Epstein-Barr Virus-Specific Adoptive Immunotherapy for Recurrent, Metastatic Nasopharyngeal Carcinoma

被引:78
作者
Huang, Julian
Fogg, Mark [2 ]
Wirth, Lori J. [3 ]
Daley, Heather
Ritz, Jerome
Posner, Marshall R. [4 ]
Wang, Fred C.
Lorch, Jochen H. [1 ]
机构
[1] Harvard Med Sch, Dana Farber Canc Inst, Dept Med Oncol, 450 Brookline Ave, Boston, MA 02215 USA
[2] Abzena, Cambridge, England
[3] Massachusetts Gen Hosp, Dept Med, Div Hematol & Oncol, Boston, MA 02114 USA
[4] Icahn Sch Med Mt Sinai, Tisch Canc Inst, Div Hematol & Med Oncol, New York, NY 10029 USA
关键词
adoptive T-cell immunotherapy; clinical trials; Epstein-Barr virus; nasopharyngeal carcinoma; phase; 1/2; CYTOTOXIC T-CELLS; PHASE-II TRIAL; COMBINATION; CARBOPLATIN; CHEMOTHERAPY; PACLITAXEL; PATHOGENESIS; GEMCITABINE; LYMPHOCYTES; MANAGEMENT;
D O I
10.1002/cncr.30541
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Early-stage and intermediate-stage nasopharyngeal cancer (NPC) generally carry a good prognosis, but for patients with recurrent, metastatic disease, options are limited. In the current study, the authors present a phase 1/2 study to evaluate the efficacy of Epstein-Barr virus (EBV)-stimulated cytotoxic T-lymphocyte (EBV-CTL) immunotherapy in this patient population. METHODS: Screening for patients with active, recurrent, metastatic EBV-associated NPC began in February 2007, and the study was closed to accrual in January 2012. After informed consent was obtained, patients had their blood drawn to initiate manufacturing of the EBV-CTL product. During product manufacturing, patients were placed on interim standard-of-care chemotherapy, and only after disease progression on the interim chemotherapy did patients receive investigational immunotherapy. Patients were restaged every 2 months until disease progression and then followed for survival. RESULTS: A total of 28 patients were enrolled, and 21 patients were treated. There was 1 complete response achieved, and at the time of last follow-up, the patient had been in remission for >8 years since treatment. The median progression-free survival was 2.2 months, and the median overall survival was 16.7 months. Two other patients, after failing EBV-CTL immunotherapy, unexpectedly demonstrated strong responses to the chemotherapy regimens they had previously failed. Patient EBV viral load and EBV-CTL specificity for tumor-associated viral antigens did not appear to correlate with clinical response. CONCLUSIONS: A durable response was observed with EBV-CTL immunotherapy, but the overall response rate for patients with recurrent, metastatic NPC was low. Further research is necessary to increase the efficacy of EBV-specific immunotherapy in patients with incurable NPC, and to characterize mechanisms for refacilitation to chemotherapy. (C) 2017 American Cancer Society.
引用
收藏
页码:2642 / 2650
页数:9
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