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Intermediate-dose cytarabine is an effective therapy for adults with non-Langerhans cell histiocytosis.

Authors :
Liu T
Cai HC
Cai H
Chen M
Zhang W
Li J
Zhou DB
Cao XX
Source :
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Feb 07; Vol. 17 (1), pp. 39. Date of Electronic Publication: 2022 Feb 07.
Publication Year :
2022

Abstract

Background: Non-Langerhans cell histiocytosis, including Erdheim-Chester disease (ECD), Rosai-Dorfman disease (RDD), indeterminate cell histiocytosis (ICH), and unclassified histiocytosis, is a rare disorder lacking a standard treatment strategy. We report our experience using intermediate-dose cytarabine as the first or subsequent therapy in non-Langerhans cell histiocytosis.<br />Results: Nine ECD patients, 5 RDD patients, 1 ICH patient and 1 unclassified histiocytosis patient were enrolled. Intermediate-dose cytarabine therapy was administered as 0.5-1.0 g/m <superscript>2</superscript> of intravenous cytarabine every 12 h for 3 days every 5 weeks. The median age at cytarabine initiation was 47.5 years (range 18-70 years). The median number of cycles of cytarabine administered was 5.5 (range 2-6). The overall response rate (ORR) was 87.5% in the overall cohort, including 12.5% with complete response and 75.0% with partial response. One patient experienced disease recurrence 19 months after cytarabine therapy. The median follow-up duration for the entire cohort was 15.5 months (range 6-68 months). The estimated 2-year progression-free survival and overall survival rates were 85.6% and 92.3%, respectively. The most common toxicity was haematological adverse events, including grade 4 neutropenia and grade 3-4 thrombocytopenia. No treatment-related deaths occurred.<br />Conclusions: Intermediate-dose cytarabine is an efficient treatment option for non-Langerhans cell histiocytosis patients, especially for those with CNS involvement.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1750-1172
Volume :
17
Issue :
1
Database :
MEDLINE
Journal :
Orphanet journal of rare diseases
Publication Type :
Academic Journal
Accession number :
35130950
Full Text :
https://doi.org/10.1186/s13023-022-02193-0