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Grand RoundsWeekly Evidence Brief

Hematology

Edition

30-Second Takeaway

  • ELN-DAVID 2025 formalizes standardized, genetics-aligned MRD use in AML, including NGS-based FLT3-ITD monitoring.
  • Asciminib provides superior molecular responses and tolerability versus standard TKIs as frontline therapy in CML-CP.
  • PD-1–based salvage before ASCT improves post-transplant PFS in relapsed/refractory Hodgkin lymphoma.

Week ending December 20, 2025

Targeted therapy, MRD-driven risk, and supportive care updates across hematologic malignancies

ELN-DAVID 2025: standardized, genetics-aligned AML MRD guidance

BLOODDec 15, 2025

This ELN-DAVID update issues 56 consensus recommendations for AML MRD assessment, aligned with ELN 2022 genetic risk groups. MRD responses are newly categorized qualitatively as optimal, warning, or high risk of treatment failure to guide clinical decisions. Recommendations are tailored by prognostic and genetic subsets, embedding MRD into routine risk assessment and post-therapy monitoring. Ultrahigh-sensitivity NGS-based MRD is specifically recommended for FLT3-ITD–mutated AML after intensive chemotherapy and before allogeneic transplantation.

ASC4FIRST: asciminib surpasses standard TKIs in newly diagnosed CML-CP

BLOODDec 15, 2025

In ASC4FIRST, asciminib achieved higher week-96 major molecular response than investigator-selected TKIs in newly diagnosed CML-CP (74.1% vs 52.0%). Asciminib also clearly outperformed imatinib (76.2% vs 47.1% MMR at week 96), meeting key secondary endpoints. Compared with second-generation TKIs, asciminib yielded higher MMR (72.0% vs 56.9%), though this secondary endpoint was not powered for definitive significance. Dose reductions and interruptions occurred less often with asciminib than with second-generation TKIs, indicating better long-term tolerability.

PD-1–based salvage before ASCT improves outcomes in R/R cHL

BLOODDec 17, 2025

This multicenter retrospective cohort included 1,280 relapsed/refractory classical Hodgkin lymphoma patients undergoing ASCT between 2010 and 2022. Twenty-five percent received PD-1 inhibitor–based therapy pre-ASCT, including 10% treated with PD-1 plus chemotherapy. Any PD-1 exposure before ASCT yielded higher 2-year PFS than brentuximab-based salvage or chemotherapy alone (88.2% vs 70.2% and 67.4%; p<0.0001). The PFS benefit persisted in patients already in complete response at transplant, suggesting an effect beyond CR attainment.

References

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Additional Reads

Optional additional studies from this edition.

Edition context

Clinical signal

  • Integrated MRD and genomic tools are sharpening prognosis and transplant decision-making in AML, B-ALL, and MDS.
  • Frontline asciminib is poised to reshape CML-CP management by coupling deeper molecular responses with fewer toxicity-driven discontinuations.
  • Cellular and immune therapies require heightened vigilance for rare but lethal IEC-HS and long-term second malignancies.