Clinical Trial | ACCORD07 | CROSS | Stahl 2009 |
---|---|---|---|
Number of patients randomized | 224 | 368 | 126 |
Patients with at least grade 3 toxicity | 38% | Hematologic: 7.6% All other: 13% | Unspecified |
Grade 3 – and 4 toxicity in control arm | - | - | 5% (CT arm as control arm) |
Grade 3–4 leukopenia during CT/CRT | 5.5% | 6% | 12% |
Grade 3–4 neutropenia during CT/CRT | 20.2% | 2% | unspecified |
Grade 3–4 thrombocytopenia during CT/CRT | 5.5% | 1% | 5% |
Progressive disease during preoperative therapy | 11% | Absolute number unspecified; 7 patients (4%) did not undergo surgery because of disease progression | 10% |
Deaths during CT/CRT | 1% | 1% | One patient (2%) died in CT group; none died in CRT group |