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临床试验/JPRN-jRCT1021230030
JPRN-jRCT1021230030招募中Unknown

Multicenter Study to Evaluate the Usefulness of TCR Repertoire as a Prognostic Marker in Postoperative Adjuvant Atezolizumab for Non-Small Cell Lung Cancer - SEATRAI

Suzuki Hiroyuki0 个研究点目标入组 20 人开始时间: 2023年10月31日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • (1) Patients must be at least 18 years of age at the time of consent.
  • (ii) Patients with a clinical diagnosis of c-stage I-III non-small cell lung cancer that can be completely resected and who will undergo surgery
  • (iii) Patients with performance status 0-1 judged by physician to be tolerant to postoperative adjuvant chemotherapy including cisplatin
  • (iv) Patients judged by physician to be tolerant of adjuvant atezolizumab therapy.
  • (v) Patients who have consented to participate in this study
  • (vi) Patients whose postoperative pathology diagnosis is p-stage II-IIIA and who have been treated with atezolizumab as adjuvant therapy will be included in the analysis.
  • (7) Patients who fulfill the above conditions and newly consent to this study among those who have collected and stored peripheral blood mononuclear cells and tumor-infiltrating lymphocytes prior to surgery in a previous study (Ethics Committee approval number: General 30163) will also be included.

排除标准

  • (i) Pregnant or lactating women
  • (ii) Patients with a history of interstitial lung disease or pulmonary inflammation
  • (iii) Patients with active autoimmune diseases
  • (iv) Patients with postoperative pathological diagnosis other than p-stage II-IIIA
  • 5) Patients with positive postoperative residual disease
  • (vi) Patients with PD-L1 TPS<1% (regardless of the type of anti-PD-L1 antibody used for immunostaining)
  • (vii) Patients who did not receive postoperative adjuvant therapy with atezolizumab

研究者

发起方
Suzuki Hiroyuki

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