Oxaliplatin before autologous transplantation in combination with high-dose cytarabine and rituximab provides longer disease control than cisplatin or carboplatin in patients with mantle-cell lymphoma: results from the LyMA prospective trial.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
07 2021
Historique:
received: 07 10 2020
accepted: 10 12 2020
pubmed: 5 3 2021
medline: 27 7 2021
entrez: 4 3 2021
Statut: ppublish

Résumé

LyMA trial has demonstrated the benefit of rituximab maintenance after autologous stem cell transplantation (ASCT) in previously untreated mantle-cell lymphoma patients (MCL). Induction consisted of four courses of R-DHAP (rituximab, dexamethasone, high-dose cytarabine, and platinum derivative). The platinum derivative (PD) choice was free: R-DHA-cisplatin, R-DHA-carboplatin, or R-DHA-oxaliplatin. We investigated the prognostic impact of each PD. PFS and OS calculated from inclusion and investigated in an intention-to-treat (ITT) (= 298) and per-protocol analyses (PP) (n = 227). R-DHACis, R-DHACa, or R-DHAOx were used at first cycle in 184, 76, and 38 patients, respectively. Overall, 71 patients (59 in the R-DHACis) required a change in PD, mainly because of PD toxicity. In ITT-analysis, PFS in the R-DHACis and R-DHACa groups were similar (4-year PFS of 65%), while R-DHAOx had a better PFS (4-year PFS of 65% versus 86.5%, respectively, HR = 0.44, p = 0.02). The 4-year OS was 92% for R-DHAOx versus 75.9% for R-DHACis/DHACa (HR = 0.37, p = 0.03). Similar results were yielded in the PP analysis. Low MIPI and R-DHAOx were independent favorable prognostic markers for both PFS (HR = 0.44, p = 0.035) and OS (HR = 0.36, p = 0.045). In vitro and in silico analyses confirmed that oxaliplatin has an anti-MCL cytotoxic effect that differs from that of other PD. R-DHAOx before ASCT provides better outcome in transplantation eligible young MCL patients.

Identifiants

pubmed: 33658645
doi: 10.1038/s41409-020-01198-2
pii: 10.1038/s41409-020-01198-2
doi:

Substances chimiques

Cytarabine 04079A1RDZ
Oxaliplatin 04ZR38536J
Rituximab 4F4X42SYQ6
Carboplatin BG3F62OND5
Cisplatin Q20Q21Q62J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1700-1709

Références

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Auteurs

Benoit Tessoulin (B)

Department of Clinical Hematology, Nantes University Hospital, Nantes, France.
CRCINA, INSERM, CNRS, Angers University, Nantes University, Nantes, France.

David Chiron (D)

CRCINA, INSERM, CNRS, Angers University, Nantes University, Nantes, France.

Catherine Thieblemont (C)

Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Hemato-Oncology, Paris, France.
Sorbonne Paris Cité, Diderot University, Paris, France.

Lucie Oberic (L)

Department of Clinical Hematology, Purpan University Hospital, Toulouse, France.

Kamal Bouadballah (K)

Department of Clinical Hematology, Bordeaux University Hospital, Bordeaux, France.

Emmanuel Gyan (E)

Department of Clinical Hematology, Tours University Hospital, Tours, France.
Inserm UMR 1415, Tours University, Tours, France.

Gandhi Damaj (G)

Department of Clinical Hematology, Amiens University Hospital, Amiens, France.
Department of Clinical Hematology, Caen University Hospital, Caens, France.

Vincent Ribrag (V)

Department of Hematology, Institut Gustave Roussy, Villejuif, France.

Rémy Gressin (R)

Department of Clinical Hematology, Grenoble University Hospital, Grenoble, France.

Pierre Feugier (P)

Department of Clinical Hematology, Nancy University Hospital, INSERM 1256, Nancy, France.

Olivier Casasnovas (O)

Service d'Hématologie Clinique, Centre Hospitalier Universitaire Dijon, INSERM UMR1231, Dijon, France.

Hacène Zerazhi (H)

Department of Hematology, Centre Hospitalier d'Avignon, Avignon, France.

François Lemonnier (F)

Unité Hémopathies Lymphoïdes, AP-HP Hôpital Henri Mondor, Créteil, France.

Hervé Maisonneuve (H)

Department of Clinical Hematology, Vendée Hospital Center, La Roche sur Yon, France.

Clementine Joubert (C)

Department of Biostatistics, LYSARC, Lyon, France.

Eric Van Den Neste (E)

Cliniques Universitaires Saint-Luc, Université de Louvain, Brussels, Belgium.

Thierry Lamy (T)

Department of Clinical Hematology, MICA Research Unit, Rennes University Hospital, Rennes, France.

Hervé Tilly (H)

Department of Hematology, Centre Henri Becquerel, University Rouen, INSERM U1245, Rouen, France.

Anne Moreau (A)

Department of Pathology, Nantes University Hospital, Nantes, France.

Olivier Hermine (O)

Hôpital Necker, Institut Imagine, Assistance Publique-Hôpitaux de Paris, University Paris Descartes, Paris, France.

Steven Le Gouill (S)

Department of Clinical Hematology, Nantes University Hospital, Nantes, France. steven.legouill@chu-nantes.fr.
CRCINA, INSERM, CNRS, Angers University, Nantes University, Nantes, France. steven.legouill@chu-nantes.fr.

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