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Consolidation and Maintenance in Newly Diagnosed Multiple Myeloma.
Sonneveld, Pieter; Dimopoulos, Meletios A; Beksac, Meral; van der Holt, Bronno; Aquino, Sara; Ludwig, Heinz; Zweegman, Sonja; Zander, Thilo; Zamagni, Elena; Wester, Ruth; Hajek, Roman; Pantani, Lucia; Dozza, Luca; Gay, Francesca; Cafro, AnneMaria; De Rosa, Luca; Morelli, Annamaria; Gregersen, Henrik; Gulbrandsen, Nina; Cornelisse, Petra; Troia, Rosella; Oliva, Stefania; van de Velden, Vincent; Wu, KaLung; Ypma, Paula F; Bos, Gerard; Levin, Mark-David; Pour, Luca; Driessen, Christoph; Broijl, Annemiek; Croockewit, Alexandra; Minnema, Monique C; Waage, Anders; Hveding, Cecilie; van de Donk, Niels W C J; Offidani, Massimo; Palumbo, Giuseppe A; Spencer, Andrew; Boccadoro, Mario; Cavo, Michele.
Afiliación
  • Sonneveld P; Department of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Dimopoulos MA; Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
  • Beksac M; Department of Hematology, Ankara University School of Medicine, Ankara, Turkey.
  • van der Holt B; Department of Hematology, HOVON Data Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Aquino S; IRCCS Azienda Ospedaliera Universitaria San Martino, IST Instituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
  • Ludwig H; Wilhelminen Cancer Research Institute, c/o Wilhelminenspital, Vienna, Austria.
  • Zweegman S; Department of Hematology, Amsterdam UMC, Cancer Center Amsterdam, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
  • Zander T; Medical Oncology, Luzerner Kantonshospital, Luzern, Switzerland.
  • Zamagni E; IRCCS Azienda Ospedaliero-Universitaria di Bologna Istituto di Ematologia "Seràgnoli" and Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale Università di Bologna, Bologna, Italy.
  • Wester R; Department of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Hajek R; University Hospital Ostrava, Ostrava, Czech Republic.
  • Pantani L; IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli," Bologna, Italy.
  • Dozza L; Department of Experimental, Diagnostic and Experimental Medicine, Seràgnoli Institute of Hematology, Bologna University School of Medicine, S. Orsola Malpighi Hospital, Bologna, Italy.
  • Gay F; Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Torino, Italy.
  • Cafro A; ASST Grande Ospedale Metropolitano, Niguarda, Milan, Italy.
  • De Rosa L; Ospedale San Camillo Forlanini, Rome, Italy.
  • Morelli A; Department of Hematology, Transfusion Medicine and Biotechnology Santo Spirito, Civic Hospital, Pescara, Italy.
  • Gregersen H; Department of Haematology, Aalborg University Hospital, Aalborg, Denmark.
  • Gulbrandsen N; Department of Hematology, Oslo University Hospital, Oslo, Norway.
  • Cornelisse P; HOVON Data Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Troia R; Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Torino, Italy.
  • Oliva S; Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Torino, Italy.
  • van de Velden V; Department of Immunology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Wu K; Department of Hematology, ZNA Stuivenberg, Antwerp, Belgium.
  • Ypma PF; Department of Hematology, Haga Ziekenhuis, The Hague, the Netherlands.
  • Bos G; Maastricht University Medical Center, Maastricht, the Netherlands.
  • Levin MD; Albert Schweitzer Ziekenhuis, Dordrecht, the Netherlands.
  • Pour L; University Hospital Brno, Brno, Czech Republic.
  • Driessen C; Department of Oncology/Hematology, Kantonsspital, St Gallen, Switzerland.
  • Broijl A; Department of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Croockewit A; Department of Hematology, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Minnema MC; Department of Hematology, University Medical Centre Utrecht, the Netherlands.
  • Waage A; Department of Hematology, St Olav Hospital, Trondheim, Norway.
  • Hveding C; Sahlgrenska University Hospital, Gothenburg, Sweden.
  • van de Donk NWCJ; Department of Hematology, Amsterdam UMC, Cancer Center Amsterdam, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
  • Offidani M; Clinica di Ematologia, AOU Ospedali Riuniti di Ancona, Ancona, Italy.
  • Palumbo GA; Department of Scienze Mediche Chirurgiche e Tecnologie Avanzate "G.F. Ingrassia," University of Catania, Catania, Italy.
  • Spencer A; Department of Haematology, Alfred Hospital-Monash University, Melbourne, Australia.
  • Boccadoro M; Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Torino, Italy.
  • Cavo M; IRCCS S.Orsola-Malpighi, Istituto di Ematologia "Seràgnoli," Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università degli Studi di Bologna, Bologna, Italy.
J Clin Oncol ; 39(32): 3613-3622, 2021 11 10.
Article en En | MEDLINE | ID: mdl-34520219
ABSTRACT

PURPOSE:

To address the role of consolidation treatment for newly diagnosed, transplant eligible patients with multiple myeloma in a controlled clinical trial. PATIENTS AND

METHODS:

The EMN02/HOVON95 trial compared consolidation treatment with two cycles of bortezomib, lenalidomide, and dexamethasone (VRD) or no consolidation after induction and intensification therapy, followed by continuous lenalidomide maintenance. Primary study end point was progression-free survival (PFS).

RESULTS:

Eight hundred seventy-eight eligible patients were randomly assigned to receive VRD consolidation (451 patients) or no consolidation (427 patients). At a median follow-up of 74.8 months, median PFS with adjustment for pretreatment was prolonged in patients randomly assigned to VRD consolidation (59.3 v 42.9 months, hazard ratio [HR] = 0.81; 95% CI, 0.68 to 0.96; P = .016). The PFS benefit was observed across most predefined subgroups, including revised International Staging System (ISS) stage, cytogenetics, and prior treatment. Revised ISS3 stage (HR, 2.00; 95% CI, 1.41 to 2.86) and ampl1q (HR, 1.67; 95% CI, 1.37 to 2.04) were significant adverse prognostic factors. The median duration of maintenance was 33 months (interquartile range 13-86 months). Response ≥ complete response (CR) after consolidation versus no consolidation before start of maintenance was 34% versus 18%, respectively (P < .001). Response ≥ CR on protocol including maintenance was 59% with consolidation and 46% without (P < .001). Minimal residual disease analysis by flow cytometry in a subgroup of 226 patients with CR or stringent complete response or very good partial response before start of maintenance demonstrated a 74% minimal residual disease-negativity rate in VRD-treated patients. Toxicity from VRD was acceptable and manageable.

CONCLUSION:

Consolidation treatment with VRD followed by lenalidomide maintenance improves PFS and depth of response in newly diagnosed patients with multiple myeloma as compared to maintenance alone.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Dexametasona / Protocolos de Quimioterapia Combinada Antineoplásica / Bortezomib / Lenalidomida / Mieloma Múltiple Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Límite: Adolescent / Adult / Aged / Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Clin Oncol Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Dexametasona / Protocolos de Quimioterapia Combinada Antineoplásica / Bortezomib / Lenalidomida / Mieloma Múltiple Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Límite: Adolescent / Adult / Aged / Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Clin Oncol Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos