Lenalidomide in relapsed and refractory multiple myeloma disease: feasibility and benefits of long-term treatment

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Lenalidomide in relapsed and refractory multiple myeloma disease: feasibility and benefits of long-term treatment. / Zago, Manola; Oehrlein, Katharina; Rendl, Corinna; Hahn-Ast, Corinna; Kanz, Lothar; Weisel, Katja.

in: ANN HEMATOL, Jahrgang 93, Nr. 12, 12.2014, S. 1993-9.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{79fb524197084b0fbff60b464fbbd1a5,
title = "Lenalidomide in relapsed and refractory multiple myeloma disease: feasibility and benefits of long-term treatment",
abstract = "Lenalidomide in combination with dexamethasone is an effective and well-established treatment of relapsed or refractory multiple myeloma (rrMM) disease. Due to the scarcity of reports assessing benefit and risk of long-term lenalidomide treatment in non-selected rrMM patients, we retrospectively analysed the long-term outcome in patients with rrMM treated with lenalidomide and dexamethasone. Sixty-seven patients (pts) who were treated with lenalidomide/dexamethasone for rrMM in the approved indication from 2007 to 2011 were included in this retrospective, single-centre analysis. Kaplan-Meier survival estimates were compared between total population, patients on lenalidomide for more than 12 months (mo) and patients discontinuing therapy earlier than 12 months. Median overall survival (OS) of the total patient population was 33.2 mo. OS of pts treated beyond 12 mo was 42.9 mo compared to 20.2 mo (p = 0.027) for pts stopping lenalidomide earlier than 12 mo for other reasons than progression disease (PD). OS of pts >12 mo on lenalidomide treatment did not significantly differ between pts who had received previous autologous transplantation, allogeneic transplantation or conventional therapy. Main non-hematologic toxicities were infections of grade 3/4 in 25 % and thrombembolic events of all grades in 18 % of patients. To the best of our knowledge, this is the first report on feasibility and efficacy of long-term lenalidomide treatment in a non-selected patient cohort. OS of pts >12 mo on lenalidomide is superior when compared to pts discontinued earlier for reasons other than PD. Our data confirm the current use of lenalidomide as a continuous long-term treatment strategy.",
keywords = "Adult, Aged, Aged, 80 and over, Allografts, Antineoplastic Combined Chemotherapy Protocols, Boronic Acids, Bortezomib, Chromosome Aberrations, Dexamethasone, Disease Progression, Drug Evaluation, Feasibility Studies, Female, Hematologic Diseases, Hematopoietic Stem Cell Transplantation, Humans, Kaplan-Meier Estimate, Lenalidomide, Male, Middle Aged, Multiple Myeloma, Pyrazines, Recurrence, Retrospective Studies, Salvage Therapy, Sensation Disorders, Thalidomide, Thromboembolism, Transplantation, Autologous, Journal Article, Research Support, Non-U.S. Gov't",
author = "Manola Zago and Katharina Oehrlein and Corinna Rendl and Corinna Hahn-Ast and Lothar Kanz and Katja Weisel",
year = "2014",
month = dec,
doi = "10.1007/s00277-014-2149-2",
language = "English",
volume = "93",
pages = "1993--9",
journal = "ANN HEMATOL",
issn = "0939-5555",
publisher = "Springer",
number = "12",

}

RIS

TY - JOUR

T1 - Lenalidomide in relapsed and refractory multiple myeloma disease: feasibility and benefits of long-term treatment

AU - Zago, Manola

AU - Oehrlein, Katharina

AU - Rendl, Corinna

AU - Hahn-Ast, Corinna

AU - Kanz, Lothar

AU - Weisel, Katja

PY - 2014/12

Y1 - 2014/12

N2 - Lenalidomide in combination with dexamethasone is an effective and well-established treatment of relapsed or refractory multiple myeloma (rrMM) disease. Due to the scarcity of reports assessing benefit and risk of long-term lenalidomide treatment in non-selected rrMM patients, we retrospectively analysed the long-term outcome in patients with rrMM treated with lenalidomide and dexamethasone. Sixty-seven patients (pts) who were treated with lenalidomide/dexamethasone for rrMM in the approved indication from 2007 to 2011 were included in this retrospective, single-centre analysis. Kaplan-Meier survival estimates were compared between total population, patients on lenalidomide for more than 12 months (mo) and patients discontinuing therapy earlier than 12 months. Median overall survival (OS) of the total patient population was 33.2 mo. OS of pts treated beyond 12 mo was 42.9 mo compared to 20.2 mo (p = 0.027) for pts stopping lenalidomide earlier than 12 mo for other reasons than progression disease (PD). OS of pts >12 mo on lenalidomide treatment did not significantly differ between pts who had received previous autologous transplantation, allogeneic transplantation or conventional therapy. Main non-hematologic toxicities were infections of grade 3/4 in 25 % and thrombembolic events of all grades in 18 % of patients. To the best of our knowledge, this is the first report on feasibility and efficacy of long-term lenalidomide treatment in a non-selected patient cohort. OS of pts >12 mo on lenalidomide is superior when compared to pts discontinued earlier for reasons other than PD. Our data confirm the current use of lenalidomide as a continuous long-term treatment strategy.

AB - Lenalidomide in combination with dexamethasone is an effective and well-established treatment of relapsed or refractory multiple myeloma (rrMM) disease. Due to the scarcity of reports assessing benefit and risk of long-term lenalidomide treatment in non-selected rrMM patients, we retrospectively analysed the long-term outcome in patients with rrMM treated with lenalidomide and dexamethasone. Sixty-seven patients (pts) who were treated with lenalidomide/dexamethasone for rrMM in the approved indication from 2007 to 2011 were included in this retrospective, single-centre analysis. Kaplan-Meier survival estimates were compared between total population, patients on lenalidomide for more than 12 months (mo) and patients discontinuing therapy earlier than 12 months. Median overall survival (OS) of the total patient population was 33.2 mo. OS of pts treated beyond 12 mo was 42.9 mo compared to 20.2 mo (p = 0.027) for pts stopping lenalidomide earlier than 12 mo for other reasons than progression disease (PD). OS of pts >12 mo on lenalidomide treatment did not significantly differ between pts who had received previous autologous transplantation, allogeneic transplantation or conventional therapy. Main non-hematologic toxicities were infections of grade 3/4 in 25 % and thrombembolic events of all grades in 18 % of patients. To the best of our knowledge, this is the first report on feasibility and efficacy of long-term lenalidomide treatment in a non-selected patient cohort. OS of pts >12 mo on lenalidomide is superior when compared to pts discontinued earlier for reasons other than PD. Our data confirm the current use of lenalidomide as a continuous long-term treatment strategy.

KW - Adult

KW - Aged

KW - Aged, 80 and over

KW - Allografts

KW - Antineoplastic Combined Chemotherapy Protocols

KW - Boronic Acids

KW - Bortezomib

KW - Chromosome Aberrations

KW - Dexamethasone

KW - Disease Progression

KW - Drug Evaluation

KW - Feasibility Studies

KW - Female

KW - Hematologic Diseases

KW - Hematopoietic Stem Cell Transplantation

KW - Humans

KW - Kaplan-Meier Estimate

KW - Lenalidomide

KW - Male

KW - Middle Aged

KW - Multiple Myeloma

KW - Pyrazines

KW - Recurrence

KW - Retrospective Studies

KW - Salvage Therapy

KW - Sensation Disorders

KW - Thalidomide

KW - Thromboembolism

KW - Transplantation, Autologous

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1007/s00277-014-2149-2

DO - 10.1007/s00277-014-2149-2

M3 - SCORING: Journal article

C2 - 24974802

VL - 93

SP - 1993

EP - 1999

JO - ANN HEMATOL

JF - ANN HEMATOL

SN - 0939-5555

IS - 12

ER -