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New England Journal of Medicine· 2018Q1

Yetişkin Relaps veya Refrakter Diffüz Büyük B Hücreli Lenfoma Hastalarında Tisagenlecleucel

Tisagenlecleucel in Adult Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Stephen J. Schuster, Michael Bishop, Constantine S. Tam, Edmund K. Waller ve diğerleri

Kısa özet

Tisagenlecleucel, bir CAR T-hücre tedavisi, kök hücre nakli için uygun olmayan relaps/refrakter diffüz büyük B hücreli lenfomalı yetişkinlerde %52 genel yanıt oranı (%40 tam yanıt) elde etti.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Tisagenlecleucel, relaps/refrakter diffüz büyük B hücreli lenfomalı 93 yetişkin hastada %52 genel yanıt oranı gösterdi.
  • Tam yanıt oranı %40, kısmi yanıt oranı ise %12 olarak kaydedildi.
  • 12. ayda yanıt sonrası nüks etmeme sağkalım oranı genel olarak %65 ve tam yanıt verenlerde %79 idi.
  • Yaygın ciddi yan etkiler arasında sitokin salınım sendromu (%22) ve nörolojik olaylar (%12) yer aldı.
  • Tisagenlecleucel, sitokin salınım sendromu veya serebral ödeme bağlı ölüm bildirilmedi.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (abstract)

BACKGROUND: Patients with diffuse large B-cell lymphoma that is refractory to primary and second-line therapies or that has relapsed after stem-cell transplantation have a poor prognosis. The chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel targets and eliminates CD19-expressing B cells and showed efficacy against B-cell lymphomas in a single-center, phase 2a study. METHODS: We conducted an international, phase 2, pivotal study of centrally manufactured tisagenlecleucel involving adult patients with relapsed or refractory diffuse large B-cell lymphoma who were ineligible for or had disease progression after autologous hematopoietic stem-cell transplantation. The primary end point was the best overall response rate (i.e., the percentage of patients who had a complete or partial response), as judged by an independent review committee. RESULTS: A total of 93 patients received an infusion and were included in the evaluation of efficacy. The median time from infusion to data cutoff was 14 months (range, 0.1 to 26). The best overall response rate was 52% (95% confidence interval, 41 to 62); 40% of the patients had complete responses, and 12% had partial responses. Response rates were consistent across prognostic subgroups. At 12 months after the initial response, the rate of relapse-free survival was estimated to be 65% (79% among patients with a complete response). The most common grade 3 or 4 adverse events of special interest included cytokine release syndrome (22%), neurologic events (12%), cytopenias lasting more than 28 days (32%), infections (20%), and febrile neutropenia (14%). Three patients died from disease progression within 30 days after infusion. No deaths were attributed to tisagenlecleucel, cytokine release syndrome, or cerebral edema. No differences between response groups in tumor expression of CD19 or immune checkpoint-related proteins were found. CONCLUSIONS: In this international study of CAR T-cell therapy in relapsed or refractory diffuse large B-cell lymphoma in adults, high rates of durable responses were produced with the use of tisagenlecleucel. (Funded by Novartis; JULIET ClinicalTrials.gov number, NCT02445248 .).

Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2018 · DOI ↗

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Alan: Onkoloji

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