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Updated: Dec 26, 2025

Isolation and Transplantation of Different Aged Murine Thymic Grafts.
Published on: May 13, 2015
Microtransplantation in older patients with AML: A pilot study of safety, efficacy and immunologic effects
Anthony D Sung1, Shekeab Jauhari1, Sharareh Siamakpour-Reihani1
1Duke University School of Medicine, Durham, North Carolina, USA.
Abstract:
Older AML patients have low remission rates and poor survival outcomes with standard chemotherapy. Microtransplantation (MST) refers to infusion of allogeneic hematopoietic stem cells without substantial engraftment. MST has been shown to improve clinical outcomes compared with chemotherapy alone. This is the first trial reporting on broad correlative studies to define immunologic mechanisms of action of MST in older AML patients. Older patients with newly diagnosed AML were eligible for enrollment, receiving induction chemotherapy with cytarabine (100 mg/m2) on days 1-7 and idarubicin (12 mg/m2) on days 1-3 (7 + 3). MST was administered 24 hours later. Patients with complete response (CR) were eligible for consolidation with high dose cytarabine (HiDAC) and a second cycle of MST. Responses were evaluated according to standard criteria per NCCN. Immune correlative studies were performed. Sixteen patients were enrolled and received 7 + 3 and MST (median age 73 years). Nine (56%) had high-risk and seven (44%) had standard-risk cytogenetics. Ten episodes of CRS were observed. No cases of GVHD or treatment-related mortality were reported. Event-free survival (EFS) was 50% at 6 months and 19% at 1 year. Overall survival (OS) was 63% at 6 months and 44% at 1 year. Donor microchimerism was not detected. Longitudinal changes were noted in NGS, TCR sequencing, and cytokine assays. Addition of MST to induction and consolidation chemotherapy was well tolerated in older AML patients. Inferior survival outcomes in our study may be attributed to a higher proportion of very elderly patients with high-risk features. Potential immunologic mechanisms of activity of MST include attenuation of inflammatory cytokines and emergence of tumor-specific T cell clones.
Insights
Microtransplantation (MST) with chemotherapy is safe for older AML patients. This approach may work by reducing inflammation and boosting anti-tumor T cells, though survival outcomes need further study.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Older patients with Acute Myeloid Leukemia (AML) exhibit poor outcomes with standard chemotherapy.
- Microtransplantation (MST), involving infusion of allogeneic hematopoietic stem cells without engraftment, shows promise in improving outcomes.
- The immunologic mechanisms underlying MST's efficacy in older AML patients remain largely undefined.
Purpose of the Study:
- To investigate the safety and tolerability of MST combined with chemotherapy in older AML patients.
- To explore the immunologic mechanisms of action of MST in this patient population.
- To assess preliminary clinical outcomes, including event-free survival (EFS) and overall survival (OS).
Main Methods:
- Older adults with newly diagnosed AML received induction chemotherapy (cytarabine and idarubicin) followed by MST.
- Patients achieving complete response (CR) underwent consolidation with high-dose cytarabine (HiDAC) and a second MST cycle.
- Extensive immune correlative studies, including next-generation sequencing (NGS), TCR sequencing, and cytokine assays, were performed.
Main Results:
- The combination of 7+3 chemotherapy and MST was well-tolerated, with no cases of graft-versus-host disease (GVHD) or treatment-related mortality.
- Ten episodes of cytokine release syndrome (CRS) were observed.
- Event-free survival (EFS) was 50% at 6 months and 19% at 1 year; overall survival (OS) was 63% at 6 months and 44% at 1 year.
Conclusions:
- MST is a safe and tolerable addition to chemotherapy for older AML patients.
- Observed survival outcomes may be influenced by the high proportion of elderly patients with high-risk cytogenetic features.
- Potential immunologic mechanisms include attenuation of inflammatory cytokines and the emergence of tumor-specific T cell clones.

