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
Conditions
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| 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
| Measure | Time frame | Description |
|---|---|---|
| Clinical characteristics form | Baseline 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 form | Baseline 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