Autologous Stem Cell Transplantation (ASCT)
Definition
- A procedure where a patient’s own hematopoietic stem cells are collected, stored, and then reinfused after the patient receives high-dose chemotherapy (conditioning regimen, e.g., BEAM, MEL200, TBC, etc.).
- Unlike allogeneic SCT, no donor is used → eliminates risk of graft-versus-host disease (GVHD).
Indications (major oncology uses)
- Hematologic Malignancies
- Hodgkin lymphoma (relapsed/refractory)
- Non-Hodgkin lymphoma (DLBCL, mantle cell, follicular)
- Multiple myeloma (standard of care in transplant-eligible patients)
- Other
Steps in ASCT
- Mobilization & Collection
- Growth factors: G-CSF (filgrastim, pegfilgrastim) ± plerixafor (CXCR4 inhibitor, for poor mobilizers)
- Leukapheresis: Peripheral blood stem cells (PBSCs) collected
- Goal: ≥ 2–5 × 10⁶ CD34+ cells/kg
- Cryopreservation
- Stem cells frozen (usually with DMSO as cryoprotectant) until reinfusion
- Conditioning Chemotherapy
- Stem Cell Infusion (“Day 0”)
- Thawed stem cells reinfused IV (like a blood transfusion)
- Side effect: DMSO toxicity → nausea, garlic/creamed-corn odor, bradycardia, hypotension
- Engraftment & Recovery
- Supportive care during aplastic phase (≈10–14 days)
- Engraftment: recovery of ANC > 500/µL for 3 consecutive days
Supportive Care (Pharmacist Focus)
- Antimicrobial prophylaxis:
- Bacterial: fluoroquinolones (sometimes)
- Fungal: fluconazole (or posaconazole if high risk)
- Viral: acyclovir
- PCP: TMP-SMX post-engraftment
- Growth factors:
- Filgrastim post-transplant to accelerate engraftment
- Transfusions:
- Platelets and RBC support as needed
- Other considerations:
Advantages vs Allogeneic SCT
- Lower treatment-related mortality
- No GVHD
- No graft-versus-leukemia/lymphoma effect (relapse is main limitation)
Key Complications
- Early (first 30 days): mucositis, neutropenic fever, infections, organ toxicities
- Intermediate (1–6 months): infections (viral reactivations, fungal)
- Late (>6 months): relapse of primary disease, secondary malignancies

