Borthakur GM, Cortes JE, Ravandi F, és mtsai. Fludarabine, Cytarabine, G-CSF and Gemtuzumab Ozogamicin (FLAG-GO) regimen results in better molecular response and relapse-free survival in core binding factor acute myeloid leukemia than FLAG and Idarubicin (FLAG-Ida). Blood 2019. November 13; 134(Supplement_1): 290.
Senapati J, Kantarjian HM, Ayoub E, és mtsai. Gemtuzumab Ozogamicin added to Fludarabine, Cytarabine and G-CSF (FLAG-GO) leads to superior molecular response and survival outcomes than idarubicin (FLAG-IDA): 200 patients long-term follow up. Blood [Internet]. 2024. November 5. [idézi 2025. január 26.]; 144(Supplement 1): 1513. Elérhető: https://ashpublications.org/blood/article/144/Supplement%201/1513/532742/Gemtuzumab-Ozogamicin-Added-to-Fludarabine.
Stone RM, Yin J, Mandrekar SJ, és mtsai. 10 Year follow-up of CALGB 10603/ratify: Midostaurin versus placebo plus intensive chemotherapy in newly diagnosed FLT3 mutant acute myeloid leukemia patients aged 18–60 years. Blood [Internet] 2024. November 5. [idézi 2025. január 26.]; 144(Supplement 1): 218–218. Elérhető: https://doi.org/10.1182/blood-2024-201058.
Luger S, Chen L, Pratz KW, és mtsai. Gilteritinib results in higher remission and transplant rates than midostaurin but does not increase the post-induction mutational MRD negative rate: results of the phase 2 randomized precog 0905 study in newly diagnosed FLT3 mutated AML. Blood [Internet] 2024. November 5. [idézi 2025. január 26.]; 144(Supplement 1): 221–221. Elérhető: https://doi.org/10.1182/blood-2024-201595.
Levis MJ, Hamadani M, Logan B, és mtsai. Gilteritinib as post-transplant maintenance for AML with internal tandem duplication mutation of FLT3. J Clin Oncol [Internet] 2024. május 20. [idézi 2025. január 26.]; 42(15): 1766–75. Elérhető: https://pubmed.ncbi.nlm.nih.gov/38471061/.
Heuser M, Shahswar R. Mutation- and MRD-informed treatment decisions for the transplant-eligible AML patient. Hematol Am Soc Hematol Educ Program [Internet] 2024. November 25. [idézi 2025. január 26.]; 2024(1): 158–67. Elérhető: https://pubmed.ncbi.nlm.nih.gov/39644001/.
Short NJ, Loghavi S, Yilmaz M, és mtsai. Long-term survival outcomes and cytogenetic/molecular patterns of relapse in adults with FLT3-mutated AML receiving frontline triplet therapy with a hypomethylating agent, venetoclax and FLT3 inhibitor. Blood [Internet] 2024. November 5. [idézi 2025. január 26.]; 144(Supplement 1): 220–220. Elérhető: https://doi.org/10.1182/blood-2024-210891.
Rausch C, Rothenberg-Thurley M, Dufour A, és mtsai. Validation and refinement of the 2022 European LeukemiaNet genetic risk stratification of acute myeloid leukemia. Leuk [Internet] 2023. június 1. [idézi 2025. január 26.]; 37(6): 1234–44. Elérhető: https://pubmed.ncbi.nlm.nih.gov/37041198/.
Othman J, Tiong IS, O’Nions J, és mtsai. Molecular MRD is strongly prognostic in patients with NPM1-mutated AML receiving venetoclax-based nonintensive therapy. Blood [Internet] 2024. január 25. [idézi 2025. január 26.]; 143(4): 336–41. Elérhető: https://pubmed.ncbi.nlm.nih.gov/37647641/.
Döhner H, Pratz KW, DiNardo CD, és mtsai. Genetic risk stratification and outcomes among treatment-naive patients with AML treated with venetoclax and azacitidine. Blood [Internet] 2024. November 21. [idézi 2025. január 26.]; 144(21). Elérhető: https://pubmed.ncbi.nlm.nih.gov/39133921/.
Paper: Venetoclax combined with „7+3” induction chemotherapy induces high MRD-negative response rates in newly diagnosed AML patients fit for intensive chemotherapy across ages [Internet]. [idézi 2025. január 26.]. Elérhető: https://ash.confex.com/ash/2024/webprogram/Paper211685.html.
Paper: A retrospective analysis of intensive chemotherapy Vs. Venetoclax/hypomethylating agents for patients aged 60–75 with favorable-risk, NPM1-mutated AML [Internet]. [idézi 2025. január 26.]. Elérhető: https://ash.confex.com/ash/2024/webprogram/Paper210320.html.
Paper: Prognostic value of the measurable residual disease (MRD) in AML treatment with venetoclax in combination with hypomethylating agents: validation of the ELN 2021 MRD recommendations [Internet]. [idézi 2025. január 26.]. Elérhető: https://ash.confex.com/ash/2024/webprogram/Paper204503.html.
Aldoss I, Issa GC, Blachly JS, és mtsai. Updated results and longer follow-up from the AUGMENT-101 phase 2 study of revumenib in all patients with relapsed or refractory (R/R) KMT2Ar acute leukemia. Blood [Internet] 2024. November 5. [idézi 2025. január 26.]; 144(Supplement 1): 211–211. Elérhető: https://doi.org/10.1182/blood-2024-194384.
DiPersio JF, Koehne G, Shah NN, és mtsai. A CD33-deleted allograft (Trem-cel) enables post-hematopoietic cell transplant (HCT) maintenance dosing of gemtuzumab ozogamicin (GO) with therapeutic levels of drug exposure and low hematologic and hepatic toxicity in patients with high-risk acute myeloid leukemia (AML). Blood [Internet]. 2024 November 5. [idézi 2025. január 26.]; 144(Supplement 1): 2873–2873. Elérhető: https://doi.org/10.1182/blood-2024-205641.