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Case report: Bridging radiation therapy before chimeric antigen receptor T-cell therapy induces sustained remission in patients with relapsed/refractory double-expressor diffuse large B-cell lymphoma with localized compressive symptoms. | LitMetric

AI Article Synopsis

  • - A 66-year-old woman had a type of cancer called double-expressor diffuse large B-cell lymphoma, which didn't get better after two rounds of regular treatments.
  • - She received special CAR-T cell therapy after a type of radiation therapy that helped target her cancer, and she stayed cancer-free for over 9 months.
  • - The patient didn’t have any serious side effects from the radiation or the CAR-T treatment, showing it could be a good option for others with similar cancer.

Article Abstract

Background: High-risk double-expressor diffuse large B-cell lymphoma has an inferior prognosis following standard first-line therapy. After failure of second-line therapy, treatment options are limited if accompanied by localized compressive symptoms. Chimeric Antigen Receptor T cell (CAR-T) therapy preceded by bridging radiotherapy may be an effective emerging therapy.

Case Presentation: We report a 66-year-old female patient diagnosed with stage IV double-expressor diffuse large B-cell lymphoma. The patient achieved progressive disease after two cycles of rituximab, cyclophosphamide, liposomal doxorubicin, vincristine, and prednisone and continued to develop cervical lymph node recurrence after second-line therapy. The patient was infused with CAR-T cells after receiving focal bridging radiotherapy and remained in complete response more than 9 months after treatment. In addition, the patients did not experience serious adverse reactions related to radiotherapy as well as CAR-T cell therapy.

Conclusions: In this article, we describe a patient with double-expressor diffuse large B-cell lymphoma with localized compression symptoms after second-line treatment failure who benefited from CAR-T combined with focal bridging radiotherapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11405209PMC
http://dx.doi.org/10.3389/fimmu.2024.1441404DOI Listing

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