Prospective pilot study of adoptive immunotherapy with autologous αβT cells for five cases of advanced and/or recurrent esophageal squamous cell carcinoma
Autor: | Tatsuki Nanami, Seiko Otsuka, Satoshi Yajima, Takashi Kamigaki, Makoto Sumazaki, Hideaki Shimada, Shigenori Goto, Takashi Suzuki, Fumiaki Shiratori, Hironori Kaneko, Yoko Oshima |
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Rok vydání: | 2017 |
Předmět: |
Oncology
medicine.medical_specialty business.industry medicine.medical_treatment Gastroenterology Recurrent Esophageal Squamous Cell Carcinoma Immunotherapy Esophageal cancer medicine.disease Peripheral blood mononuclear cell Clinical trial Cell therapy 03 medical and health sciences 0302 clinical medicine medicine.anatomical_structure Tumor progression 030220 oncology & carcinogenesis Internal medicine Medicine 030211 gastroenterology & hepatology Esophagus business |
Zdroj: | Esophagus. 14:303-308 |
ISSN: | 1612-9067 1612-9059 |
DOI: | 10.1007/s10388-017-0577-5 |
Popis: | Although several clinical trials of vaccination and cellular immunotherapy for esophageal cancer have been reported, clinical trials of anti-CD3-activated autologous αβT cell therapy for patients with esophageal squamous cell carcinoma are limited. A total of five patients with recurrent esophageal squamous cell carcinoma were enrolled in this prospective pilot study. Peripheral blood mononuclear cells from the patients were cultured with immobilized anti-CD3 antibody and interleukin-2 for approximately 14 days, and 5 × 109 lymphocytes were harvested. Expanded lymphocytes were intravenously infused every 2 weeks for six courses. All patients were followed up until death. The treatment response was assessed by the number of lymphocytes, CD4/CD8 ratio, serum tumor markers, and computed tomography scan. A total of 23 courses of treatment were completed. Three of the five patients (cases 2, 3, and 4) completed six courses of cell therapy according to the protocol. However, case 1 quit treatment after three courses and case 5 quit treatment after two courses because of tumor progression. There were no adverse effects related to cell therapy. Although cases 1 and 5 did not show any treatment benefits, cases 2, 3, and 4 showed some treatment benefits. Cases 2 and 4 showed long-term survived for more than 1 year. These results might suggest the safety and benefits of anti-CD3-activated autologous αβT cell therapy for the part of the patients with esophageal squamous cell carcinoma. |
Databáze: | OpenAIRE |
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