Table 1.
Patient | Age | Gender | Stage | Prior Surgery* | Prior Radiation | PriorImmunotherapy | Dose Received | Toxicity Event | Number of Events | Grade of Event† |
---|---|---|---|---|---|---|---|---|---|---|
PT 01 | 66 | F | IV | Yes | No | Yes | 30 mcg | Erythematous Skin Rash | 1 | 1 |
PT 02 | 79 | M | IV | Yes | Yes | Yes | 60 mcg | None | 0 | 0 |
PT 03 | 74 | F | IV | Yes | No | No | 90 mcg | None | 0 | 0 |
PT 04 | 81 | F | IV | No | Yes | Yes | 120 mcg | None | 0 | 0 |
PT 05 | 72 | F | IV | Yes | Yes | Yes | 180 mcg | None | 0 | 0 |
PT 06 | 36 | F | IV | Yes | Yes | Yes | 180 mcg | None | 0 | 0 |
PT 07 | 46 | F | IIIC | Yes | Yes | Yes | 180 mcg | Fever + Hyperhidrosis | 5 + 1 | 1 |
PT 08 | 85 | F | IV | No | Yes | Yes | 180 mcg | None | 0 | 0 |
PT 09 | 48 | M | IV | No | Yes | Yes | 180 mcg | None | 0 | 0 |
PT 10 | 60 | F | IIIC | Yes | Yes | Yes | 180 mcg | None | 0 | 0 |
For therapeutic Intent
No grade 2 or higher adverse events occurred in the cohort