Authors (reference) | Bataller [2] | Yu [3] | Ruhnke [4] | Zarnegar-Lumley [5] | Hu [6] |
---|---|---|---|---|---|
Regimen | VEN + CPX-351 | VEN + CAG | VEN + HAM | VEN + selinexor + FLA(G) | VEN + MTO + HHT + olverembatinib |
Study type | Phase Ib/II | N/A | Phase-I/II | Phase I | N/A |
NCT number | NCT03629171 | N/A | NCT04330820 | NCT04898894 | N/A |
Study period | 2018–2022 | 2016–2023 | 2020–2023 | N/A | N/A |
Patients number | 33 | 37 | 38 | 14 | 18 |
Male | 13 (39.4%) | 24 (64.8%) | N/A | 9 (64.3%) | 9 (50.0%) |
Age range (years) | 26–72 | 18–68 | 26–74 | 3–17 | 0.3–13 |
Median prior lines of therapies | 1 (1–7) | N/A | N/A | N/A | N/A |
Prior exposure to VEN | 19 (57.6%) | N/A | N/A | N/A | N/A |
Response rate | ORR 45%,CR/CRi 39% | CRc 78.4% | CR/CRi 81.6% | CR/CRi 41.7 | ORR 94.4%,CR/CRi 72.2% |
Grade ≥ 3 AEs | Infections 45% | febrile neutropenia 67.6% | febrile neutropenia ≥ 10% | febrile neutropenia 16.7% | Neutropenia 100% |
Follow-up (months) | 20.7 | N/A | N/A | N/A | N/A |
Survival | Median OS 6.4 months | The one-year OS 78.4% | N/A | N/A | The 8-month mean EFS 60.1% and the OS 100% |