Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 May;37(5):1103-1112.
doi: 10.1038/s41375-023-01864-6. Epub 2023 Mar 17.

Therapy-related MDS dissected based on primary disease and treatment-a nationwide perspective

Affiliations

Therapy-related MDS dissected based on primary disease and treatment-a nationwide perspective

Daniel Moreno Berggren et al. Leukemia. 2023 May.

Abstract

In this population-based study, we aimed to characterize and compare subgroups of therapy-related Myelodysplastic syndromes (t-MDS) and define the implications of type of previous treatment and primary disease. We combined data from MDS patients, diagnosed between 2009 and 2017 (n = 2705), in the nationwide Swedish MDS register, with several health registers. Furthermore, using matched population controls, we investigated the prevalence of antecedent malignancies in MDS patients in comparison with the general population. This first ever nationwide study on t-MDS confirms a shorter median survival for t-MDS compared to de novo MDS (15.8 months vs 31.1 months, p < 0.001). T-MDS patients previously treated with radiation only had disease characteristics with a striking resemblance to de novo-MDS, in sharp contrast to patients treated with chemotherapy who had a significantly higher risk profile. IPSS-R and the WHO classification differentiated t-MDS into different risk groups. As compared with controls, MDS patients had a six-fold increased prevalence of a previous hematological malignancy but only a 34% increased prevalence of a previous solid tumor. T-MDS patients with a previous hematological malignancy had a dismal prognosis, due both to mortality related to their primary disease and to high-risk MDS.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. OS of de novo-MDS and subgroups of t-MDS.
a OS by different treatments for the primary disease. b OS by type of primary disease.
Fig. 2
Fig. 2. OS by IPSS-R risk group.
a OS of patients with de novo-MDS. b OS of all patients with t-MDS. c OS of patients with t-MDS treated with chemotherapy only. d OS of patients with t-MDS treated with radiation only. e OS of patients with t-MDS treated with chemotherapy in combination with radiation. f OS of patients with t-MDS with a solid tumor as a primary disease. g OS of patients with t-MDS with a hematological malignancy as a primary disease. h OS of patients with t-MDS with a non-malignant disease as a primary disease.
Fig. 3
Fig. 3. OS by WHO risk group.
a OS of patients with de novo-MDS. b OS of all patients with t-MDS. c OS of patients with t-MDS treated with chemotherapy only. d OS of patients with t-MDS treated with radiation only. e OS of patients with t-MDS treated with chemotherapy in combination with radiation. f OS of patients with t-MDS with a solid tumor as a primary disease. g OS of patients with t-MDS with a hematological malignancy as a primary disease. h OS of patients with t-MDS with a non-malignant disease as a primary disease.
Fig. 4
Fig. 4
Multivariate analyses of the all-cause mortality of t-MDS patients by patient and disease characteristics.

References

    1. Zeidan AM, Al Ali N, Barnard J, Padron E, Lancet JE, Sekeres MA, et al. Comparison of clinical outcomes and prognostic utility of risk stratification tools in patients with therapy-related vs de novo myelodysplastic syndromes: a report on behalf of the MDS Clinical Research Consortium. Leukemia. 2017;31:1391–7. doi: 10.1038/leu.2017.33. - DOI - PubMed
    1. Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016;127:2391–405. doi: 10.1182/blood-2016-03-643544. - DOI - PubMed
    1. Smith SM, Le Beau MM, Huo D, Karrison T, Sobecks RM, Anastasi J, et al. Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series. Blood. 2003;102:43–52. doi: 10.1182/blood-2002-11-3343. - DOI - PubMed
    1. Chung J, Sallman DA, Padron E. TP53 and therapy-related myeloid neoplasms. Best Pract Res Clin Haematol. 2019;32:98–103. doi: 10.1016/j.beha.2019.02.009. - DOI - PubMed
    1. Rowland JH, Bellizzi KM. Cancer survivorship issues: life after treatment and implications for an aging population. J Clin Oncol: Off J Am Soc Clin Oncol. 2014;32:2662–8. doi: 10.1200/JCO.2014.55.8361. - DOI - PMC - PubMed

Publication types

MeSH terms