Table 2.
Treatment-related adverse events related to ramucirumab and docetaxel among patients in the UM Cohort.
| Toxicity Variable | All Grades (%) | Grade 3+ (%) |
|---|---|---|
| Hypertension (Ram) | 2 (5.7) | – |
| Proteinuria (Ram) | 2 (5.7) | – |
| Bleeding (Ram) | 1 (2.9) | 1 (2.9) |
| Fatigue (Ram) | 1 (2.9) | – |
| Dose-reduction of Ram | 1 (2.9) | 1 (2.9) |
| Fatigue (Doc) | 15 (42.9) | 1 (2.9) |
| Skin/nail changes (Doc) | 3 (8.6) | – |
| Myalgias (Doc) | 1 (2.9) | 1 (2.9) |
| Neutropenia (Doc) | 2 (5.7) | 1 (2.9) |
| Anemia (Doc) | 4 (11.4) | – |
| Neuropathy (Doc) | 4 (11.4) | 1 (2.9) |
| Cough/COPD Exacerbation (Doc) | 2 (5.7) | – |
| Dose-reduction of Doc | 2 (5.7) | 2 (5.7) |
| Dose-reduction of Ram + Doc | 2 (5.7) | 2 (5.7) |
| Arthralgia (IO) | 1 (2.9) | – |
This symbol means no value.