Table 3.
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 |
Side effects and toxicity in GEJ carcinoma trials; in CROSS- and ACCORD07 trial, surgery only was defined as control arm; in Stahl 2009, CT arm was considered as control arm, CRT was considered as CT/CRT arm.