Response-adapted therapy with infusional EPOCH chemotherapy plus rituximab in HIV-associated, B-cell non-Hodgkin's lymphoma.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 03 2021
Historique:
received: 19 11 2019
pubmed: 29 2 2020
medline: 28 5 2021
entrez: 29 2 2020
Statut: epublish

Résumé

Four cycles of rituximab plus CHOP chemotherapy is as effective as 6 cycles in low-risk diffuse large B-cell lymphoma (DLBCL). Here we report a post-hoc analysis of a prospective clinical trial in patients with HIV-associated DLBCL and high-grade lymphoma treated with 4-6 cycles of EPOCH plus rituximab based a response-adapted treatment strategy. 106 evaluable patients with HIV-associated DLBCL or high-grade CD20-positive non-Hodgkin's lymphoma were randomized to receive rituximab (375 mg/m2) given either concurrently prior to each infusional EPOCH cycle, or sequentially (weekly for 6 weeks) following completion of EPOCH. EPOCH consisted of a 96-hour IV infusion of etoposide, doxorubicin, and vincristine plus oral prednisone followed by IV bolus cyclophosphamide every 21 days for 4 to 6 cycles. Patients received 2 additional cycles of therapy after documentation of a complete response (CR) by computerized tomography after cycles 2 and 4. 64 of 106 evaluable patients (60%, 95% CI 50%, 70%) had a CR in both treatment arms. The 2-year event-free survival (EFS) rates were similar in the 24 patients with CR who received 4 or fewer EPOCH cycles (78%, 95% confidence intervals [55%, 90%]) due to achieving a CR after 2 cycles, compared with those who received 5-6 cycles of EPOCH (85%, 95% CI 70%, 93%) because a CR was first documented after cycle 4. A response-adapted strategy may permit a shorter treatment duration without compromising therapeutic efficacy in patients with HIV-associated lymphoma treated with EPOCH plus rituximab, which merits further evaluation in additional prospective trials. Clinical Trials.gov identifier NCT00049036.

Identifiants

pubmed: 32107337
pii: haematol.2019.243386
doi: 10.3324/haematol.2019.243386
pmc: PMC7927888
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Etoposide 6PLQ3CP4P3
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT00049036']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

730-735

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA121947
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA121947
Pays : United States

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Auteurs

Joseph A Sparano (JA)

Montefiore-Einstein Cancer Center, Montefiore Medical Center, Bronx, NY, USA.

Jeannette Y Lee (JY)

University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Lawrence D Kaplan (LD)

University of California, San Francisco, San Francisco, CA, USA.

Juan Carlos Ramos (JC)

University of Miami, Sylvester Comprehensive Cancer Center, Miami, USA.

Richard F Ambinder (RF)

Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, MD, USA.

William Wachsman (W)

Moores University of California, San Diego Cancer Center, La Jolla, CA, USA.

David Aboulafia (D)

Virginia Mason Cancer Institute, Seattle, WA, USA.

Ariela Noy (A)

Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY, USA.

David H Henry (DH)

University of Pennsylvania, Pennsylvania Hospital, Philadelphia, PA, USA.

Lee Ratner (L)

Washington University, St. Louis, MO, USA.

Ethel Cesarman (E)

Weill Medical College of Cornell University, New York, NY, USA.

Amy Chadburn (A)

Weill Cornell Medical College, New York, NY, USA.

Ronald Mitsuyasu (R)

University of California, Los Angeles Medical Center, Los Angeles, CA, USA.

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Classifications MeSH