Geriatric assessment predicts survival and toxicities in elderly myeloma patients: an International Myeloma Working Group report

We conducted a pooled analysis of 869 individual newly diagnosed elderly patient data from 3 prospective trials. At diagnosis, a geriatric assessment had been performed. An additive scoring system (range 0-5), based on age, comorbidities, and cognitive and physical conditions, was developed to ident...

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Vydané v:Blood Ročník 125; číslo 13; s. 2068
Hlavní autori: Palumbo, Antonio, Bringhen, Sara, Mateos, Maria-Victoria, Larocca, Alessandra, Facon, Thierry, Kumar, Shaji K, Offidani, Massimo, McCarthy, Philip, Evangelista, Andrea, Lonial, Sagar, Zweegman, Sonja, Musto, Pellegrino, Terpos, Evangelos, Belch, Andrew, Hajek, Roman, Ludwig, Heinz, Stewart, A Keith, Moreau, Philippe, Anderson, Kenneth, Einsele, Hermann, Durie, Brian G M, Dimopoulos, Meletios A, Landgren, Ola, San Miguel, Jesus F, Richardson, Paul, Sonneveld, Pieter, Rajkumar, S Vincent
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 26.03.2015
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ISSN:1528-0020, 1528-0020
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Abstract We conducted a pooled analysis of 869 individual newly diagnosed elderly patient data from 3 prospective trials. At diagnosis, a geriatric assessment had been performed. An additive scoring system (range 0-5), based on age, comorbidities, and cognitive and physical conditions, was developed to identify 3 groups: fit (score = 0, 39%), intermediate fitness (score = 1, 31%), and frail (score ≥2, 30%). The 3-year overall survival was 84% in fit, 76% in intermediate-fitness (hazard ratio [HR], 1.61; P = .042), and 57% in frail (HR, 3.57; P < .001) patients. The cumulative incidence of grade ≥3 nonhematologic adverse events at 12 months was 22.2% in fit, 26.4% in intermediate-fitness (HR, 1.23; P = .217), and 34.0% in frail (HR, 1.74; P < .001) patients. The cumulative incidence of treatment discontinuation at 12 months was 16.5% in fit, 20.8% in intermediate-fitness (HR, 1.41; P = .052), and 31.2% in frail (HR, 2.21; P < .001) patients. Our frailty score predicts mortality and the risk of toxicity in elderly myeloma patients. The International Myeloma Working group proposes this score for the measurement of frailty in designing future clinical trials. These trials are registered at www.clinicaltrials.gov as #NCT01093136 (EMN01), #NCT01190787 (26866138MMY2069), and #NCT01346787 (IST-CAR-506).
AbstractList We conducted a pooled analysis of 869 individual newly diagnosed elderly patient data from 3 prospective trials. At diagnosis, a geriatric assessment had been performed. An additive scoring system (range 0-5), based on age, comorbidities, and cognitive and physical conditions, was developed to identify 3 groups: fit (score = 0, 39%), intermediate fitness (score = 1, 31%), and frail (score ≥2, 30%). The 3-year overall survival was 84% in fit, 76% in intermediate-fitness (hazard ratio [HR], 1.61; P = .042), and 57% in frail (HR, 3.57; P < .001) patients. The cumulative incidence of grade ≥3 nonhematologic adverse events at 12 months was 22.2% in fit, 26.4% in intermediate-fitness (HR, 1.23; P = .217), and 34.0% in frail (HR, 1.74; P < .001) patients. The cumulative incidence of treatment discontinuation at 12 months was 16.5% in fit, 20.8% in intermediate-fitness (HR, 1.41; P = .052), and 31.2% in frail (HR, 2.21; P < .001) patients. Our frailty score predicts mortality and the risk of toxicity in elderly myeloma patients. The International Myeloma Working group proposes this score for the measurement of frailty in designing future clinical trials. These trials are registered at www.clinicaltrials.gov as #NCT01093136 (EMN01), #NCT01190787 (26866138MMY2069), and #NCT01346787 (IST-CAR-506).
We conducted a pooled analysis of 869 individual newly diagnosed elderly patient data from 3 prospective trials. At diagnosis, a geriatric assessment had been performed. An additive scoring system (range 0-5), based on age, comorbidities, and cognitive and physical conditions, was developed to identify 3 groups: fit (score = 0, 39%), intermediate fitness (score = 1, 31%), and frail (score ≥2, 30%). The 3-year overall survival was 84% in fit, 76% in intermediate-fitness (hazard ratio [HR], 1.61; P = .042), and 57% in frail (HR, 3.57; P < .001) patients. The cumulative incidence of grade ≥3 nonhematologic adverse events at 12 months was 22.2% in fit, 26.4% in intermediate-fitness (HR, 1.23; P = .217), and 34.0% in frail (HR, 1.74; P < .001) patients. The cumulative incidence of treatment discontinuation at 12 months was 16.5% in fit, 20.8% in intermediate-fitness (HR, 1.41; P = .052), and 31.2% in frail (HR, 2.21; P < .001) patients. Our frailty score predicts mortality and the risk of toxicity in elderly myeloma patients. The International Myeloma Working group proposes this score for the measurement of frailty in designing future clinical trials. These trials are registered at www.clinicaltrials.gov as #NCT01093136 (EMN01), #NCT01190787 (26866138MMY2069), and #NCT01346787 (IST-CAR-506).We conducted a pooled analysis of 869 individual newly diagnosed elderly patient data from 3 prospective trials. At diagnosis, a geriatric assessment had been performed. An additive scoring system (range 0-5), based on age, comorbidities, and cognitive and physical conditions, was developed to identify 3 groups: fit (score = 0, 39%), intermediate fitness (score = 1, 31%), and frail (score ≥2, 30%). The 3-year overall survival was 84% in fit, 76% in intermediate-fitness (hazard ratio [HR], 1.61; P = .042), and 57% in frail (HR, 3.57; P < .001) patients. The cumulative incidence of grade ≥3 nonhematologic adverse events at 12 months was 22.2% in fit, 26.4% in intermediate-fitness (HR, 1.23; P = .217), and 34.0% in frail (HR, 1.74; P < .001) patients. The cumulative incidence of treatment discontinuation at 12 months was 16.5% in fit, 20.8% in intermediate-fitness (HR, 1.41; P = .052), and 31.2% in frail (HR, 2.21; P < .001) patients. Our frailty score predicts mortality and the risk of toxicity in elderly myeloma patients. The International Myeloma Working group proposes this score for the measurement of frailty in designing future clinical trials. These trials are registered at www.clinicaltrials.gov as #NCT01093136 (EMN01), #NCT01190787 (26866138MMY2069), and #NCT01346787 (IST-CAR-506).
Author Kumar, Shaji K
Moreau, Philippe
Musto, Pellegrino
Terpos, Evangelos
Zweegman, Sonja
Mateos, Maria-Victoria
Stewart, A Keith
Offidani, Massimo
Sonneveld, Pieter
San Miguel, Jesus F
Rajkumar, S Vincent
Dimopoulos, Meletios A
McCarthy, Philip
Palumbo, Antonio
Evangelista, Andrea
Lonial, Sagar
Ludwig, Heinz
Anderson, Kenneth
Richardson, Paul
Landgren, Ola
Bringhen, Sara
Facon, Thierry
Hajek, Roman
Larocca, Alessandra
Durie, Brian G M
Belch, Andrew
Einsele, Hermann
Author_xml – sequence: 1
  givenname: Antonio
  surname: Palumbo
  fullname: Palumbo, Antonio
  organization: Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy
– sequence: 2
  givenname: Sara
  surname: Bringhen
  fullname: Bringhen, Sara
  organization: Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy
– sequence: 3
  givenname: Maria-Victoria
  surname: Mateos
  fullname: Mateos, Maria-Victoria
  organization: Servicio de Hematología, Hospital Universitario de Salamanca, Centro de Investigación del Cáncer, Instituto de Biología Molecular y Celular del Cáncer, Universidad de Salamanca-Centro Superior de Investigaciones Científicas, Salamanca, Spain
– sequence: 4
  givenname: Alessandra
  surname: Larocca
  fullname: Larocca, Alessandra
  organization: Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy
– sequence: 5
  givenname: Thierry
  surname: Facon
  fullname: Facon, Thierry
  organization: Department of Hematology, University Hospital, Lille, France
– sequence: 6
  givenname: Shaji K
  surname: Kumar
  fullname: Kumar, Shaji K
  organization: Division of Hematology, College of Medicine, Mayo Clinic, Rochester, MN
– sequence: 7
  givenname: Massimo
  surname: Offidani
  fullname: Offidani, Massimo
  organization: Clinica di Ematologia, Azienda Ospedaliero-Universitaria Ospedali Riuniti di Ancona, Ancona, Italy
– sequence: 8
  givenname: Philip
  surname: McCarthy
  fullname: McCarthy, Philip
  organization: Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY
– sequence: 9
  givenname: Andrea
  surname: Evangelista
  fullname: Evangelista, Andrea
  organization: Unit of Clinical Epidemiology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy
– sequence: 10
  givenname: Sagar
  surname: Lonial
  fullname: Lonial, Sagar
  organization: Department of Hematology and Medical Oncology, Emory University, Atlanta, GA
– sequence: 11
  givenname: Sonja
  surname: Zweegman
  fullname: Zweegman, Sonja
  organization: Department of Hematology, VU University Medical Center, Amsterdam, The Netherlands
– sequence: 12
  givenname: Pellegrino
  surname: Musto
  fullname: Musto, Pellegrino
  organization: Scientific Direction, Istituto di Ricovero e Cura a Carattere Scientifico, Referral Cancer Center of Basilicata, Rionero in Vulture, Italy
– sequence: 13
  givenname: Evangelos
  surname: Terpos
  fullname: Terpos, Evangelos
  organization: Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece
– sequence: 14
  givenname: Andrew
  surname: Belch
  fullname: Belch, Andrew
  organization: Department of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, AB, Canada
– sequence: 15
  givenname: Roman
  surname: Hajek
  fullname: Hajek, Roman
  organization: Department of Haematooncology and Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic
– sequence: 16
  givenname: Heinz
  surname: Ludwig
  fullname: Ludwig, Heinz
  organization: Department of Oncology, Hematology and Palliative Care, Wilhelminen, Vienna, Austria
– sequence: 17
  givenname: A Keith
  surname: Stewart
  fullname: Stewart, A Keith
  organization: Division of Hematology-Oncology, Mayo Clinic, Scottsdale, AZ
– sequence: 18
  givenname: Philippe
  surname: Moreau
  fullname: Moreau, Philippe
  organization: Department of Hematology, University Hospital Hôtel-Dieu, Nantes, France
– sequence: 19
  givenname: Kenneth
  surname: Anderson
  fullname: Anderson, Kenneth
  organization: Department of Hematology/Oncology, Dana-Farber Cancer Institute, Boston, MA
– sequence: 20
  givenname: Hermann
  surname: Einsele
  fullname: Einsele, Hermann
  organization: Medical Clinic and Polyclinic II, Department of Internal Medicine II, University Hospital, Wuerzburg, Germany
– sequence: 21
  givenname: Brian G M
  surname: Durie
  fullname: Durie, Brian G M
  organization: Department of Hematology/Oncology, Cedars-Sinai Comprehensive Cancer Center, Los Angeles, CA
– sequence: 22
  givenname: Meletios A
  surname: Dimopoulos
  fullname: Dimopoulos, Meletios A
  organization: Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece
– sequence: 23
  givenname: Ola
  surname: Landgren
  fullname: Landgren, Ola
  organization: Multiple Myeloma section, National Cancer Institute, Bethesda, MD
– sequence: 24
  givenname: Jesus F
  surname: San Miguel
  fullname: San Miguel, Jesus F
  organization: Clínica Universidad de Navarra, Centro de Investigaciones Médicas Aplicadas, Pamplona, Spain
– sequence: 25
  givenname: Paul
  surname: Richardson
  fullname: Richardson, Paul
  organization: Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA; and
– sequence: 26
  givenname: Pieter
  surname: Sonneveld
  fullname: Sonneveld, Pieter
  organization: Department of Hematology, Erasmus Medical Center and HOVON Data Center, Rotterdam, The Netherlands
– sequence: 27
  givenname: S Vincent
  surname: Rajkumar
  fullname: Rajkumar, S Vincent
  organization: Division of Hematology, College of Medicine, Mayo Clinic, Rochester, MN
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25628469$$D View this record in MEDLINE/PubMed
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References 25814486 - Blood. 2015 Mar 26;125(13):2014-5. doi: 10.1182/blood-2015-02-626408
29732537 - Br J Haematol. 2018 Jul;182(2):165-167. doi: 10.1111/bjh.15260
31265505 - Blood. 2016 Aug 18;128(7):1020. doi: 10.1182/blood-2016-07-727081
31265500 - Blood. 2016 Mar 3;127(9):1213. doi: 10.1182/blood-2016-01-693390
Blood. 2016 Mar 3;127(9):1213
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– reference: 31265500 - Blood. 2016 Mar 3;127(9):1213. doi: 10.1182/blood-2016-01-693390
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Snippet We conducted a pooled analysis of 869 individual newly diagnosed elderly patient data from 3 prospective trials. At diagnosis, a geriatric assessment had been...
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Aged, 80 and over
Antineoplastic Agents - adverse effects
Antineoplastic Agents - therapeutic use
Clinical Trials as Topic
Cohort Studies
Frail Elderly
Geriatric Assessment
Humans
Multiple Myeloma - drug therapy
Multiple Myeloma - mortality
Prognosis
Withholding Treatment - statistics & numerical data
Title Geriatric assessment predicts survival and toxicities in elderly myeloma patients: an International Myeloma Working Group report
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