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Current Status of BTKi Treatment for CLL/SLL in China

Current Status and Influencing Factors of Chinese Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Undergoing Treatment With Bruton's Tyrosine Kinase Inhibitors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06508684
Enrollment
1000
Registered
2024-07-18
Start date
2024-07-13
Completion date
2025-07-12
Last updated
2024-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CLL/SLL

Brief summary

BTKi has become the standard treatment regimen for CLL/SLL,there is a lack of large-scale real-world studies on the use status and related influencing factors of BTK inhibitors. Therefore, we plan to conduct this multicenter retrospective cross-sectional study to understand the current situation of BTK inhibitor treatment for CLL/SLL patients in China and the related influencing factors, and to explore more suitable treatment patterns based on this.

Interventions

BTKi can refer to Orelabrutinib, Ibrutinib, Zanubrutinib, and Acalabrutinib

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years; * Patients with a confirmed diagnosis of CLL/SLL; * Received BTK inhibitor treatment between February 2023 and February 2024.

Exclusion criteria

* Patients with other types of lymphoma; * Cases deemed unsuitable for inclusion in this study by the investigators.

Design outcomes

Primary

MeasureTime frameDescription
Patient characteristics of those receiving BTKi treatmentup to one yearDescribe the patient characteristics of those receiving BTKi treatment, including age, gender, etc

Secondary

MeasureTime frameDescription
overall response rateup to one yearAssessed according to the iwCLL2018 criteria
Incidence of adverse reactionsup to one yearAssessed according to the CTCAE 5.0 criteria

Countries

China

Contacts

Primary ContactHuayuan Zhu, MD
huayuan.zhu@hotmail.com025-58530260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026