Table 3.
Study | NK cell infusion regimen | Results | |
In non-transplant setting | |||
In advanced AML | Miller, 2014 | Haplo-NK, activated with IL-2, Flu/Cy | Five of 19 (26%) patients achieved CR |
Bachanova, 2014 | Haplo-NK, depletion of Tregs, activation of IL-2, Flu/Cy | Eight of 15 patients (53%) achieved remission at day 28, CR (n = 3), (CRp; n = 2), and CRi (n = 3) | |
Cooley, 2019 | Haplo-NK cells given with rhIL-15, Flu/Cy | Fourteen of 40 patients (35%) achieved CR/CRi | |
In MRD positive AML | Zhao, 2020 | IL-21/4-1BBL-expanded NK cellchemotherapy with Flu/Cy or anthracyclines/Cy | Effective rates were 50% or 60% in Flu/Cy (n = 10) or anthracyclines/Cy (n = 10); DFS was clearly better in the NK group than in the historical group |
As consolidation or maintenance | Jiang, 2019 | IL-21/4-1BBL-expanded NK cell infusion during 4 to 7 courses of chemotherapy | The 3-year LFS was better in the NK group than in the control group (65.1% vs. 43.5%, P = 0.047) |
Nguyen, 2019 | Haplo-NK, activated with IL-2, Flu/Cy | NK cells did not improve EFS (60.7% vs. 69.1%; P = 0.553) over chemotherapy alone | |
In transplant setting | |||
Post-HSCT | Choi, 2014 | Donor-derived, IL-15 plus IL-21-stimulated CD3-depleted NK cells on days 14 and 21 post HSCT | Post-transplantation NK cells significantly decreased leukemia progression (74% to 46%, P = 0.038) |
Choi, 2016 | Additional donor NK-cell infusions given on days 6 and 9 in addition to 14 and 21 post HSCT | Compared with the above study findings, an additional NK infusion on days 6 and 9 was not associated with less leukemia progression | |
Pre-HSCT | Lee, 2016 | IL-2 activated NK cell infusion after conditioning chemotherapy and before stem cell infusion | Durable CR occurred in 5 of 21 patients |
Ciurea, 2017 | mbIL21 ex vivo expanded donor-derived NK cells on days −2, +7, and +28 | The incidence was significantly lower in the NK group than in the control group for CMV reactivation (30.8%) (70.4%, P = 0.01) |
CRp, CR without platelet recovery; CRi, CR with incomplete recovery.