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A Retrospective Study on Extranodal Lymphoma or Lymphoma of Rare Pathological Types

A Retrospective Study on Extranodal Lymphoma or Lymphoma of Rare Pathological Types

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05907447
Enrollment
10000
Registered
2023-06-18
Start date
2023-07-01
Completion date
2024-10-01
Last updated
2023-06-18

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

Conditions

Anaplastic Large Cell Lymphoma, Angioimmunoblastic T-cell Lymphoma, Diffuse Large B Cell Lymphoma, Extranodal Lymphoma, Intravascular Large B-Cell Lymphoma, Lymphoma, Marginal Zone Lymphoma, Mucosa-Associated Lymphoid Tissue Lymphoma, NK/T-Cell Lymphoma, Nasal and Nasal-Type

Keywords

LYMPHOMA, EXTRANODAL

Brief summary

The aim of this study is to retrospectively collect clinical information on patients with extranodal or rare lymphomas, and to explore the best treatment strategy for these lymphomas in the real-world population.

Detailed description

Lymphoma is a highly common malignant tumor in Asia. For specific extra-abdominal sites or rare pathological subtypes of lymphoma, traditional chemotherapy protocols often cannot provide satisfactory results for patients. This study aims to retrospectively collect clinical information on patients with extranodal lymphoma or rare pathological subtype lymphoma, including the distribution of involved sites, clinical and molecular characteristics of different lymphoma subtypes, clinical treatment protocols, and prognosis, to explore the best treatment strategy for these lymphomas in the real-world population.

Interventions

No interventions need to be specified for this study

Sponsors

Nanfang Hospital, Southern Medical University
CollaboratorOTHER
Fujian Medical University Union Hospital
CollaboratorOTHER
Peking University Third Hospital
CollaboratorOTHER
Peking University People's Hospital
CollaboratorOTHER
Peking Union Medical College Hospital
CollaboratorOTHER
Beijing Hospital
CollaboratorOTHER_GOV
The Second Affiliated Hospital of Dalian Medical University
CollaboratorOTHER
The First Affiliated Hospital of Guangzhou Medical University
CollaboratorOTHER
Henan Provincial People's Hospital
CollaboratorOTHER
Hunan Cancer Hospital
CollaboratorOTHER
Henan Cancer Hospital
CollaboratorOTHER_GOV
The First Hospital of Jilin University
CollaboratorOTHER
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
CollaboratorOTHER
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
CollaboratorOTHER
Affiliated Hospital of Nantong University
CollaboratorOTHER
The First Affiliated Hospital of Xiamen University
CollaboratorOTHER
Shandong Provincial Hospital
CollaboratorOTHER_GOV
Shanxi Province Cancer Hospital
CollaboratorOTHER
RenJi Hospital
CollaboratorOTHER
Beijing Friendship Hospital
CollaboratorOTHER
West China Hospital
CollaboratorOTHER
The First Affiliated Hospital of Soochow University
CollaboratorOTHER
Tongji Hospital
CollaboratorOTHER
Second Affiliated Hospital, School of Medicine, Zhejiang University
CollaboratorOTHER
Sun Yat-sen University
CollaboratorOTHER
Chongqing University Cancer Hospital
CollaboratorOTHER
Anhui Provincial Cancer Hospital
CollaboratorOTHER
The General Hospital of Northern Theater Command
CollaboratorOTHER
Qilu Hospital of Shandong University
CollaboratorOTHER
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
The Affiliated Hospital Of Guizhou Medical University
CollaboratorOTHER
Wuhan TongJi Hospital
CollaboratorOTHER
General Hospital of Ningxia Medical University
CollaboratorOTHER
The First Affiliated Hospital of Nanchang University
CollaboratorOTHER
The First Affiliated Hospital with Nanjing Medical University
CollaboratorOTHER
Anshan Central Hospital
CollaboratorOTHER
Hainan Cancer Hospital
CollaboratorOTHER
Fifth Affiliated Hospital of Guangzhou Medical University
CollaboratorOTHER
The First Affiliated Hospital of Anhui Medical University
CollaboratorOTHER
The Affiliated Hospital of Xuzhou Medical University
CollaboratorOTHER
First Affiliated Hospital of Harbin Medical University
CollaboratorOTHER
Zhujiang Hospital
CollaboratorOTHER
Ruijin Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

1. Age ≥ 18 years (including 18 years old). 2. Patients newly diagnosed with non-Hodgkin lymphoma with extranodal involvement, whether it is primary, secondary, or cannot be determined; Or patients newly diagnosed with non-Hodgkin lymphoma of rare pathological types, including IVLBCL, SMZL, ALCL, AITL, MALTL. 3. Patients who have received systematic clinical treatment. 4. Patients with measurable lesions, at least containing one effective evaluation of efficacy.

Exclusion criteria

1. Patients who only receive supportive treatment. 2. Patients who cannot obtain effective evaluation data of efficacy.

Design outcomes

Primary

MeasureTime frameDescription
Progression Free Survival (PFS)Baseline up to data cut-off (up to approximately 1 year)Progression-Free Survival (PFS) will be defined from the date of starting therapy and the date of disease progression, relapse or death from any cause.
Overall Survival (OS)Baseline up to data cut-off (up to approximately 1 year)Overall Survival (OS) will be defined from the start date of therapy to the date of death from any cause.

Secondary

MeasureTime frameDescription
Clinical characteristics formBaseline up to data cut-off (up to approximately 1 year)Clinical characteristics from data filled into registry forms by physicians and data managers, including but not limited to values of lactate dehydrogenase, clinical stage, performance status, age ≥ 60 years and number and location of extranodal localizations.
Biological characteristics formBaseline up to data cut-off (up to approximately 1 year)Biological characteristics from data filled into registry forms by physicians and data managers, such as immunohistochemical differences and genetic mutation characteristics of non-hodgkin´s lymphomas.

Countries

China

Contacts

Primary ContactWeili Prof. Zhao
zwl_trial@163.com+862164370045
Backup ContactPengpeng Prof. Xu
pengpeng_xu@126.com+862164370045

Outcome results

None listed

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