Table IV.
Patient characteristics | Grade of adverse eventsa | |||||||
---|---|---|---|---|---|---|---|---|
| ||||||||
Age (years) | Gender | UGT1A1 | PS | Pathology | cStage | FN | Diarrhea | Other severe NH toxicitiesb |
|
|
|||||||
73 | Female | Non-test | 1 | SCC | IV | 4 | - | - |
83 | Male | Non-test | 1 | NSCLC | IIIB | 5 | 5 | - |
56 | Male | Wild-type | 1 | Adenocarcinoma | IV | - | - | 5c |
69 | Male | Wild-type | 1 | SCC | IV | - | - | 5c |
72 | Male | Wild-type | 1 | Adenocarcinoma | IV | 5 | 5 | - |
73 | Male | Wild-type | 1 | SCC | IV | 4 | 3 | - |
77 | Male | *28 heterozygous | 0 | Adenocarcinoma | IV | 4 | 4 | - |
67 | Male | *6 heterozygous | 1 | LCNEC | IV | - | - | 4d |
78 | Male | *6 heterozygous | 1 | SCLC | IV | 4 | 3 | - |
Adverse events ≥grade 3.
Other grade 4 and 5 adverse events.
Interstitial pneumonitis.
Bowel perforation.
LCNEC, large-cell neuroendocrine carcinoma; FN, febrile neutropenia; NH, non-hematological; UGT1A1, UDP glucuronosyltransferase 1 family, polypeptide A1; PS, performance status; SCC, squamous cell carcinoma; SCLC, small-cell lung cancer; NSCLC, non-small-cell lung cancer.