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Survival outcomes of hypomethylating agents maintenance therapy in new diagnosed AML patients: Real experience data

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info:eu-repo/semantics/openAccess

Date

2022

Author

Karakuş, Volkan
Maral, Senem
Kaya, Egemen
Gemici, Aliihsan
Dere, Yelda
Sevindik, Ömür Gökmen

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Karakuş, V., Maral, S., Kaya, E., Gemici, A., Dere, Y. ve Sevindik, Ö. G. (2022). Survival outcomes of hypomethylating agents maintenance therapy in new diagnosed AML patients: Real experience data. Northern Clinics of Istanbul, 9(4), 331-336. https://doi.org/10.14744/nci.2021.42800

Abstract

OBJECTIVE: Acute myeloid leukemia (AML) is a hematological malignancy that frequently affects elderly population. With introducing the hypomethylating agents (HMAs) in elderly AML treatment, survival rates and quality of life have improved. However, long-term management in elderly and frail patients is still a challenge. In the present study, we aimed to determine whether HMA maintenance therapy is required until disease progression in frail and elderly AML patients by examining with a real-life data.METHODS: In a multicenter study, we analyzed non-promyelocytic elderly AML patients who were treated with first-line azacitidine or decitabine monotherapy in two different groups, retrospectively. While patients were treated with HMA until progression in the maintenance group, 6+3 cycles of azacitidine or decitabine were administered as a standard care of elderly AML patients in the non-maintenance group. Survival outcomes were compared between the groups.RESULTS: HMA therapy was maintained until progression in 20 patients, and HMA therapy was terminated after 6+3 cycles in 21 patients. Patients received a median of 6 (1-14) HMA cycles during follow-up time. The median 7.5 months of overall survival were observed (2-17 months) in maintenance and 3 months (1-13 months) in non-maintenance groups (p=0.001).CONCLUSION: Despite long-term exposure to HMA may appear as a risk factor for complications and toxicities in elderly and frail AML patients, the maintenance of therapy until disease progression provides a significant survival advantage. Therefore, we suggest that HMA therapy should continue until disease progression regardless the sort of HMA.

Source

Northern Clinics of Istanbul

Volume

9

Issue

4

URI

https://doi.org/10.14744/nci.2021.42800
https://hdl.handle.net/20.500.12511/9897

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  • Makale Koleksiyonu [3204]
  • PubMed İndeksli Yayınlar Koleksiyonu [3497]
  • TR-Dizin İndeksli Yayınlar Koleksiyonu [1898]
  • WoS İndeksli Yayınlar Koleksiyonu [5545]



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