Relapsed childhood acute lymphoblastic leukaemia
D Bhojwani, CH Pui - The lancet oncology, 2013 - thelancet.com
With steadily improved cure rates for children with newly diagnosed acute lymphoblastic
leukaemia (ALL), treating relapsed ALL has become increasingly challenging largely due to …
leukaemia (ALL), treating relapsed ALL has become increasingly challenging largely due to …
Pediatric acute lymphoblastic leukemia
WL Carroll, D Bhojwani, DJ Min, E Raetz… - ASH Education …, 2003 - ashpublications.org
The outcome for children with acute lymphoblastic leukemia (ALL) has improved dramatically
with current therapy resulting in an event free survival exceeding 75% for most patients. …
with current therapy resulting in an event free survival exceeding 75% for most patients. …
Biology of childhood acute lymphoblastic leukemia
D Bhojwani, JJ Yang, CH Pui - Pediatric Clinics, 2015 - pediatric.theclinics.com
Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy, accounting
for 25% of all childhood cancers. In the United States, approximately 3000 children aged 1 …
for 25% of all childhood cancers. In the United States, approximately 3000 children aged 1 …
Phase I/phase II study of blinatumomab in pediatric patients with relapsed/refractory acute lymphoblastic leukemia
…, MM O'brien, B Brethon, D Bhojwani… - Journal of Clinical …, 2016 - ascopubs.org
… /m 2 /d and a stepwise dosage of 15/30 µg/m 2 /d (15 µg/m 2 /d for the first 7 days and 30
µg/m 2 /d thereafter). After determining the recommended dosage (stepwise 5/15 µg/m 2 /d), we …
µg/m 2 /d thereafter). After determining the recommended dosage (stepwise 5/15 µg/m 2 /d), we …
Long-term results of St Jude Total Therapy Studies 11, 12, 13A, 13B, and 14 for childhood acute lymphoblastic leukemia
…, C Cheng, SC Howard, ML Metzger, D Bhojwani… - Leukemia, 2010 - nature.com
We analyzed the long-term outcome of 1011 patients treated in five successive clinical trials
(Total Therapy Studies 11, 12, 13A, 13B, and 14) between 1984 and 1999. The event-free …
(Total Therapy Studies 11, 12, 13A, 13B, and 14) between 1984 and 1999. The event-free …
NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity
…, T Isobe, Z Chen, EKH Chiew, D Bhojwani… - Nature …, 2016 - nature.com
… of 14 d) before metabolite measurements and then correlated with NUDT15 diplotype (as
normal, intermediate or low NUDT15 activity) using a linear regression model (two-sided) (c,d). …
normal, intermediate or low NUDT15 activity) using a linear regression model (two-sided) (c,d). …
[HTML][HTML] Methotrexate-induced neurotoxicity and leukoencephalopathy in childhood acute lymphoblastic leukemia
Purpose Methotrexate (MTX) can cause significant clinical neurotoxicity and asymptomatic
leukoencephalopathy. We sought to identify clinical, pharmacokinetic, and genetic risk factors …
leukoencephalopathy. We sought to identify clinical, pharmacokinetic, and genetic risk factors …
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
…, SC Chen, G Song, J Cheng, P Meyers, D Bhojwani… - Nature …, 2013 - nature.com
Somatic alterations of the lymphoid transcription factor gene PAX5 (also known as BSAP) are
a hallmark of B cell precursor acute lymphoblastic leukemia (B-ALL) 1 , 2 , 3 , but inherited …
a hallmark of B cell precursor acute lymphoblastic leukemia (B-ALL) 1 , 2 , 3 , but inherited …
Identification of novel cluster groups in pediatric high-risk B-precursor acute lymphoblastic leukemia with gene expression profiling: correlation with genome-wide …
To resolve the genetic heterogeneity within pediatric high-risk B-precursor acute lymphoblastic
leukemia (ALL), a clinically defined poor-risk group with few known recurring cytogenetic …
leukemia (ALL), a clinically defined poor-risk group with few known recurring cytogenetic …
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse
… (b,d) Early treatment response measured by MRD at the end of induction was also related
to genotype at rs3824662 in both the COG P9906 (b) and COG P9905 (d) cohorts, with P …
to genotype at rs3824662 in both the COG P9906 (b) and COG P9905 (d) cohorts, with P …