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Published on: May 15, 2019
Pomalidomide, Cyclophosphamide, and Dexamethasone for Relapsed/Refractory Multiple Myeloma: A Single-Center
Ioannis Ntanasis-Stathopoulos1, Panagiotis Malandrakis1, Charalampos Filippatos1
1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
The PCd regimen (pomalidomide, cyclophosphamide, and dexamethasone) shows promising efficacy in relapsed/refractory multiple myeloma (RRMM) patients. High-risk cytogenetics negatively impacted outcomes, while neutropenia was the most common severe toxicity.
Area of Science:
- Hematology
- Oncology
- Clinical Therapeutics
Background:
- Pomalidomide, a third-generation immunomodulatory drug (IMiD), is effective in relapsed/refractory multiple myeloma (RRMM).
- The combination of pomalidomide, cyclophosphamide, and dexamethasone (PCd) is being investigated for RRMM treatment.
Purpose of the Study:
- To evaluate the efficacy and safety of the PCd regimen in patients with relapsed/refractory multiple myeloma.
- To identify factors influencing treatment outcomes in RRMM patients receiving PCd.
Main Methods:
- Retrospective analysis of 45 RRMM patients treated with PCd.
- Patients received at least one prior therapy and had experienced disease progression.
- Outcomes assessed included overall response rate (ORR), disease control rate (DCR), time to treatment not-given (TTNT), progression-free survival (PFS), and overall survival (OS).
Main Results:
- The PCd regimen achieved an ORR of 46.7% and a DCR of 66.7%.
- Median TTNT, PFS, and OS were 14.6, 9.0, and 21.0 months, respectively.
- High-risk cytogenetics were associated with worse PFS and DCR. Neutropenia was the most frequent severe toxicity.
Conclusions:
- The addition of cyclophosphamide to pomalidomide and dexamethasone (PCd) demonstrates promising efficacy in pretreated RRMM patients.
- PCd represents a viable therapeutic option in real-world settings for RRMM.
- Further investigation into PCd's role in RRMM management is warranted.
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