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ð äžé éé»
- 22E:
- Revumenib (Revuforj, FDA 2024) menin inhibitor for KMT2A + NPM1
- Olutasidenib IDH1 (FDA 2022 R/R AML)
- Quizartinib (Vanflyta, FDA 2023) FLT3-ITD; +chemo + maintenance (QuANTUM-First)
- Venetoclax + AZA standard older AML; expanding to other settings
- MRD-driven HSCT decision + post-HSCT MRD monitoring
- WHO 2022 + ICC 2022 harmonized classification (driver-defined)
- Taiwan: å¥ä¿ 7+3, HiDAC, ATRA, arsenic, midostaurin (FLT3+), gemtuzumab (æ¢ä»¶), venetoclax + AZA æ¢ä»¶; gilteritinib + ivosidenib + enasidenib + revumenib + olutasidenib + quizartinib + CPX-351 èªè²» å€ / æ¢ä»¶ limited
ð Pearls (12)
- WHO 2022 vs ICC 2022: ICC requires 10% blasts for AML if recurrent abnormality (vs WHO no threshold for some)
- CR vs CRh vs MRDneg CR: hierarchy of remission depth; MRD predictor
- Day 14 BM: if > 5% blasts â consider re-induction; varies by protocol
- Quizartinib + 7+3 + maintenance for FLT3-ITD (QuANTUM-First; FDA 2023)
- Olutasidenib (Rezlidhia, FDA 2022) IDH1 inhibitor â alternative to ivosidenib
- Revumenib menin inhibitor: blocks menin-KMT2A interaction; effective in KMT2A-rearranged + NPM1-mutated R/R
- Differentiation syndrome with menin inhibitor (revumenib): similar to ATRA + IDH inhibitors
- Hyperleukocytosis / leukostasis: leukapheresis + cytoreduction; avoid RBC transfusion until WBC reduced
- Tumor lysis syndrome venetoclax: slow 5-day ramp + monitor; especially CLL but also AML
- HSCT post-CR: MRD-positive â HSCT in 1st CR even favorable risk; MRD-negative + favorable â consolidation only
- Therapy-related AML: dismal prognosis; CPX-351 (Vyxeos) better than 7+3
- CAR-T for AML: CD33, CD123, CLL-1 in trials; not yet standard
ð Taiwan + å¥ä¿
- å¥ä¿ 7+3 (cytarabine + idarubicin/daunorubicin)
- å¥ä¿ HiDAC consolidation
- å¥ä¿ ATRA + arsenic for APL
- å¥ä¿ azacitidine + decitabine
- å¥ä¿ midostaurin for FLT3+ frontline æ¢ä»¶
- å¥ä¿ venetoclax + AZA for older AML æ¢ä»¶ (æ°)
- å¥ä¿ gemtuzumab ozogamicin for CBF / CD33+ æ¢ä»¶
- å¥ä¿ HSCT æ¢ä»¶
- Gilteritinib (Xospata), ivosidenib (Tibsovo), enasidenib (Idhifa), revumenib (Revuforj), olutasidenib (Rezlidhia), quizartinib (Vanflyta), CPX-351 (Vyxeos), glasdegib (Daurismo) èªè²» å€ / æ¢ä»¶ limited
- å¥ä¿ NGS panel æ¢ä»¶ (æ°, AML)
- åžæ: TSH (Taiwan Society of Hematology) + åå®¶è¡çç ç©¶é¢ leukemia consortium
ð å
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æ (12)
- WHO 2022 + ICC 2022 driver-defined classification
- ELN 2022 risk stratification + MRD
- APL low vs high risk Sanz + Lo-Coco
- APL DIC + DS prophylaxis
- 7+3 induction + targeted addition (FLT3 midostaurin/quizartinib)
- Older AML venetoclax + AZA (VIALE-A)
- FLT3 R/R: gilteritinib (ADMIRAL)
- IDH1: ivosidenib + olutasidenib; IDH2: enasidenib
- KMT2A/NPM1: revumenib menin inhibitor (22E)
- HSCT decision + MRD-driven
- Therapy-related AML + CPX-351
- CAR-T trials + future
â ïž AI èçš¿ã