2009
DOI: 10.1016/j.transci.2009.01.015
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Peripheral blood progenitor cell collection without close monitoring of peripheral blood CD34+ cells: A feasible strategy for multiple myeloma or pre-treated Non-Hodgkin’s Lymphoma patients mobilized with low-dose cyclophosphamide plus G-CSF

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Cited by 10 publications
(5 citation statements)
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“…Despite absolute circulating CD34+ cell count being the gold standard for predicting a successful PBSC collection, the cost of CD34+ determination is still a significant concern for many patients and/or institutions. Some studies attempted to create protocols for initiating an effective PBSC collection on a fixed day [30]. Our study demonstrated that some conventional, less costly and easily obtained parameters were reliable predictors for a successful PBSC harvest.…”
Section: Discussionmentioning
confidence: 63%
“…Despite absolute circulating CD34+ cell count being the gold standard for predicting a successful PBSC collection, the cost of CD34+ determination is still a significant concern for many patients and/or institutions. Some studies attempted to create protocols for initiating an effective PBSC collection on a fixed day [30]. Our study demonstrated that some conventional, less costly and easily obtained parameters were reliable predictors for a successful PBSC harvest.…”
Section: Discussionmentioning
confidence: 63%
“…Further, peripheral blood CD341 cell enumeration does not account for variables such as patient weight, blood volume processed, and collection efficiency, which also affect the number of CD341 cells collected [23]. Some institutions may only have limited access to flow cytometry facilities and daily peripheral CD341 monitoring may be costly [25]. For these reasons, as well as practical issues of timely performance of this test, many transplant institutions do not use preapheresis blood CD341 cell count to determine when to start collection.…”
Section: Discussionmentioning
confidence: 99%
“…In multiple myeloma, patients with poor collections immediately received CY pulsing to enhance yield. 39,45 These patients generally were in first partial response with only 4 months of prior induction therapy. In the lymphoma cohort, collection attempts began after proof of chemosensitive disease after relapse by using either rituximab with ifosfamide, carboplatin, and etoposide or rituximab with dexamethasone, cytarabine, and cisplatin.…”
Section: Discussionmentioning
confidence: 99%