Low-Dose Cyclophosphamide versus Intermediate-High-Dose Cyclophosphamide versus Granulocyte Colony-Stimulating Factor Alone for Stem Cell Mobilization in Multiple Myeloma in the Era of Novel Agents: A Multicenter Retrospective Study

Autor: Daniele Laszlo, Claudia Cellini, Federica Monaco, Martina Chiarucci, Massimo Martino, Attilio Guarini, Elisabetta Fabbri, Eliana Zuffa, Beatrice Anna Zannetti, Attilio Olivieri, Francesco Lanza, Manuela Imola, Patrizia Tosi, Francesco Saraceni
Rok vydání: 2020
Předmět:
Melphalan
medicine.medical_specialty
Cyclophosphamide
High-dose cyclophosphamide
Urology
Antigens
CD34

Autologous stem cell transplantation
NO
chemistry.chemical_compound
G-CSF priming
Autologous stem-cell transplantation
Heterocyclic Compounds
Granulocyte Colony-Stimulating Factor
medicine
Immunology and Allergy
Humans
Multiple myeloma
Lenalidomide
Retrospective Studies
Transplantation
Stem cell mobilization
Multiple myeloma
Plerixafor
Low-dose cyclophosphamide
High-dose cyclophosphamide
G-CSF priming
Autologous stem cell transplantation

Low-dose cyclophosphamide
business.industry
Plerixafor
Cell Biology
Hematology
medicine.disease
Carfilzomib
Hematopoietic Stem Cell Mobilization
Granulocyte colony-stimulating factor
chemistry
Stem cell mobilization
Molecular Medicine
business
Multiple Myeloma
medicine.drug
Zdroj: Transplantation and cellular therapy. 27(3)
ISSN: 2666-6367
Popis: The optimal stem cell (SC) mobilization strategy for patients with multiple myeloma (MM) remains a matter of debate. Possible approaches include low or high doses of cyclophosphamide (Cy), other chemotherapeutic agents, or granulocyte colony-stimulating factor (G-CSF) alone. The scope of the study was to compare low-dose Cy plus G-CSF versus intermediate-high-dose Cy plus G-CSF versus G-CSF alone for SC mobilization in MM, in terms of efficacy and safety. We retrospectively analyzed 422 MM patients undergoing SC mobilization in 6 Italian centers, including 188 patients who received low-dose Cy (LD-Cy group, defined as 2 g/m2), 163 patients who received intermediate-high-dose Cy (HD-Cy group, defined as ≥ 3 g/m2), and 71 patients who received G-CSF alone (G-CSF group). The median peak of circulating CD34+ cells was 77/µL in the LD-Cy group, 92/µL in the HD-Cy group, and 55/µL in the G-CSF group (P = .0001). The median amount of SCs collected was 9.1 × 106/kg, 9.7 × 106/kg, and 5.6 × 106/kg in the 3 groups, respectively (P = .0001). The rate of mobilization failure (defined as failure to collect ≥2 × 106/kg) was 3.7% in the LD-Cy group, 3.4% in the HD-Cy group, and 4.3% in the G-CSF group (P = .9). The target SC dose of at least 4 × 106/kg was reached in 90.4%, 91.1%, and 78.6% of the patients in these 3 groups, respectively (P = .014). The "on demand" use of plerixafor was higher in the G-CSF group (76%) compared with the LD-Cy group (19%) and the HD-Cy group (6%). In multivariate analysis, G-CSF mobilization and previous use of melphalan or radiotherapy were independently associated with failure to collect the target SC dose of ≥4 × 106/kg. No impacts of age, blood counts, or previous treatment with lenalidomide, bortezomib, or carfilzomib were observed. Our results suggest that LD-Cy may be considered for successful SC mobilization in patients with MM.
Databáze: OpenAIRE