TY - JOUR
T1 - Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis
T2 - results of an international phase 2 study
AU - Salvage Group of the Histiocyte Society
AU - Donadieu, Jean
AU - Bernard, Frederic
AU - van Noesel, Max
AU - Barkaoui, Mohamed
AU - Bardet, Odile
AU - Mura, Rosella
AU - Arico, Maurizio
AU - Piguet, Christophe
AU - Gandemer, Virginie
AU - Armari Alla, Corinne
AU - Clausen, Niels
AU - Jeziorski, Eric
AU - Lambilliote, Anne
AU - Weitzman, Sheila
AU - Henter, Jan Inge
AU - Van Den Bos, Cor
N1 - © 2015 by The American Society of Hematology.
PY - 2015/9/17
Y1 - 2015/9/17
N2 - An international phase 2 study combining cladribine and cytarabine (Ara-C) was initiated for patients with refractory, risk-organ-positive Langerhans cell histiocytosis (LCH) in 2005. The protocol, comprising at least two 5-day courses of Ara-C (1 g/m(2) per day) plus cladribine (9 mg/m(2) per day) followed by maintenance therapy, was administered to 27 patients (median age at diagnosis, 0.7 years; median follow-up, 5.3 years). At inclusion, all patients were refractory after at least 1 course of vinblastine (VBL) plus corticosteroid, all had liver and spleen involvement, and 25 patients had hematologic cytopenia. After 2 courses, disease status was nonactive (n = 2), better (n = 23), or stable (n = 2), with an overall response rate of 92%. Median disease activity scores decreased from 12 at the start of therapy to 3 after 2 courses (P < .0001). During maintenance therapy, 4 patients experienced reactivation in risk organs. There were 4 deaths; 2 were related to therapy toxicity and 2 were related to reactivation. All patients experienced severe toxicity, with World Health Organization grade 4 hematologic toxicity and 6 documented severe infections. The overall 5-year survival rate was 85% (95% confidence interval, 65.2%-94.2%). Thus, the combination of cladribine/Ara-C is effective therapy for refractory multisystem LCH but is associated with high toxicity.
AB - An international phase 2 study combining cladribine and cytarabine (Ara-C) was initiated for patients with refractory, risk-organ-positive Langerhans cell histiocytosis (LCH) in 2005. The protocol, comprising at least two 5-day courses of Ara-C (1 g/m(2) per day) plus cladribine (9 mg/m(2) per day) followed by maintenance therapy, was administered to 27 patients (median age at diagnosis, 0.7 years; median follow-up, 5.3 years). At inclusion, all patients were refractory after at least 1 course of vinblastine (VBL) plus corticosteroid, all had liver and spleen involvement, and 25 patients had hematologic cytopenia. After 2 courses, disease status was nonactive (n = 2), better (n = 23), or stable (n = 2), with an overall response rate of 92%. Median disease activity scores decreased from 12 at the start of therapy to 3 after 2 courses (P < .0001). During maintenance therapy, 4 patients experienced reactivation in risk organs. There were 4 deaths; 2 were related to therapy toxicity and 2 were related to reactivation. All patients experienced severe toxicity, with World Health Organization grade 4 hematologic toxicity and 6 documented severe infections. The overall 5-year survival rate was 85% (95% confidence interval, 65.2%-94.2%). Thus, the combination of cladribine/Ara-C is effective therapy for refractory multisystem LCH but is associated with high toxicity.
KW - Antineoplastic Agents/adverse effects
KW - Child, Preschool
KW - Cladribine/adverse effects
KW - Cytarabine/adverse effects
KW - Female
KW - Histiocytosis, Langerhans-Cell/diagnosis
KW - Humans
KW - Immunosuppressive Agents/adverse effects
KW - Infant
KW - Langerhans Cells/drug effects
KW - Liver/drug effects
KW - Male
KW - Recurrence
KW - Spleen/drug effects
KW - Survival Analysis
KW - Survival Rate
KW - Vinblastine/therapeutic use
UR - http://www.scopus.com/inward/record.url?scp=84942922162&partnerID=8YFLogxK
U2 - 10.1182/blood-2015-03-635151
DO - 10.1182/blood-2015-03-635151
M3 - Article
C2 - 26194764
SN - 0006-4971
VL - 126
SP - 1415
EP - 1423
JO - Blood
JF - Blood
IS - 12
ER -