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. Author manuscript; available in PMC: 2011 Oct 28.
Published in final edited form as: Clin Cancer Res. 2007 Mar 15;13(6):1775–1782. doi: 10.1158/1078-0432.CCR-06-1863

Table 3.

Adverse events (all cycles)

Daily × 5
Daily × 3
Grade 1 Grade 2 Grade 3 Grade 4 Grade 1 Grade 2 Grade 3 Grade 4
No. patients 17 15
No. courses 50 55
Adverse events
 Nausea 9 (53%) 1 (6%) 6 (40%) 1 (7%) 1 (7%)
 Emesis 5 (29%) 1 (6%) 2 (13%) 1 (7%) 1 (7%)
 Diarrhea 3 (18%) 1 (6%) 1 (6%) 5 (33%) 3 (20%)
 AST 6 (35%) 2 (12%) 1 (6%) 1 (6%) 6 (40%) 4 (27%)
 ALT 5 (29%) 1 (6%) 1 (6%) 1 (6%) 6 (40%) 2 (13%) 1 (7%)*
 Platelets 3 (18%) 1 (6%) 4 (27%) 1 (7%)
Days 1, 4, 8, and 11
Days 1 and 4 weekly
Grade 1 Grade 2 Grade 3 Grade 4 Grade 1 Grade 2 Grade 3 Grade 4
No. patients 16 6
No. courses 56 33
Adverse events
 Nausea 6 (38%) 4 (25%) 1 (17%) 2 (33%)
 Emesis 4 (25%) 2 (13%) 1 (17%)
 Diarrhea 5 (31%) 3 (19%) 1 (6%) 3 (50%) 1 (17%)
 AST 4 (25%) 4 (25%) 1 (17%) 1 (17%) 2 (33%) 1 (17%)
 ALT 4 (25%) 1 (6%) 1 (17%) 4 (67%)
 Platelets 2 (13%) 1 (17%)
*

Abnormal lab value in this patient likely attributable to antibiotic therapy.