Alliance QUANTUM Trial to Study Bispecific Immunotherapy for Rare Leukemia
New trial evaluates whether post-transplant consolidation therapy with teclistamab can improve survival in patients with primary plasma cell leukemia
July 30 - The Alliance for Clinical Trials in Oncology today announced the activation of The QUANTUM Trial (Alliance A062401), a clinical study designed to test a novel, immune-targeting approach for patients newly diagnosed with primary plasma cell leukemia (PCL).
Plasma cell leukemia is a rare but aggressive form of blood cancer with about 1,200 new cases diagnosed in the U.S. each year. It is characterized by high numbers of malignant plasma cells circulating in the bloodstream and long-term survival remains poor.
Because current therapies are often cannot produce durable remissions, researchers are evaluating whether teclistamab—a novel bispecific antibody—can improve outcomes when used as consolidation therapy after stem cell transplantation compared with standard post-transplant treatments. Teclistamab is a next-generation immunotherapy that is FDA-approved for certain patients with multiple myeloma. It works by activating the body’s immune system to target and destroy cancer cells.

“Plasma cell leukemia progresses rapidly and remains one of the most difficult blood cancers to treat effectively,” said Douglas Sborov, MD, MS, Professor of Medicine at the University of Utah-Huntsman Cancer Institute, Department of Internal Medicine- Division of Hematology and Hematologic Malignancies and principal investigator of the trial. “By introducing the bispecific antibody teclistamab right after stem cell transplantation, the QUANTUM trial aims to harness the patient’s own immune system to clear residual cancer cells and with the ultimate goal of meaningfully improving long-term survival.”
Participants in the QUANTUM study undergo a multi-phase treatment plan that combines established therapies with a novel bispecific antibody approach:
- Step 1-Induction Phase: All patients will receive four cycles of quadruplet induction therapy consisting of daratumumab, carfilzomib, lenalidomide, and dexamethasone called D-KRd to rapidly reduce cancer cell counts. These drugs work to stop cancer cells from reproducing while mobilizing the patient’s immune system against the disease.
- Step 2-Stem Cell Transplant: After induction therapy, patients undergo stem cell mobilization and collection followed by high-dose chemotherapy and an autologous stem cell transplant to rebuild healthy blood-forming cells. This process uses the patient’s own healthy blood stem cells to rebuild bone marrow that has been damaged by chemotherapy.
- Step 3-Targeted Consolidation (Key Trial Focus): Following transplantation, patients are randomly assigned to one of two treatment groups. Patients in the experimental arm receive teclistamab while patients in the standard-of-care arm continue D-KRd therapy. The trial is evaluating whether teclistamab consolidation can improve overall survival compared to standard D-KRd treatment.
- Step 4-Maintenance Phase: After consolidation, patients in both treatment groups receive long-term maintenance therapy with carfilzomib and lenalidomide intended to help maintain disease control and delay relapse.
The QUANTUM Trial is sponsored by the National Cancer Institute (NCI) and conducted by the Alliance for Clinical Trials in Oncology. This Phase II study aims to enroll 74 adults at participating cancer centers and medical clinics across the United States.
Reference: Alliance A062401-Quadruplet Induction Followed by Teclistamab Consolidation and Doublet Maintenance in Patients with Primary Plasma Cell Leukemia: The QUANTUM Trial, https://clinicaltrials.gov/study/NCT07605416.
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The Alliance for Clinical Trials in Oncology is a national leader in advancing cancer research, uniting more than 26,000 cancer specialists at 112 main institutions and 1,400 affiliates across the U.S. and Canada. As part of the National Clinical Trials Network and a leading research base for the NCI Community Oncology Research Program, the Alliance conducts pioneering, practice-changing clinical trials that improve outcomes and reshape standards of care. Our work has led to multiple FDA approvals, influenced national guidelines, and produced hundreds of high-impact publications. More than 40,000 participants have taken part in Alliance studies, and our growing biospecimen repository now includes more than 1.5 million samples, collected over the past 30 years. Learn more at allianceforclinicaltrialsinoncology.org.


