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临床试验/NCT07310186
NCT07310186尚未招募不适用

Salvage Treatment Strategies and Clinical Outcomes in Diffuse Large B-cell Lymphoma After Failure of Polatuzumab Vedotin-based Combination Therapy: A Multi-center, Retro- and Prospective, Observational, Real-World Study

Peking Union Medical College Hospital0 个研究点目标入组 200 人开始时间: 2025年12月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
200
主要终点
complete response rate

研究概览

简要总结

Diffuse Large B-cell Lymphoma (DLBCL) is a common hematologic malignancy. Even after standard first-line treatment, approximately 40% of patients will experience relapse. Currently, polatuzumab vedotin (pola) has been incorporated into DLBCL treatment (both for newly diagnosed and relapsed cases). However, for patients whose disease progresses after pola-containing regimens, the subsequent treatment options, efficacy, and survival outcomes remain unclear. Understanding these real-world scenarios is of great significance, as it can guide clinicians in developing better and more tailored treatment strategies for patients in the future.

Therefore, we plan to conduct this real-world study titled "Salvage Treatment Strategies and Clinical Outcomes in Diffuse Large B-cell Lymphoma After Failure of Polatuzumab Vedotin-based Combination Therapy", aiming to obtain real-world data from the Chinese population.

详细描述

This is a retro- and prospective, observational study

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with DLBCL
  • Age ≥18 years
  • Prior treatment with a polatuzumab vedotin (pola)-containing regimen and confirmed disease progression (refractory/relapsed) after this therapy.
  • Availability of complete electronic medical records and ability to be contacted via telephone.
  • Full understanding of the study, voluntary participation, and willingness to sign the informed consent form.

排除标准

  • Patients who have not received pola-based regimen treatment.
  • Incomplete electronic medical records or unreachable by telephone.

结局指标

主要结局

complete response rate

时间窗: through study completion, an average of 2 years

the ratio of patients achieves complete response

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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