Moving Average Of Immature Platelet Fraction Predict Late Platelet Engraftment After Reduced-Intensity Cord Blood Transplantation: A Single-Institutional Study

Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 4583-4583
Author(s):  
Kanichi Iwama ◽  
Jun Aoki ◽  
Noriyuki Tadera ◽  
Daisuke Sinoda ◽  
Kouichi Kaziwara ◽  
...  

Introduction Platelet engraftment is an important marker of successful allogeneic stem cell transplantation and platelet is the last to be regenerated in bone marrow after stem cell transplantation. Especially, platelet engraftment is far slower in reduced-intensity conditioning regimen(RIC) in cord blood transplant(CBT). Early prediction of platelet engraftment in RIC-CBT can be helpful to proper treatment. Recent retrospective studies suggested immature platelet fraction(IPF) can be useful to predict platelet engraftment. However, the role of IPF in RIC-CBT is not be sufficiently investigated. In addition, these studies included patients undergoing bone marrow or peripheral blood transplantation. Therefore, we analyzed cases in our database to evaluate the impact of IPF and Reticulocyte count(RET%) on the outcome of platelet engraftment in consecutive patients who were treated with RIC-CBT over the past 4 years at our institution in Tokyo, Japan. Patients and Methods We included 53 consecutive patients treated at our institution between April 2008 and May 2013. The study population consisted of 29 male and 23 female patients with a median age of 57 years old (range: 36-69). Patient in this cohort underwent RIC-CBT as a part of therapy for myeloid malignancies(N=28) and lymphoid malignancies (N=24). 21 patients were treated with Flu+Cy+TBI(2gy), and 31 patients were treated with Flu+Bu+TBI(2Gy). All patients received calcineurin inhibitor plus MMF for GVHD prophylaxis. Due to the influence of blood transfusion on IPF and RET% and overall estimation of IPF and RET% movement, IPF and RET% were assessed by using the 5-day moving average ,and then we compared movement of the fifth moving average between patients with platelet engraftment and patients without platelet engraftment. The fifth moving average was calculated from the time of day4 after transplantation until the date of platelet engraftment or death from any cause or the date on which the patient was received next chemotherapy. Platelet engraftment was defined as independent from platelet transfusion. Result Among 53 patient, 29 patieunt achieved platelet engraftment. The median time of platelet engraftment was day +42 (range:24-203day), and median time of follow up periods of patients without platelet engraftment was 47 days. 16 patients achieved platelet engraftment after day +40. Baseline characteristics according to patients who achieved platelet engraftment, or did not achieve were similar among RIC-regimen, patient diagnosis. Patients' age, sex, total cell count andCD34 cell count in donor cord blood has no impact on pletelet engraftment. Maximum value of IPF did not have significant impact on platelet engrafment. As shown figure 1, The mean of the 5-day moveing average in IPF show similar curve from day +4 to day +30 between patient with platelet engraftment and without, and after +30 days the curve of patient with platelet engraftment gradually highter than the curve of patient without platelet engraftment. The difference of these curves was larger after day +50. In the RET% case, it was almost same. the 5-day moveing average of IPF and RET% in platelet engraftment patient were raising after day +40, while those in non-engraftment patient were decreasing in this period. Provided the 5-day moving average of IPF are blow 6.0 from day +40 to day +50, It is highly likely that platelet engraftment can't be expected (p=0.001 in univariate analyses). Likewise, provided the 5-day moving average RET% are blow 1.5 from day +40 to day +50, platelet engraftment significantly can't be expected (p=0.002). Conclusion The results of the present study highlighted the importance of the fifth-moving average of IPF and RET% after day +40, and IPF and RET% can be useful tools to predict platelet engraftment in RIC-CBT. Disclosures: No relevant conflicts of interest to declare.

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 4981-4981
Author(s):  
Shinsuke Takagi ◽  
Kazuya Ishiwata ◽  
Masanori Tsuji ◽  
Hisashi Yamamoto ◽  
Daisuke Kato ◽  
...  

Abstract Blood stream infection (BSI) is a major cause of transplant-related mortality (TRM) following allogeneic hematopoietic stem cell transplantation, and to overcome it, reduced-intensity preparative regimens were developed in recent years. However, little information has been reported on BSI after reduced-intensity cord blood transplantation (RI-CBT). To clarify the characteristics of BSI after RI-CBT, we compared the incidence of microbiologically documented BSI before day 100 between RI-CBT and reduced-intensity non-cord blood allogeneic hematopoietic stem cell transplant (RI-non-CBT) recipients in Toranomon hospital, Japan. RI-non-CBT group includes related bone marrow (rBM), related peripheral blood stem cell (rPBSC) and unrelated bone marrow (uBM) transplantation. We retrospectively reviewed the first events of BSI in 211 consecutive adult patients between Jan 2004 and July 2006. One hundred and fifteen patients received RI-CBT and 96 patients received RI-non-CBT (4 from rBM, 34 from rPBSC and 58 from uBM). The median ages of patients in both groups were 55 years. All of the preparative regimens were fludarabine-based and prophylaxis against GVHD was tacrolimus alone in most of the RI-CBT recipients and combination of calcinurin inhibitor and short-term methotrexate in most of the RI-non-CBT recipients. The median time to achieve neutrophil engraftment was delayed in RI-CBT group (day 20 vs. day15). The cumulative incidence of engraftment at day 60 was 73.0% in RI-CBT group versus 90.6% in RI-non-CBT group. The cumulative incidence of BSI was 39.3% at day 100 and RI-CBT group tended to have more BSI compared to RI-non-CBT group (46.1% vs. 31.3%, p=0.0122), particularly at the early points after transplantation. Median day of positive culture for bacteremia was earlier (day 9 vs. day 14) in RI-CBT group. In spite of reduced-intensity preparative regimen, RI-CBT in adults is associated with higher rates of BSI at early time points after transplantation.


Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 1073-1073
Author(s):  
Kazuya Ishiwata ◽  
Naoyuki Uchida ◽  
Hisashi Yamamoto ◽  
Shinsuke Takagi ◽  
Daisuke Kato ◽  
...  

Abstract Background Late-onset hemorrhagic cystitis (HC) is a common viral infections after allogeneic hematopoietic stem cell transplantation (HSCT). Most cases of HC occurring after HSCT are self-limited, but they can cause pain, pollakiuria, and prolonged hospitalization. In cases with progression of HC, ureteral stenosis has occurred and occasionaly resulted in obstructive renal failure. Several risk factors associated with HC after bone marrow transplantation(BMT) and peripheral blood stem cell transplantation(PBSCT) have been reported in several studies. However, most of these risk factors for HC after cord blood transplantation(CBT) have not been observed in detail. Subjects and methods We retrospectively analyzed the clinical records of 461 patients who underwent HSCT at Toranomon Hospital between November 2002 and December 2006. Median age of the patients was 53 years (range 17– 79). Source of HSCT was peripheral blood (PB) in 79 patients (17%), cord blood (CB) in 281 patients (61%), bone marrow (BM) in 101 patients (22%). Underlying diseases were AML(n= 146), ALL(n=61), MDS(n=68), ATL(n=34), CML(n=8), NHL (n=109), other(n=35). The most frequently used conditioning regimens were fludarabine (Flu), alkylating agent (melphalan, busulfan or cyclophosphamide) with total body irradination (TBI).The most frequently used prophylaxis regimens for graft-versus-host disease (GVHD) were calcineurin inhibitor (CI) alone or CI plus methotrexate. HC was defined as the presence of sustained microscopic hematuria for more than 7 days at least 10 days after HSCT in the absence of other conditions such as gynecologic-related bleeding, multiple organ dysfunction, or sepsis. HC was graded according to the following criteria: grade0 = no HC, grade1 = microscopic hematuria, grade2 = macroscopic hematuria, grade3 = macroscopic hematuria with clots, grade4 = macroscopic hematuria requiring instrumentation for clot evacuation or causing urinary retention. BK virus and adenovirus were detected by PCR on urinary samples in all patients who developed HC. Results Overall, 73 patients (16%) developed HC. The median day of presentation was 55 days (range 10 to 505 days). HC cases were graded as follows: grade 1 (8%), grade 2 (64%), grade 3 (24%), grade 4 (4%). The following variables were associated with a higher incidence of HC: CB source vs BM vs PB (14.2% vs 19.8% vs 16.5%, p<0.01). Adenovirus was detected in 27 patients (ADV type11 in 16 patients). BK virus was detected in 42 patients. Both virus was detected in 9 patients. The incidence of HC was significantly associated with grade II to IV acute GVHD in CBT (p<0.01). Conclusion We concluded that there is no significant disparity in the rate of HC among CBT and other HSCT, and immune reconstitution in parallel with BK and adenovirus viruria after CBT stand comparison with other HSCT.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 5346-5346
Author(s):  
Sachiko Seo ◽  
Naoyuki Uchida ◽  
Hisashi Yamamoto ◽  
Naofumi Matsuno ◽  
Yoshiko Matsuhashi ◽  
...  

Abstract Backgrounds: For more than 10 years, umbilical cord blood has become an alternative stem cell source for the patients with hematological malignancies requiring allogeneic stem cell transplantation. Cord blood transplantation (CBT) can be performed more quickly than other stem cell transplantation, since cord blood units are preserved in the deep freeze and 1–3 HLA mismatched donors are acceptable. Considering these advantage, we examined the feasibility of cord blood transplantation using reduced-intensity regimens (RI-CBT) for adult relapsed patients after allogeneic tranplantation. Patients/methods: We reviewed medical records of 26 patients who received RI-CBT at Toranomon Hospital between November 2003 and June 2006. Median age of the patients was 36 years (range, 20–66). Underlying diseases were acute leukemia (n=17), myelodysplastic syndrome (n=4) and lymphoma (n=5). The stem cell source of the first transplantation were bone marrow from sibling donor (n=2), bone marrow from unrelated (n=5) donor, peripheral blood stem cell from sibling donor (n=5) and unrelated cord blood (n=14). Conditioning regimens comprised fludarabine 125–180 mg/m2 in several combination with melphalan 80–140 mg/m2, Busulfan 8–16mg/kg and total body irradiation (TBI) (4–8 Gy). Graft-versus-host disease (GVHD) prophylaxis was cyclosporine (n=5) or tacrolimus (n=21). Median number of total nucleated cells and CD34+ cells was 2.56×106 cells/kg (1.91–5.94), and 0.86×105 cells/kg (0.57–1.77) respectively. HLA disparities were 5/6 (n=2), 4/6 (n=22), and 3/6 (n=2). Results: Median observation period was 58 days (range, 32–380). Overall survival for 1 year was 15% and 16 patients were died of disease progression (n=5) and infection (n=11). The infection in 4 patients was considered to be caused by regimen related toxicity (RRT). No grade IV toxicities (NCI-CTC Ver.3.0) were observed. The duration between two transplantations was longer in surviving patients compared to dead patients (98 days (range, 39–2108) and 262 days (range, 95–901), respectively), although significant difference was not detected. The stage of the disease in the second transplantation, conditioning regimens and HLA disparities did not influence to the outcome. Discussion: We demonstrated that RI-CBT could be an available and feasible treatment for the relapsed patients after stem cell transplantation. Moreover, the RRT is acceptable even in the patients with an advanced disease.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3142-3142
Author(s):  
Jakub Tolar ◽  
Carmem Bonfim ◽  
Satkiran Grewal ◽  
Paul Orchard

Abstract Autosomal recessive osteopetrosis (OP) is a disease characterized by osteoclast dysfunction, leading to multisystem morbidity and death of most affected children. Hematopoietic stem cell transplantation (HSCT) is the treatment of choice for OP, but this patient population is particularly prone to post-transplant complications and death after myeloablative conditioning. To determine the potential of achieving improved overall outcomes in these patients by decreasing pre-transplant mortality, we investigated engraftment and survival following a reduced intensity regimen including busulfan, fludarabine and total lymphoid irradiation. We report outcomes in 11 patients: Age years Graft and HLA match NC dose (x108) CD34 dose (x106) Follow-up (years) Donor chimerism 1 2.1 URD BM 5/6 3 1.4 0.8 (dead) 100% 2 0.6 UCB 4/6 0.9 0.4 2.5 (dead) Transient partial 3 24 REL PBSC 6/6 12.1 9.2 3.25 (alive) 100% 4 1 URD PBSC 6/6 47 29.6 3 (alive) 100% 5 2.5 UCB 6/6 0.7 0.2 0.2 (dead) No donor engraftment 6 0.9 UCB 5/6 0.8 NK 2.25 (dead) No donor engraftment 7 0.6 UCB 5/6 0.9 0.2 4 (alive) No donor engraftment 8 1 URD PBSC 6/6 15
 7.5
 24.4 6
 3
 7 1.9 (alive) Transient partial
 No donor engr.
 78% donor 9 0.5 UCB 5/6, 4/6 3.5 5.3 0.75 (alive) Transient partial 10 4.4 UCB 4/6 1.1 0.7 0.6 (dead) 100% 11 2 URD BM 6/6 5 2.7 5.2 (alive) 100% Legend: NC, nucleated cell; URD, unrelated donor; REL, related donor; BM, bone marrow; UCB, umbilical cord blood; PBSC, peripheral blood stem cells; engr., engraftment; NK, not known; HLA matching is reported for 6 antigens. All six patients who received a bone marrow or peripheral stem cell graft engrafted with > 75% donor chimerism. In contrast, all five recipients of unrelated cord blood as a stem cell source for a first graft failed to demonstrate donor hematopoietic chimerism. The day 100 and 6 month mortality was low at 9%. At 1-year after HSCT, 6 of 11 patients (55%) were surviving. Our data suggests that this regimen results in low peri-transplant mortality without compromising engraftment when a marrow or peripheral stem cell graft is used. An umbilical cord blood graft, however, should be used with caution for patients with OP when this or similar reduced intensity regimen is used.


2020 ◽  
pp. OP.20.00170
Author(s):  
Amandeep Godara ◽  
Nauman S. Siddiqui ◽  
Satish Munigala ◽  
Rishi Dhawan ◽  
Ankit J. Kansagra ◽  
...  

PURPOSE: Patients who undergo allogeneic hematopoietic stem-cell transplantation (allo-HSCT) usually require a prolonged hospital stay that varies greatly across patients. Limited information exists on the factors associated with hospital length of stay (LOS) after allo-HSCT and the impact on transplant-related costs. The objective of this study was to determine predictors for longer LOS for allo-HSCT and to assess their impact on the cost of transplant stay. METHODS: Using the National Inpatient Sample database, adult patients hospitalized for allo-HSCT were identified using International Classification of Diseases, Ninth Revision, primary and secondary procedure codes. RESULTS: Between 2002 and 2015, 68,296 hospitalizations for allo-HSCT were identified. Peripheral blood was the most common stem-cell source (80%) followed by bone marrow (15%) and cord blood (5%). Median LOS was 25.8 days (interquartile range [IQR], 21-34.0 days), and the overall inpatient mortality rate was 8%. Stem-cell source was a significant predictor for longer LOS, being significantly longer for cord blood (median, 36.9 days; IQR, 26.7-49.9 days) compared with bone marrow (median, 27.2 days; IQR, 21.5-35.2 days) and peripheral blood (median 25.4 days; IQR, 20.8-32.7 days). Other predictors for longer LOS were patient characteristics such as age and race, transplant/post-transplant characteristics, and complications such as total body irradiation use, acute graft-versus-host disease, and infections. Longer LOS was also found to be associated with higher hospital costs. CONCLUSION: In patients who undergo allo-HSCT, LOS can be predicted using patient- and transplant-related characteristics as well as post-transplant complications. LOS is also a driver for increased cost, and further efforts are needed to mitigate transplant complications and resource utilization.


2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Fredrick Hogan ◽  
Melhem Solh

Immune mediated demyelinating disease after allogeneic stem cell transplantation is a rare entity with unclear etiology. Acute inflammatory demyelinating polyneuropathy (AIDP) has been reported after related and adult unrelated allogeneic stem cell transplantation but no such case has been reported after unrelated cord blood transplantation. We hereby present the first case of AIDP after double umbilical cord blood transplantation (DUCBT). A 55-year-old man with chronic lymphocytic leukemia (CLL) received a cord blood transplant for relapsed refractory disease with high risk cytogenetics. On day 221, patient presented with skin rash, tingling in both lower extremites, and ascending paralysis that progressed rapidly over the course of 2 days. The workup resulted in a diagnosis of AIDP and administration of intravenous immunoglobulins plus steroids was initiated. Motor and sensory powers were fully recovered and his chronic GVHD was managed for several months with single agent sirolimus.


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