Prognosis
Surveillance, Epidemiology, and End Results (SEER) Program data (2000-2020) report the following relative survival rates (all stages) by time since diagnosis:[77]
92.4% (2-year survival)
84.8% (5-year survival)
71.8% (10-year survival)
Targeted therapies, particularly Bruton tyrosine kinase (BTK) inhibitors (e.g., ibrutinib, acalabrutinib, zanubrutinib), B-cell lymphoma-2 protein (BCL2) inhibitors (e.g., venetoclax), and phosphoinositide 3-kinase (PI3K) inhibitors (e.g., duvelisib, idelalisib), are particularly useful in patients with a poor prognosis (del(17p) or TP53 mutation; relapsed/refractory disease).[75] Survival among patients with a poor prognosis may now exceed 8 years.[78]
Prognostic outcomes are likely to improve with increasing availability of targeted therapies.
Использование этого контента попадает под действие нашего заявления об отказе от ответственности