2009
DOI: 10.1002/pbc.21992
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Progressive neurocognitive impairment in young adult survivors of childhood acute lymphoblastic leukemia

Abstract: Survivors of childhood ALL suffer from long-lasting progressive neuropsychological impairment, especially when treatment includes cranial irradiation.

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Cited by 65 publications
(78 citation statements)
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References 43 publications
(55 reference statements)
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“…Of the 42 studies, 13 were excluded because patients were less than 5 years since diagnosis or 2 years since the end of treatment, 8 because they lacked a healthy control group, 6 because some/all patients received cranial radiation, and 5 because they did not directly assess neurocognitive outcomes of interest (summarized in Figure 1). Ten studies 11,19,[26][27][28][29][30][31][32][33][34] remained that met all the predefined inclusion criteria (Table 1).…”
Section: Resultsmentioning
confidence: 99%
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“…Of the 42 studies, 13 were excluded because patients were less than 5 years since diagnosis or 2 years since the end of treatment, 8 because they lacked a healthy control group, 6 because some/all patients received cranial radiation, and 5 because they did not directly assess neurocognitive outcomes of interest (summarized in Figure 1). Ten studies 11,19,[26][27][28][29][30][31][32][33][34] remained that met all the predefined inclusion criteria (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…Four studies evaluated verbal memory, the ability to encode and retrieve verbally presented information, 11,27,28,30 Only 2 of the studies found diminished verbal memory functioning in the ALL survivor group compared with the healthy control group.…”
Section: Verbal and Visual Memorymentioning
confidence: 99%
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“…There is a clear role for emergent cranial radiation therapy in moribund patients with bulky CNS disease at presentation (Cuvelier et al, 2008). However cranial radiation therapy for childhood ALL is associated with an increased risk of neurocognitive deficits, particularly in younger children, which may be progressive (Spiegler et al, 2006;Harila et al, 2009). There is recent data supporting the use of dasatinib for Ph+ CNS disease (Porkka et al, 2008), and the introduction of dasatinib and intensive induction therapy led to rapid regression of bulky intracranial disease and steady neurological recovery in both cases.…”
mentioning
confidence: 99%