{"title":"SOHO State of the Art Updates and Next Questions | The Evolving Landscape of Prognostic Models in Chronic Lymphocytic Leukemia.","authors":"Stefano Molica, Ahmad Ibrahim, David Allsup","doi":"10.1016/j.clml.2025.05.010","DOIUrl":null,"url":null,"abstract":"<p><p>The advent of targeted therapies has profoundly altered the prognostic landscape of chronic lymphocytic leukemia (CLL), demanding a reassessment of established predictive models. Initial frameworks, such as the CLL International Prognostic Index (CLL-IPI), primarily relied on clinical and genetic parameters. However, the growing clinical utility of targeted agents highlights the ongoing need to refine these prognostic tools. Although the CLL-IPI remains a valuable metric for progression-free survival (PFS), its capacity to accurately predict overall survival (OS) has been attenuated by the evolution of therapeutic approaches. Novel prognostic models hold promise by leveraging advanced technologies, sophisticated statistical methods, and computational analytics to improve risk stratification. These innovations address the inherent limitations of conventional models, enabling more precise and individualized prognostic assessments. To maintain clinical utility, however, these models must continuously adapt alongside the rapidly advancing therapeutic landscape of CLL. Optimizing patient outcomes requires a fundamental paradigm shift that integrates a broader and more dynamic array of patient-specific data into prognostic evaluations.</p>","PeriodicalId":10348,"journal":{"name":"Clinical Lymphoma, Myeloma & Leukemia","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Lymphoma, Myeloma & Leukemia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.clml.2025.05.010","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The advent of targeted therapies has profoundly altered the prognostic landscape of chronic lymphocytic leukemia (CLL), demanding a reassessment of established predictive models. Initial frameworks, such as the CLL International Prognostic Index (CLL-IPI), primarily relied on clinical and genetic parameters. However, the growing clinical utility of targeted agents highlights the ongoing need to refine these prognostic tools. Although the CLL-IPI remains a valuable metric for progression-free survival (PFS), its capacity to accurately predict overall survival (OS) has been attenuated by the evolution of therapeutic approaches. Novel prognostic models hold promise by leveraging advanced technologies, sophisticated statistical methods, and computational analytics to improve risk stratification. These innovations address the inherent limitations of conventional models, enabling more precise and individualized prognostic assessments. To maintain clinical utility, however, these models must continuously adapt alongside the rapidly advancing therapeutic landscape of CLL. Optimizing patient outcomes requires a fundamental paradigm shift that integrates a broader and more dynamic array of patient-specific data into prognostic evaluations.
期刊介绍:
Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.