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Published on: February 17, 2022
Rituximab for primary cutaneous diffuse large B-cell lymphoma-leg type.
Marion Fenot1, Gaelle Quereux, Anabelle Brocard
1Department of Dermato-Oncology, Nantes University Hospital Centre, Nantes Cedex, France.
European Journal of Dermatology : EJD
|October 20, 2010
Summary
Single-agent rituximab shows good initial response rates for primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT). However, all patients relapsed, indicating limited long-term efficacy despite excellent tolerance.
Area of Science:
- Oncology
- Hematology
- Dermatology
Background:
- Primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT) is a rare, aggressive non-Hodgkin lymphoma.
- Elderly patients are predominantly affected, often with a poor prognosis.
- Rituximab, an anti-CD20 monoclonal antibody, is effective in nodal lymphomas but its role in PCDLBCL-LT requires further evaluation.
Purpose of the Study:
- To evaluate the risk-benefit ratio of single-agent rituximab for PCDLBCL-LT.
- To assess objective response rates, adverse effects, disease-free survival, and overall survival.
Main Methods:
- Retrospective study of 8 patients with PCDLBCL-LT treated with single-agent rituximab.
- Evaluation of clinical endpoints including objective response rate, adverse events, and survival data.
Main Results:
- Objective response rate of 75% after 4 courses of rituximab.
- 100% of patients experienced relapse, with a median disease-free survival of 5.25 months.
- Excellent tolerance observed, with only one Grade I adverse event.
Conclusions:
- Single-agent rituximab demonstrates a high initial objective response rate in PCDLBCL-LT but lacks durable therapeutic effects, with all patients relapsing.
- While less effective than combination therapy, rituximab monotherapy offers superior tolerance and may be suitable for short-term palliative care in select patients.
- The risk-benefit profile suggests rituximab monotherapy is a well-tolerated option for palliative treatment, though not curative.