The DOI matches its Crossref record; 34 of the 35 references it cites were found in a registry or an index.
Clonal Selection with RAS Pathway Activation Mediates Secondary Clinical Resistance to Selective FLT3 Inhibition in Acute Myeloid Leukemia
Open accessPublished version of a preprint
Abstract
Gilteritinib is a potent and selective FLT3 kinase inhibitor with single-agent clinical efficacy in relapsed/refractory FLT3-mutated acute myeloid leukemia (AML). In this context, however, gilteritinib is not curative, and response duration is limited by the development of secondary resistance. To evaluate resistance mechanisms, we analyzed baseline and progression samples from patients treated on clinical trials of gilteritinib. Targeted next-generation sequencing at the time of AML progression on gilteritinib identified treatment-emergent mutations that activate RAS/MAPK pathway signaling, most commonly in NRAS or KRAS. Less frequently, secondary FLT3-F691L gatekeeper mutations or BCR–ABL1 fusions were identified at progression. Single-cell targeted DNA sequencing revealed diverse patterns of clonal selection and evolution in response to FLT3 inhibition, including the emergence of RAS mutations in FLT3-mutated subclones, the expansion of alternative wild-type FLT3 subclones, or both patterns simultaneously. These data illustrate dynamic and complex changes in clonal architecture underlying response and resistance to mutation-selective tyrosine kinase inhibitor therapy in AML. Significance: Comprehensive serial genotyping of AML specimens from patients treated with the selective FLT3 inhibitor gilteritinib demonstrates that complex, heterogeneous patterns of clonal selection and evolution mediate clinical resistance to tyrosine kinase inhibition in FLT3-mutated AML. Our data support the development of combinatorial targeted therapeutic approaches for advanced AML. See related commentary by Wei and Roberts, p. 998. This article is highlighted in the In This Issue feature, p. 983
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“However, clinical response duration to FLT3 inhibitor treatment remains short partially due to the development of secondary resistance [130].”
From Proteolysis targeting chimeras (PROTACs) are emerging therapeutics for hematologic malignancies (2020) · cites this paper as [130]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nowell, P. C. (1976) · Science · doi:10.1126/science.959840 · Cited by 6,471
Genomic classification and prognosis in acute myeloid leukemia
Papaemmanuil, E., Gerstung, M., Bullinger, L., Gaidzik, V. I., Paschka, P., Roberts, N. D., Potter, N. E., Heuser, M., Thol, F., Bolli, N., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1516192 · Cited by 4,350
Midostaurin plus Chemotherapy for Acute Myeloid Leukemia with a FLT3 Mutation
Stone, R. M., Mandrekar, S. J., Sanford, B. L., Laumann, K., Geyer, S., Bloomfield, C. D., Thiede, C., Prior, T. W., Döhner, K., Marcucci, G., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1614359 · Cited by 2,250
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
Ding, L., Ley, T. J., Larson, D. E., Miller, C. A., Koboldt, D. C., Welch, J. S., Ritchey, J. K., Young, M. A., Lamprecht, T., McLellan, M. D., et al. (2012) · Nature · doi:10.1038/nature10738 · Cited by 1,993
Grimwade, D. J., Hills, R. K., Moorman, A. V., Walker, H., Chatters, S., Goldstone, A. H., Wheatley, K., Harrison, C. J., & Burnett, A. K. (2010) · Blood · doi:10.1182/blood-2009-11-254441 · Cited by 1,936
Retinoic Acid and Arsenic Trioxide for Acute Promyelocytic Leukemia
Lo-Coco, F., Avvisati, G., Vignetti, M., Thiede, C., Orlando, S. M., Iacobelli, S., Ferrara, F., Fazi, P., Cicconi, L., Di Bona, E., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1300874 · Cited by 1,611
The origin and evolution of mutations in acute myeloid leukemia
Welch, J. S., Ley, T. J., Link, D. C., Miller, C. A., Larson, D. E., Koboldt, D. C., Wartman, L. D., Lamprecht, T. L., Liu, F., Xia, J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.023 · Cited by 1,575
Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies
Yamamoto, Y. (2001) · Blood · doi:10.1182/blood.v97.8.2434 · Cited by 1,152
Fröhling, S., Schlenk, R. F., Breitruck, J., Benner, A., Kreitmeier, S., Tobis, K., Döhner, H., & Döhner, K. (2002) · Blood · doi:10.1182/blood-2002-05-1440 · Cited by 873
Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia
Smith, C. C., Wang, Q., Chin, C.-S., Salerno, S. N., Damon, L. E., Levis, M. J., Perl, A. E., Travers, K. J., Wang, S., Hunt, J. P., et al. (2012) · Nature · doi:10.1038/nature11016 · Cited by 738
Self-citation
Flagged first, then by citations
1 of the 35 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Cortes, 2018, Quizartinib significantly prolongs overall survival in patients with FLT3-internal tandem duplication–mutated relapsed/refractory AML in the phase 3, randomized, controlled QuANTUM-R trial [abstract]
Cited by
Sorted by citations
Items 101–200 of 447
Jen, W., Kantarjian, H. M., Kadia, T. M., Dinardo, C. D., Issa, G. C., Short, N. J., Yilmaz, M. E., Borthakur, G. M., Ravandi, F., & Daver, N. G. (2024) · British Journal of Haematology · doi:10.1111/bjh.19519 · Cited by 38
Overcoming Resistance: FLT3 Inhibitors Past, Present, Future and the Challenge of Cure
Capelli, D., Menotti, D., Fiorentini, A., Saraceni, F., & Olivieri, A. (2022) · Cancers · doi:10.3390/cancers14174315 · Cited by 36
TP-0903 is active in models of drug-resistant acute myeloid leukemia
Jeon, J. Y., Buelow, D. R., Garrison, D. A., Niu, M., Eisenmann, E. D., Huang, K. M., Thomas, M. E. Z., Weber, R. H., Whatcott, C. J., Warner, S. L., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.140169 · Cited by 35
Kawashima, N., Ishikawa, Y., Kim, J. H., Ushijima, Y., Akashi, A., Yamaguchi, Y., Hattori, H., Nakashima, M., Ikeno, S., Kihara, R., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29304-6 · Cited by 38
Genetic heterogeneity and clonal evolution in acute myeloid leukemia
Romer-Seibert, J. S., & Meyer, S. E. (2020) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000626 · Cited by 33
Post, S. M., Ma, H., Malaney, P., Zhang, X., Aitken, M. J. L., Mak, P. Y., Ruvolo, V. R., Yasuhiro, T., Kozaki, R., Chan, L. E., et al. (2021) · Haematologica · doi:10.3324/haematol.2021.278369 · Cited by 33
New Therapeutic Strategies for Adult Acute Myeloid Leukemia
Ishii, H., & Yano, S. (2022) · Cancers · doi:10.3390/cancers14112806 · Cited by 33
Loo, S., Roberts, A. W., Anstee, N. S., Kennedy, G., He, S., Schwarer, A. P., Enjeti, A. K., D’Rozario, J., Marlton, P. V., Bilmon, I., et al. (2023) · Blood · doi:10.1182/blood.2023020301 · Cited by 32
Rivera, D., Kim, K., Kanagal‐Shamanna, R., Borthakur, G. M., Bravo, G. M., Daver, N. G., Dinardo, C. D., Short, N. J., Yilmaz, M. E., Pemmaraju, N., et al. (2022) · American Journal of Hematology · doi:10.1002/ajh.26731 · Cited by 32
Resistance to targeted therapies in acute myeloid leukemia
Mecklenbrauck, R., & Heuser, M. (2022) · Clinical & Experimental Metastasis · doi:10.1007/s10585-022-10189-0 · Cited by 31
Karthika, C., Sureshkumar, R., Zehravi, M., Akter, R., Ali, F., Ramproshad, S., Mondal, B., Kundu, M. K., Dey, A., Rahman, M. H., et al. (2022) · Life · doi:10.3390/life12060811 · Cited by 30
FLT3-targeted treatment for acute myeloid leukemia
Arai, Y., Chi, S., Minami, Y., & Yanada, M. (2022) · International Journal of Hematology · doi:10.1007/s12185-022-03374-0 · Cited by 30
Developments and challenges of FLT3 inhibitors in acute myeloid leukemia
Ge, S., Liu, S., & Xue, S. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.996438 · Cited by 30
Dumas, P., Raffoux, E., Bérard, E., Bertoli, S., Heiblig, M., Desbrosses, Y., Bonmati, C., Pautas, C., Lambert, J., Orvain, C., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01742-7 · Cited by 34
Venditti, A., Palmieri, R., Maurillo, L., Röllig, C., Wierzbowska, A., de Leeuw, D. C., Efficace, F., Curti, A., Ngai, L. L., Tettero, J. M., et al. (2025) · Blood Advances · doi:10.1182/bloodadvances.2024013744 · Cited by 32
Self-citationTiong, I. S., & Loo, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054790 · Cited by 30
Clonal competition within complex evolutionary hierarchies shapes AML over time
Sandén, C., Lilljebjörn, H., Orsmark‐Pietras, C., Henningsson, R., Saba, K. H., Landberg, N., Thorsson, H., von Palffy, S., Peña‐Martínez, P., Högberg, C., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14106-0 · Cited by 30
Application of omics in the diagnosis, prognosis, and treatment of acute myeloid leukemia
Zhang, Z., Huang, J., Zhang, Z., Shen, H., Tang, X., Wu, D., Bao, X., Xu, G., & Chen, S. (2024) · Biomarker Research · doi:10.1186/s40364-024-00600-1 · Cited by 30
The transcriptional regulation of normal and malignant blood cell development
Edginton‐White, B., & Bonifer, C. (2021) · FEBS Journal · doi:10.1111/febs.15735 · Cited by 27
Single-cell sequencing technology in tumor research
Bai, X., Li, Y., Zeng, X., Zhao, Q., & Zhang, Z. (2021) · Clinica Chimica Acta · doi:10.1016/j.cca.2021.03.013 · Cited by 30
Decroocq, J., Birsen, R., Montersino, C., Chaskar, P., Mano, J., Poulain, L., Friedrich, C., Alary, A., Guermouche, H., Sahal, A., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01541-0 · Cited by 30
Tan, Y., Xin, L., Wang, Q., Xu, R., Tong, X., Chen, G., Ma, L., Yang, F., Jiang, H., Zhang, N., et al. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.216933 · Cited by 27
Alotaibi, A. S., Yilmaz, M. E., Loghavi, S., Dinardo, C. D., Borthakur, G. M., Kadia, T. M., Thakral, B., Pemmaraju, N., Issa, G. C., Konopleva, M. Y., et al. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.588876 · Cited by 27
Clonal Architecture and Evolutionary Dynamics in Acute Myeloid Leukemias
Duchmann, M., Laplane, L., & Itzykson, R. (2021) · Cancers · doi:10.3390/cancers13194887 · Cited by 31
The Multi-Dimensional Biomarker Landscape in Cancer Immunotherapy
Lee, J. Y., Kannan, B., Lim, B. Y., Li, Z., Lim, A. H., Loh, J. W., Ko, T. K., Ng, C. C. Y., & Chan, J. Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147839 · Cited by 29
Neoantigen-specific TCR-T cell-based immunotherapy for acute myeloid leukemia
Zhou, W., Yu, J., Li, Y., & Wang, K. (2022) · Experimental Hematology and Oncology · doi:10.1186/s40164-022-00353-3 · Cited by 27
Clonal evolution and hierarchy in myeloid malignancies
Takahashi, K., & Tanaka, T. N. (2023) · Trends in cancer · doi:10.1016/j.trecan.2023.05.004 · Cited by 28
Mapping the proteogenomic landscape enables prediction of drug response in acute myeloid leukemia
Pino, J. C., Posso, C., Joshi, S. K., Nestor, M. D., Moon, J., Hansen, J., Hutchinson-Bunch, C. M., Gritsenko, M., Weitz, K., Watanabe‐Smith, K., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101359 · Cited by 26
Application of high-throughput single-nucleus DNA sequencing in pancreatic cancer
Zhang, H., Karnoub, E.-R. R., Umeda, S., Chaligné, R., Masilionis, I., McIntyre, C. A., Sashittal, P., Hayashi, A., Zucker, A., Mullen, K. M., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36344-z · Cited by 24
Gilteritinib: The Story of a Proceeding Success into Hard-to-Treat FLT3-Mutated AML Patients
Molica, M., Perrone, S., & Rossi, M. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12113647 · Cited by 26
The Role of Somatic Mutations in Acute Myeloid Leukemia PathogenesisPreprint
Kishtagari, A., & Levine, R. L. (2020) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a034975 · Cited by 26
Aptamers against cancer drug resistance: Small fighters switching tactics in the face of defeat
Sanati, M., Afshari, A. R., Ahmadi, S. S., Kesharwani, P., & Sahebkar, A. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166720 · Cited by 27
Levis, M. J., Perl, A. E., Schiller, G. J., Fathi, A. T., Roboz, G. J., Wang, E. S., Altman, J. K., Rajkhowa, T., Ando, M., Suzuki, T., et al. (2024) · Blood Advances · doi:10.1182/bloodadvances.2023010619 · Cited by 25
Self-citationPerrone, S., Ottone, T., Zhdanovskaya, N., & Molica, M. (2023) · Cancer Drug Resistance · doi:10.20517/cdr.2022.130 · Cited by 26
Abdel‐Aziz, A. K., Dokla, E. M. E., & Saadeldin, M. K. (2023) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2023.104139 · Cited by 24
Cerrano, M., Duchmann, M., Kim, R., Vasseur, L., Hirsch, P., Thomas, X., Quentin, S., Pasanisi, J., Passet, M., Rabian, F., et al. (2020) · Leukemia · doi:10.1038/s41375-020-0932-8 · Cited by 24
Charlet, A., Kappenstein, M., Keye, P., Kläsener, K., Endres, C., Poggio, T., Gorantla, S. P., Kreutmair, S., Sänger, J., Illert, A. L., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01462-4 · Cited by 24
Ciotti, G., Marconi, G., & Martinelli, G. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2021.810387 · Cited by 23
Yamatani, K., Ai, T., Saito, K., Suzuki, K., Hori, A., Kinjo, S., Ikeo, K., Ruvolo, V. R., Zhang, W., Mak, P. Y., et al. (2022) · Translational Oncology · doi:10.1016/j.tranon.2022.101354 · Cited by 22
Zhang, Y., Wang, P., Wang, Y., & Shen, Y. (2023) · Biomarker Research · doi:10.1186/s40364-022-00447-4 · Cited by 22
Meyers, S., Servera, L. A., Gielen, O., Erard, M., Swings, T., Bie, J. D., Michaux, L., Dewaele, B., Boeckx, N., Uyttebroeck, A., et al. (2022) · HemaSphere · doi:10.1097/hs9.0000000000000700 · Cited by 21
Single-cell methods in myeloproliferative neoplasms: old questions, new technologies
O’Sullivan, J., Mead, A. J., & Psaila, B. (2022) · Blood · doi:10.1182/blood.2021014668 · Cited by 24
Garciaz, S., & Hospital, M. (2023) · OncoTargets and Therapy · doi:10.2147/ott.s236740 · Cited by 21
FLT3 inhibitors in the treatment of acute myeloid leukemia: current status and future perspectives
Orgueira, A. M., Pérez, L. B., Torre, A. M., Raíndo, A. P., López, M. C., Arias, J. Á. D., Ferro, R. F., Rodríguez, B. A., González, M. S., Ferreiro, M. A., et al. (2020) · Minerva Medica · doi:10.23736/s0026-4806.20.06989-x · Cited by 21
Lachowiez, C. A., Dinardo, C. D., & Loghavi, S. (2023) · Cancers · doi:10.3390/cancers15051617 · Cited by 20
Microfluidic design in single-cell sequencing and application to cancer precision medicine
Han, X., Xu, X. J., Yang, C. J., & Liu, G. (2023) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100591 · Cited by 21
Yen, S., Chen, L., Huang, H.-L., HuangFu, W., Chen, Y.-Y., Lin, T. E., Lien, S.-T., Tseng, H.-J., Sung, T.-Y., Hsieh, J., et al. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.105675 · Cited by 20
Liu, S., Zhou, J. H. S., Ye, X., Chen, D., Chen, W., Lin, Y., Chen, Z., Chen, B., & Shang, J. (2023) · Leukemia · doi:10.1038/s41375-023-01923-y · Cited by 20
Sung, P. J., Selvam, M., Riedel, S. S., Xie, H. M., Bryant, K. M., Manning, B. S., Wertheim, G. B. W., Kulej, K., Pham, L., Bowman, R. L., et al. (2024) · Leukemia · doi:10.1038/s41375-023-02131-4 · Cited by 20
Self-citationGilteritinib for the treatment of relapsed and/or refractory FLT3-mutated acute myeloid leukemia
McMahon, C. M., & Perl, A. E. (2019) · Expert Review of Clinical Pharmacology · doi:10.1080/17512433.2019.1657009 · Cited by 20
Self-citationLoschi, M. L., Sammut, R., Chiche, E., & Cluzeau, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115873 · Cited by 20
Refining AML Treatment: The Role of Genetics in Response and Resistance Evaluation to New Agents
Halik, A., Arends, C. M., Bullinger, L., Damm, F., & Frick, M. (2022) · Cancers · doi:10.3390/cancers14071689 · Cited by 20
Lv, M., Hu, W., Zhang, S., He, L., Hu, C., & Yang, S. (2022) · Cancer Letters · doi:10.1016/j.canlet.2022.215716 · Cited by 19
Update on Small Molecule Targeted Therapies for Acute Myeloid Leukemia
Wang, J., Tomlinson, B. K., & Lazarus, H. M. (2023) · Current Treatment Options in Oncology · doi:10.1007/s11864-023-01090-3 · Cited by 18
Cytogenetics and genomics of acute myeloid leukemia
Snaith, O., Poveda-Rogers, C., Laczko, D. I., Yang, G., & Morrissette, J. J. D. (2023) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2023.101533 · Cited by 23
Self-citationSingle-cell sequencing in hematology
Brierley, C. K., & Mead, A. J. (2019) · Current Opinion in Oncology · doi:10.1097/cco.0000000000000613 · Cited by 19
Targeted Single-Cell RNA and DNA Sequencing With Fluorescence-Activated Droplet Merger
Clark, I. C., Delley, C. L., Sun, C., Thakur, R. A., Stott, S. L., Thaploo, S., Li, Z., Quintana, F. J., & Abate, A. R. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c03059 · Cited by 19
Khoury, J. D., Tashakori, M., Yang, H. Y., Loghavi, S., Wang, Y., Wang, J., Piya, S., & Borthakur, G. M. (2020) · Cancers · doi:10.3390/cancers12123511 · Cited by 19
Oncogenic N-Ras Mitigates Oxidative Stress–Induced Apoptosis of Hematopoietic Stem Cells
Ney, G. M., Yang, K. B., Ng, V., Liu, L., Zhao, M., Kuk, W., Alaka, L., Sampang, L., Ross, A., Jones, M. A., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-0118 · Cited by 19
Momelotinib is a highly potent inhibitor of FLT3-mutant AML
Azhar, M., Kincaid, Z., Kesarwani, M., Ahmed, A., Wunderlich, M., Latif, T., Starczynowski, D. T., & Azam, M. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021004611 · Cited by 19
Targeted therapy in acute myeloid leukemia: Resistance and overcoming strategy
Song, F., Lin, S., Xu, T., Yang, C., Sharavyn, B., Naranmandura, H., Zhang, Y., & Huang, P. C. (2025) · Drug Resistance Updates · doi:10.1016/j.drup.2025.101286 · Cited by 21
Achi, H. E., & Kanagal‐Shamanna, R. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.748250 · Cited by 21
BMX kinase mediates gilteritinib resistance in FLT3 -mutated AML through microenvironmental factors
Buelow, D. R., Bhatnagar, B., Orwick, S. J., Jeon, J. Y., Eisenmann, E. D., Stromatt, J. C., Pabla, N., Blachly, J. S., Baker, S. D., & Blaser, B. W. (2022) · Blood Advances · doi:10.1182/bloodadvances.2022007952 · Cited by 19
From Bench to Bedside and Beyond: Therapeutic Scenario in Acute Myeloid Leukemia
Gurnari, C., Voso, M. T., Maciejewski, J. P., & Visconte, V. (2020) · Cancers · doi:10.3390/cancers12020357 · Cited by 18
Emerging Targeted Therapy for Specific Genomic Abnormalities in Acute Myeloid Leukemia
Chi, S., & Minami, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042362 · Cited by 16
Which FLT3 Inhibitor for Treatment of AML?
Senapati, J., & Kadia, T. M. (2022) · Current Treatment Options in Oncology · doi:10.1007/s11864-022-00952-6 · Cited by 18
Brinton, L. T., Sher, S., Williams, K., Canfield, D., Orwick, S. J., Wasmuth, R., Cempre, C. B., Skinner, J. N., Lehman, A., Blachly, J. S., et al. (2020) · Cancers · doi:10.3390/cancers12061574 · Cited by 18
Overcoming Secondary Mutations of Type II Kinase Inhibitors
Wang, X., DeFilippis, R. A., Yan, W., Shah, N. P., & Li, H. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.3c01629 · Cited by 18
Self-citationBall, B. J., Hsu, M., Devlin, S. M., Arcila, M. E., Roshal, M., Zhang, Y., Famulare, C., Goldberg, A. D., Cai, S. F., Dunbar, A. J., et al. (2021) · American Journal of Hematology · doi:10.1002/ajh.26146 · Cited by 17
FLT3 targeting in the modern era: from clonal selection to combination therapies
Kennedy, V. E., & Smith, C. C. (2023) · International Journal of Hematology · doi:10.1007/s12185-023-03681-0 · Cited by 17
Self-citationTargeting CCL2/CCR2 Signaling Overcomes MEK Inhibitor Resistance in Acute Myeloid Leukemia
Modak, R. V., Rebola, K. G. D. O., McClatchy, J., Mohammadhosseini, M., Damnernsawad, A., Kurtz, S. E., Eide, C. A., Wu, G., Laderas, T., Nechiporuk, T., et al. (2024) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-23-2654 · Cited by 18
A novel combination regimen of BET and FLT3 inhibition for FLT3-ITD acute myeloid leukemia
Lee, L., Hizukuri, Y., Severson, P. L., Powell, B., Zhang, C., Ma, Y., Narahara, M., Sumi, H., Hernandez, D., Rajkhowa, T., et al. (2021) · Haematologica · doi:10.3324/haematol.2020.247346 · Cited by 17
A noncanonical FLT3 gatekeeper mutation disrupts gilteritinib binding and confers resistance
Joshi, S. K., Sharzehi, S., Pittsenbarger, J., Bottomly, D., Tognon, C. E., McWeeney, S. K., Druker, B. J., & Traer, E. A. (2021) · American Journal of Hematology · doi:10.1002/ajh.26174 · Cited by 17
Chen, P., Wang, C., Tsao, E.-C., Chen, Y., Wu, M., Ho, C., & Yen, J.-H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137392 · Cited by 17
Umeda, M., Hiltenbrand, R., Michmerhuizen, N. L., Barajas, J. M., Thomas, M. E., Arthur, B., Walsh, M. P., Song, G., Ma, J., Westover, T., et al. (2025) · Blood · doi:10.1182/blood.2025028993 · Cited by 16
Pratz, K. W., Kaplan, J. B., Levy, M. Y., Bixby, D. L., Burke, P. W., Erba, H. P., Wise-Draper, T. M., Roboz, G. J., Papadantonakis, N., Rajkhowa, T., et al. (2022) · Haematologica · doi:10.3324/haematol.2022.281216 · Cited by 16
Methyltransferase DNMT3B in leukemia
Zhang, H., Ying, H., & Wang, X. (2019) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2019.1666377 · Cited by 16
Kim, B.-R., Jung, S., Han, A., Park, G., Kim, H., Yuan, B., Battula, V. L., Andreeff, M., Konopleva, M. Y., Chung, Y., et al. (2020) · Cancers · doi:10.3390/cancers12071737 · Cited by 16
Smith, C. C., Viny, A. D., Massi, E., Kandoth, C., Socci, N. D., Rapaport, F., Najm, M., Medina-Martinez, J. S., Papaemmanuil, E., Tarver, T. C., et al. (2021) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-20-3458 · Cited by 17
Self-citationMechanisms of Resistance to Small Molecules in Acute Myeloid Leukemia
Lang, T. J. L., Damm, F., Bullinger, L., & Frick, M. (2023) · Cancers · doi:10.3390/cancers15184573 · Cited by 16
Recent advancements in biomarkers, therapeutics, and associated challenges in acute myeloid leukemia
Prajapati, S. K., Neha, K., Bhowmik, D., & Gupta, R. (2024) · Annals of Hematology · doi:10.1007/s00277-024-05963-x · Cited by 15
Advances in the pathogenesis of FLT3-mutated acute myeloid leukemia and targeted treatments
Travaglini, S., Gurnari, C., Ottone, T., & Voso, M. T. (2024) · Current Opinion in Oncology · doi:10.1097/cco.0000000000001094 · Cited by 15
FGFR Signaling as a Candidate Therapeutic Target for Cancers Resistant to Carbon Ion Radiotherapy
Darwis, N. D. M., Nachankar, A., Sasaki, Y., Matsui, T., Noda, S., Murata, K., Tamaki, T., Ando, K., Okonogi, N., Shiba, S., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184563 · Cited by 15
Targeted Therapies for the Evolving Molecular Landscape of Acute Myeloid Leukemia
Ahmadmehrabi, K., Haque, A. R., Aleem, A., Griffiths, E. A., & Roloff, G. W. (2021) · Cancers · doi:10.3390/cancers13184646 · Cited by 14
A precision medicine classification for treatment of acute myeloid leukemia in older patients
Mims, A. S., Kohlschmidt, J., Borate, U., Blachly, J. S., Orwick, S. J., Eisfeld, A., Papaioannou, D., Nicolet, D., Mrózek, K., Stein, E. M., et al. (2021) · Journal of Hematology & Oncology · doi:10.1186/s13045-021-01110-5 · Cited by 14
Self-citationKurata, M., Antony, M. L., Noble-Orcutt, K. E., Rathe, S. K., Lee, Y., Furuno, H., Ishibashi, S., Ikeda, M., Yamamoto, K., Kitagawa, M., et al. (2022) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-22-0109 · Cited by 14
Clinical implications of NUP98::NSD1 fusion at diagnosis in adult FLT3‐ITD positive AML
Miyajima, T., Onozawa, M., Yoshida, S. Y., Miyashita, N., Kimura, H., Takahashi, S., Yokoyama, S., Matsukawa, T., Goto, H., Sugita, J., et al. (2023) · European Journal Of Haematology · doi:10.1111/ejh.14055 · Cited by 14
Venetoclax and Cobimetinib in Relapsed/Refractory AML: A Phase 1b Trial
Konopleva, M. Y., Dail, M., Daver, N. G., Garcia, J. S., Jonas, B. A., Yee, K. W. L., Kelly, K. R., Vey, N., Assouline, S. E., Roboz, G. J., et al. (2024) · Clinical Lymphoma Myeloma & Leukemia · doi:10.1016/j.clml.2024.01.007 · Cited by 14
Mohebbi, A., Shahriyary, F., Farrokhi, V., Bandar, B., & Saki, N. (2024) · Leukemia Research · doi:10.1016/j.leukres.2024.107505 · Cited by 14
Wei, T., Wang, Z., Lu, M., Xu, Y., Yang, J., Ni, X.-F., Yang, C., Zhang, M., Liu, J., Li, Q., et al. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c00529 · Cited by 14
Eisfelder, B. J., Saygin, C., Wynne, J. P., Cove, M. C., Fischietti, M., Beauchamp, E. M., Cheng, J. X., Odenike, O. M., Roboz, G. J., Alachkar, H., et al. (2021) · Blood Cancer Journal · doi:10.1038/s41408-021-00433-3 · Cited by 14
Mechanisms of resistance to targeted therapies for relapsed or refractory acute myeloid leukemia
Kropp, E. M., & Li, Q. (2022) · Experimental Hematology · doi:10.1016/j.exphem.2022.04.001 · Cited by 14
Popescu, B. O., Stahlhut, C. E., Tarver, T. C., Wishner, S., Lee, B. J., Peretz, C. A. C., Luck, C., Phojanakong, P. J., Cámara, J. A., Hongo, H., et al. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101290 · Cited by 12
Self-citationTherapeutic biomarkers in acute myeloid leukemia: functional and genomic approaches
Bhatia, K. S., Sandhu, V., Wong, M. H., Iyer, P., & Bhatt, S. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1275251 · Cited by 13
Targeting FLT3 for treating diseases: FLT3 inhibitors
Rong, Q.-Y., Lu, Y., Zhang, W., Rao, G.-W., & Zheng, Q. (2025) · Drug Discovery Today · doi:10.1016/j.drudis.2025.104367 · Cited by 13
Altman, J. K., Perl, A. E., Hill, J. E., Rosales, M., Bahceci, E., & Levis, M. J. (2020) · Cancer Medicine · doi:10.1002/cam4.3652 · Cited by 13
Self-citationTien, F., Tsai, C., Huang, S.-C., Liu, J., Chen, C., Kuo, Y., Chuang, Y., Tseng, M., Peng, Y., Liu, M.-C., et al. (2021) · Bone Marrow Transplantation · doi:10.1038/s41409-021-01454-z · Cited by 13
Biavasco, F., & Zeiser, R. (2022) · International Journal of Hematology · doi:10.1007/s12185-022-03352-6 · Cited by 12
JAK2 inhibition mediates clonal selection of RAS pathway mutations in myeloproliferative neoplasms
Maslah, N., Kaci, N., Roux, B., Alexe, G., Marie, R., Pasquer, H., Verger, E., Oliveira, R. D. D., Culeux, C., Mlayah, B., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60884-1 · Cited by 16
Popescu, B., Jones, M. F., Piao, M., Tran, E., Koh, A., Lomeli, I., Peretz, C. A. C., Murad, N. F., Abelson, S., Morales, C. E., et al. (2025) · Blood · doi:10.1182/blood.2025030558 · Cited by 16
Self-citation
Metadata
- Authors
- McMahon, C. M., Ferng, T., Canaani, J., Wang, E. S., Morrissette, J. J. D., Eastburn, D. J., Pellegrino, M., Durruthy-Durruthy, R., Watt, C. D., Asthana, S., Lasater, E. A., DeFilippis, R., Peretz, C. A. C., McGary, L. H. F., Deihimi, S., Logan, A. C., Luger, S. M., Shah, N. P., Carroll, M., Smith, C. C., & Perl, A. E.
- Affiliations
- University of Pennsylvania (US)
- University of California, San Francisco (US)
- Tel Aviv University (IL)
- Roswell Park Comprehensive Cancer Center (US)
- Mission Bio (United States) (US)
- United States Department of Veterans Affairs (US)
- ORCID
- Venue
- Cancer Discovery
- Published
- 2019-08-01
- Volume
- 9
- Issue
- 8
- Pages
- 1050-1063
- ISSN
- 2159-8274 (ISSN-L)
- 2159-8290
- PMC
- PMC11994087
- OpenAlex
- W2946259536
- Cited by
- 446
- References
- 35
- Citations by year
- 2026: 35 · 2025: 55 · 2024: 56 · 2023: 62 · 2022: 91 · 2021: 61 · 2020: 68 · 2019: 16
- FWCI
- 41.51
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cancer Discovery (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- HHS | NIH | National Center for Advancing Translational SciencesHHS | NIH | National Center for Advancing Translational Sciences (NCATS) (TL1TR001880)
- American Society of Clinical OncologyAmerican Society of Clinical Oncology (ASCO)
- HHS | NIH | National Cancer InstituteHHS | NIH | National Cancer Institute (NCI) (R21 CA198621, R01 CA198089, R01 CA166616, K08 CA187577)
- Damon Runyon Cancer Research FoundationDamon Runyon Cancer Research Foundation (Damon Runyon) (CI-99-18)
- Biff Ruttenberg Foundation
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Health Sciences › Medicine › Hematology › Chronic Myeloid Leukemia Treatments
- Keywords
- acute myeloid leukemia, FLT3 mutation, gilteritinib, FLT3 inhibitor resistance, clonal selection, clonal evolution, NRAS mutation, KRAS mutation, BCR-ABL fusion gene, tyrosine kinase inhibitor resistance, single-cell DNA sequencing
- MeSH terms
- Adult, Aged, Aged, 80 and over, Aniline Compounds, Female, Humans, Male, Middle Aged, Mutation, Pyrazines, Signal Transduction, Leukemia, Myeloid, Acute, ras Proteins, Drug Resistance, Neoplasm, Protein Kinase Inhibitors, fms-Like Tyrosine Kinase 3, Young Adult, Single-Cell Analysis, High-Throughput Nucleotide Sequencing, Clonal Evolution
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review