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

Author:

Rozema Johanne12ORCID,Hoogendoorn Mels3,Kibbelaar Robby4,van den Berg Eva5ORCID,Veeger Nic67,van Roon Eric12

Affiliation:

1. Unit of Pharmacotherapy, Epidemiology and Economics, Department of Pharmacy, University of Groningen, Groningen, The Netherlands;

2. Department of Clinical Pharmacy and Pharmacology and

3. Department of Internal Medicine, Medical Center Leeuwarden, Leeuwarden, The Netherlands;

4. Pathology Friesland, Leeuwarden, The Netherlands;

5. Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands;

6. Science Bureau, Medical Center Leeuwarden, Leeuwarden, The Netherlands; and

7. Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands

Abstract

Abstract Population-based studies that contain detailed clinical data on patients with myelodysplastic syndrome (MDS) are scarce. This study focused on the real-world overall survival (OS) of MDS patients in association with comorbidities, specifically malignancies. An observational population-based study using the HemoBase registry was performed, including all patients with MDS diagnosed between 2005 and 2017 in Friesland, a Dutch province. Detailed information about diagnosis, patient characteristics, previous treatment of malignancies, and comorbidities according to the Charlson Comorbidity Index (CCI) was collected from electronic health records. Patients were followed up until June 2019. Kaplan-Meier plots and Cox regression analyses were used to study survival differences. In the 291 patients diagnosed with MDS, the median OS was 25.3 months (95% confidence interval [CI], 20.3-30.2). OS was significantly better for patients with CCI score <4, age <65 years, female sex, and low-risk MDS. Fifty-seven patients (20%) had encountered a prior malignancy (excluding nonmelanoma skin cancer), and a majority (38 patients; 67%) were therapy related. Both therapy-related and secondary MDSs were associated with worse OS (hazard ratio, 1.51; 95% CI, 1.02-2.23 and 1.58; 95% CI, 0.95-2.65, respectively), as compared with de novo MDS patients (P = .04). Patients in remission at time of MDS diagnosis had a similar median OS compared with patients with de novo MDS (25.5 vs 28.3 months). This population-based study involving all newly diagnosed MDS patients over a 13-year period in Friesland showed that multiple comorbidities, including previous malignancies, are associated with shorter OS. OS was not related to the use of radiotherapy or chemotherapy.

Publisher

American Society of Hematology

Subject

Hematology

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