30-Second Takeaway
- Post-allo-HSCT AIHA is uncommon (**0.72%**) but carries substantial mortality risk and responds better to steroids plus rituximab.
- HMA+venetoclax uptake for first-line AML rose after 2018 with real-world remission rates comparable to trials.
Latest - Week ending May 2, 2026
Grand Rounds: Selected 2026 hematology evidence briefs
Calibrating prognostic dialogue to support double awareness in hematologic malignancies
This qualitative study of 25 recorded serious-illness conversations describes how clinicians tailor prognostic depth and timing to patient and caregiver readiness. Preparatory materials and structured openings facilitated prognostic dialogue and supported patients' capacity for double awareness. Clinicians used prognostic uncertainty as a communicative resource rather than a barrier to discussion. Findings apply to hematologic malignancy patients, caregivers, and clinicians trained in serious-illness communication.
Incidence, risk factors, and outcomes of AIHA after allo‑HSCT
In a nested case-control cohort (61 cases), post-allo-HSCT autoimmune hemolytic anemia incidence was 0.72%. Unrelated donor increased AIHA risk (HR 2.323) while prior acute GVHD was protective (HR 0.340). Corticosteroids plus rituximab significantly improved response rates without observed treatment-related mortality. Age, LDH, and CRP were independent predictors of mortality; mononuclear cell dose correlated with AIHA relapse.
Real-world first-line AML treatments and outcomes in the United States
Among 2,516 newly diagnosed AML patients, cytarabine-based intensive chemotherapy remained the most used first-line regimen. Overall complete remission was 45%, highest with IC w/cytarabine (61%) and investigational therapies (62%). Use of HMA plus venetoclax increased after 2018 approval, with real-world outcomes similar to clinical trials. Survival differences favoring intensive cytarabine regimens are confounded by baseline patient selection.
References
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Additional Reads
Optional additional studies from this edition.