Table 1.
Summary of case reports, case series, and completed clinical trials.
Report | Type | #cAS (%) | ORR | Duration of response | PFS | OS | Notes |
---|---|---|---|---|---|---|---|
Sindu et al. (29) | Case report | 1 (100) | n/a | Ongoing | n/a | n/a | |
Hamacher et al. (30) | Case report | 1 (100) | n/a | Ongoing | n/a | n/a | |
Florou et al. (31) | Case series | 5 (100) | 80% | Ongoing in 4 patients, 14 weeks in 1 patient | n/a | n/a | |
Rosenbaum et al. (32) | Retrospective study | 15 (42.9) | n/a | n/a | cAS, median: 17.9 weeks | cAS: Not reached | |
Phase II SWOG S1609 (DART) trial (33) | Study | Head and neck cAS: 5 (31.3) | Head and neck cAS: 60% Overall: 25% | n/a | 6 m PFS rate: 38% (95% Cl 20 to 70%) | Overall: Not reached | 3 of 5 head and neck cAS patients had a confirmed objective response to treatment. 2 radiation induced breast cAS patients were excluded from this table. |
Phase II study of durvalumab plus tremelimumab (NCT02815995) (34) | Study | 1 (1.8) | Overall: 12% | n/a | Overall, median: 12.2 weeks | Overall, median: 93.9 weeks | The 1 cAS patient had a partial response and was the only responder of 5 AS patients. |
Phase II study of TVEC and pembrolizumab (NCT03069378) (35) | Study | 3 (15) | Overall: 35% | Overall: 56.1 weeks | Overall, median: 17.1 weeks | Overall, disease specific survival: 74.6 weeks | Partial response in 2 cAS patients. Both completed 52 weeks of study therapy. |