## Abstract ## BACKGROUND. The management of recurrent or refractory Hodgkin lymphoma (HL) remains challenging. The objective of this phase 2 trial was to investigate the activity of gemcitabine in combination with rituximab in patients with recurring or refractory HL. ## METHODS. Patients were
A pilot study of rituximab in patients with recurrent, classic Hodgkin disease
โ Scribed by Anas Younes; Jorge Romaguera; Frederick Hagemeister; Peter McLaughlin; Maria Alma Rodriguez; Paolo Fiumara; Andre Goy; Sima Jeha; John T. Manning Jr.; Dan Jones; Lynne V. Abruzzo; L. Jeffrey Medeiros
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 152 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
BACKGROUND
To explore the potential role of infiltrating benign B cells in classic Hodgkin disease (HD) lesions in supporting the survival of malignant Hodgkin and ReedโSternberg (H/RS) cells, the authors initiated a pilot study of rituximab. Rituximab is used to primarily deplete normal B cells from HD lesions.
METHODS
Patients with recurrent, classic HD who had received a minimum of two prior treatment regimens, regardless of whether H/RS cells expressed CD20, were treated with 6 weekly doses of 375 mg/m^2^ rituximab to selectively deplete infiltrating benign B cells. Objective tumor response was determined 3 weeks after completion of the last dose of rituximab and every 3 months thereafter. Serum samples were collected from patients before they started rituximab therapy and 3 weeks after the final course of rituximab. Serum cytokine levels of interleukin 6 (ILโ6), ILโ10, ILโ12, ILโ13, and interferon ฮณ were determined using commercially available enzymeโlinked immunosorbent assay kits.
RESULTS
Twentyโtwo patients with nodular sclerosis histology were evaluable for treatment response. Five patients (22%) achieved partial or complete remission that lasted for a median of 7.8 months (range, 3.3โ14.9 months). Remissions were observed in patients only at lymph node and splenic sites, but not at extranodal sites, and were irrespective of CD20 expression by H/RS cells. Furthermore, systemic (B) symptoms resolved in six of seven patients after therapy. In two patients, partial remissions were associated with a decline in serum ILโ6 levels.
CONCLUSIONS
The current data suggest that rituximab therapy in patients with recurrent, classic HD can alter serum ILโ6 cytokine levels, can improve B symptoms, and may result in clinical remissions. Cancer 2003;98:310โ4. ยฉ 2003 American Cancer Society.
DOI 10.1002/cncr.11511
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