphoma, and 1 unclassifiable NHL. VOR was escalated from 300 to 400 mg using a standard 3 + 3 design based on dose-limiting toxicity observed in cycle 1 of R-EPOCH.<br />Results: The recommended phase II dose of VOR was 300 mg, with dose-limiting toxicity in 2 of 6 patients at 400 mg (grade 4 thrombocytopenia, grade 4 neutropenia), and 1 of 6 treated at 300 mg (grade 4 sepsis from tooth abscess). Neither VOR, nor cART regimen, significantly altered chemotherapy steady-state concentrations. VOR chemotherapy did not negatively impact CD4+ cell counts or HIV viral loads, which decreased or remained undetectable in most patients during treatment. The response rate in high-risk patients with NHL treated with VOR(R)-EPOCH was 100% (complete 83% and partial 17%) with a 1-year event-free survival of 83% (95% confidence interval, 51.6%-97.9%).<br />Conclusion: VOR combined with R-EPOCH was tolerable and seemingly efficacious in patients with aggressive HIV-NHL.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Antineoplastic Agents pharmacology
Antineoplastic Combined Chemotherapy Protocols pharmacology
Cyclophosphamide pharmacology
Doxorubicin pharmacology
Etoposide pharmacology
Female
HIV Infections pathology
Humans
Lymphoma, Non-Hodgkin pathology
Male
Prednisone pharmacology
Vincristine pharmacology
Vorinostat pharmacology
Antineoplastic Agents therapeutic use
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Cyclophosphamide therapeutic use
Doxorubicin therapeutic use
Etoposide therapeutic use
HIV Infections drug therapy
Lymphoma, Non-Hodgkin drug therapy
Prednisone therapeutic use
Vincristine therapeutic use
Vorinostat therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 2152-2669
- Volume :
- 18
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Clinical lymphoma, myeloma & leukemia
- Publication Type :
- Academic Journal
- Accession number :
- 29426719
- Full Text :
- https://doi.org/10.1016/j.clml.2018.01.004