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Treatment Effectiveness with Venetoclax-Based Therapy after Bruton Tyrosine Kinase Inhibitors in Chronic Lymphocytic Leukemia: An International Real-World Study
Abstract
Introduction: Venetoclax has demonstrated consistent efficacy and manageable toxicity in patients with previously untreated or relapsed/refractory (R/R) chronic lymphocytic leukemia/small lymphocytic leukemia (CLL/SLL). However, evidence on venetoclax use in patients previously treated with Bruton tyrosine kinase inhibitors (BTKi) is limited. This real-world evidence (RWE) study assessed clinical outcomes of patients who received venetoclax after covalent BTKi (cBTKi) therapy, i.e., response rates, time to next treatment or death (TTNT-D), and progression-free survival (PFS), overall and stratified by line of therapy. Methods: The CLL Collaborative Study of Real-World Evidence (CORE), a retrospective, international, observational study (23 centers) provided data for this analysis. Adult patients diagnosed with CLL/SLL were included if they received a venetoclax-based regimen after discontinuation of a cBTKi-based regimen. Baseline characteristics at venetoclax initiation were summarized using descriptive statistics. Overall response rate (ORR) was calculated as the proportion of patients with complete response (CR) or partial response (PR) among patients with documented responses as recorded in the patients' medical charts based on physician assessment. TTNT-D was measured from date of venetoclax initiation to change of treatment/death (event) or end of follow-up, while PFS was measured from date of venetoclax initiation to disease progression/death (event) or end of follow-u…
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“These results suggest that venetoclax is effective following cBTKi therapy particularly when used as second or third line treatment (61).”
From Resistance Mechanisms and Approach to Chronic Lymphocytic Leukemia after BTK Inhibitor Therapy (2025) · cites this paper as [61]
In the citing paper
“Of 127 (69.0%)patients evaluable for response, the ORR was 78.0% (CR rate 43.3%) and the median PFS was 43.2 months (95% CI, 31.9 to NR).”
From Resistance Mechanisms and Approach to Chronic Lymphocytic Leukemia after BTK Inhibitor Therapy (2025) · cites this paper as [61]
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Self-citationA Review of Resistance Mechanisms to Bruton’s Kinase Inhibitors in Chronic Lymphocytic Leukemia
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Roeker, L. E., Burke, J. M., Rhodes, J. M., Emechebe, N. C., Jawaid, D., Manzoor, B. S., Jensen, C. E., Ryland, L. K., Liu, Y., Marx, S. E., et al. (2025) · Cancers · doi:10.3390/cancers17050799 · Cited by 8
Self-citationResistance Mechanisms and Approach to Chronic Lymphocytic Leukemia after BTK Inhibitor Therapy
Gruessner, C., Wiestner, A., & Sun, C. (2025) · Leukemia & Lymphoma · doi:10.1080/10428194.2025.2466101 · Cited by 6
“%] due to progression) and initiated venetoclax-based therapy (115 venetoclax monotherapy and 69 venetoclax combined with rituximab or obinutuzumab) [60].”
InfluentialJain, N., Eyre, T. A., Winfree, K. B., Bhandari, N. R., Khanal, M., Sugihara, T., Chen, Y., Abada, P., & Patel, K. (2025) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2025.2482132 · Cited by 5
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Metadata
- Authors
- Ghosh, N., Lamanna, N., Eyre, T. A., Coombs, C. C., Manzoor, B. S., Brown, J. R., Tuncer, H. H., Ujjani, C. S., Leslie, L. A., Roeker, L. E., Davids, M. S., Rhodes, J. M., Skarbnik, A., Emechebe, N., Fleury, I., Hill, B. T., Fox, C. P., Barr, P. M., Jawaid, D., Sinai, W. J., Pearson, L. K., Lansigan, F., Choi, Y., Jensen, C. E., Schuster, S. J., Kennard, K., Pivneva, I., Watson, T., Guerin, A., & Shadman, M.
- Affiliations
- Levine Cancer Institute (US)
- Columbia University (US)
- Churchill Hospital (GB)
- University of California, Irvine (US)
- AbbVie (United States) (US)
- Dana-Farber Cancer Institute (US)
- Fred Hutch Cancer Center (US)
- Hackensack University Medical Center (US)
- Memorial Sloan Kettering Cancer Center (US)
- Rutgers Cancer Institute (US)
- 11Novant Health Cancer Institute, Lymphoma and CLL Program, Charlotte, NC
- Hôpital Maisonneuve-Rosemont (CA)
- Cleveland Clinic (US)
- University of Nottingham (GB)
- University of Rochester Medicine (US)
- University of Massachusetts Chan Medical School (US)
- Dartmouth–Hitchcock Medical Center (US)
- Tufts Medical Center (US)
- University of North Carolina at Chapel Hill (US)
- University of Pennsylvania (US)
- Concordia University (CA)
- 21Analysis Group, Inc., Montreal, Canada
- ORCID
- Ghosh, Nilanjan
- Lamanna, Nicole
- Eyre, Toby A.
- Coombs, Catherine C
- Manzoor, Beenish S
- Brown, Jennifer R.
- Tuncer, Hande H.
- Ujjani, Chaitra S
- Leslie, Lori A
- Roeker, Lindsey E.
- Davids, Matthew S
- Rhodes, Joanna M.
- Skarbnik, Alan
- Fleury, Isabelle
- Hill, Brian T.
- Fox, Christopher P.
- Barr, Paul M.
- Lansigan, Frederick
- Choi, Yun
- Jensen, Christopher E.
- Schuster, Stephen J.
- Pivneva, Irina
- Shadman, Mazyar
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2023-11-02
- Volume
- 142
- Issue
- Supplement 1
- Pages
- 1908-1908
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W4389248231
- Cited by
- 6
- References
- 0
- Citations by year
- 2025: 4 · 2024: 2
- Type
- conference abstract
- Language
- en
- Open access
- closed
- Locations
- Blood (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Chronic Lymphocytic Leukemia Research
- Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphoma Diagnosis and Treatment
- Health Sciences › Medicine › Hematology › Acute Lymphoblastic Leukemia research
- Keywords
- venetoclax, BTK inhibitors, chronic lymphocytic leukemia, small lymphocytic leukemia, relapsed/refractory CLL, treatment discontinuation, progression-free survival, time to next treatment, overall response rate, rituximab, obinutuzumab, ibrutinib, zanubrutinib, acalabrutinib
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