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Cladribine Combined with Low-Dose Cytarabine as Frontline Treatment for Unfit Elderly Acute Myeloid Leukemia Patients: Results from a Prospective Multicenter Study of Polish Adult Leukemia Group (PALG).

Authors :
Budziszewska BK
Salomon-Perzyński A
Pruszczyk K
Barankiewicz J
Pluta A
Helbig G
Janowska A
Kuydowicz M
Bołkun Ł
Piszcz J
Patkowska E
Wątek M
Małecki P
Kościołek-Zgódka S
Cichocka E
Charliński G
Irga-Staniukiewicz A
Zaucha JM
Piekarska A
Gromek T
Hus M
Wójcik K
Raźny M
Sędzimirska M
Puła B
Giebel S
Grosicki S
Wierzbowska A
Lech-Marańda E
Source :
Cancers [Cancers (Basel)] 2021 Aug 20; Vol. 13 (16). Date of Electronic Publication: 2021 Aug 20.
Publication Year :
2021

Abstract

Acute myeloid leukemia (AML) in older unfit patients is a therapeutic challenge for clinical hematologists. We evaluated the efficacy and safety of a novel low-intensity regimen consisting of low-dose cytarabine and cladribine (LD-AC+cladribine) in first-line treatment of elderly (≥60 years) AML patients not eligible for intensive chemotherapy (IC) who had either the Eastern Cooperative Oncology Group performance status (ECOG PS) ≥2 or the hematopoietic cell transplantation comorbidity index (HCT-CI) score ≥3. The induction phase included two cycles of LD-AC+cladribine. Patients who achieved at least partial remission (PR) received maintenance treatment with LD-AC alone. Overall, 117 patients with a median age of 70 years were enrolled. Adverse cytogenetics, ECOG PS ≥2 and HCT-CI score ≥3 was observed in 43.5%, 60%, and 58% of patients, respectively. The response rate (≥PR) was 54% (complete remission [CR], 32%; CR with incomplete hematologic recovery [CRi], 5%). A median overall survival (OS) was 21 and 8.8 months in CR/CRi and PR group, respectively. Advanced age (≥75 years) and adverse cytogenetics had a negative impact on OS. The 56-day mortality rate was 20.5%. In conclusion, LD-AC+cladribine is a beneficial therapeutic option with a predictable safety profile in elderly AML patients not eligible for IC.

Details

Language :
English
ISSN :
2072-6694
Volume :
13
Issue :
16
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
34439342
Full Text :
https://doi.org/10.3390/cancers13164189