Skip to main content

Advertisement

Advertisement

Advertisement

Advertisement

ADVERTISEMENT

Chronic Lymphocytic Leukemia Specialty Channel

Chronic Lymphocytic Leukemia
Specialty Channel
Moritz Furstenau, MD
Conference Coverage
06/26/2024

Featuring Moritz Furstenau, MD

Featuring Moritz Furstenau, MD ...
At the 65th ASH Annual Meeting, Moritz Furstenau, MD, presented a follow-up analysis of the CLL2-Baag trial on the efficacy and ctDNA analysis of acalabrutinib, venetoclax, and obinutuzumab combination therapy after optional debulking with...
At the 65th ASH Annual Meeting, Moritz Furstenau, MD, presented a follow-up analysis of the CLL2-Baag trial on the efficacy and ctDNA analysis of acalabrutinib, venetoclax, and obinutuzumab combination therapy after optional debulking with...
At the 65th ASH Annual Meeting,...
06/26/2024
Oncology
News
04/18/2024

Amber Denham

Amber Denham
According to phase 3b results from the VENICE-1 trial, venetoclax monotherapy demonstrates durable responses in adult patients with relapsed/refractory chronic lymphocytic leukemia, including BCRi-pretreated patients.
According to phase 3b results from the VENICE-1 trial, venetoclax monotherapy demonstrates durable responses in adult patients with relapsed/refractory chronic lymphocytic leukemia, including BCRi-pretreated patients.
According to phase 3b results...
04/18/2024
Oncology
FDA Approval
03/25/2024

Amber Denham

Amber Denham
The FDA granted accelerated approval to lisocabtagene maraleucel for adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who have received at least 2 prior lines of therapy, including a BTK...
The FDA granted accelerated approval to lisocabtagene maraleucel for adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who have received at least 2 prior lines of therapy, including a BTK...
The FDA granted accelerated...
03/25/2024
Oncology
News
03/15/2024

Amber Denham

Amber Denham
According to 5-year follow-up data, ibrutinib plus fludarabine, cyclophosphamide, and rituximab followed by 2 years of ibrutinib maintenance led to durably deep responses in patients with previously untreated chronic lymphocytic leukemia with...
According to 5-year follow-up data, ibrutinib plus fludarabine, cyclophosphamide, and rituximab followed by 2 years of ibrutinib maintenance led to durably deep responses in patients with previously untreated chronic lymphocytic leukemia with...
According to 5-year follow-up...
03/15/2024
Oncology
News
02/05/2024

Amber Denham

Amber Denham
Venetoclax-obinutuzumab achieved frequent, durable, and safe responses among patients with relapsed/refractory chronic lymphocytic leukemia/small lymphocytic leukemia, according to a retrospective, real-world study.
Venetoclax-obinutuzumab achieved frequent, durable, and safe responses among patients with relapsed/refractory chronic lymphocytic leukemia/small lymphocytic leukemia, according to a retrospective, real-world study.
Venetoclax-obinutuzumab achieved...
02/05/2024
Oncology
News
02/05/2024

Amber Denham

Amber Denham
Measurable residual disease-directed ibrutinib–venetoclax treatment improved progression-free survival compared with fludarabine–cyclophosphamide–rituximab treatment for patients with untreated chronic lymphocytic leukemia, according to a...
Measurable residual disease-directed ibrutinib–venetoclax treatment improved progression-free survival compared with fludarabine–cyclophosphamide–rituximab treatment for patients with untreated chronic lymphocytic leukemia, according to a...
Measurable residual...
02/05/2024
Oncology
News
01/24/2024

Amber Denham

Amber Denham
CD19 CAR T-cell therapy achieved durable responses among a subset of patients with high-risk, R/R chronic lymphocytic leukemia, according to a phase 1/2 study which explored factors associated with long-term outcomes.
CD19 CAR T-cell therapy achieved durable responses among a subset of patients with high-risk, R/R chronic lymphocytic leukemia, according to a phase 1/2 study which explored factors associated with long-term outcomes.
CD19 CAR T-cell therapy achieved...
01/24/2024
Oncology
Adrian Wiestner, MD
Conference Coverage
01/12/2024

Featuring Adrian Wiestner, MD

Featuring Adrian Wiestner, MD
At the 65th ASH Annual Meeting, Adrian Wiestner, MD, discusses exciting possibilities for the future of chronic lymphocytic leukemia treatment, including the prospect of time-limited treatment periods and T-cell-engaging bispecific antibodies.
At the 65th ASH Annual Meeting, Adrian Wiestner, MD, discusses exciting possibilities for the future of chronic lymphocytic leukemia treatment, including the prospect of time-limited treatment periods and T-cell-engaging bispecific antibodies.
At the 65th ASH Annual Meeting,...
01/12/2024
Oncology
News
11/20/2023

Amber Denham

Amber Denham
Phase 1/2 trial results demonstrated that lisocabtagene maraleucel treatment induced complete response or remission, including with incomplete marrow recovery, among patients with R/R chronic lymphocytic leukemia or small lymphocytic lymphoma.
Phase 1/2 trial results demonstrated that lisocabtagene maraleucel treatment induced complete response or remission, including with incomplete marrow recovery, among patients with R/R chronic lymphocytic leukemia or small lymphocytic lymphoma.
Phase 1/2 trial results...
11/20/2023
Oncology
Quiz
10/31/2023
The addition of venetoclax therapy among patients with high-risk chronic lymphocytic leukemia who had received at least ___ months or more of ibrutinib treatment achieved a high rate of undetectable measurable residual disease (U-MRD) in the...
The addition of venetoclax therapy among patients with high-risk chronic lymphocytic leukemia who had received at least ___ months or more of ibrutinib treatment achieved a high rate of undetectable measurable residual disease (U-MRD) in the...
The addition of venetoclax...
10/31/2023
Oncology
Quiz
10/05/2023
The addition of venetoclax therapy yielded high rates of undetectable measurable residual disease (U-MRD) in the bone marrow among patients with CLL who had received ibrutinib for ≥12 months and had high-risk features, including ___.
The addition of venetoclax therapy yielded high rates of undetectable measurable residual disease (U-MRD) in the bone marrow among patients with CLL who had received ibrutinib for ≥12 months and had high-risk features, including ___.
The addition of venetoclax...
10/05/2023
Oncology

Advertisement

News

Moritz Furstenau, MD
Conference Coverage
06/26/2024

Featuring Moritz Furstenau, MD

Featuring Moritz Furstenau, MD ...
At the 65th ASH Annual Meeting, Moritz Furstenau, MD, presented a follow-up analysis of the CLL2-Baag trial on the efficacy and ctDNA analysis of acalabrutinib, venetoclax, and obinutuzumab combination therapy after optional debulking with...
At the 65th ASH Annual Meeting, Moritz Furstenau, MD, presented a follow-up analysis of the CLL2-Baag trial on the efficacy and ctDNA analysis of acalabrutinib, venetoclax, and obinutuzumab combination therapy after optional debulking with...
At the 65th ASH Annual Meeting,...
06/26/2024
Oncology
News
04/18/2024

Amber Denham

Amber Denham
According to phase 3b results from the VENICE-1 trial, venetoclax monotherapy demonstrates durable responses in adult patients with relapsed/refractory chronic lymphocytic leukemia, including BCRi-pretreated patients.
According to phase 3b results from the VENICE-1 trial, venetoclax monotherapy demonstrates durable responses in adult patients with relapsed/refractory chronic lymphocytic leukemia, including BCRi-pretreated patients.
According to phase 3b results...
04/18/2024
Oncology
FDA Approval
03/25/2024

Amber Denham

Amber Denham
The FDA granted accelerated approval to lisocabtagene maraleucel for adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who have received at least 2 prior lines of therapy, including a BTK...
The FDA granted accelerated approval to lisocabtagene maraleucel for adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who have received at least 2 prior lines of therapy, including a BTK...
The FDA granted accelerated...
03/25/2024
Oncology
News
03/15/2024

Amber Denham

Amber Denham
According to 5-year follow-up data, ibrutinib plus fludarabine, cyclophosphamide, and rituximab followed by 2 years of ibrutinib maintenance led to durably deep responses in patients with previously untreated chronic lymphocytic leukemia with...
According to 5-year follow-up data, ibrutinib plus fludarabine, cyclophosphamide, and rituximab followed by 2 years of ibrutinib maintenance led to durably deep responses in patients with previously untreated chronic lymphocytic leukemia with...
According to 5-year follow-up...
03/15/2024
Oncology
News
02/05/2024

Amber Denham

Amber Denham
Venetoclax-obinutuzumab achieved frequent, durable, and safe responses among patients with relapsed/refractory chronic lymphocytic leukemia/small lymphocytic leukemia, according to a retrospective, real-world study.
Venetoclax-obinutuzumab achieved frequent, durable, and safe responses among patients with relapsed/refractory chronic lymphocytic leukemia/small lymphocytic leukemia, according to a retrospective, real-world study.
Venetoclax-obinutuzumab achieved...
02/05/2024
Oncology
News
02/05/2024

Amber Denham

Amber Denham
Measurable residual disease-directed ibrutinib–venetoclax treatment improved progression-free survival compared with fludarabine–cyclophosphamide–rituximab treatment for patients with untreated chronic lymphocytic leukemia, according to a...
Measurable residual disease-directed ibrutinib–venetoclax treatment improved progression-free survival compared with fludarabine–cyclophosphamide–rituximab treatment for patients with untreated chronic lymphocytic leukemia, according to a...
Measurable residual...
02/05/2024
Oncology
News
01/24/2024

Amber Denham

Amber Denham
CD19 CAR T-cell therapy achieved durable responses among a subset of patients with high-risk, R/R chronic lymphocytic leukemia, according to a phase 1/2 study which explored factors associated with long-term outcomes.
CD19 CAR T-cell therapy achieved durable responses among a subset of patients with high-risk, R/R chronic lymphocytic leukemia, according to a phase 1/2 study which explored factors associated with long-term outcomes.
CD19 CAR T-cell therapy achieved...
01/24/2024
Oncology
Adrian Wiestner, MD
Conference Coverage
01/12/2024

Featuring Adrian Wiestner, MD

Featuring Adrian Wiestner, MD
At the 65th ASH Annual Meeting, Adrian Wiestner, MD, discusses exciting possibilities for the future of chronic lymphocytic leukemia treatment, including the prospect of time-limited treatment periods and T-cell-engaging bispecific antibodies.
At the 65th ASH Annual Meeting, Adrian Wiestner, MD, discusses exciting possibilities for the future of chronic lymphocytic leukemia treatment, including the prospect of time-limited treatment periods and T-cell-engaging bispecific antibodies.
At the 65th ASH Annual Meeting,...
01/12/2024
Oncology
News
11/20/2023

Amber Denham

Amber Denham
Phase 1/2 trial results demonstrated that lisocabtagene maraleucel treatment induced complete response or remission, including with incomplete marrow recovery, among patients with R/R chronic lymphocytic leukemia or small lymphocytic lymphoma.
Phase 1/2 trial results demonstrated that lisocabtagene maraleucel treatment induced complete response or remission, including with incomplete marrow recovery, among patients with R/R chronic lymphocytic leukemia or small lymphocytic lymphoma.
Phase 1/2 trial results...
11/20/2023
Oncology
News
09/21/2023

Jordan Kadish

Jordan Kadish
A phase 2 trial found that ibrutinib plus rituximab demonstrated efficacy among patients with CLL and steroid refractory autoimmune cytopenias such as autoimmune hemolytic anemia and pure red cell aplasia.
A phase 2 trial found that ibrutinib plus rituximab demonstrated efficacy among patients with CLL and steroid refractory autoimmune cytopenias such as autoimmune hemolytic anemia and pure red cell aplasia.
A phase 2 trial found that...
09/21/2023
Oncology

Interactive Features

Quiz
10/31/2023
The addition of venetoclax therapy among patients with high-risk chronic lymphocytic leukemia who had received at least ___ months or more of ibrutinib treatment achieved a high rate of undetectable measurable residual disease (U-MRD) in the...
The addition of venetoclax therapy among patients with high-risk chronic lymphocytic leukemia who had received at least ___ months or more of ibrutinib treatment achieved a high rate of undetectable measurable residual disease (U-MRD) in the...
The addition of venetoclax...
10/31/2023
Oncology
Quiz
10/05/2023
The addition of venetoclax therapy yielded high rates of undetectable measurable residual disease (U-MRD) in the bone marrow among patients with CLL who had received ibrutinib for ≥12 months and had high-risk features, including ___.
The addition of venetoclax therapy yielded high rates of undetectable measurable residual disease (U-MRD) in the bone marrow among patients with CLL who had received ibrutinib for ≥12 months and had high-risk features, including ___.
The addition of venetoclax...
10/05/2023
Oncology
Quiz
09/01/2023
True or False: Results of the phase 3 GLOW trial indicated that ibrutinib plus venetoclax treatment did not improve progression-free survival compared to treatment with chlorambucil and obinutuzumab among older patients with previously...
True or False: Results of the phase 3 GLOW trial indicated that ibrutinib plus venetoclax treatment did not improve progression-free survival compared to treatment with chlorambucil and obinutuzumab among older patients with previously...
True or False: Results of the...
09/01/2023
Oncology
Quiz
05/23/2023
The FDA approved zanubrutinib for CLL or SLL based on efficacy results from the ALPINE trial, which indicated that the overall response rate among patients who received this treatment was ____.
The FDA approved zanubrutinib for CLL or SLL based on efficacy results from the ALPINE trial, which indicated that the overall response rate among patients who received this treatment was ____.
The FDA approved zanubrutinib...
05/23/2023
Oncology
Quiz
12/01/2022
What was the overall survival rate of venetoclax plus rituximab treatment in patients with relapsed/refractory CLL at 3 years following cessation, according to a 5-year update of a phase 3 trial? 
What was the overall survival rate of venetoclax plus rituximab treatment in patients with relapsed/refractory CLL at 3 years following cessation, according to a 5-year update of a phase 3 trial? 
What was the overall survival...
12/01/2022
Oncology
Quiz
12/01/2022
True or false: Obinutuzumab is well-tolerated in patients with chronic lymphocytic leukemia that responded to chemo-immunotherapy, according to a phase 2/3 trial.
True or false: Obinutuzumab is well-tolerated in patients with chronic lymphocytic leukemia that responded to chemo-immunotherapy, according to a phase 2/3 trial.
True or false: Obinutuzumab is...
12/01/2022
Oncology
Quiz
10/12/2022
True or False: Zanubrutinib significantly improved progression-free survival vs bendamustine–rituximab as a frontline therapy for CLL and SLL.
True or False: Zanubrutinib significantly improved progression-free survival vs bendamustine–rituximab as a frontline therapy for CLL and SLL.
True or False: Zanubrutinib...
10/12/2022
Oncology
Quiz
09/05/2022
True or false: MRD-guided, time-limited treatment with ibrutinib plus venetoclax may be beneficial for patients with relapsed/refractory CLL, according to a phase 2 trial.
True or false: MRD-guided, time-limited treatment with ibrutinib plus venetoclax may be beneficial for patients with relapsed/refractory CLL, according to a phase 2 trial.
True or false: MRD-guided,...
09/05/2022
Oncology
Quiz
08/05/2022
True or false: Long-term RESONATE-2 data revealed continual benefit with first-line ibrutinib treatment for CLL, including for patients who have high-risk genomic features?
True or false: Long-term RESONATE-2 data revealed continual benefit with first-line ibrutinib treatment for CLL, including for patients who have high-risk genomic features?
True or false: Long-term...
08/05/2022
Oncology
qqq
Test Your Knowledge
11/22/2021
True or false: the phase 3 UNITY-CLL study found umbralisib plus ublituximab has a tolerable safety profile and prolonged PFS compared to CIT in patients with both TN and PT CLL.
True or false: the phase 3 UNITY-CLL study found umbralisib plus ublituximab has a tolerable safety profile and prolonged PFS compared to CIT in patients with both TN and PT CLL.
True or false: the phase 3...
11/22/2021
Oncology

Advertisement

Advertisement

Advertisement

Advertisement