Abstract 4551

Background:

In a recent phase IIa open-label, randomized, cross-over design study, we evaluated the pharmacokinetics of Propylene Glycol-Free Melphalan (PG-free Mel) HCL and Alkeran in multiple myeloma patients undergoing transplantation. In this study, we have shown through statistical tests of the geometric means of AUC that PG-free Mel was bioequivalent to Alkeran, and provided marginally higher blood drug levels.

Hypothesis:

Because this new formulation is associated with marginally higher blood drug levels and because melphalan is associated with a linear dose-response curve, we speculated that patients treated on study would have a better multiple myeloma response compared to matched controls.

Goal:

To assess day +100 multiple myeloma responses from the study patients (n=24) receiving PG-free Mel conditioning in combination with Alkeran. Responses were assessed based on International Uniform Response Criteria for Multiple Myeloma. Comparison was made to a matched cohort of patients who received conventional melphalan.

Methods:

We compared the study patient responses to matched controls (n=24) treated exclusively with Alkeran or generic melphalan conditioning within the same time frame in a case-control study design. The controls were matched to study population based on disease stage, age, and pre-transplant response.

Results:

The study population and the control cohort were well matched in terms of age, gender, disease stage, and pre-transplant response. However, the study population had more patients with high-risk cytogenetics (10 vs 3). Overall response (CR, VGPR, and PR) was higher in the study population (22 vs 19). While no patient on the study progressed within 100 days of transplant, 3 patients in the matched cohort progressed within 100 days. The median duration of follow up of surviving patients was 650 days in the study cohort and 409 days in the matched control cohort. Twenty three study patients and 22 patients in the matched control cohort were reported alive. On the other hand, 7 study patients and 8 patients in the matched cohort progressed during follow up.

Conclusion:

Compared to matched controls, PG-free Mel, as part of the melphalan conditioning regimen, resulted in higher remission rates and less disease progression at day 100 post autologous transplant for multiple myeloma.

Disclosures:

Off Label Use: Propylene glycol free melphalan for high-dose therapy and autologous transplant for multiple myeloma.

Author notes

*

Asterisk with author names denotes non-ASH members.

Sign in via your Institution