scholarly journals Preventive Versus Curative Platelet Transfusion Strategies in the Treatment of Acute Myeloid Leukemia Patients: A Comparative Study

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 4288-4288 ◽  
Author(s):  
Aude Charbonnier ◽  
Michel Raba ◽  
Patrick Ladaique ◽  
Laurence Augey ◽  
Lilian Laborde ◽  
...  

Abstract Different transfusion care strategies are considered for the treatment of acute thrombopenia due to low or absence of production of platelets in Acute Myeloid Leukemia (AML) patients with controversies about both threshold of platelets to consider prior to transfusion and the quality of the product to transfuse. In addition, despite two recent studies (Wandt et al, Lancet. 2012 Oct 13;380:1309; Stanworth and al. N Engl J Med. 2013 May 9;368:1771), the choice between preventive (based upon the number of platelets) and curative (based on clinical symptoms) care, as discussed in 2004 by Slichter and al. (Transfus Med Rev. 2004 Jul;18(3):153), still remains a concern although preventive care is commonly used. In this study, we compared the treatment of AML patients at the Institut Paoli-Calmettes (Marseille, France, that elicited curative transfusion care strategy) herein called IPC, and Centre Hospitalier Lyon Sud (Pierre Benite, France, that elicited preventive transfusion care strategy) herein called CHLS, between January 2001 and December 2010, considering the use of transfusion product during induction, and death due to hemorrhage. At the time of study, the curative transfusion care strategy at the IPC relied on the analysis of three complete blood counts a week, clinical examination of the patients (Pt) at least twice a day, and platelet transfusion in case of mucosal hemorrhage syndrome, headaches, fever, and high blood pressure. At the CHLS, the preventive transfusion care strategy relied on blood count, daily clinical examination of the Pt, and platelet transfusion when platelet number was found below 20 G/L. Both IPC and CHLS used Platelet Concentrate (PC) obtained from apheresis from single donor (CPA) or multiple donors (MCPS) and a threshold of 80 g/l Hb was considered for red blood cell transfusion. AML patients were treated by cytarabine combined with anthracycline (induction regimen), with subtle differences between CHLS and IPC and according to recommendation at the time of treatment. Our analysis covered a 45 day induction time, and the 6 first months (185 days) of treatment. Between January 2001 and December 2010, 884 patients (median age 59 with 80% < 70) and 524 patients (median age 52 with 94% <70) were treated at the IPC and at the CHLS, respectively. 74% vs 82% of the patients underwent complete remission (CR) following one or two induction regimens, and 39% vs 40% are still alive. During induction, patients at the IPC and the CHLS received 5,1 ± 3,9 (mean ± Standard Deviation) and 10,2 ± 7 PC, with 4,4 and 9,8 CPA and 1,3 and 1,3 MCPS, respectively. During this period, the number of packed red blood cell unit used was 5.7 ± 4,6 and 10.6 ± 5,8, respectively, and 21 Pts deceased from hemorrhage at the IPC versus 2 at the CHLS, with 9 Pts refractory to platelet transfusion versus 1. When not considering Pts refractory to transfusion and Pts with disseminated intravascular coagulation (DIC), 7 Pts died at the IPC (at a median of 12 days after diagnosis) versus 1 patient at the CHLS at day 16 after diagnosis. Of note, ≥ grade 3 sepsis supported in intensive care unit was observed in 5 over 7 patients at the IPC. This retrospective study confirms the results suggested in the TOPPS and German studies that have compared preventive and curative platelet transfusion strategies for leukemia patients. Two fold less platelet products are used in a curative strategy, but more patients deceased from hemorrhage, most of them earlier during the treatment and with high grade sepsis. Unexpectedly, two fold more packed red blood cell units are used in the preventive strategy. This study also suggests that increase of the number of platelet concentrate infused without regard to ABO typing could decrease the therapeutical impact of red blood cell transfusion. At the IPC, high number of patients deceased from hemorrhage in context of DIC or refractoriness to transfusion may be relied to the platelet and plasma transfusion strategy elicited in these particular situations. Altogether, these results suggest that risk factors like sepsis, have to be considered to elicit a preventive versus curative platelet transfusion strategy in the treatment of AML Patient. Six months results and further statistical analyses are in progress and will be presented. Disclosures Prebet: Celgene Corporation: Honoraria. Vey:BMS: Honoraria.

Blood ◽  
1998 ◽  
Vol 91 (10) ◽  
pp. 3601-3606 ◽  
Author(s):  
Hannes Wandt ◽  
Markus Frank ◽  
Gerhard Ehninger ◽  
Christiane Schneider ◽  
Norbert Brack ◽  
...  

Abstract In 105 consecutive patients with de novo acute myeloid leukemia (French-American-British M3 excluded), we compared prospectively the risk of bleeding complications, the number of platelet and red blood cell transfusions administered, and the costs of transfusions using two different prophylactic platelet transfusion protocols. Two hundred sixteen cycles of induction or consolidation chemotherapy and 3,843 days of thrombocytopenia less than 25 × 109/L were evaluated. At the start of the study, each of the 17 participating centers decided whether they would use a 10 × 109/L prophylactic platelet transfusion trigger (group A/8 centers) or a 20 × 109/L trigger (group B/9 centers). Bleeding complications (World Health Organization grade 2-4) during treatment cycles were comparable in the two groups: 20 of 110 (18%) in group A and 18 of 106 (17%) in group B (P = .8). Serious bleeding events (grade 3-4) were generally not related to the patient's platelet count but were the consequence of local lesions and plasma coagulation factor deficiencies due to sepsis. Eighty-six percent of the serious bleeding episodes occurred during induction chemotherapy. No patient died of a bleeding complication. There were no significant differences in the number of red blood cell transfusions administered between the two groups, but there were significant differences in the number of platelet transfusions administered per treatment cycle: pooled random donor platelet concentrates averaged 15.4 versus 25.4 (P < .01) and apheresis platelets averaged 3.0 versus 4.8 (P < .05) for group A versus group B, respectively. This resulted in the cost of platelet therapy being one third lower in group A compared with group B without any associated increase in bleeding risk.


Blood ◽  
1998 ◽  
Vol 91 (10) ◽  
pp. 3601-3606 ◽  
Author(s):  
Hannes Wandt ◽  
Markus Frank ◽  
Gerhard Ehninger ◽  
Christiane Schneider ◽  
Norbert Brack ◽  
...  

In 105 consecutive patients with de novo acute myeloid leukemia (French-American-British M3 excluded), we compared prospectively the risk of bleeding complications, the number of platelet and red blood cell transfusions administered, and the costs of transfusions using two different prophylactic platelet transfusion protocols. Two hundred sixteen cycles of induction or consolidation chemotherapy and 3,843 days of thrombocytopenia less than 25 × 109/L were evaluated. At the start of the study, each of the 17 participating centers decided whether they would use a 10 × 109/L prophylactic platelet transfusion trigger (group A/8 centers) or a 20 × 109/L trigger (group B/9 centers). Bleeding complications (World Health Organization grade 2-4) during treatment cycles were comparable in the two groups: 20 of 110 (18%) in group A and 18 of 106 (17%) in group B (P = .8). Serious bleeding events (grade 3-4) were generally not related to the patient's platelet count but were the consequence of local lesions and plasma coagulation factor deficiencies due to sepsis. Eighty-six percent of the serious bleeding episodes occurred during induction chemotherapy. No patient died of a bleeding complication. There were no significant differences in the number of red blood cell transfusions administered between the two groups, but there were significant differences in the number of platelet transfusions administered per treatment cycle: pooled random donor platelet concentrates averaged 15.4 versus 25.4 (P < .01) and apheresis platelets averaged 3.0 versus 4.8 (P < .05) for group A versus group B, respectively. This resulted in the cost of platelet therapy being one third lower in group A compared with group B without any associated increase in bleeding risk.


2013 ◽  
Vol 20 (4) ◽  
pp. 392-402 ◽  
Author(s):  
Vaidehi Agrawal ◽  
Jung Hee Woo ◽  
Gautham Borthakur ◽  
Hagop Kantarjian ◽  
Arthur E. Frankel

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 3686-3686 ◽  
Author(s):  
Kerstin Schaefer-Eckart ◽  
Knut Wendelin ◽  
Bettina Pilz ◽  
Michael Kramer ◽  
Gerhard Ehninger ◽  
...  

Abstract Background: Between 2005 und 2010 we conducted a multicenter randomized study comparing a therapeutic and a prophylactic (morning platelet (ptl) trigger < 10/nl) platelet transfusion strategy in patients with hematological disorders. (The Lancet Vol 380, No 9850, pp 1309-16). Briefly, we could show that a therapeutic plt transfusion strategy, where platelets are transfused in clinical stable patients (pts) only if bleeding ≥ WHO grade II occurs is safe in patients after autologous transplantation. In patients with acute myeloid leukemia (AML) we observed significantly more severe bleedings (WHO IV°) with the therapeutic regimen. To proof, if there is a difference in bleeding risk related to the remission status of the patients, we conducted a post-hoc analysis to compare the risk of severe bleeding (WHO III° and IV°) in induction with consolidation therapy. Patients and Methods: We analyzed 175 pts with 175 cycles of induction therapy, 90 with a prophylactic transfusion regimen and 85 cycles with a therapeutic regimen. 131 pts received 268 cycles of consolidation therapy, 155 with a prophylactic and 113 with a therapeutic transfusion strategy. Results: Bleedings WHO III° were neither different between the two strategies nor between induction and consolidation therapy. In contrast, there were significantly more bleedings WHO IV° in induction (7,4%) compared to consolidation therapy (1,5%; p=0,01). In addition, there were significantly more bleedings WHO IV° with the therapeutic regimen (11,8%) compared to the prophylactic strategy (3,3%) in induction therapy (p=0,012). This difference was less pronounced in consolidation therapy. But even in the prophylactic arm most WHO IV° bleedings occurred in pts with more than 10/nl ptl, which shows, that the morning platelet count should not be the only trigger for a platelet transfusion. Conclusions: In consolidation therapy the risk of bleeding is significantly less compared to induction therapy, even with a therapeutic platelet transfusion strategy. During induction therapy the prophylactic strategy should remain the standard of care. The therapeutic transfusion strategy in consolidation therapy will be proven prospectively in an ongoing multicenter study. Disclosures No relevant conflicts of interest to declare.


2013 ◽  
Vol 20 (4) ◽  
pp. 392-402 ◽  
Author(s):  
Vaidehi Agrawal ◽  
Jung Hee Woo ◽  
Gautham Borthakur ◽  
Hagop Kantarjian ◽  
Arthur E. Frankel

2021 ◽  
Vol 10 (7) ◽  
pp. 1349
Author(s):  
Kamila Czubak-Prowizor ◽  
Jacek Trelinski ◽  
Paulina Stelmach ◽  
Piotr Stelmach ◽  
Agnieszka Madon ◽  
...  

Chronic oxidative stress (OS) can be an important factor of acute myeloid leukemia (AML) progression; however, there are no data on the extent/consequence of OS after transfusion of packed red blood cells (pRBCs) and platelet concentrates (PCs), which are commonly used in the treatment of leukemia-associated anemia and thrombocytopenia. We aimed to investigate the effects of pRBC/PC transfusion on the OS markers, i.e., thiol and carbonyl (CO) groups, 3-nitrotyrosine (3-NT), thiobarbituric acid reactive substances (TBARS), advanced glycation end products (AGE), total antioxidant capacity (TAC), SOD, GST, and LDH, in the blood plasma of AML patients, before and 24 h post-transfusion. In this exploratory study, 52 patients were examined, of which 27 were transfused with pRBCs and 25 with PCs. Age-matched healthy subjects were also enrolled as controls. Our results showed the oxidation of thiols, increased 3-NT, AGE levels, and decreased TAC in AML groups versus controls. After pRBC transfusion, CO groups, AGE, and 3-NT significantly increased (by approximately 30, 23, and 35%; p < 0.05, p < 0.05, and p < 0.01, respectively) while thiols reduced (by 18%; p < 0.05). The PC transfusion resulted in the raise of TBARS and AGE (by 45%; p < 0.01 and 31%; p < 0.001), respectively). Other variables showed no significant post-transfusion changes. In conclusion, transfusion of both pRBCs and PCs was associated with an increased OS; however, transfusing the former may have more severe consequences, since it is associated with the irreversible oxidative/nitrative modifications of plasma proteins.


Haematologica ◽  
2011 ◽  
Vol 96 (9) ◽  
pp. 1310-1317 ◽  
Author(s):  
H. J. M. de Jonge ◽  
P. J. M. Valk ◽  
E. S. J. M. de Bont ◽  
J. J. Schuringa ◽  
G. Ossenkoppele ◽  
...  

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