Bortezomib-based induction, high-dose melphalan and lenalidomide maintenance in myeloma up to 70 years of age.


Journal

Leukemia
ISSN: 1476-5551
Titre abrégé: Leukemia
Pays: England
ID NLM: 8704895

Informations de publication

Date de publication:
03 2021
Historique:
received: 29 03 2020
accepted: 06 07 2020
revised: 29 06 2020
pubmed: 21 7 2020
medline: 23 3 2021
entrez: 21 7 2020
Statut: ppublish

Résumé

Intensive upfront therapy in newly-diagnosed multiple myeloma (MM) including induction therapy (IT), high-dose melphalan (MEL200), and autologous blood stem cell transplantation (ASCT) followed by consolidation and/or maintenance is mostly restricted to patients up to 65 years of age. Prospective phase III trial data in the era of novel agents for patients up to 70 years of age are not available. The GMMG-MM5 trial included 601 patients between 18 and 70 years of age, divided in three groups for the present analysis: ≤60 years (S1, n = 353), 61-65 years (S2, n = 107) and 66-70 years (S3, n = 141). Treatment consisted of a bortezomib-containing IT, MEL200/ASCT, consolidation, and maintenance with lenalidomide. Adherence to treatment was similar among patients of the three age groups. Overall toxicity during all treatment phases was increased in S2 and S3 compared to S1 (any adverse event/any serious adverse event: S1:81.7/41.8% vs. S2:90.7/56.5% vs. S3:87.2/68.1%, p = 0.05/<0.001). With respect to progression-free survival (log-rank p = 0.73), overall survival (log-rank p = 0.54) as well as time-to-progression (Gray's p = 0.83) and non-relapse mortality (Gray's p = 0.25), no differences were found between the three age groups. Our results imply that an intensive upfront therapy with a bortezomib-containing IT, MEL200/ASCT, lenalidomide consolidation, and maintenance should be applied to transplant-eligible MM patients up to 70 years of age.

Identifiants

pubmed: 32684633
doi: 10.1038/s41375-020-0976-9
pii: 10.1038/s41375-020-0976-9
pmc: PMC8318883
doi:

Substances chimiques

Bortezomib 69G8BD63PP
Lenalidomide F0P408N6V4

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

809-822

Commentaires et corrections

Type : ErratumIn

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Auteurs

Elias K Mai (EK)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.
National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg, Germany.

Kaya Miah (K)

Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Uta Bertsch (U)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.
National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg, Germany.

Jan Dürig (J)

Department of Hematology, University Clinic Essen, Essen, Germany.

Christof Scheid (C)

Department of Internal Medicine I, University Hospital Cologne, Cologne, Germany.

Katja C Weisel (KC)

Department of Oncology, Hematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Hematology, Oncology and Immunology, University Hospital Tübingen, Tübingen, Germany.

Christina Kunz (C)

Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Institute of Child Nutrition, Max Rubner Institute, Federal Research Institute of Nutrition and Food, Karlsruhe, Germany.

Markus Munder (M)

Department of Internal Medicine III, University Medical Center Mainz, Mainz, Germany.

Hans-Walter Lindemann (HW)

Department of Hematology and Oncology, Katholisches Krankenhaus Hagen, Hagen, Germany.

Maximilian Merz (M)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.

Dirk Hose (D)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.

Anna Jauch (A)

Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.

Anja Seckinger (A)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.

Steffen Luntz (S)

Coordination Centre for Clinical Trials, University Hospital Heidelberg, Heidelberg, Germany.

Sandra Sauer (S)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.

Stephan Fuhrmann (S)

Department of Hematology and Oncology, Helios Hospital Berlin Buch, Berlin, Germany.

Peter Brossart (P)

University Hospital Bonn, Bonn, Germany.

Ahmet Elmaagacli (A)

Department of Hematology and Oncology, Asklepios Hospital Hamburg St. Georg, Hamburg, Germany.

Martin Goerner (M)

Department of Hematology, Oncology and Palliative Care, Klinikum Bielefeld, Bielefeld, Germany.

Helga Bernhard (H)

Department of Internal Medicine V, Klinikum Darmstadt, Darmstadt, Germany.

Martin Hoffmann (M)

Medical Clinic A, Klinikum Ludwigshafen, Ludwigshafen, Germany.

Marc S Raab (MS)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.

Igor W Blau (IW)

Medical Clinic, Charité University Medicine Berlin, Berlin, Germany.

Mathias Hänel (M)

Department of Internal Medicine III, Klinikum Chemnitz, Chemnitz, Germany.

Axel Benner (A)

Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Hans J Salwender (HJ)

Department of Hematology and Oncology, Asklepios Hospital Hamburg Altona, Hamburg, Germany.

Hartmut Goldschmidt (H)

Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany. hartmut.goldschmidt@med.uni-heidelberg.de.
National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg, Germany. hartmut.goldschmidt@med.uni-heidelberg.de.

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