Table 2.
Summary of confirmed tumor response per RECIST v1.1 by investigator assessment.
| MK-4830 monotherapy | MK-4830 + pembrolizumab | Crossover to MK-4830 + pembrolizumab | |
|---|---|---|---|
| Confirmed response, n (%) | n = 50 | n = 34 | n = 18 |
| ORR | 1 (2)a | 8 (24)b | 1 (6)c |
| CR | 0 | 1 (3) | 0 |
| PR | 1 (2) | 7 (21) | 1 (6) |
| SD | 11 (22) | 9 (26) | 1 (6) |
| SD with PFS ≥6 months | 5 (1) | 6 (18) | 0 |
| PD | 34 (68) | 16 (47) | 3 (17) |
| No RECIST assessmentd | 4 (8) | 1 (3) | 13 (72)e |
Abbreviations: CR, complete response; ORR, objective response rate; PFS, progression-free survival; PR, partial response; RECIST v1.1, Response Evaluation Criteria in Solid Tumors version 1.1; SD, stable disease.
aPatient had high-grade serous ovarian cancer.
bPatients had microsatellite-high colorectal cancer (n = 2), gastric cancer (n = 2), head and neck squamous cell carcinoma (n = 1), Merkel cell carcinoma (n = 1), non–small cell lung cancer (n = 1), and papillary thyroid (n = 1).
cPatient had microsatellite-high colorectal cancer.
dIncludes patients who had the opportunity to have a postbaseline assessment based on the date of their first dose but did not have any postbaseline assessment by the data cutoff date.
eEleven patients have been evaluated by immune Response Evaluation Criteria in Solid Tumors.