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. Author manuscript; available in PMC: 2011 May 26.
Published in final edited form as: Future Oncol. 2010 Apr;6(4):563–585. doi: 10.2217/fon.10.17

Table 3. Polymorphic variation in UGT associated with irinotecan toxicity (p < 0.05).

UGT allele Clinical effect
UGT1A1*28 Increased severe neutropenia in Caucasians [32,34-38,46,88] and
Japanese populations [41,42]
Increased leukopenia in Japanese populations [39-41]
Decreased ANC nadir in Caucasians [31,32]
Increased severe diarrhea in Caucasians [38,43-46] and Japanese
populations [39,40]
UGT1A1*60 G/G genotype was associated with severe hematologic toxicity when
compared with T/T at frst cycle in Caucasians [70] but was not
confirmed in multivariate analysis
UGT1A1*93 Increased severe neutropenia in Caucasians [32,37,69]
Decreased ANC nadir in Caucasians [32]
UGT1A1*6 Increased severe neutropenia in Japanese populations [41,42,48,49,60,64],
Koreans [48,49] and Chinese populations [59]
Increased leukopenia in Japanese populations [41]
UGT1A7*2 Lack of severe neutropenia or diarrhea in Caucasians [47]
UGT1A7*3 Lack of severe neutropenia or diarrhea in Caucasians [47]
Increased severe hematologic toxicity in Caucasians [70]
Increased severe diarrhea in Koreans [48,49]
UGT1A7*4 Increased severe neutropenia and/or diarrhea in Caucasians [46]
UGT1A9*1b Increased severe neutropenia or diarrhea in Caucasians [47]
Increased severe neutropenia in Japanese populations [60]
Severe hematologic toxicity in Caucasians [70]
Decreased severe diarrhea in Koreans [48,49]

ANC: Absolute neutrophil count; UGT: Uridine 5′-diphosphoglucuronosyltransferase.