Assessment of Allogeneic Hematopoietic Cell Transplantation in Medicare Beneficiaries With Multiple Myeloma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorCenter for International Blood and Marrow Transplant Research

About this trial

Multiple myeloma (MM) is the second most common hematologic malignancy in adults. The current standard of care for MM patients fit to undergo high dose conditioning chemotherapy is an autologous HCT (autoHCT). Allogeneic HCT (alloHCT) is the only potentially curative therapy available to patients with MM. However, the significant morbidity and mortality of this procedure historically limited its application in older patients.

Thus, although potentially curative, standard risk MM patients have excellent prognoses in the era of novel therapies which reduces the overall benefit of alloHCT. However, because the outcomes for high-risk MM remain poor despite the best available standard therapies (overall survival of 24-36 months), initial data suggest that alloHCT should be explored in this subset.

Eligibility criteria

Qualifiers

Medicare beneficiary

Stage II or III multiple myeloma and/or primary plasma cell leukemia

Eligible to receive an allogeneic HCT from any suitable allogeneic donor (as determined by the transplant center) including umbilical cord blood

Will receive allogeneic HCT at a US transplant center

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Allogeneic Hematopoietic Stem Cell Transplant

Treatment groups

544 Participants
are divided into 2 treatment groups

Sponsors and collaborators