{"title":"Fixed Duration Ibrutinib-Venetoclax, a Redefinition of the CLL Treatment Landscape","authors":"Stefano Molica, David Allsup","doi":"10.1002/hon.70088","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>The fixed-duration combination of ibrutinib and venetoclax (IV) has emerged as a highly effective therapeutic strategy for treating chronic lymphocytic leukemia (CLL), marking a significant shift in the treatment paradigm for this disease. Preclinical studies have demonstrated the synergistic anti-leukemic effects of the elements of this regimen and therefore provide a strong rationale for their combined use in the clinical setting. Clinical trial data of IV has demonstrated substantial improvements in progression-free survival (PFS) rates across both treatment-naïve and relapsed/refractory CLL. Notably, a considerable proportion of patients have achieved undetectable measurable residual disease (uMRD), a key marker of deep remission. However, several critical questions remain unanswered, including the optimal duration of IV and the prognostic significance of uMRD, particularly in high-risk CLL subsets. Whilst uMRD is widely considered a surrogate for deep remission, the precise correlation of this parameter with long-term survival outcomes in IV-treated patients requires further clarification. Moreover, emergent evidence suggests that a prolonged duration of IV therapy, beyond that currently employed, may enhance MRD clearance. Future research should focus on the optimization of BTKi/venetoclax fixed-duration regimens, particularly for elderly and medically unfit patients. In this context, the development of more selective BTKis that minimize adverse events whilst maintaining effective disease control will be crucial.</p>\n </div>","PeriodicalId":12882,"journal":{"name":"Hematological Oncology","volume":"43 3","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hematological Oncology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/hon.70088","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 fixed-duration combination of ibrutinib and venetoclax (IV) has emerged as a highly effective therapeutic strategy for treating chronic lymphocytic leukemia (CLL), marking a significant shift in the treatment paradigm for this disease. Preclinical studies have demonstrated the synergistic anti-leukemic effects of the elements of this regimen and therefore provide a strong rationale for their combined use in the clinical setting. Clinical trial data of IV has demonstrated substantial improvements in progression-free survival (PFS) rates across both treatment-naïve and relapsed/refractory CLL. Notably, a considerable proportion of patients have achieved undetectable measurable residual disease (uMRD), a key marker of deep remission. However, several critical questions remain unanswered, including the optimal duration of IV and the prognostic significance of uMRD, particularly in high-risk CLL subsets. Whilst uMRD is widely considered a surrogate for deep remission, the precise correlation of this parameter with long-term survival outcomes in IV-treated patients requires further clarification. Moreover, emergent evidence suggests that a prolonged duration of IV therapy, beyond that currently employed, may enhance MRD clearance. Future research should focus on the optimization of BTKi/venetoclax fixed-duration regimens, particularly for elderly and medically unfit patients. In this context, the development of more selective BTKis that minimize adverse events whilst maintaining effective disease control will be crucial.
期刊介绍:
Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged:
-Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders
-Diagnostic investigations, including imaging and laboratory assays
-Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases
-Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies
-Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems.
Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.