TY - JOUR
T1 - An Allogeneic Multiple Myeloma GM-CSF-Secreting Vaccine with Lenalidomide Induces Long-term Immunity and Durable Clinical Responses in Patients in Near Complete Remission
AU - Biavati, Luca
AU - Ann Huff, Carol
AU - Ferguson, Anna
AU - Sidorski, Amy
AU - Stevens, M. Amanda
AU - Rudraraju, Lakshmi
AU - Zucchinetti, Cristina
AU - Abbas Ali, Syed
AU - Imus, Philip
AU - Gocke, Christian B.
AU - Gittelman, Rachel M.
AU - Johnson, Sarah
AU - Sanders, Catherine
AU - Vignali, Marissa
AU - Gandhi, Anita
AU - Ye, Xiaobu
AU - Noonan, Kimberly A.
AU - Borrello, Ivan
N1 - Funding Information:
C.A. Huff reports grants from Celgene (now BMS) during the conduct of the study and personal fees from Sanofi Genzyme, AstraZeneca, GlaxoSmithKline, Oncopep-tides, and Jansssen outside the submitted work. A. Sidorski reports personal fees from Genentech, Amgen, AbbVie, Sanofi Genzyme, Bristol Myers Squibb, Glaxo Smith Kline, and Janssen Biotech outside the submitted work. S.A. Ali reports grants from Celgene/BMS and Aduro Biotech during the conduct of the study as well as personal fees from Celgene/BMS, Aduro Biotech, Amgen, Oncopeptides, Janssen, and Sanofi outside the submitted work. R.M. Gittelman reports personal fees from Adaptive Biotechnologies during the conduct of the study. S. Johnson reports other support from Adaptive Biotechnologies outside the submitted work. M. Vignali reports other support from Adaptive Biotechnologies outside the submitted work. A. Gandhi reports other support from Bristol Myers Squib outside the submitted work. K.A. Noonan reports other support from Aduro Bio during the conduct of the study as well as other support from Aduro Bio/Meridian Therapeutics outside the submitted work; in addition, K.A. Noonan has a patent for Bystander Vaccine issued and with royalties paid from Meridian Therapeutics. I. Borrello reports grants from Aduro Biotech and Celgene and non-financial support from Adaptive Biotechnology during the conduct
Funding Information:
This study was supported by Celgene Corporation (now BMS). It was also funded in part by P30 CA006973 (PI: William Nelson) and the Kathryn Zugby Myeloma Research Fund.
Publisher Copyright:
© 2021 American Association for Cancer Research.
PY - 2021/12/15
Y1 - 2021/12/15
N2 - Purpose: This proof-of-principle clinical trial evaluated whether an allogeneic multiple myeloma GM-CSF-secreting vaccine (MMGVAX) in combination with lenalidomide could deepen the clinical response in patients with multiple myeloma in sustained near complete remission (nCR). Patients and Methods: Fifteen patients on lenalidomide were treated with MM-GVAX and pneumococcal conjugate vaccine (PCV; Prevnar) at 1, 2, 3, and 6 months. Results: Eight patients (53.3%) achieved a true CR. With a median follow-up of 5 years, the median progression-free survival had not been reached, and the median overall survival was 7.8 years from enrollment. MM-GVAX induced clonal T-cell expansion and measurable cytokine responses that persisted up to 7 years in all patients. At baseline, a higher minimal residual disease was predictive of early relapse. After vaccination, a lack of both CD27_DNAM1_CD8 T cells and antigen-presenting cells was associated with disease progression. Conclusions: MM-GVAX, along with lenalidomide, effectively primed durable immunity and resulted in long-term disease control, as suggested by the reappearance of a detectable, fluctuating Mspike without meeting the criteria for clinical relapse. For patients in a nCR, MM-GVAX administration was safe and resulted in prolonged clinical responses.
AB - Purpose: This proof-of-principle clinical trial evaluated whether an allogeneic multiple myeloma GM-CSF-secreting vaccine (MMGVAX) in combination with lenalidomide could deepen the clinical response in patients with multiple myeloma in sustained near complete remission (nCR). Patients and Methods: Fifteen patients on lenalidomide were treated with MM-GVAX and pneumococcal conjugate vaccine (PCV; Prevnar) at 1, 2, 3, and 6 months. Results: Eight patients (53.3%) achieved a true CR. With a median follow-up of 5 years, the median progression-free survival had not been reached, and the median overall survival was 7.8 years from enrollment. MM-GVAX induced clonal T-cell expansion and measurable cytokine responses that persisted up to 7 years in all patients. At baseline, a higher minimal residual disease was predictive of early relapse. After vaccination, a lack of both CD27_DNAM1_CD8 T cells and antigen-presenting cells was associated with disease progression. Conclusions: MM-GVAX, along with lenalidomide, effectively primed durable immunity and resulted in long-term disease control, as suggested by the reappearance of a detectable, fluctuating Mspike without meeting the criteria for clinical relapse. For patients in a nCR, MM-GVAX administration was safe and resulted in prolonged clinical responses.
UR - http://www.scopus.com/inward/record.url?scp=85122395505&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122395505&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-21-1916
DO - 10.1158/1078-0432.CCR-21-1916
M3 - Article
C2 - 34667029
AN - SCOPUS:85122395505
SN - 1078-0432
VL - 27
SP - 6696
EP - 6708
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 24
ER -