Romidepsin Plus CHOP Versus CHOP in Patients With Previously Untreated Peripheral T-Cell Lymphoma: Results of the Ro-CHOP Phase III Study (Conducted by LYSA).


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 01 2022
Historique:
pubmed: 30 11 2021
medline: 22 2 2022
entrez: 29 11 2021
Statut: ppublish

Résumé

Romidepsin, a histone deacetylase inhibitor, has demonstrated activity in relapsed or refractory peripheral T-cell lymphoma (PTCL) as a single agent. Cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) therapy is widely used as first-line treatment of PTCL; however, it has limited efficacy. Results from a phase Ib and II study showed the feasibility of combining romidepsin with CHOP (Ro-CHOP). This study is a randomized phase III study of Ro-CHOP versus CHOP in adult patients with previously untreated PTCL. All patients received CHOP in 3-week cycles for six cycles. Romidepsin, 12 mg/m Between January 2013 and December 2017, 421 patients were enrolled (Ro-CHOP, n = 211; CHOP, n = 210). The median PFS for Ro-CHOP versus CHOP was 12.0 months (95% CI, 9.0 to 25.8) versus 10.2 months (95% CI, 7.4 to 13.2) with a hazard ratio of 0.81 ( The addition of romidepsin to CHOP did not improve PFS, response rates, nor overall survival and increased the frequency for grade ≥ 3 treatment-emergent adverse events. Ro-CHOP does not represent a significant advance in the standard of care for patients with previously untreated PTCL.

Identifiants

pubmed: 34843406
doi: 10.1200/JCO.21.01815
doi:

Substances chimiques

Depsipeptides 0
Histone Deacetylase Inhibitors 0
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
romidepsin CX3T89XQBK
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT01796002']

Types de publication

Clinical Trial, Phase III Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

242-251

Subventions

Organisme : Austrian Science Fund FWF
ID : I 4154
Pays : Austria
Organisme : Austrian Science Fund FWF
ID : I 4156
Pays : Austria

Commentaires et corrections

Type : CommentIn

Auteurs

Emmanuel Bachy (E)

Hospices Civils de Lyon, Lyon, France.
Claude Bernard Lyon 1 University, Lyon, France.

Vincent Camus (V)

Department of Hematology, Centre Henri Becquerel, Rouen, France.

Catherine Thieblemont (C)

APHP, Hôpital Saint-Louis, Service d'hémato-oncologie, DMU DHI, Université de Paris, Paris, France.

David Sibon (D)

Service d'Hématologie adultes, Hopital Universitaire Necker Enfants Malades, AP-HP, Paris, France.

René-Olivier Casasnovas (RO)

Department of Hematology, CHU Dijon-Bourgogne and INSERM 1231, Dijon, France.

Loïc Ysebaert (L)

IUCT Oncopole, Toulouse, France.

Gandhi Damaj (G)

Hematology Institute, University Hospital, Normandy University, School of Medicine, Caen, France.

Stéphanie Guidez (S)

Service d'Hématologie, CHU de Poiters, Poiters, France.

Gian Matteo Pica (GM)

Department of Hematology, Centre Hospitalier Métropole Savoie Chambéry, Chambéry, France.

Won Seog Kim (WS)

Samsung Medical Center, Seoul, South Korea.

Soon Thye Lim (ST)

National Cancer Centre Singapore, Singapore.

Marc André (M)

Department of Hematology, CHU UCL Namur, Yvoir, Belgium.

Alejandro Martín García-Sancho (AM)

Hospital Universitario de Salamanca, IBSAL, CIBERONC, Salamanca, Spain.

Maria Jesus Penarrubia (MJ)

Hospital Clinico Universitario de Valladolid, Valladolid, Spain.

Philipp B Staber (PB)

Division of Hematology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Judith Trotman (J)

Concord Repatriation General Hospital, University of Sydney, Concord, Australia.

Andreas Hüttmann (A)

Department of Hematology and Stem Cell Transplantation, West German Cancer Center Essen, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Vittorio Stefoni (V)

Policlinico Sant'Orsola-Malpighi, Bologna, Italy.

Alessandro Re (A)

Hematology Division, Spedali Civili di Brescia, Brescia, Italy.

Philippe Gaulard (P)

Department of Pathology and Inserm U955, University Hospital Henri Mondor, Créteil, France.

Marie-Helene Delfau-Larue (MH)

Department of Immunobiology and Inserm U955, Université Hôpital Henri Mondor, Créteil, France.

Laurence de Leval (L)

Institute of Pathology, Lausanne University Hospital, Lausanne University, Lausanne, Switzerland.

Michel Meignan (M)

LYSA Imaging, APHP, Hôpital Henri Mondor, Université Paris Est, Créteil, France.

Ju Li (J)

Bristol Myers Squibb Company, Princeton, NJ.

Franck Morschhauser (F)

Univ. Lille, CHU Lille, ULR 7365 - GRITA - Groupe de Recherche sur les Formes Injectables et les Technologies Associées, Lille, France.

Richard Delarue (R)

Service d'Hématologie adultes, Hopital Universitaire Necker Enfants Malades, AP-HP, Paris, France.
Celgene, a Bristol Myers Squibb Company, Boudry, Switzerland.

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Classifications MeSH