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Long-term cryopreservation of bone marrow for autologous transplantation

Bone Marrow Transplant

Key Findings

This study confirms that long-term cryopreservation of bone marrow for up to 7.8 years does not negatively impact hematopoietic stem cell viability or engraftment success.

Results indicate that early-stage marrow collection can effectively preserve stem cell quality before cumulative damage from chemotherapy or radiation occurs. This research supports the long-term storage of autologous bone marrow as a reliable option for future transplantation.

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Long-term cryopreservation of bone marrow for autologous transplantation

Little is known about the effect of long-term cryopreservation on the viability of hematopoietic stem cells (HSC) or on the success of autologous bone marrow transplantation. Although progenitor cell assays, such as the culture of CFU-GM after thawing, can be predictive of engraftment, the most rigorous assay for the cryosurvival of HSC is engraftment after reinfusion of stem cells.

Study Methodology and Patient Demographics

Researchers retrospectively evaluated the engraftment data for 36 patients with hematologic malignancies or solid tumors treated at the Fred Hutchinson Cancer Research Center between 1981 and 1993. These patients received bone marrows stored for 2 years or more. The median duration of cryopreservation for this study group was 2.7 years, with a range spanning 2.0 to 7.8 years.

Comparative Engraftment Results

  • Granulocyte Recovery: 97% of the study group achieved a count of ≥ 0.5 x 1.0(9)/1 at a median of 19 days, compared to 86% of the control group at 20 days (P = 0.14).

  • Platelet Recovery: 70% of the study group achieved a count ≥ 20 x 10(9)/1 at a median of 27 days, compared to 74% of the control group at 23 days (P = 0.47).

  • Progenitor Culture: Samples from 28 marrows stored for a median of 4.4 years showed that storage length was not predictive for the quantity of colonies formed (BFU-E P = 0.57; CFU-GM P = 0.65).

Conclusion

The study found no consistent detrimental effect of long-term cryopreservation on the success rate of autologous bone marrow transplantation. This report confirms that marrow cells cryopreserved for several years remain capable of engrafting. Consequently, bone marrow cells may be stored at an early appropriate time before the cumulative side-effects of multiple cycles of chemotherapy and radiotherapy on hematopoietic tissues are incurred.

Research Details

Source

Bone Marrow Transplant

Publication Date

Cite this article: Bone Marrow Transplant. "Long-term cryopreservation of bone marrow for autologous transplantation". Published August 14, 2025. Available at: http://www.ncbi.nlm.nih.gov/pubmed/8704699

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Autologous hematopoietic stem cell transplantation in multiple sclerosis: a phase II trial

OBJECTIVE To assess in multiple sclerosis (MS) the effect of intense immunosuppression followed by autologous hematopoietic stem cells transplantation (AHSCT) vs mitoxantrone (MTX) on disease activity measured by MRI. METHODS We conducted a multicenter, phase II, randomized trial including patients with secondary progressive or relapsing-remitting MS, with a documented increase in the last year on the Expanded Disability Status Scale, in spite of conventional therapy, and presence of one or more gadolinium-enhancing (Gd+) areas. Patients were randomized to receive intense immunosuppression (mobilization with cyclophosphamide and filgrastim, conditioning with carmustine, cytosine-arabinoside, etoposide, melphalan, and anti-thymocyte globulin) followed by AHSCT or MTX 20 mg every month for 6 months. The primary endpoint was the cumulative number of new T2 lesions in the 4 years following randomization. Secondary endpoints were the cumulative number of Gd+ lesions, relapse rate, and disability progression. Safety and tolerability were also assessed. Twenty-one patients were randomized and 17 had postbaseline evaluable MRI scans. RESULTS AHSCT reduced by 79% the number of new T2 lesions as compared to MTX (rate ratio 0.21, p = 0.00016). It also reduced Gd+ lesions as well as the annualized relapse rate. No difference was found in the progression of disability. CONCLUSION Intense immunosuppression followed by AHSCT is significantly superior to MTX in reducing MRI activity in severe cases of MS. These results strongly support further phase III studies with primary clinical endpoints.

Neurology
Long-term cryopreservation of bone marrow for autologous transplantation - Research Article | ForeverLabs