clofarabine

1
Reactions 1453 - 25 May 2013 S Clofarabine Myelosuppression, infectious complications and liver disorders in paediatric patients: 6 case reports Four boys and two girls, aged 4 months to 5 years, were identified from a retrospective study after they developed myelosuppression, infectious complications and liver disorders while receiving clofarabine [routes and durations of treatment to reaction onsets not stated]. One patient later died. The patients, who had refractory high-risk Langerhans cell histiocytosis (LCH), received 6–8 cycles of clofarabine 20–35 mg/m 2 for 3–5 days per cycle. The cycles were administered approximately every 4 weeks. All patients developed myelosuppression, including grade 4 neutropenia and/or grade 3 febrile neutropenia requiring admission. Three patients developed four episodes of bacteraemia due to Enterococcus, Staphylococcus epidermidis or Bacillus species and one patient experienced a dental abscess. One boy developed transient grade 2 liver enzyme elevation and grade 4 direct hyperbilirubinaemia after cycles 1 and 2. Five patients required transfusions of RBCs and platelets with most clofarabine cycles, and four patients received filgrastim to reduce the duration of neutropenia following clofarabine administration. Subsequent cycles were started after absolute neutrophil count recovery in most cases. Myelosuppression was also managed with clofarabine dose reduction. One boy had persistently increased liver transaminase levels and hepatomegaly 1.5 years after treatment; liver biopsy showed stage 1 portal fibrosis [outcome not stated]. One girl later received palliative therapy with clofarabine after recurrence of LCH; she subsequently died of progressive disease. Author comment: "[In this study] there were no clofarabine-related deaths, and the most common toxicity was myelosuppression. . . The only lasting toxicity in this cohort possibly attributable to clofarabine is stage 1 portal fibrosis in [one patient]." Abraham A, et al. Clofarabine salvage therapy for refractory high-risk langerhans cell histiocytosis. Pediatric Blood and Cancer 60: E19-E22, No. 6, Jun 2013. Available from: URL: http://dx.doi.org/10.1002/pbc.24436 - USA 803087344 1 Reactions 25 May 2013 No. 1453 0114-9954/10/1453-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

Upload: b-m

Post on 23-Dec-2016

214 views

Category:

Documents


1 download

TRANSCRIPT

Page 1: Clofarabine

Reactions 1453 - 25 May 2013

SClofarabine

Myelosuppression, infectious complications andliver disorders in paediatric patients: 6 case reports

Four boys and two girls, aged 4 months to 5 years, wereidentified from a retrospective study after they developedmyelosuppression, infectious complications and liverdisorders while receiving clofarabine [routes and durations oftreatment to reaction onsets not stated]. One patient later died.

The patients, who had refractory high-risk Langerhans cellhistiocytosis (LCH), received 6–8 cycles of clofarabine20–35 mg/m2 for 3–5 days per cycle. The cycles wereadministered approximately every 4 weeks. All patientsdeveloped myelosuppression, including grade 4 neutropeniaand/or grade 3 febrile neutropenia requiring admission. Threepatients developed four episodes of bacteraemia due toEnterococcus, Staphylococcus epidermidis or Bacillus speciesand one patient experienced a dental abscess. One boydeveloped transient grade 2 liver enzyme elevation andgrade 4 direct hyperbilirubinaemia after cycles 1 and 2.

Five patients required transfusions of RBCs and plateletswith most clofarabine cycles, and four patients receivedfilgrastim to reduce the duration of neutropenia followingclofarabine administration. Subsequent cycles were startedafter absolute neutrophil count recovery in most cases.Myelosuppression was also managed with clofarabine dosereduction. One boy had persistently increased livertransaminase levels and hepatomegaly 1.5 years aftertreatment; liver biopsy showed stage 1 portal fibrosis[outcome not stated]. One girl later received palliative therapywith clofarabine after recurrence of LCH; she subsequentlydied of progressive disease.

Author comment: "[In this study] there were noclofarabine-related deaths, and the most common toxicitywas myelosuppression. . . The only lasting toxicity in thiscohort possibly attributable to clofarabine is stage 1 portalfibrosis in [one patient]."Abraham A, et al. Clofarabine salvage therapy for refractory high-risk langerhanscell histiocytosis. Pediatric Blood and Cancer 60: E19-E22, No. 6, Jun 2013.Available from: URL: http://dx.doi.org/10.1002/pbc.24436 - USA 803087344

1

Reactions 25 May 2013 No. 14530114-9954/10/1453-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved