Publications by authors named "O S Frankfurt"

Article Synopsis
  • * In a phase 2b study involving 65 patients averaging 75 years old, aspacytarabine was administered, resulting in a complete remission rate of 36.9% without the serious side effects typically associated with high doses of cytarabine.
  • * The median overall survival for patients was 9 months, with all responders showing recovery in blood cell counts by day 26, indicating aspacytarabine may be an effective and less toxic treatment option for AML in vulnerable populations.
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Stress is becoming increasingly commonplace in modern times, making it important to have accurate and effective detection methods. Currently, detection methods such as self-evaluation and clinical questionnaires are subjective and unsuitable for long-term monitoring. There have been significant studies into biomarkers such as HRV, cortisol, electrocardiography, and blood biomarkers, but the use of multiple electrodes for electrocardiography or blood tests is impractical for real-time stress monitoring.

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Omidubicel is an umbilical cord blood (UCB)-derived ex vivo-expanded cellular therapy product that has demonstrated faster engraftment and fewer infections compared with unmanipulated UCB in allogeneic hematopoietic cell transplantation. Although the early benefits of omidubicel have been established, long-term outcomes remain unknown. We report on a planned pooled analysis of 5 multicenter clinical trials including 105 patients with hematologic malignancies or sickle cell hemoglobinopathy who underwent omidubicel transplantation at 26 academic transplantation centers worldwide.

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This phase 2 study describes long-term clinical and immunological effects of fixed-duration ofatumumab (anti-CD20) and alemtuzumab (anti-CD52) combination immunotherapy in 52 patients with previously untreated CLL. The median age was 65 years (range 45-79), 60% had Rai stage 3-4, 40% were IgHV unmutated and 25% had del(17p)/TP53 mutation. Alemtuzumab was given subcutaneously (30 mg tiw, 18 weeks) and ofatumumab intravenously (300-2000 mg) starting week 3 q2 weeks (8 doses).

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Article Synopsis
  • The trial was a phase 3 study comparing enasidenib, an oral IDH2 inhibitor, to standard care regimens in older patients with late-stage acute myeloid leukemia (AML) who had already undergone multiple treatments.
  • The primary goal was to evaluate overall survival (OS), but while the OS results were similar (6.5 months for enasidenib vs. 6.2 months for standard care), enasidenib showed significant improvements in secondary outcomes like event-free survival (EFS), overall response rate (ORR), and transfusion independence (TI).
  • Despite not meeting the primary endpoint for OS, the findings suggest that enasidenib could offer important benefits in managing relapsed or refractory AML in
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