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Oncology Communications Skills
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Medical Learning Institute Inc
Home
CME Activities
Educational Series
Featured Educational Series
Oncology Communications Skills
Shedding Light on T2D
The Evolution of HCT: NMPD Series
Vaccines in Older Adults Series
Accreditation
About MLI Accreditation
About Us
About MLI
Societies and Partners
CE Coordinator Incentive Program (CECIP)
Contact Us
Please fill out the pre-assessment below before the session begins.
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1. Which of the following has been shown to improve survival in patients with newly diagnosed FLT3-ITD mutated AML?
*
A. Addition of quizartinib to the initial induction chemotherapy
B. Addition of revumenib to the initial induction chemotherapy
C. Autologous stem cell transplant as a component of salvage therapy
D. Gilteritinib in combination with intensive chemotherapy
2. Which of the following statements regarding the use of menin inhibitors in AML is correct?
A. Addition of menin inhibitors to frontline induction regimens has clearly demonstrated higher response in patients with NPM1 mutated or KMT2A rearranged AML
B. Menin inhibitors have proven efficacy in the treatment of patients with relapsed NPM1 mutated or KMT2A rearranged AML
C. Menin inhibitor therapy has not been associated with differentiation syndrome
D. Menin inhibitors cannot be combined with other agents due to their significant toxicity profile
3. Which of the following statements regarding low intensity therapy in patients with AML is true?
A. Lower intensity therapy with hypomethylating agents and venetoclax should be offered to all newly diagnosed patients with AML.
B. Addition of a third agent such as IDH inhibitors or FLT3 inhibitors to the combination of HMA and venetoclax has been associated with lower response rates and should be avoided.
C. MRD monitoring is not appropriate in the setting of lower intensity therapy as the responses are not deep enough.
D. The response and long-term survival associated with HMA plus venetoclax are highly dependent on AML biology and molecular profile.
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