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    Out-of-pocket fees are a barrier to follow-up care after an abnormal cervical cancer screening test. Among commercially insured Virginians, out-of-pocket costs for follow-up services averaged $144/patient; 34% of cervical cancer screenings were classified as low value. Reallocating low-value cervical cancer screening expenditures to enhance coverage for follow-up care can improve screening…

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    • July issue— Rockwell et al. show that reallocating resources from low-value #cervicalcancer spending to fund more generous coverage of necessary follow-up care is a feasible approach to enhancing cervical cancer prevention equity and outcomes. https://t.co/WfYNIYbxnV @vtcsom https://t.co/YiDuvaqZOf https://t.co/WPOqvh3Y7L

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    Abstract. Several FGFR inhibitors are approved or in clinical development for the treatment of FGFR-driven urothelial cancer, and molecular mechanisms of resistance leading to patient relapses have not been fully explored. We identified 21 FGFR-driven urothelial cancer patients treated with selective FGFR inhibitors and analyzed post-progression tissue and/or circulating tumor DNA (ctDNA). We…

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    • #ICYMI— Resistance to Selective #FGFR Inhibitors in FGFR-driven #UrothelialCancer, by Francesco Facchinetti, @Luc_Friboulet et al. https://t.co/Z9E646JlA7 @GustaveRoussy https://t.co/7yEe8HbBgS

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    Abstract. Oncogenic point mutants of isocitrate dehydrogenases 1 and 2 (IDH2) generate 2-hydroxyglutarate (2HG), which inhibits lysine demethylases and increases heterochromatin. Tumor cells expressing IDH mutants are sensitive to poly(ADP) ribose polymerase (PARP) inhibitors, offering an opportunity to eliminate IDH-driven tumor cells in therapy. Expression of an oncogenic IDH1 mutant in cells…

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    • Online now: Read the In The Spotlight Commentary— Heterochromatin-dependent Replication Stress: A Lesson from IDH1/2 Mutants, by @LeeZou8 discussing a recent @MolecularCell paper from Craig Thompson et al. https://t.co/7sNg4JeTlD https://t.co/0YhXgFxQSa