Table 2. SLAM members implicated in anti-cancer clinical trials.
SLAM family | Pathology | Treatment type | Treatment name | Study phase | References |
---|---|---|---|---|---|
SLAMF1 | ALL | Oncolytic MV vaccine strains | CAM-70 | Preclinical | [28] |
Non-Hodgkin’s lymphoma | MVVAC2NIS | Preclinical | [29] | ||
SLAMF2 | CLL | anti-SLAMF2 Ab | WM-63 | Phase 1 clinical trial | [35] |
B lymphoma | HuLy-m3 | Preclinical | [36] | ||
MM | 1B4 | Preclinical | [37] | ||
SLAMF4 | Leukemia | 2B4 chimeric receptor | 2B4-ζ | Preclinical | [57] |
SLAMF6 | CLL and lymphoma | anti-SLAMF6 Ab | 994.1 and 480.12 | Preclinical | [67] |
CLL | αSLAMF6 and Ibrutinib | Preclinical | [68] | ||
SLAMF7 | MM | CS1-specific peptide | CS1239–247 | Preclinical | [75] |
anti-SLAMF7 Ab | HuLuc63 | Preclinical | [70, 72] | ||
Elotuzumab combined to Bortezomib | Preclinical | [71] | |||
Elotuzumab combined to Bortezomib | Phase 1 clinical trial | [77] | |||
Elotuzumab combined to Lenalidomide and Dexamethasone | Phase 1 clinical trial | [79] | |||
Elotuzumab combined to Lenalidomide and Dexamethasone | Phase 3 clinical trial | (ELOQUENT-1, NCT01335399) | |||
MM with renal impairment | anti-SLAMF7 Ab | 10 mg/Kg Elotuzumab, 5-25 mg Lenalidomide and 40 mg Dexamethasone | Phase 1b clinical trial | [81] | |
Refractory or relapsed MM | anti-SLAMF7 Ab | Elotuzumab | Phase 1 clinical trial | [76] | |
10 or 20 mg Elotuzumab, 25 mg Lenalidomide and 40 mg Dexamethasone | Phase1b-2 clinical trial | [80] | |||
10 mg/Kg Elotuzumab, 25 mg Lenalidomide and 40 mg Dexamethasone | Phase 3 clinical trial | [82] | |||
10 mg/Kg Elotuzumab, 1,3 mg Bortezomib and 20 mg Dexamethasone | Phase 2 clinical trial | [78] | |||
10 mg/Kg Elotuzumab, 200 mg Thalidomide and 40 mg Dexamethasone | Phase 2 clinical trial | [83] | |||
Elotuzumab in combination with Lenalidomide and Dexamethasone obtained FDA in November 2015 |
Abbreviations: MM: Multiple Myeloma; CLL: Chronic Lymphocytic Leukemia; ALL: Acute Lymphocytic Leukemia.