| Literature DB >> 29925908 |
Meinolf Suttorp1, Philipp Schulze2, Ingmar Glauche2, Gudrun Göhring3, Nils von Neuhoff3,4, Markus Metzler5, Petr Sedlacek6, Eveline S J M de Bont7,8, Adriana Balduzzi9, Birgitte Lausen10, Olga Aleinikova11, Sabina Sufliarska12, Günter Henze13, Gabriele Strauss13,14, Angelika Eggert13, Bernhard Kremens4, Andreas H Groll15, Frank Berthold16, Christoph Klein17, Ute Groß-Wieltsch18, Karl Walter Sykora19, Arndt Borkhardt20, Andreas E Kulozik21, Martin Schrappe22, Christina Nowasz23, Manuela Krumbholz5, Josephine T Tauer23,24, Alexander Claviez22, Jochen Harbott25, Hans H Kreipe26, Brigitte Schlegelberger3, Christian Thiede27.
Abstract
A total of 156 patients (age range 1.3-18.0 years, median 13.2 years; 91 (58.3%) male) with newly diagnosed CML (N = 146 chronic phase (CML-CP), N = 3 accelerated phase (CML-AP), N = 7 blastic phase (CML-BP)) received imatinib up-front (300, 400, 500 mg/m2, respectively) within a prospective phase III trial. Therapy response, progression-free survival, causes of treatment failure, and side effects were analyzed in 148 children and adolescents with complete data. Event-free survival rate by 18 months for patients in CML-CP (median follow-up time 25 months, range: 1-120) was 97% (95% CI, 94.2-99.9%). According to the 2006 ELN-criteria complete hematologic response by month 3, complete cytogenetic response (CCyR) by month 12, and major molecular response (MMR) by month 18 were achieved in 98, 63, and 59% of the patients, respectively. By month 36, 86% of the patients achieved CCyR and 74% achieved MMR. Thirty-eight patients (27%) experienced imatinib failure because of unsatisfactory response or intolerance (N = 9). In all, 28/148 patients (19%) underwent stem cell transplantation (SCT). In the SCT sub-cohort 2/23 patients diagnosed in CML-CP, 0/1 in CML-AP, and 2/4 in CML-BP, respectively, died of relapse (N = 3) or SCT-related complications (N = 2). This large pediatric trial extends and confirms data from smaller series that first-line imatinib in children is highly effective.Entities:
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Year: 2018 PMID: 29925908 DOI: 10.1038/s41375-018-0179-9
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528