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1138 North American Cooperative Group Members' Patterns of Blood Products Transfusion for Patients with Acute Leukemia

Basic Science and Clinical Practice in Blood Transfusion
Program: Oral and Poster Abstracts
Session: 401. Basic Science and Clinical Practice in Blood Transfusion: Poster I
Saturday, December 5, 2015, 5:30 PM-7:30 PM
Hall A, Level 2 (Orange County Convention Center)

Alexander B Pine, MD PhD1*, Eun-Ju Lee, MD2, Mikkael A. Sekeres, MD, MS3,4, David P. Steensma, MD5, Thomas Prebet, MD6, Amy E. DeZern, MD, MHS7, Rami S. Komrokji, MD8, Mark R Litzow, MD9, Selina Luger, MD10, Richard M. Stone, MD11, Harry P. Erba, MD, PhD12, Guillermo Garcia-Manero, MD13, Alfred I Lee, MD, PhD6*, Nikolai A. Podoltsev, MD, PhD6, Lisa Barbarotta, APRN-BC6*, Jeanne E. Hendrickson, MD14, Steven D. Gore, MD15 and Amer M. Zeidan, MBBS, MHS15

1Yale New Haven Hospital, New Haven, CT
2Hematology, Yale University School of Medicine, New Haven, CT
3Leukemia Program, Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH
4Leukemia Program, Cleveland Clinic, Cleveland, OH
5Dana-Farber Cancer Institute, Boston, MA
6Dept of Internal Medicine, Section of Hematology, Yale University School of Medicine, New Haven, CT
7The Johns Hopkins School of Medicine, Baltimore, MD
8H. Lee Moffitt Cancer Center, Tampa, FL
9Division of Hematology, Mayo Clinic, Rochester, MN
10Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA
11Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA
12Internal Medicine, Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL
13Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
14Laboratory Medicine, Yale University School of Medicine, New Haven, CT
15Yale University School of Medicine, New Haven, CT

Background. Transfusion of blood products is an integral component of the management of patients with acute leukemias. However, high-quality evidence and clinical trial data to support specific practices of blood product transfusion in this population are limited. We hypothesized that there is wide variation in blood product transfusion practices among providers in North America who manage patients with acute leukemia.

Methods. A 30-question web-based survey about transfusion practices was emailed to members of the Eastern Cooperative Oncology Group (ECOG)-ACRIN Cancer Research Group, Alliance for Clinical Trials in Oncology (Alliance), and the Southwest Oncology Group (SWOG), and the Cancer Trials Support Unit (CTSU) on 7/6/2015 with 4 subsequent weekly reminders. The distribution list included 9,859 recipients, of whom at least 741 were providers who treated patients with acute leukemia. Responses were anonymous, and the survey distribution was approved by the respective cooperative group chairs. Descriptive statistics were used to analyze the data.

Results. Of 254 responses received, 113 were excluded as they were returned by recipients not directly treating patients with acute leukemia. Another 30 responses were excluded due to incomplete data, leaving 111 responses (43.7%) eligible for the primary analysis. Of those, 109 responders were from North America representing 83 institutions in 33 states and the province of Ontario. Eighty-four of the included responders (75.7%) were physicians, and 44 (39.6%) were females. Median age of responders was 44 years (range, 26-76). A hemoglobin (Hb) level of ≤7 g/dL was the most commonly used threshold (44%) for red blood cell (RBCs) transfusions to asymptomatic stable hospitalized patients, followed closely by 8 g/dL (38%) (Figure 1). In the outpatient setting, the most commonly reported threshold was 8 gm/dL (49%) (Figure 1). Most providers reported that they “always” use leukocyte-reduced (93%) and irradiated (79%) RBCs. A platelet level of 10,000/µL was the threshold for platelet transfusions in the stable non-bleeding hospitalized patients cited by the majority of responders (76%) (Figure 2). This platelet level remained the most common threshold for platelet transfusions for non-bleeding patients in the outpatient setting (49%), although 31% of responders reported a higher threshold of 20,000/µL. A preference for single-donor apheresis platelets was reported by 81% respondents, and 57% use these products exclusively. Most providers (70%) reported always using irradiated platelets. With respect to cryoprecipitate and plasma infusions, nearly half of the respondents reported a threshold fibrinogen level of 100 mg/dL as a trigger for administering a product to a stable non-bleeding patient (Figure 3). The most commonly reported platelet threshold for performing a bone marrow biopsy (BMB) was 10,000/μL (69% of responders), followed by 20,000 (21%), 50,000 (6%), and 30,000 (4%). Therapeutic anticoagulation was held by most responders (80%) before performing a BMB. Most responders (73%) reported a platelet level of 50,000/µL as the lowest level for performing a lumbar puncture (LP) without prophylactic platelet transfusion.

Conclusions. This survey demonstrates wide variability in blood product transfusion patterns among providers who treat patients with acute leukemias. A platelet level of 10,000/µL is the most common trigger for platelet transfusions for stable non-bleeding patients in both inpatient and outpatient settings. This, along with a platelet threshold of 50,000/µL for performing an LP, appear to be most widely accepted practices. Our findings emphasize the need to obtain high-quality data to develop consensus evidence-based guidelines for transfusion practices in acute leukemia with the goal of limiting unnecessary transfusions without compromising patient outcomes.

Figure 1.  The most common reported hemoglobin level thresholds for red blood cell transfusions in the inpatient and outpatient settings.

Figure 2. The most common reported platelet level thresholds for platelet transfusions in the inpatient and outpatient settings.

Figure 3. The most common reported fibrinogen level thresholds for cryoprecipitate or plasma transfusions in the inpatient and outpatient settings.

 

Disclosures: Sekeres: Celgene Corporation: Membership on an entity’s Board of Directors or advisory committees ; TetraLogic: Membership on an entity’s Board of Directors or advisory committees ; Amgen: Membership on an entity’s Board of Directors or advisory committees . Steensma: Onconova: Consultancy ; Incyte: Consultancy ; Amgen: Consultancy ; Celgene: Consultancy . Prebet: CELGENE: Research Funding . Komrokji: Celgene: Consultancy , Research Funding ; Incite: Consultancy ; Novartis: Speakers Bureau ; GSK: Research Funding . Stone: Merck: Consultancy ; AROG: Consultancy ; Celgene: Consultancy ; Sunesis: Consultancy , Other: DSMB for clinical trial ; Abbvie: Consultancy ; Novartis: Research Funding ; Juno: Consultancy ; Amgen: Consultancy ; Roche/Genetech: Consultancy ; Celator: Consultancy ; Agios: Consultancy ; Karyopharm: Consultancy ; Pfizer: Consultancy . Erba: Astellas: Research Funding ; Amgen: Consultancy , Research Funding ; Pfizer: Consultancy ; Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited: Research Funding ; Celator: Research Funding ; Janssen: Consultancy ; Sunesis: Consultancy ; Novartis: Consultancy , Speakers Bureau ; Celgene: Consultancy , Speakers Bureau ; Incyte: Consultancy , Speakers Bureau ; Seattle Genetics: Consultancy , Research Funding ; Daiichi Sankyo: Consultancy ; Ariad: Consultancy ; Agios: Research Funding . Barbarotta: Celgene, BMS, Novartis: Speakers Bureau . Gore: Celgene: Consultancy , Honoraria , Research Funding .

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*signifies non-member of ASH