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. Author manuscript; available in PMC: 2011 Jun 29.
Published in final edited form as: Br J Haematol. 2010 Jul 7;150(4):438–445. doi: 10.1111/j.1365-2141.2010.08265.x

Table III.

AEs Occurring in ≥20% of all patients and selected AEs of interest.

AEs, n (%) Tanespimycin dose, mg/m2
150 n = 4 220 n = 9 275 n = 3 340 n = 7 420 n = 3 525 n = 3 All dose cohorts N = 29
Any 4 (100) 9 (100) 3 (100) 7 (100) 3 (100) 3 (100) 29 (100)
Non-haematological*
 Diarrhoea 2 (50) 3 (33) 3 (100) 4 (57) 3 (100) 2 (67) 17 (59)
 Back pain 3 (75) 1 (11) 2 (67) 2 (29) 2 (67) 0 10 (35)
 Fatigue 1 (25) 2 (22) 2 (67) 2 (29) 2 (67) 2 (67) 11 (38)
 Nausea 1 (25) 1 (11) 1 (33) 2 (29) 3 (100) 2 (67) 10 (35)
 AST increased 1 (25) 1 (11) 1 (33) 2 (29) 2 (67) 2 (67) 9 (31)
 Muscle spasms 1 (25) 3 (33) 0 3 (43) 1 (33) 0 8 (28)
 ALT increased 1 (25) 1 (11) 0 2 (29) 2 (67) 1 (33) 7 (24)
 Constipation 2 (50) 1 (11) 0 2 (29) 1 (33) 0 6 (21)
 Dyspnea 0 1 (11) 0 4 (57) 0 1 (33) 6 (21)
 Pain in extremity 2 (50) 3 (33) 0 0 1 (33) 0 6 (21)
 Neuropathy 0 0 0 1 (14) 0 0 0
Haematological
 Anaemia 1 (25) 3 (33) 1 (33) 1 (14) 1 (33) 0 7 (24)
 Thrombocytopenia 1 (25) 1 (11) 0 3 (43) 1 (33) 0 6 (21)
 Neutropenia 0 0 0 0 0 0 0

AEs, adverse events; ALT, alanine aminotransferase; AST, aspartate aminotransferase.

*

AEs affecting at least 20% of the total group.