patient assignment
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2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Alice S. Mims ◽  
Jessica Kohlschmidt ◽  
Uma Borate ◽  
James S. Blachly ◽  
Shelley Orwick ◽  
...  

Abstract Background Older patients (≥ 60 years) with acute myeloid leukemia (AML) often have multiple, sequentially acquired, somatic mutations that drive leukemogenesis and are associated with poor outcome. Beat AML is a Leukemia and Lymphoma Society-sponsored, multicenter umbrella study that algorithmically segregates AML patients based upon cytogenetic and dominant molecular abnormalities (variant allele frequencies (VAF) ≥ 0.2) into different cohorts to select for targeted therapies. During the conception of the Beat AML design, a historical dataset was needed to help in the design of the genomic algorithm for patient assignment and serve as the basis for the statistical design of individual genomic treatment substudies for the Beat AML study. Methods We classified 563 newly diagnosed older AML patients treated with standard intensive chemotherapy on trials conducted by Cancer and Leukemia Group B based on the same genomic algorithm and assessed clinical outcomes. Results Our classification identified core-binding factor and NPM1-mutated/FLT3-ITD-negative groups as having the best outcomes, with 30-day early death (ED) rates of 0 and 20%, respectively, and median overall survival (OS) of > 1 year and 3-year OS rates of ≥ 20%. All other genomic groups had ED rates of 17–42%, median OS ≤ 1 year and 3-year OS rates of ≤ 15%. Conclusions By classifying patients through this genomic algorithm, outcomes were poor and not unexpected from a non-algorithmic, non-dominant VAF approach. The exception is 30-day ED rate typically is not available for intensive induction for individual genomic groups and therefore difficult to compare outcomes with targeted therapeutics. This Alliance data supported the use of this algorithm for patient assignment at the initiation of the Beat AML study. This outcome data was also used for statistical design for Beat AML substudies for individual genomic groups to determine goals for improvement from intensive induction and hopefully lead to more rapid approval of new therapies. Trial registration ClinicalTrials.gov Identifiers: NCT00048958 (CALGB 8461), NCT00900224 (CALGB 20202), NCT00003190 (CALGB 9720), NCT00085124 (CALGB 10201), NCT00742625 (CALGB 10502), NCT01420926 (CALGB 11002), NCT00039377 (CALGB 10801), and NCT01253070 (CALGB 11001).


Author(s):  
Lorenzo Barberis Canonico ◽  
Nathan J. McNeese ◽  
Marissa L. Shuffler

Hospitals are plagued with a multitude of logistical challenges amplified by a time-sensitive and high intensity environment. These conditions have resulted in burnout among both doctors and nurses as they work tirelessly to provide critical care to patients in need. We propose a new machine-learning-powered matching mechanism that manages the surgeon-nurse-patient assignment process in an efficient way that saves time and energy for hospitals, enabling them to focus almost entirely on delivering effective care. Through this design, we show how incorporating artificial intelligence into management systems enables teams of all sizes to meaningfully coordinate in highly chaotic and complex environments.


2018 ◽  
Vol 36 (8) ◽  
pp. 1367-1371 ◽  
Author(s):  
Stephen J. Traub ◽  
Soroush Saghafian ◽  
Adam C. Bartley ◽  
Matthew R. Buras ◽  
Christopher F. Stewart ◽  
...  
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