CD34(+)-selected stem cell boost for delayed or insufficient engraftment after allogeneic stem cell transplantation.

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CD34(+)-selected stem cell boost for delayed or insufficient engraftment after allogeneic stem cell transplantation. / Oyekunle, Aa; Koehl, U; Schieder, H; Ayuketang Ayuk, Francis; Renges, H; Fehse, N; Zabelina, Tatjana; Fehse, Boris; Klingebiel, T; Sputtek, Andreas; Zander, Axel R.; Kröger, Nicolaus.

In: CYTOTHERAPY, Vol. 8, No. 4, 4, 2006, p. 375-380.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Oyekunle, A, Koehl, U, Schieder, H, Ayuketang Ayuk, F, Renges, H, Fehse, N, Zabelina, T, Fehse, B, Klingebiel, T, Sputtek, A, Zander, AR & Kröger, N 2006, 'CD34(+)-selected stem cell boost for delayed or insufficient engraftment after allogeneic stem cell transplantation.', CYTOTHERAPY, vol. 8, no. 4, 4, pp. 375-380. <http://www.ncbi.nlm.nih.gov/pubmed/16923613?dopt=Citation>

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Bibtex

@article{229e50c3005b4561b86051a059fdc50f,
title = "CD34(+)-selected stem cell boost for delayed or insufficient engraftment after allogeneic stem cell transplantation.",
abstract = "BACKGROUND: Poor graft function without rejection may occur after stem cell transplantation (SCT). CD34(+) stem cell boost (SCB) can restore marrow function but may induce or exacerbate GvHD. We therefore investigated the feasibility and efficacy of CD34(+)-selected SCB in some patients with poor graft function. We present the results for eight patients (median age 46 years) transplanted initially for myelofibrosis, acute leukemia, myeloma and NHL. Six patients had received HLA-matched and two mismatched grafts (PB, BM; n=5, 3). After a median of 128 days post-transplant, the median leukocyte and platelet counts were, respectively, 2.05/nL and 18/nL. None had achieved platelet counts >50/nL even though donor chimerism was >95% in seven recipients. METHODS: Positive selection of CD34(+) stem cells was performed on a CliniMACS device, observing GMP and achieving a median of 98.5% purity. The patients received a median of 1.7 x 10(6)/kg CD34(+) cells and 2.5 x 10(3)/kg CD3(+) T lymphocytes. RESULTS: Hemograms at days +30, +60 and +90, respectively, showed steadily increasing median leukocyte (2.55, 3.15 and 4.20/nL) and platelet (29, 39 and 95/nL) counts. After a median follow-up of 144 days, five patients remained alive. No patient had developed acute or chronic GvHD. One patient died of leukemic relapse and two others of systemic mycosis. DISCUSSION: These preliminary results point to the possibility of safely improving graft function using CD34(+) positively selected stem cells without necessarily increasing the incidence of GvHD in patients with poor graft function post-SCT. Experience with more patients and longer follow-up should clarify the optimal role for this procedure.",
author = "Aa Oyekunle and U Koehl and H Schieder and {Ayuketang Ayuk}, Francis and H Renges and N Fehse and Tatjana Zabelina and Boris Fehse and T Klingebiel and Andreas Sputtek and Zander, {Axel R.} and Nicolaus Kr{\"o}ger",
year = "2006",
language = "Deutsch",
volume = "8",
pages = "375--380",
journal = "CYTOTHERAPY",
issn = "1465-3249",
publisher = "informa healthcare",
number = "4",

}

RIS

TY - JOUR

T1 - CD34(+)-selected stem cell boost for delayed or insufficient engraftment after allogeneic stem cell transplantation.

AU - Oyekunle, Aa

AU - Koehl, U

AU - Schieder, H

AU - Ayuketang Ayuk, Francis

AU - Renges, H

AU - Fehse, N

AU - Zabelina, Tatjana

AU - Fehse, Boris

AU - Klingebiel, T

AU - Sputtek, Andreas

AU - Zander, Axel R.

AU - Kröger, Nicolaus

PY - 2006

Y1 - 2006

N2 - BACKGROUND: Poor graft function without rejection may occur after stem cell transplantation (SCT). CD34(+) stem cell boost (SCB) can restore marrow function but may induce or exacerbate GvHD. We therefore investigated the feasibility and efficacy of CD34(+)-selected SCB in some patients with poor graft function. We present the results for eight patients (median age 46 years) transplanted initially for myelofibrosis, acute leukemia, myeloma and NHL. Six patients had received HLA-matched and two mismatched grafts (PB, BM; n=5, 3). After a median of 128 days post-transplant, the median leukocyte and platelet counts were, respectively, 2.05/nL and 18/nL. None had achieved platelet counts >50/nL even though donor chimerism was >95% in seven recipients. METHODS: Positive selection of CD34(+) stem cells was performed on a CliniMACS device, observing GMP and achieving a median of 98.5% purity. The patients received a median of 1.7 x 10(6)/kg CD34(+) cells and 2.5 x 10(3)/kg CD3(+) T lymphocytes. RESULTS: Hemograms at days +30, +60 and +90, respectively, showed steadily increasing median leukocyte (2.55, 3.15 and 4.20/nL) and platelet (29, 39 and 95/nL) counts. After a median follow-up of 144 days, five patients remained alive. No patient had developed acute or chronic GvHD. One patient died of leukemic relapse and two others of systemic mycosis. DISCUSSION: These preliminary results point to the possibility of safely improving graft function using CD34(+) positively selected stem cells without necessarily increasing the incidence of GvHD in patients with poor graft function post-SCT. Experience with more patients and longer follow-up should clarify the optimal role for this procedure.

AB - BACKGROUND: Poor graft function without rejection may occur after stem cell transplantation (SCT). CD34(+) stem cell boost (SCB) can restore marrow function but may induce or exacerbate GvHD. We therefore investigated the feasibility and efficacy of CD34(+)-selected SCB in some patients with poor graft function. We present the results for eight patients (median age 46 years) transplanted initially for myelofibrosis, acute leukemia, myeloma and NHL. Six patients had received HLA-matched and two mismatched grafts (PB, BM; n=5, 3). After a median of 128 days post-transplant, the median leukocyte and platelet counts were, respectively, 2.05/nL and 18/nL. None had achieved platelet counts >50/nL even though donor chimerism was >95% in seven recipients. METHODS: Positive selection of CD34(+) stem cells was performed on a CliniMACS device, observing GMP and achieving a median of 98.5% purity. The patients received a median of 1.7 x 10(6)/kg CD34(+) cells and 2.5 x 10(3)/kg CD3(+) T lymphocytes. RESULTS: Hemograms at days +30, +60 and +90, respectively, showed steadily increasing median leukocyte (2.55, 3.15 and 4.20/nL) and platelet (29, 39 and 95/nL) counts. After a median follow-up of 144 days, five patients remained alive. No patient had developed acute or chronic GvHD. One patient died of leukemic relapse and two others of systemic mycosis. DISCUSSION: These preliminary results point to the possibility of safely improving graft function using CD34(+) positively selected stem cells without necessarily increasing the incidence of GvHD in patients with poor graft function post-SCT. Experience with more patients and longer follow-up should clarify the optimal role for this procedure.

M3 - SCORING: Zeitschriftenaufsatz

VL - 8

SP - 375

EP - 380

JO - CYTOTHERAPY

JF - CYTOTHERAPY

SN - 1465-3249

IS - 4

M1 - 4

ER -