Chemoresponse of de novo Acute Myeloid Leukemia to "7+3" Induction can Be Predicted by c-Myc-facilitated Cytogenetics
Background: Identifying patients with de novo acute myeloid leukemia (AML) who will probably respond to the "7 + 3" induction regimen remains an unsolved clinical challenge. This study aimed to identify whether c-Myc could facilitate cytogenetics to predict a "7 + 3" induction ch...
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Frontiers Media S.A.,
2021-04-01T00:00:00Z.
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001 | doaj_8c202f7fc4614b8197ae2142b0b5fe3c | ||
042 | |a dc | ||
100 | 1 | 0 | |a Tzu-Hung Hsiao |e author |
700 | 1 | 0 | |a Ren Ching Wang |e author |
700 | 1 | 0 | |a Ren Ching Wang |e author |
700 | 1 | 0 | |a Tsai-Jung Lu |e author |
700 | 1 | 0 | |a Chien-Hung Shih |e author |
700 | 1 | 0 | |a Yu-Chen Su |e author |
700 | 1 | 0 | |a Jia-Rong Tsai |e author |
700 | 1 | 0 | |a Pei-Pei Jhan |e author |
700 | 1 | 0 | |a Cai-Sian Lia |e author |
700 | 1 | 0 | |a Han-Ni Chuang |e author |
700 | 1 | 0 | |a Kuang-Hsi Chang |e author |
700 | 1 | 0 | |a Kuang-Hsi Chang |e author |
700 | 1 | 0 | |a Kuang-Hsi Chang |e author |
700 | 1 | 0 | |a Chieh-Lin Teng |e author |
700 | 1 | 0 | |a Chieh-Lin Teng |e author |
700 | 1 | 0 | |a Chieh-Lin Teng |e author |
245 | 0 | 0 | |a Chemoresponse of de novo Acute Myeloid Leukemia to "7+3" Induction can Be Predicted by c-Myc-facilitated Cytogenetics |
260 | |b Frontiers Media S.A., |c 2021-04-01T00:00:00Z. | ||
500 | |a 1663-9812 | ||
500 | |a 10.3389/fphar.2021.649267 | ||
520 | |a Background: Identifying patients with de novo acute myeloid leukemia (AML) who will probably respond to the "7 + 3" induction regimen remains an unsolved clinical challenge. This study aimed to identify whether c-Myc could facilitate cytogenetics to predict a "7 + 3" induction chemoresponse in de novo AML.Methods: We stratified 75 untreated patients (24 and 51 from prospective and retrospective cohorts, respectively) with de novo AML who completed "7 + 3" induction into groups with and without complete remission (CR). We then compared Myc-associated molecular signatures between the groups in the prospective cohort after gene set enrichment analysis. The expression of c-Myc protein was assessed by immunohistochemical staining. We defined high c-Myc-immunopositivity as > 40% of bone marrow myeloblasts being c-Myc (+).Results: Significantly more Myc gene expression was found in patients who did not achieve CR by "7 + 3" induction than those who did (2439.92 ± 1868.94 vs. 951.60 ± 780.68; p = 0.047). Expression of the Myc gene and c-Myc protein were positively correlated (r = 0.495; p = 0.014). Although the non-CR group did not express more c-Myc protein than the CR group (37.81 ± 25.13% vs. 29.04 ± 19.75%; p = 0.151), c-Myc-immunopositivity could be a surrogate to predict the "7 + 3" induction chemoresponse (specificity: 81.63%). More importantly, c-Myc-immunopositivity facilitated cytogenetics to predict a "7 + 3" induction chemoresponse by increasing specificity from 91.30 to 95.92%.Conclusion: The "7 + 3" induction remains the standard of care for de novo AML patients, especially for those without a high c-Myc-immunopositivity and high-risk cytogenetics. However, different regimens might be considered for patients with high c-Myc-immunopositivity or high-risk cytogenetics. | ||
546 | |a EN | ||
690 | |a induction chemotherapy | ||
690 | |a "7+3" | ||
690 | |a myc (c-Myc) | ||
690 | |a acute myeloid leukemia | ||
690 | |a chemoresponse | ||
690 | |a Therapeutics. Pharmacology | ||
690 | |a RM1-950 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Frontiers in Pharmacology, Vol 12 (2021) | |
787 | 0 | |n https://www.frontiersin.org/articles/10.3389/fphar.2021.649267/full | |
787 | 0 | |n https://doaj.org/toc/1663-9812 | |
856 | 4 | 1 | |u https://doaj.org/article/8c202f7fc4614b8197ae2142b0b5fe3c |z Connect to this object online. |