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. 2007 Feb 6;96(4):559–566. doi: 10.1038/sj.bjc.6603606

Table 4b. Number of patients with any treatment-related haematological toxicity grade 3 or 4 according to the NCI-common toxicity criteria (CTC) at cycle 1 and post cycle 1.

Dose levela 350/6 500/6 600/6 600/5 All
Number of evaluable patients 4 3 4 5 16
CTC grade 3 4 3 4 3 4 3 4 3 4
Cycle 1
 Platelets 0 0 1 0 1 2 3 1 5 (31%) 3 (19%)
 Neutrophils 0 0 0 0 1 1 0 1 1 (6%) 2 (13%)
 Leucocytes 0 0 0 0 1 0 1 1 2 (13%) 1 (6%)
 Lymphocytes 0 0 0 0 0 0 1 0 1 (6%) 0 (0%)
 Haemoglobin 0 0 0 0 0 1 2 0 2 (13%) 1 (6%)
                     
Post cycle 1
 Platelets 3 0 2 1 1 2 4 1 10 (63%) 4 (25%)
 Neutrophils 2 0 2 1 3 2 2 4 9 (56%) 7 (44%)
 Leucocytes 2 0 1 0 1 0 4 2 8 (50%) 2 (13%)
 Lymphocytes 1 0 0 0 0 0 3 0 4 (25%) 0 (0%)
 Haemoglobin 2 0 1 0 2 0 2 0 7 (44%) 0 (0%)
a

Indisulam (mg m−2)/carboplatin (mg min ml−1).