Cited by 1,564Acute Lymphoblastic Leukemia researchLymphoma Diagnosis and TreatmentChronic Lymphocytic Leukemia Research

Acute lymphoblastic leukaemia

Pui, Ching-Hon, Robison, Leslie L, Look, A Thomas·2008·The Lancet

Abstract

Acute lymphoblastic leukaemia, a malignant disorder of lymphoid progenitor cells, affects both children and adults, with peak prevalence between the ages of 2 and 5 years. Steady progress in development of effective treatments has led to a cure rate of more than 80% in children, creating opportunities for innovative approaches that would preserve past gains in leukaemia-free survival while reducing the toxic side-effects of current intensive regimens. Advances in our understanding of the pathobiology of acute lymphoblastic leukaemia, fuelled by emerging molecular technologies, suggest that drugs specifically targeting the genetic defects of leukaemic cells could revolutionise management of this disease. Meanwhile, studies are underway to ascertain the precise events that take place in the genesis of acute lymphoblastic leukaemia, to enhance the clinical application of known risk factors and antileukaemic agents, and to identify treatment regimens that might boost the generally low cure rates in adults and subgroups of children with high-risk leukaemia.

Integrity signals

Registry

Crossref · 10.1016/s0140-6736(08)60457-2

Cites

3 of 3 references verified0 citation errors · 0 not checkable

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  • ALL patients are treated with a combination of ~10 different chemotherapy agents through several phases lasting 2-3 years.

    “ALL patients are treated with a combination of ~10 different chemotherapy agents through several phases lasting 2–3 years (Inaba et al., 2013; Pui, Robison, & Look, 2008; Pui et al., 2009).”

    From Brain structure, working memory and response inhibition in childhood leukemia survivors (2017) · cites this paper as Pui, Robison, & Look, 2008

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Authors
Pui, C.-H., Robison, L. L., & Look, A. T.
Affiliations
  • St. Jude Children's Research Hospital (US)
  • Harvard University (US)
Corresponding author
Pui, Ching-Hon
Venue
The Lancet
Publisher
Elsevier BV
Published
2008-03
Volume
371
Issue
9617
Pages
1030-1043
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
OpenAlex
W2105435030
Cited by
1,564
References
3
Citations by year
2026: 29 · 2025: 49 · 2024: 65 · 2023: 62 · 2022: 66 · 2021: 55 · 2020: 74 · 2019: 73 · 2018: 89 · 2017: 100 · 2016: 102 · 2015: 101 · 2014: 124 · 2013: 93 · 2012: 127
FWCI
17.13
Type
journal article
Language
en
Open access
closed
Locations
  • The Lancet (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Sanofi
  • National Cancer Institute (R01CA052259, CA 36401, CA90246, CA06516, CA 68484, CA 78224, CA-51001, P01CA068484, CA60419, CA21765, R01CA090246, R01CA078224, P30CA021765, P30CA006516, CA 52259)
  • National Institute of Nursing Research (NR07610, R01NR007610)
  • National Institute of General Medical Sciences (GM61393, U01GM061393)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Acute Lymphoblastic Leukemia research
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphoma Diagnosis and Treatment
  • Health Sciences › Medicine › Genetics › Chronic Lymphocytic Leukemia Research
Keywords
acute lymphoblastic leukemia, pediatric leukemia, adult leukemia, targeted therapy, leukemogenesis, risk factors, treatment toxicity, cure rate
MeSH terms
Adolescent, Adult, Age Factors, Antineoplastic Agents, Child, Child, Preschool, Humans, Pharmacogenetics, Translocation, Genetic, Randomized Controlled Trials as Topic, Treatment Outcome, Risk Assessment, Disease-Free Survival, Precursor Cell Lymphoblastic Leukemia-Lymphoma

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