Long-term follow-up of patients with hairy cell leukaemia after treatment with pentostatin or cladribine

Citation
Ce. Dearden et al., Long-term follow-up of patients with hairy cell leukaemia after treatment with pentostatin or cladribine, BR J HAEM, 106(2), 1999, pp. 515-519
Citations number
12
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BRITISH JOURNAL OF HAEMATOLOGY
ISSN journal
00071048 → ACNP
Volume
106
Issue
2
Year of publication
1999
Pages
515 - 519
Database
ISI
SICI code
0007-1048(199908)106:2<515:LFOPWH>2.0.ZU;2-1
Abstract
We report the long-term follow-up results on two groups of patients with ha iry cell leukaemia (HCL) treated with either pentostatin (deoxycoformycin) or cladribine (2-chlorodeoxyadenosine). 165 HCL patients received treatment with pentostatin (between 1986 and 1994), and 45 were treated with cladrib ine (between 1992 and 1997). Age and sex characteristics were similar in th e two groups. 38 patients in the pentostatin group and 12 in the cladribine group were previously untreated. 22 patients in the cladribine group had r eceived prior treatment with pentostatin; four were resistant, 17 had relap sed following partial (four) or complete (13) responses, and one was not ev aluable for response. The response rates were the same in the two groups: 8 2% complete response (CR), 15% partial response (PR) for pentostatin and 84 % CR, 16% PR for cladribine. Relapse rates were 24% for pentostatin and 29% for cladribine after median follow-up of 71 and 45 months respectively. At 45 months, however, the relapse rate for pentostatin was only 9.7%. We fou nd a statistically significant difference in the disease-free interval (DFI ) between the two groups suggesting that patients may relapse more quickly after cladribine. The majority of relapsed patients achieved second remissi ons following further therapy with either pentostatin or cladribine, with n o evidence of cross resistance between the two agents. The 5-year survival for all patients was 97% and treatment-related toxicity was low We conclude that both pentostatin and cladribine induce durable remissions in the majo rity of HCL patients. Longer follow-up is required to establish whether som e patients are cured as there is no plateau in DFI, and which of these two agents may be the treatment of choice.