scholarly journals CD34+ cell content of 126 341 cord blood units in the US inventory: implications for transplantation and banking

2019 ◽  
Vol 3 (8) ◽  
pp. 1267-1271 ◽  
Author(s):  
Juliet N. Barker ◽  
Jane Kempenich ◽  
Joanne Kurtzberg ◽  
Claudio G. Brunstein ◽  
Colleen Delaney ◽  
...  

Abstract CD34+ cell dose is critical for cord blood (CB) engraftment. However, the CD34+ content of the CB inventory in the United States is unknown. We examined the CD34+ cell content of 126 341 red blood cell–depleted US units banked from January 2007 to September 2017 with a total nucleated cell (TNC) count of ≥90 × 107 and a cryovolume of 24-55 mL. Median pre-cryopreservation TNC content was 127 × 107 (interquartile range [IQR], 108-156 × 107); CD34+ cell content was 44 × 105 (IQR, 29 to 67 × 105). The median CD34+:TNC ratio was 0.34%. TNC and CD34+ cell content correlation was weak (r = 0.24). Of 7125 units with TNCs of ≥210 × 107, only 47% had CD34+ content of ≥100 × 105. However, some units had high CD34+ content for a given TNC count. Only 4% of CB units were acceptable as single-unit grafts (TNCs, ≥2.5 × 107/kg; CD34+ cells, ≥1.5 × 105/kg) for 70-kg patients; 22% of units were adequate for 70-kg patients using lower dose criteria (TNCs, ≥1.5 × 107/kg; CD34+ cells, ≥1.0 × 105/kg) suitable for a double-unit graft. These findings highlight that units with the highest TNC dose may not have the highest CD34+ dose, units with unexpectedly high CD34+ content (a ratio of >1.0%) should be verified, and the US CB inventory of adequately sized single units for larger patients is small. They also support the ongoing use of double-unit grafts, a focus on banking high-dose units, and development of expansion technologies.

Transfusion ◽  
2017 ◽  
Vol 57 (7) ◽  
pp. 1644-1655 ◽  
Author(s):  
Mark H. Yazer ◽  
Ralph Vassallo ◽  
Meghan Delaney ◽  
Marc Germain ◽  
Matthew S. Karafin ◽  
...  

Transfusion ◽  
2017 ◽  
Vol 58 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Mark H. Yazer ◽  
Waseem Q. Anani ◽  
Gregory A. Denomme ◽  
Matthew S. Karafin ◽  
Merlyn Sayers ◽  
...  

2016 ◽  
Vol 26 (1) ◽  
pp. 45 ◽  
Author(s):  
Paul D. Loprinzi ◽  
Jeremy P. Loenneke ◽  
Haitham M. Ahmed ◽  
Michael J. Blaha

<p><strong>Objective</strong>: Red blood cell distribution width (RDW) has been shown to associate with increased risk of cardiovascular and non-cardiovascular death. To our knowledge, no study has examined secular trends in RDW over the last decade.</p><p><strong>Design</strong>: Serial cross-sectional design. <strong></strong></p><p><strong>Setting</strong>: Data from the National Health and Nutrition Examination Survey (NHANES), 1999-2012, were used.</p><p><strong>Patients</strong>: 34,171 adults. <strong></strong></p><p><strong>Main Outcome Measure</strong>: RDW was assessed from a blood sample derived from the coefficient of variation of the red cell volume distribution histogram and reported as a percent.  Elevated RDW was defined as an RDW &gt; 14.6%.</p><p><strong>Results</strong>: The overall age-adjusted mean RDW increased progressively and significantly (P&lt;.05) from 12.59% in 1999-2000 to 12.89% in 2011-2012. The overall age-adjusted prevalence of elevated RDW increased progressively and significantly (P&lt;.05) from 4.01% in 1999-2000 to 6.25% in 2011-2012. Statistically significant increases over this time period also occurred among non-Hispanic White women, non-Hispanic Black men and women, and Mexican American men and women. Across all sex and race-ethnicity combinations, women, compared with men, had higher RDW and larger increases over time in mean and elevated RDW.  </p><p><strong>Conclusion</strong>: Mean and elevated RDW has progressively increased from 1999-2012 among adults in the United States, with increases observed among non-Hispanic Whites, Blacks, and Mexican Americans. Future research is needed to describe the determinants and implications of this RDW rise, as well as explanations for why a greater RDW change has occurred among women. <em>Ethn Dis. </em>2016;26(1):45-50; doi:10.18865/ed.26.1.45</p>


JAMA ◽  
2018 ◽  
Vol 319 (8) ◽  
pp. 825 ◽  
Author(s):  
Ruchika Goel ◽  
Meera R. Chappidi ◽  
Eshan U. Patel ◽  
Paul M. Ness ◽  
Melissa M. Cushing ◽  
...  

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 1157-1157
Author(s):  
Jens Klaus ◽  
Doris Herrmann ◽  
Ute Hegenbart ◽  
Gerlinde Egerer ◽  
Friedrich W. Cremer ◽  
...  

Abstract Background: The optimum number of CD34+ cells to be reinfused in patients undergoing peripheral blood stem cell (PBSC) transplantation (PBSCT) after high-dose chemotherapy is still unknown. Patients and Methods: Hematologic reconstitution was analyzed with respect to the number of CD34+ cells reinfused in 768 patients with advanced MM or AL-amyloidosis treated by PBSCT between 06/1992 and 06/2004. 539 transplantations were performed upfront and 229 transplantations after relapse. Endpoints of the study were the number of days from PBSCT until neutrophil recovery (&gt;1.0x10e9/L), and platelet recovery (&gt;20x10e9/L and &gt;50x10e9/L). A multivariable analysis was performed using Cox proportional hazards regression to model the dependence of neutrophil and platelet recovery on CD34+ cell dose reinfusion (included as continuous variable), age at PBSCT, number of previous regimens, number of cycles with alkylating agents, response status prior to PBSCT (CR or not), CD34+ enrichment, total body irradiation and previous partial irradiation. Results: The number of CD34+ cells reinfused was the only factor being statistically significant for neutrophil as well as platelet recovery (p&lt;0.001). In view of previously reported cut-offs, three groups were defined (low: &lt;=2.5x10e6; high: &gt;8x10e6 CD34+ cells/kg; and intermediate). In the patients treated by PBSCT up-front, the 100 patients of the high-group experienced a shorter median time until neutrophil recovery (low/intermediate/high CD34+:14/14/12 days), platelet recovery &gt;20x10e9 (low/intermediate/high CD34+: 11/11/9 days), and platelet recovery &gt;50x10e9/L (low/intermediate/high CD34+: 13/13/11 days) compared to patients of the intermediate and low groups. These 100 patients required less platelet and red blood cell transfusions, experienced a shorter hospitalization, had fewer days with antibiotic and antimycotic treatment, and required less partial and total parenteral nutrition. In the patients treated by PBSCT at relapse, the 29 patients of the high-group also experienced a shorter median time until neutrophil (low/intermediate/high CD34+: 13/14/12 days), platelet recovery &gt;20x10e9 (low/intermediate/high CD34+: 12/11/9 days), and platelet recovery &gt;50x10e9/L (low/intermediate/high CD34+: 15/14/11 days) compared to patients of the intermediate and low groups. The advantages for the 29 high group relapse-patients regarding the supportive care after PBSC transplantation were similar to those observed in the 100 upfront-patients: shorter duration of hospitalization, fewer days of antibiotic and antimycotic treatment, fewer days of partial parenteral nutrition and total parenteral nutrition, less platelet and red blood cell transfusions. Conclusion: The number of CD34+ cells reinfused significantly influences time until neutrophil as well as platelet recovery. Comparison of groups suggests that reinfusion of more than 8x10e6 CD34+ cells/kg after high-dose chemotherapy for advanced MM or AL-amlyoidosis shortens hematopoietic reconstitution, reduces platelet and red blood cell transfusions, and reduces days of hospitalization.


2019 ◽  
Vol 54 (11) ◽  
pp. 1836-1846 ◽  
Author(s):  
Takaaki Konuma ◽  
Maki Oiwa-Monna ◽  
Mai Mizusawa ◽  
Masamichi Isobe ◽  
Seiko Kato ◽  
...  

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