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- W4311338538 abstract "Testing for poor prognostic factors such as del(17p) chromosomal anomaly, mutated TP53 or NOTCH1, and unmutated IGHV has significant relevance in guiding therapy in CLL as these markers have significant impact on outcomes and progression. Although, international and national guidelines are widely available, little is known about real-world testing. Here, we investigated real-world clinical practices on CLL prognostic testing in Belgium, France, Germany, Italy, the Netherlands, Spain, Sweden, and the United Kingdom." @default.
- W4311338538 created "2022-12-25" @default.
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- W4311338538 date "2022-12-01" @default.
- W4311338538 modified "2023-09-27" @default.
- W4311338538 title "RWD38 Genetic Mutational Testing in CLL Patients in the Routine Care of Eight EU Member States" @default.
- W4311338538 doi "https://doi.org/10.1016/j.jval.2022.09.2263" @default.
- W4311338538 hasPublicationYear "2022" @default.
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