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CC-122 immunomodulatory effects in refractory patients with diffuse large B-cell lymphoma
Carolina Cubillos-Zapata1, Raúl Cordoba2, José Avendaño-Ortiz3
1The Innate Immune Response Group, IdiPAZ, La Paz University Hospital, Madrid, Spain; Tumor Immunology Laboratory, IdiPAZ, Madrid, Spain; Center for Biomedical Research Network, CIBEres, Madrid, Spain.
Oncoimmunology
|March 4, 2017
Summary
CC-122, a novel compound, shows immunomodulatory effects in diffuse large B-cell lymphoma (DLBCL) patients. It may enhance immune cell activity and offers a potential alternative for refractory DLBCL.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- Diffuse large B-cell lymphoma (DLBCL) is a significant B-cell lymphoid malignancy.
- Novel therapeutic strategies are needed for DLBCL patients refractory to conventional chemotherapy.
- Pleiotropic pathway modifiers, like CC-122, are emerging as promising agents.
Purpose of the Study:
- To evaluate the immunomodulatory effects and efficacy of CC-122 in patients with DLBCL.
- To investigate the impact of CC-122 on immune cell subsets and activity.
- To explore CC-122 as a potential treatment for refractory DLBCL.
Main Methods:
- Phase I clinical trial (NCT01421524) involving three patients.
- Assessment of immunomodulatory effects of CC-122.
- Analysis of immune cell phenotypes, including NK cells, myeloid-derived suppressor cells, and Tregs.
- Monitoring of T cell activation via co-stimulatory molecule CD28.
Main Results:
- CC-122 demonstrated immunomodulatory effects in DLBCL patients.
- Observed regulation of NK cell phenotype and activity.
- Reduced accumulation of myeloid-derived suppressor cells and Tregs.
- Delayed activation of T cells through CD28 co-stimulatory molecule.
Conclusions:
- CC-122 exhibits potential as an immunomodulatory agent in DLBCL.
- The compound may re-regulate immune responses by reducing suppressive cells and enhancing T cell activity.
- CC-122 presents a potential alternative therapeutic option for DLBCL patients resistant to standard chemotherapy.

