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临床试验/NL-OMON48462
NL-OMON48462已完成2 期

Ipilimumab plus Nivolumab and ChemoRadiotherapy followed by Surgery in patients with resectable and borderline resectable T3-4N0-1 NSCLC - INCREASE

Vrije Universiteit Medisch Centrum0 个研究点目标入组 29 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
29

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Histologically confirmed NSCLC, a histological biopsy is mandatory
  • 2. T3-4, N0-1 tumors based on size or upon ingrowth into the thoracic wall,
  • mediastinum, vertebra or diaphragm
  • 3. Patients that are irresectable upfront, but expected to be resectable after
  • chemoradiotherapy induction, as per multidisciplinary tumor board evaluation
  • 4. Be willing and able to provide written informed consent for the trial.
  • 5. Be above 18 years of age on day of signing informed consent.
  • 6. Have measurable disease based on RECIST 1.1. 9.
  • 7. Have a performance status of 0-1 on the ECOG Performance Scale.
  • 8. Demonstrate adequate organ function.

排除标准

  • 1. Known oncogenic drivers such as activating EGFR or BRAF mutations or ALK or
  • ROS1 gene rearrangements
  • 2. Prior surgery and/or radiotherapy on the ipsilateral thorax
  • 3. Patients deemed inoperable
  • 4. Subjects with a condition requiring systemic treatment with either
  • corticosteroids (> 10 mg daily prednisone equivalent) or other
  • immunosuppressive medications within 14 days of day 0. Inhaled or topical
  • steroids, and adrenal replacement steroid >10 mg daily prednisone
  • equivalent, are permitted in the absence of active autoimmune disease.
  • 5. Additional malignancy that is progressing or requires active treatment.
  • Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of
  • the skin, or in situ cervical cancer that has undergone potentially curative
  • 6. Active autoimmune disease requiring systemic steroid treatment within the
  • past 3 months or a documented history of clinically severe autoimmune disease,
  • or a syndrome that requires systemic steroids.
  • 7. Evidence of interstitial lung disease or active, non-infectious pneumonitis.
  • 8. Active infection requiring systemic therapy.
  • 9. Ahistory of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
  • 10. Active Hepatitis B or C.
  • 11. Psychiatric or substance abuse disorders that would interfere with
  • cooperation with the requirements of the trial.
  • 12. Has received prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2,
  • anti-CTLA-4 antibody, or any other antibody or drug specifically targeting
  • T-cell co-stimulation or immune checkpoint pathways.
  • 13. Patient is pregnant or breastfeeding, or expecting to conceive within the
  • projected duration of the trial, starting with the pre-screening or screening
  • visit through 23 weeks after the last dose of trial treatment.
  • A Woman of Childbearing Potential (WOCBP) is defined as any female who has
  • experienced menarche and who has not undergone surgical sterilization
  • (hysterectomy or bilateral oophorectomy) and is not postmenopausal. Menopause
  • is defined as 12 months of amenorrhea in a woman over age 45 years in the
  • absence of other biological or physiological causes.
  • WOCBP receiving nivolumab will be instructed to adhere to contraception for a
  • period of 5 months after the last dose of nivolumab. Men receiving nivolumab
  • and who are sexually active with WOCBP will be instructed to adhere to
  • contraception for a period of 7 months after the last dose of nivolumab.
  • These durations have been calculated using the upper limit of the half-life for
  • nivolumab (~25 days) and are based on the recommendation that WOCBP use
  • contraception for 5 half-lives plus 30 days, and men who are sexually active
  • with WOCBP use contraception for 5 half-lives plus 90 days after the last dose
  • of nivolumab. Females should not breastfeed while receiving nivolumab and for
  • any subsequent protocol-specified period. Investigators shall counsel WOCBP and
  • male subjects who are sexually active with WOCBP on the importance of pregnancy
  • prevention and the implications of an unexpected pregnancy. Investigators shall
  • advise WOCBP and male subjects who are sexually active with WOCBP on the use of
  • highly effective methods of contraception. Highly effective methods of
  • contraception have a failure rate of < 1% when used consistently and
  • correctly. Local laws and regulations may require use of a

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