Table 5.
Summary of methods and results from selected studies concerning genetic predictive factors.
| Authors | Type of study | Age mean ± (SD or range) | Cancer location (n) | Treatment type | Studied factors | Measurements | Results | |||
|---|---|---|---|---|---|---|---|---|---|---|
| Biological tests | Assessed cognitive domains | Time of assessment | Observed cognitive impairments | Association with studied predictive factors | ||||||
| GENETIC PREDICTORS | ||||||||||
| Kamdar et al., 2011 | Prospective cohort | 4.4 ± 3.9 −12.1 ± 11.3 | ALL (n = 62) | Methotrexate chemotherapy | 6 Genotype polymorphisms (folate pathway: MTHFRa 677C>T MTHFR 1298A>C SHMTb 1420C>T MSc 2759 A>G MTRRd 66A>G TSERe2R/3R TSER3R/3R | Genotyping essay by PCR (Venipuncture) |
|
Years after end of therapy: 5.3± 4.4 | Global cognitive functioning: 44.3% of patients | Combined effect of multiple folate pathway polymorphisms (MS and MTHFR): ↗cognitive disturbance probability (attention and processing speed) |
| Krull et al., 2013a | Cohort | 7.0 ± 3.11 | ALL (n = 243) | Chemotherapy (without prophylactic cranial irradiation) | Many genetic polymorphisms | Genotyping by PCR (Venipuncture) |
|
2 years completion of consolidation therapy | Sustained attention and attention difficulties reported by parents | MS (/ MAOAf/ APOEg) polymorphisms:
|
| Small et al., 2011 | Cross-sectional, Case-control | 56.93 ± 9.01 (RT) 51.22 ± 8.63 (CT) | Breast (RT: n = 58 CT: n = 72 Healthy Controls: n = 204) | Chemotherapy and radiotherapy | COMTh Genotype COMT-Val COMT-Met | DNA collection by saliva and genotyping |
|
6 months after end of treatments |
|
COMT-Val homozygote:
|
MTHFR: 5,10-methylenetetrahydrofolate reductase.
SHMT: serine hydroxylmethyltransferase.
MS: methionine synthase.
MTRR: methionine synthase reductase.
TSER: thymidylate synthase enhancer region.
MAOA : Monoamine oxidase A.
APOE: Apolipoprotein E.
COMT: Catechol-O-Methyltransferase.