Program: Oral and Poster Abstracts
Session: 615. Acute Myeloid Leukemia: Commercially available Therapy, excluding Transplantation: Poster III
Methods: The patient data was queried from METEOR (Methodist Environment for Translational Enhancement and Outcomes Research), a clinical data warehouse and analytics environment that integrates existing business data warehouse with internal and external research databases and national registries to support clinical research and outcome studies for improving patient care cost-effectively. METEOR data warehouse contains records dating back to January 1, 2006 with over 1 million unique patients and over 4 million unique patient encounters. We queried for the diagnosis of leukemia and those that received at least one course of leukapheresis and also obtained baseline demographics, and overall outcomes.
Results: We reviewed 5585 of whom 42 patients who meet the criteria-patients, 29 of them have diagnosis of AML, 6 with CLL, 4 with ALL, and 3 with CML. The baseline demographics included 29 males and 13 females, whose median age was 52.5; 19 were Caucasians while 10 were African Americans, 5 Hispanic, 5 Asian and 3 reportedly as others.
As shown in Table 1, the population is divided into 3 groups according to WBC before leukapheresis. Group 1 has 7 patients with WBC <100,000, median of 80.460. Group 2 has 17 patients with WBC range from 100,000 to 200,000, median of 150,740. Group 3 has 18 patients with WBC above 200,000, median of 252,200.
In group 1, the average leukostatsis symptom grade is 1.43, average % decrease of WBC is 34.54%, ( blast-84%). In group 2, the average leukostatsis symptom grade is 1.88, average % decrease of WBC is 48.25%, ( blast- 69%). In group 3, the average leukostatsis symptom grade is 1.06, average % decrease of WBC is 42.81%, (blast-59.5%).
In terms of complications, in group 1, 42.86% presented with acute kidney injury (AKI), 28.57% with tumor lysis syndrome, 28.57% with disseminated intravascular coagulation (DIC), 28.57% with sepsis, 14.29% with pneumonia, 42.86% with respiratory failure, 14.29% and with acute coronary syndrome (ACS). In group 2, 17.65% presented with AKI, 47.06% with TLS, 47.06 % with DIC, 23.53% with sepsis, 11.76% with pneumonia, 41.18% with respiratory failure, and 5.88% with acute coronary syndrome. In group 3 11.10 % presented with acute kidney injury, 44.44% with TLS, 38.89 % with DIC, 22.22% with sepsis, 11.11% with pneumonia, 27.78 % with respiratory failure, and 5.56 % with ACS. The 4 weeks mortality rate are 42.86% for group 1, 29.41% for group 2, and 22.22% for group 3.
Conclusions: We have validated the Hyperleukocytosis grading schema and usefulness of leukapheresis. Our data indicates comparable mortality in pts with WBC between 100 -200,000 and > 200,000. Further statistical review of this data set will be presented at the ASH Meeting, Orlando 2015
Table 1
|
Group 1 |
Group 2 |
Group 3 |
WBC range |
<100,000 |
100,000 to 200,000 |
>200,000 |
Number of patients |
7 |
17 |
18 |
Average leukostasis symptom grade |
1.43 |
1.88 |
1.06 |
% Lymphoid leukemia |
14.29% |
17.65% |
33.33% |
Median WBC before leukapheresis |
80,460 |
150,740 |
252,200 |
Average % decrease of WBC |
34.54% |
48.25% |
42.81% |
Median % of blast before leukapheresis |
84% |
69% |
59.5% |
Average % change in %blast |
5.35% |
11.23% |
-6.55% |
Average Creatinine after Leukapheresis |
2.39 |
1.47 |
1.38 |
Average uric acid after leukapheresis |
8.77 |
6.52 |
6.75 |
Average Fibrinogen after leukapheresis |
424.25 |
336.78 |
300.56 |
% Acute kidney injury |
42.86% |
17.65% |
11.10% |
% Tumor lysis syndrome |
28.57% |
47.06% |
44.44% |
% DIC |
28.57% |
47.06% |
38.89% |
% Sepsis |
28.57% |
23.53% |
22.22% |
% Pneumonia |
14.29% |
11.76% |
11.11% |
% Respiratory failure |
42.86% |
41.18% |
27.78% |
% Acute Coronary Syndrome |
14.29% |
5.88% |
5.56% |
% 4 weeks Mortality |
42.86% |
29.41% |
22.22% |
References:
1. Novotny JR, Müller-Beissenhirtz H, Herget-Rosenthal S, Kribben A, Dührsen U. Grading of symptoms in hyperleukocytic leukaemia: a clinical model for the role of different blast types and promyelocytes in the development of leukostatsis syndrome. Eur J Haematol 2005:74:501-510
Disclosures: No relevant conflicts of interest to declare.
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