Outcomes for Relapsed and Refractory Peripheral T-Cell Lymphoma Patients after Front-Line Therapy from the COMPLETE Registry.


Journal

Acta haematologica
ISSN: 1421-9662
Titre abrégé: Acta Haematol
Pays: Switzerland
ID NLM: 0141053

Informations de publication

Date de publication:
2020
Historique:
received: 05 04 2019
accepted: 29 04 2019
pubmed: 18 7 2019
medline: 24 4 2020
entrez: 18 7 2019
Statut: ppublish

Résumé

Outcomes for patients with peripheral T-cell lymphoma (PTCL) who fail to achieve complete response (CR) or relapse after front-line therapy are poor with lack of prospective outcomes data. COMPLETE is a prospective registry of 499 patients enrolled at academic and community sites in the United States detailing patient demographics, treatment and outcomes for patients with aggressive T cell lymphomas. We report results for patients with primary refractory and relapsed disease. Primary refractory disease was defined as an evaluable best response to initial treatment (induction ± maintenance or consolidation/transplant) other than CR, and included a partial response, progressive disease, or no response/stable disease. Relapsed disease was defined as an evaluable best response to initial treatment of CR, followed by disease progression at a later date, irrespective of time to progression. Patients were included in the analysis if initial treatment began within 30 days of enrollment and treatment duration was ≥4 days. Of 420 evaluable patients, 97 met the definition for primary refractory and 58 with relapsed disease. In the second-line setting, relapsed patients received single-agent therapies more often than refractory patients (52 vs. 28%; p = 0.01) and were more likely to receive single-agent regimens (74 vs. 53%; p = 0.03). The objective response rate to second-line therapy was higher in relapsed patients (61 vs. 40%; p = 0.04) as was the proportion achieving a CR (41 vs. 14%; p = 0.002). Further, relapsed patients had longer overall survival (OS) compared to refractory patients, with a median OS of 29.1 versus 12.3 months. Despite the availability of newer active single agents, refractory patients were less likely to receive these therapies and continue to have inferior outcomes compared to those with relapsed disease. PTCL in the real world remains an unmet medical need, and improvements in front-line therapies are needed.

Sections du résumé

BACKGROUND
Outcomes for patients with peripheral T-cell lymphoma (PTCL) who fail to achieve complete response (CR) or relapse after front-line therapy are poor with lack of prospective outcomes data.
OBJECTIVES
COMPLETE is a prospective registry of 499 patients enrolled at academic and community sites in the United States detailing patient demographics, treatment and outcomes for patients with aggressive T cell lymphomas. We report results for patients with primary refractory and relapsed disease.
METHODS
Primary refractory disease was defined as an evaluable best response to initial treatment (induction ± maintenance or consolidation/transplant) other than CR, and included a partial response, progressive disease, or no response/stable disease. Relapsed disease was defined as an evaluable best response to initial treatment of CR, followed by disease progression at a later date, irrespective of time to progression. Patients were included in the analysis if initial treatment began within 30 days of enrollment and treatment duration was ≥4 days.
RESULTS
Of 420 evaluable patients, 97 met the definition for primary refractory and 58 with relapsed disease. In the second-line setting, relapsed patients received single-agent therapies more often than refractory patients (52 vs. 28%; p = 0.01) and were more likely to receive single-agent regimens (74 vs. 53%; p = 0.03). The objective response rate to second-line therapy was higher in relapsed patients (61 vs. 40%; p = 0.04) as was the proportion achieving a CR (41 vs. 14%; p = 0.002). Further, relapsed patients had longer overall survival (OS) compared to refractory patients, with a median OS of 29.1 versus 12.3 months.
CONCLUSIONS
Despite the availability of newer active single agents, refractory patients were less likely to receive these therapies and continue to have inferior outcomes compared to those with relapsed disease. PTCL in the real world remains an unmet medical need, and improvements in front-line therapies are needed.

Identifiants

pubmed: 31315113
pii: 000500666
doi: 10.1159/000500666
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

40-50

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Frederick Lansigan (F)

Dartmouth Hitchcock Medical Center, Hanover, New Hampshire, USA.

Steven M Horwitz (SM)

Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

Lauren C Pinter-Brown (LC)

University of California, Irvine, Irvine, California, USA.

Steven T Rosen (ST)

City of Hope, Duarte, California, USA.

Barbara Pro (B)

Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA.

Eric D Hsi (ED)

Cleveland Clinic, Cleveland, Ohio, USA.

Massimo Federico (M)

Centro Oncologico Modenese, Policlinico, Modena, Italy.

Christian Gisselbrecht (C)

Hôpital Saint Louis, Paris, France.

Marc Schwartz (M)

MS Biostatistics, LLC, Clermont, Florida, USA.

Lisa A Bellm (LA)

MedNet Solutions, Minnetonka, Minnesota, USA.

Mark Acosta (M)

Spectrum Pharmaceuticals Inc., Irvine, California, USA.

Andrei R Shustov (AR)

Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Ranjana H Advani (RH)

Stanford University Medical Center, Stanford, California, USA.

Tatyana Feldman (T)

Hackensack University Medical Center, Hackensack, New Jersey, USA.

Mary Jo Lechowicz (MJ)

Emory University, Atlanta, Georgia, USA.

Sonali M Smith (SM)

University of Chicago, Chicago, Illinois, USA.

Anil Tulpule (A)

University of Southern California, Los Angeles, California, USA.

Michael D Craig (MD)

West Virginia University, Morgantown, West Virginia, USA.

John P Greer (JP)

Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Brad S Kahl (BS)

Washington University School of Medicine, St. Louis, Missouri, USA.

Joseph W Leach (JW)

Virginia Piper Cancer Institute, Minneapolis, Minnesota, USA.

Neil Morganstein (N)

Overlook Medical Center, Summit, New Jersey, USA.

Carla Casulo (C)

University of Rochester, Rochester, New York, USA.

Steven I Park (SI)

Levine Cancer Institute, Chapel Hill, North Carolina, USA.

Francine M Foss (FM)

Yale University, New Haven, Connecticut, USA, Francine.foss@yale.edu.

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