Literature DB >> 26145790

Age and comorbidities deeply impact on clinical outcome of patients with myelodysplastic syndromes.

E Balleari1, C Salvetti2, L Del Corso2, R Filiberti3, A Bacigalupo2, A Bellodi2, G Beltrami2, M Bergamaschi2, G Berisso4, T Calzamiglia5, A M Carella2, M Cavalleri6, A Da Col2, S Favorini2, G L Forni7, R Goretti8, M Miglino2, L Mitscheuning2, E Molinari2, O Racchi9, M Scudeletti6, R Tassara10, M Gobbi2, R Lemoli2, M Clavio2.   

Abstract

BACKGROUND: Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal disorders, with very different prognosis in given individuals; age and comorbidities are emerging as relevant patient-related factors influencing clinical outcome in MDS. Our aim was to evaluate the impact of age, comorbidities and disease severity (IPSS and IPSS-R prognostic scores) in a "real-life" series of MDS patients.
METHODS: 318 patients with available assessment of comorbidities at diagnosis and consecutively registered into the Registro Ligure delle Mielodisplasie were analyzed. Comorbidities were evaluated according to HCT-CI and MDS-CI comorbidity indexes. Overall survival (OS) and the probability of death among patients who did not develop acute myeloid leukemia (NLD cumulative incidence) were analyzed.
RESULTS: Comorbidities were seen in 177 (55.7%) patients. An older age (>75 y) had a significant negative impact on OS (p=0.008). HCT-CI was not associated with OS. MDS-CI was of prognostic significance (p=0.001), but the association was limited to pts with IPSS or IPSS-R "lower-risk". In multivariate analysis, MDS-CI remained an independent factor associated with OS and with an increased risk of NLD both when controlling for IPSS (p=0.019 and p=0.001, respectively) and for IPSS-R (p=0.048 and p=0.002, respectively).
CONCLUSIONS: Evaluation of age and comorbidities according to a tailored tool such is MDS-CI helps to predict survival in patients with MDS and should be incorporated to current prognostic scores.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Comorbidity; Elderly; Myelodysplastic syndromes; Prognosis

Mesh:

Year:  2015        PMID: 26145790     DOI: 10.1016/j.leukres.2015.05.007

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  7 in total

1.  Integrating patient-centered factors in the risk assessment of MDS.

Authors:  Rena J Buckstein
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

2.  Comorbidities and malignancies negatively affect survival in myelodysplastic syndromes: a population-based study.

Authors:  Johanne Rozema; Mels Hoogendoorn; Robby Kibbelaar; Eva van den Berg; Nic Veeger; Eric van Roon
Journal:  Blood Adv       Date:  2021-03-09

3.  Personal history of autoimmune disease and other medical conditions and risk of myelodysplastic syndromes.

Authors:  Amy M Linabery; Michelle A Roesler; Michaela Richardson; Erica D Warlick; Phuong L Nguyen; Adina M Cioc; Jenny N Poynter
Journal:  Cancer Epidemiol       Date:  2022-01-05       Impact factor: 2.984

4.  Patients of Myelodysplastic Syndrome with Mild/Moderate Myelofibrosis and a Monosomal Karyotype are Independently Associated with an Adverse Prognosis: Long-Term Follow-Up Data.

Authors:  Na Wang; Hongzhi Xu; Qing Li; Xiaosheng Fang; Jie Liu; Xiaohui Sui; Lingyan Zhang; Yujie Jiang; Xin Wang
Journal:  Cancer Manag Res       Date:  2020-07-16       Impact factor: 3.989

Review 5.  Assessing Quality of Care for the Myelodysplastic Syndromes.

Authors:  Zachary A K Frosch; Gregory A Abel
Journal:  Curr Hematol Malig Rep       Date:  2016-12       Impact factor: 3.952

Review 6.  Myelodysplastic Syndromes and Acute Myeloid Leukemia in the Elderly.

Authors:  Heidi D Klepin
Journal:  Clin Geriatr Med       Date:  2016-02       Impact factor: 3.076

7.  Gender disparity in the survival of patients with primary myelodysplastic syndrome.

Authors:  Fangfang Wang; Jun Ni; Lei Wu; Ying Wang; Bin He; Duonan Yu
Journal:  J Cancer       Date:  2019-01-30       Impact factor: 4.207

  7 in total

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