» Articles » PMID: 3297203

CFU-GM Content of Bone Marrow Graft Correlates with Time to Hematologic Reconstitution Following Autologous Bone Marrow Transplantation with 4-hydroperoxycyclophosphamide-purged Bone Marrow

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 1987 Jul 1
PMID 3297203
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Autologous bone marrow transplants (BMTs) can repopulate the hematologic system of patients treated with marrow-ablative chemotherapy and/or radiotherapy. However, treatment of the bone marrow graft to eliminate residual tumor cells prior to reinfusion can delay the return of peripheral blood elements, presumably from damage to or loss of hematopoietic stem cells responsible for hematologic recovery. To develop a model predictive of hematologic recovery, we studied the progenitor cell contents of 4-hydroperoxycyclophosphamide (100 micrograms/mL)-purged bone marrow grafts of 40 consecutive patients undergoing autologous BMT at this center. Granulocyte-macrophage colonies (CFU-GM) were grown from all grafts after treatment with this chemotherapeutic agent, but erythroid (BFU-E) and mixed (CFU-GEMM) colonies were grown from only 44% and 33% of the grafts respectively. The recovery of CFU-GM after purging ranged from 0.07% to 23%. The logarithm of CFU-GM content of the treated grafts was linearly correlated with the time to recovery of peripheral blood leukocytes (r = -0.80), neutrophils (r = -0.79), reticulocytes (r = -0.60), and platelets (r = -0.66). The CFU-GM content of purged autologous bone marrow grafts may reflect the hematopoietic stem cell content of the grafts and thus predict the rate of hematologic recovery in patients undergoing autologous BMT.

Citing Articles

Extract Prevents Cisplatin-Induced Myelotoxicity and .

Lin S, Li M, Chuang K, Lin N, Chang C, Wu H Oxid Med Cell Longev. 2020; 2020:7353618.

PMID: 32047579 PMC: 7003270. DOI: 10.1155/2020/7353618.


Maitake beta-glucan promotes recovery of leukocytes and myeloid cell function in peripheral blood from paclitaxel hematotoxicity.

Lin H, de Stanchina E, Zhou X, Hong F, Seidman A, Fornier M Cancer Immunol Immunother. 2010; 59(6):885-97.

PMID: 20140432 PMC: 3268513. DOI: 10.1007/s00262-009-0815-3.


In vitro purging of clonogenic leukaemic cells from human bone marrow by interferon-gamma-activated monocytes.

van de Loosdrecht A, Ossenkoppele G, Beelen R, Broekhoven M, Schweitzer K, Langenhuijsen M Cancer Immunol Immunother. 1994; 38(5):346-52.

PMID: 8162617 PMC: 11038299. DOI: 10.1007/BF01525514.


Hematopoietic progenitor cell content of vertebral body marrow used for combined solid organ and bone marrow transplantation.

Rybka W, Fontes P, Rao A, Winkelstein A, Ricordi C, Ball E Transplantation. 1995; 59(6):871-4.

PMID: 7701582 PMC: 2958527. DOI: 10.1097/00007890-199503270-00012.


Release from quiescence of CD34+ CD38- human umbilical cord blood cells reveals their potentiality to engraft adults.

Cardoso A, Li M, Batard P, Hatzfeld A, Brown E, Levesque J Proc Natl Acad Sci U S A. 1993; 90(18):8707-11.

PMID: 7690969 PMC: 47427. DOI: 10.1073/pnas.90.18.8707.