NCT03253068Unknown2 期
A Phase II Study of Pembrolizumab Plus Amurubicin in Patients With Refractory Small-cell Lung Cancer
适应症
干预措施
相关药物
试验速览
- 阶段
- 2 期
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- Overall response rate
研究概览
简要总结
To explore the overall response rate (ORR) per RECIST 1.1 as assessed by investigators in subjects with refractory small cell lung cancer treated with pembrolizumab (Pembro) plus amurubicin (AMR).
详细描述
Open, uncontrolled, multi-center, phase II study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Have a histologically or cytologically confirmed diagnosis of SCLC.
- •Confirmed radiological relapse within 90 days from the last day of first-line chemotherapy.
- •Have adequate tumor tissue sample to test PD-L1 immunohistochemistry.
- •Have measurable disease based on RECIST 1.1 as determined by the site.
- •Be ≥20 years of age on day of signing informed consent.
- •Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group
- •Have adequate organ function as indicated by the following laboratory values
- •Is expected to live more than 90 days.
- •Be willing and able to provide written informed consent/assent for the trial.
- •Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours from registration.
- •Female subjects of childbearing potential must be willing to use an adequate method of contraception as outlined in Section 5.7.2 - Contraception, for the course of the study through 120 days (or longer as specified by local institutional guidelines) after the last dose of study medication.
- •Male subjects of childbearing potential must agree to use an adequate method of contraception as outlined in Section 5.7.2- Contraception, starting with the first dose of study therapy through 120 days (or longer as specified by local institutional guidelines) after the last dose of study therapy.
排除标准
- •Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigation device within 30 days from registration.
- •Is receiving systemic steroid therapy ≤ 3 days from registration or receiving any other form of immunosuppressive medication.
- •Has received prior systemic cytotoxic chemotherapy, biological therapy, OR major surgery within 3 weeks of the first dose of trial treatment; received thoracic radiation therapy of > 30 Gy within 6 months from registration.
- •Has received prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody.
- •Has symptomatic central nervous system (CNS) metastases and/or carcinomatous meningitis.
- •Active autoimmune disease that has required systemic treatment in past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs).
- •Has had an allogeneic tissue/solid organ transplant.
- •History of noninfectious pneumonitis that required steroids or current active pneumonitis, or any evidence of interstitial lung disease by CT scan.
- •Has received or will receive a live vaccine within 30 days from registration.
- •Has an active infection requiring intravenous systemic therapy and oral administration.
- •Has known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
- •Has known active Hepatitis B, or Hepatitis C.
- •Has any history of prior malignancy, with the exception of basal cell carcinoma of the skin, superficial bladder cancer, squamous cell carcinoma of the skin, in situ cervical cancer, or has undergone potentially curative therapy with no evidence of that disease recurrence for 5 years since initiation of that therapy.
- •Has Known history of serious allergy.
- •Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
- •Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
- •Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days (or longer as specified by local institutional guidelines) after the last dose of trial treatment.
- •Hypersensitivity or allergy to pembrolizumab or any of its excipients, and/or to AMR or any of its excipients.
研究组 & 干预措施
Pembrolizumab plus amurubicin
Experimental
Pembrolizumab 200mg/body plus amurubicin 40mg/m2, intravenous, every 3 weeks
干预措施: Pembrolizumab plus amurubicin (Drug)
结局指标
主要结局
Overall response rate
时间窗: Imaging will be performed every 6 weeks through study completion, an average of 6 months
Overall response rate will be assessed using RECIST ver1.1 by investigators
次要结局
未报告次要终点
研究者
Hiroaki Akamatsu
Assistant Professor
Wakayama Medical University
研究点 (1)
Loading locations...
相似试验
已完成
2 期
Pembrolizumab Plus Ramucirumab in Metastatic Gastric CancerGastric CancerNCT04632459Samsung Medical Center26
已完成
2 期
Pembrolizumab After SBRT Versus Pembrolizumab Alone in Advanced NSCLCNon-Small Cell Lung CancerNCT02492568The Netherlands Cancer Institute92
已完成
2 期
Pembrolizumab in Advanced/Metastatic Acral Lentiginous MelanomaAcral Lentiginous MelanomaNCT02875132Chinese University of Hong Kong9
终止
2 期
Phase 2 Study of Imprime PGG & Pembrolizumab in Subjects With Adv SCCHN Who Failed Pembro Monotherapy or Experiencing SDSquamous Cell Carcinoma of the Head and NeckNCT03246685HiberCell, Inc.1
已完成
2 期
Study of Imprime PGG and Pembrolizumab in Advanced Melanoma and Triple Negative Breast CancerTriple-Negative Breast CancerAdvanced MelanomaNCT02981303HiberCell, Inc.64