Transplantation of enriched CD34-positive autologous marrow into breast cancer patients following high-dose chemotherapy : influence of CD34-positive peripheral-blood progenitors and growth factors on engraftment
PURPOSE: To evaluate the capacity of enriched CD34-positive (CD34+) progenitor cells to reconstitute hematopoiesis in poor-prognosis breast cancer patients following administration of a high-dose alkylating agent chemotherapy regimen.
PATIENTS AND METHODS: Forty-four breast cancer patients received high-dose chemotherapy followed by autologous bone marrow support (ABMS) with CD34+ hematopoietic progenitor cells in five sequentially treated cohorts. Following infusion of CD34+ marrow, cohort no. 1 received no growth factor, cohort no. 2 received granulocyte colony-stimulating factor (G-CSF), and cohort no. 3 received granulocyte-macrophage colony-stimulating factor (GM-CSF). Cohort no. 4 received the CD34+ fractions of both marrow and peripheral-blood progenitor cells (PBPCs) plus G-CSF. Cohort no. 5 received only the CD34+ PBPCs plus G-CSF. Immunohistochemical staining for breast cancer was performed on all hematopoietic cell products before and after the positive selection procedure, to assess quantitatively the level of tumor-cell contamination.
RESULTS: Cohorts no. 1, 2, 3, 4, and 5 achieved a granulocyte count > or = 500 x 10(9)/L in a median of 23, 10, 16, 11, and 11 days, with a platelet count greater than 20,000 x 10(9)/L documented in a median of 22, 23, 32, 12, and 10 days, respectively. The time to granulocyte reconstitution was significantly shorter for patients who received CD34+ PBPCs alone (cohort no. 5), or in combination with CD34+ marrow (cohort no. 4), when compared with those who received only the CD34+ marrow fraction (P < .01). From 1 to greater than 4 logs of breast cancer cell depletion were documented after CD34-selection, for patients in whom tumor was initially detected.
CONCLUSION: CD34+ marrow and/or PBPCs provide reliable and timely hematopoietic reconstitution in breast cancer patients receiving high-dose chemotherapy. Contamination of both marrow and PBPCs with breast cancer cells was reduced using this positive selection technique.
Medienart: |
Artikel |
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Erscheinungsjahr: |
1994 |
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Erschienen: |
1994 |
Enthalten in: |
Zur Gesamtaufnahme - volume:12 |
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Enthalten in: |
Journal of clinical oncology : official journal of the American Society of Clinical Oncology - 12(1994), 1 vom: 01. Jan., Seite 28-36 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Shpall, E J [VerfasserIn] |
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Themen: |
Antigens, CD |
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Anmerkungen: |
Date Completed 31.01.1994 Date Revised 10.02.2017 published: Print Citation Status MEDLINE |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM074821652 |
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100 | 1 | |a Shpall, E J |e verfasserin |4 aut | |
245 | 1 | 0 | |a Transplantation of enriched CD34-positive autologous marrow into breast cancer patients following high-dose chemotherapy |b influence of CD34-positive peripheral-blood progenitors and growth factors on engraftment |
264 | 1 | |c 1994 | |
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500 | |a Date Completed 31.01.1994 | ||
500 | |a Date Revised 10.02.2017 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a PURPOSE: To evaluate the capacity of enriched CD34-positive (CD34+) progenitor cells to reconstitute hematopoiesis in poor-prognosis breast cancer patients following administration of a high-dose alkylating agent chemotherapy regimen | ||
520 | |a PATIENTS AND METHODS: Forty-four breast cancer patients received high-dose chemotherapy followed by autologous bone marrow support (ABMS) with CD34+ hematopoietic progenitor cells in five sequentially treated cohorts. Following infusion of CD34+ marrow, cohort no. 1 received no growth factor, cohort no. 2 received granulocyte colony-stimulating factor (G-CSF), and cohort no. 3 received granulocyte-macrophage colony-stimulating factor (GM-CSF). Cohort no. 4 received the CD34+ fractions of both marrow and peripheral-blood progenitor cells (PBPCs) plus G-CSF. Cohort no. 5 received only the CD34+ PBPCs plus G-CSF. Immunohistochemical staining for breast cancer was performed on all hematopoietic cell products before and after the positive selection procedure, to assess quantitatively the level of tumor-cell contamination | ||
520 | |a RESULTS: Cohorts no. 1, 2, 3, 4, and 5 achieved a granulocyte count > or = 500 x 10(9)/L in a median of 23, 10, 16, 11, and 11 days, with a platelet count greater than 20,000 x 10(9)/L documented in a median of 22, 23, 32, 12, and 10 days, respectively. The time to granulocyte reconstitution was significantly shorter for patients who received CD34+ PBPCs alone (cohort no. 5), or in combination with CD34+ marrow (cohort no. 4), when compared with those who received only the CD34+ marrow fraction (P < .01). From 1 to greater than 4 logs of breast cancer cell depletion were documented after CD34-selection, for patients in whom tumor was initially detected | ||
520 | |a CONCLUSION: CD34+ marrow and/or PBPCs provide reliable and timely hematopoietic reconstitution in breast cancer patients receiving high-dose chemotherapy. Contamination of both marrow and PBPCs with breast cancer cells was reduced using this positive selection technique | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Antigens, CD |2 NLM | |
650 | 7 | |a Antigens, CD34 |2 NLM | |
650 | 7 | |a Colony-Stimulating Factors |2 NLM | |
700 | 1 | |a Jones, R B |e verfasserin |4 aut | |
700 | 1 | |a Bearman, S I |e verfasserin |4 aut | |
700 | 1 | |a Franklin, W A |e verfasserin |4 aut | |
700 | 1 | |a Archer, P G |e verfasserin |4 aut | |
700 | 1 | |a Curiel, T |e verfasserin |4 aut | |
700 | 1 | |a Bitter, M |e verfasserin |4 aut | |
700 | 1 | |a Claman, H N |e verfasserin |4 aut | |
700 | 1 | |a Stemmer, S M |e verfasserin |4 aut | |
700 | 1 | |a Purdy, M |e verfasserin |4 aut | |
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