Low Dose, Reduced Frequency Nivolumab for the Treatment of Unresectable or Metastatic Cancer, AFFORD IO Trial
AFFORD IO: A Phase 2 Trial of Low Dose, Reduced Frequency Nivolumab (Anti-PD-1 Antibody) in Patients With Unresectable or Metastatic Cancer
研究概览
地位
条件
- 霍奇金淋巴瘤
- 转移性肺非小细胞癌
- 转移性透明细胞肾细胞癌
- 转移性皮肤黑色素瘤
- 不可切除的皮肤黑色素瘤
- 卡波西肉瘤
- III 期肺癌 AJCC v8
- IV 期肺癌 AJCC v8
- 不可切除的恶性实体肿瘤
- III 期肾细胞癌 AJCC v8
- IV 期肾细胞癌 AJCC v8
- 转移性恶性实体瘤
- 临床 III 期皮肤黑色素瘤 AJCC v8
- 转移性尿路上皮癌
- 转移性默克尔细胞癌
- 转移性皮肤鳞状细胞癌
- 转移性结直肠癌
- IV 期结直肠癌 AJCC v8
- 临床 IV 期皮肤黑色素瘤 AJCC v8
- III 期结直肠癌 AJCC v8
- 转移性头颈部鳞状细胞癌
- 不可切除的头颈部鳞状细胞癌
- 不可切除的肺非小细胞癌
- III 期宫颈癌 AJCC v8
- IV 期宫颈癌 AJCC v8
- 不可切除的肢端黑色素瘤
- 不可切除的粘膜黑色素瘤
- 不可切除的尿路上皮癌
- 不可切除的结直肠癌
- 转移性卡波西肉瘤
- 转移性宫颈癌
- 转移性粘膜黑色素瘤
- 转移性基底细胞癌
- 不可切除的宫颈癌
- 不可切除的默克尔细胞癌
- 不可切除的皮肤鳞状细胞癌
- 不可切除的基底细胞癌
- 转移性肢端黑色素瘤
- 不可切除的透明细胞肾细胞癌
- 临床 III 期皮肤默克尔细胞癌 AJCC v8
- 临床 IV 期皮肤默克尔细胞癌 AJCC v8
- 第四阶段头和颈皮肤鳞状细胞癌AJCC V8
- 第三阶段头和颈皮肤细胞癌AJCC V8
详细说明
OUTLINE:
INDUCTION PHASE: Patients receive nivolumab intravenously (IV) over approximately 30 minutes on days 1 and 45 in the absence of disease progression or unacceptable toxicity. Patients who are benefitting after 45 days proceed to Maintenance Phase.
MAINTENANCE PHASE: Patients receive nivolumab IV over approximately 30 minutes every 90 days (days 90, 180, 270 and 360) in the absence of disease progression or unacceptable toxicity.
All patients also undergo computed tomography (CT)/magnetic resonance imaging (MRI) and blood sample collection throughout the study. Patients may also undergo urine sample collection throughout the study.
After completion of study treatment, patients are followed up at 90 days and then every 12 months for up to 4 years.
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Shailender Bhatia, MD
- 电话号码:206-606-6765
- 邮箱:sbhatia@uw.edu
学习地点
-
-
-
Kampala、乌干达、3935
- Uganda Cancer Institute
-
接触:
- Jackson Orem
- 电话号码:0782 320543
- 邮箱:jackson.orem@uci.or.ug
-
首席研究员:
- Jackson Orem
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
Participants are eligible if they have one of these histologically confirmed, unresectable or metastatic cancer types listed below, based upon historical responsiveness to anti-PD-(L)1 agents
- Non-small cell lung cancer (NSCLC) with documented PD-L1 expression (combined positive score [CPS] ≥ 1) (NOTE: Participants with known driver oncogenic mutations/rearrangements, including EGFR, ALK and ROS-1, will be excluded.)
- Head and neck squamous cell carcinoma (HNSCC) with documented PD-L1 expression (CPS ≥ 1)
- Clear cell renal cell carcinoma (ccRCC) (NOTE: Other subtypes may be permitted after approval by the Medical Monitor)
- Melanoma (cutaneous, acral-lentiginous and mucosal subtypes), and non-melanoma skin cancers, (cutaneous squamous cell carcinoma [CSCC], basal cell carcinoma [BCC] and Merkel cell carcinoma [MCC])
- Hodgkin's lymphoma
- Urothelial carcinoma
- Cervical cancer with documented PD-L1 expression (CPS ≥ 1)
- Colorectal cancer with high microsatellite instability (MSI) or mismatch repair deficiency
- Kaposi sarcoma (KS) without clinical concern for multicentric Castleman's disease (MCD)
- Any cancer type with historical data suggesting an ORR > 20% with anti-PD(L)-1 agents (NOTE: All participants in this category must be approved by the Medical Monitor prior to enrollment.)
- Must have experienced disease progression after or deemed not to be a good candidate for available curative systemic therapy options
- Presence of at least one measurable tumor, per RECIST v1.1
- Age 18 or older. (NOTE: Both men and women, and members of all races and ethnic groups are eligible for this trial.)
- Eastern Cooperative Oncology Group (ECOG) performance score of 0-2
- Absolute neutrophil count (ANC) ≥ 1.0 × 10^9/L
- Platelet count ≥ 75 × 10^9/L
- Hemoglobin ≥ 9 g/dL (NOTE: Participants may have been transfused)
- Total bilirubin level ≤ 1.5 × the upper limit of normal (ULN) (or total bilirubin ≤ 2.5 × upper limit of normal [ULN] in participants with Gilbert's syndrome)
- Estimated creatinine clearance ≥ 30mL/min according to the Cockcroft-Gault formula or according to local institutional standard
- Must consent to undergo serial research blood draws at study defined timepoints, unless deemed unsafe or not feasible by the treating investigator
- Must have an ability to understand and provide consent to the institutional review board (IRB)-approved informed consent form (ICF) document(s)
- Women of childbearing potential must have a negative serum or urine pregnancy test at screening
- Both male and female participants must be willing to use highly effective contraception, as stipulated in national or local guidelines, throughout the study and for at least 180 days after the last treatment administration, if the risk of conception exists
Exclusion Criteria:
- Prior exposure to any immune-checkpoint inhibitor for any reason
- Residual adverse event(s) from prior therapy grade > 1 (National Cancer Institute [NCI]-Common Terminology Criteria for Adverse Events [CTCAE] v6.0) that could interfere with study endpoints or put participant safety at risk, as determined by the treating investigator
- Known active central nervous system (CNS) metastases and/or prior history of leptomeningeal cancer involvement
- Known history of another active malignancy (besides the eligible cancer diagnosis) within the last 3 years from day 1 of nivolumab that could interfere with study endpoints or put participant safety at risk. (NOTE: Exception will be made for adequately treated basal or squamous cell carcinoma of the skin or carcinoma in situ [skin, bladder, cervical, colorectal, breast] or low grade prostatic intraepithelial neoplasia or grade 1 prostate cancer. Any other neoplasm, which has been treated adequately and is adjudged by the treating investigator to have a low risk of progression during the study, could be enrolled only after approval from the medical monitor.)
Known active hepatitis B virus (HBV) or hepatitis C virus (HCV), defined as follows:
- Active HBV is defined as a known positive hepatitis B virus surface antigen (HBsAg) result or positive total hepatitis B virus core antibody (anti-HBc) results in the absence of hepatitis B virus surface antibody (anti-HBsAb). (NOTE: When HBsAg is negative and HBcAb is positive, HBV-DNA should be measured. When HBV-deoxyribonucleic acid [DNA] is negative, this participant could be enrolled with close monitoring of HBV activities.)
- Active hepatitis C virus (HCV) is defined as a known positive HCV antibody result and quantitative HCV-ribonucleic acid (RNA) results greater than the lower limits of detection of the assay. (NOTE: Participants who have had definitive treatment for HCV are permitted if HCV-RNA is undetectable.)
Known uncontrolled HIV infection. (NOTE: HIV-infected participants may be allowed if all the following criteria are met: CD4 count ≥ 100/μL, viral load less than 200 copies/mL, and clinically stable on antiretroviral therapy [ART] for at least 3 months.)
- These participants will be enrolled only after approval from the medical monitor
- Known active autoimmune disease or an allograft requiring systemic immunosuppression with corticosteroids (> 10 mg/day of prednisone or equivalent) or immunosuppressive drugs within the past 2 years before the first dose of nivolumab. (NOTE: Exceptions will be made for participants with autoimmune conditions such as diabetes type I, vitiligo, psoriasis, hypothyroid or hyperthyroid diseases not requiring immunosuppressive treatment; participants receiving physiologic corticosteroid replacement therapy at doses < 10 mg/day of prednisone or equivalent for adrenal or pituitary insufficiency; participants with a condition such as asthma or chronic obstructive pulmonary disease that requires intermittent use of steroids or those who require brief courses of corticosteroids for prophylaxis [e.g., contrast dye allergy], nivolumab-related standard premedication, and/or treatment of non-serious immune related adverse events. Any other situation must be discussed with the medical monitor for risk/benefit assessment.)
- Immunosuppressed status due to severe uncontrolled diabetes, concurrent uncontrolled hematological malignancy, or other comorbidities
- Known history of serious, active infections (aside from well-controlled HIV, as per exclusion criterion #6) requiring systemic antimicrobial agents within 14 days before the first dose of nivolumab. (NOTE: Chronic infections such as herpes simplex virus requiring suppressive therapy may be allowed after discussion with the medical monitor for risk/benefit assessment.)
- Known history of clinically significant interstitial lung disease, or active noninfectious pneumonitis
- Clinically significant (i.e., active) cardiovascular disease such as cerebral vascular accident or myocardial infarction within 6 months prior to first dose of nivolumab, ongoing unstable angina or congestive heart failure (New York Heart Association Classification class II-IV), or serious cardiac arrhythmia that could jeopardize participant safety on the study
- Receipt of live vaccine(s) within 30 days of planned start of nivolumab. (NOTE: Examples of live vaccines include but are not limited to measles, mumps, rubella, varicella-zoster [chickenpox], yellow fever, rabies, bacillus Calmette Guerin [BCG], and typhoid vaccines. Seasonal influenza vaccines for injection are generally killed-virus vaccines and are allowed; however, intranasal influenza vaccines are live, attenuated vaccines and are not allowed.)
- Known severe acute or chronic medical conditions such as uncontrolled seizure disorder, serious psychiatric illness, or laboratory abnormalities, that may increase the risk associated with study participation or may interfere with the interpretation of study endpoints and, in the judgment of the treating investigator, would make the participant inappropriate for entry into this study
- Known active tuberculosis (TB). (NOTE: Participants with latent TB will be allowed, provided they are receiving tuberculosis preventive therapy, after approval of the medical monitor.)
- Known allergy or hypersensitivity to any component of the study drug formulation (including excipients and additives) that could interfere with study endpoints or put participant safety at risk
- Pregnant or breast-feeding woman
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Treatment (low dose, reduced frequency nivolumab)
INDUCTION PHASE: Patients receive nivolumab IV over approximately 30 minutes on days 1 and 45 in the absence of disease progression or unacceptable toxicity. Patients who are benefitting after 45 days proceed to Maintenance Phase. MAINTENANCE PHASE: Patients receive nivolumab IV over approximately 30 minutes every 90 days (days 90, 180, 270 and 360) in the absence of disease progression or unacceptable toxicity. All patients also undergo CT/MRI and blood sample collection throughout the study. Patients may also undergo urine sample collection throughout the study. |
鉴于IV
其他名称:
进行核磁共振
其他名称:
接受CT
其他名称:
Undergo collection of urine and/or blood samples
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Objective response
大体时间:Up to 4 years after completion of study treatment
|
Defined as the best objective response of complete response (CR) or partial response (PR), as determined by investigator assessment per Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1.
|
Up to 4 years after completion of study treatment
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Duration of response (DOR)
大体时间:From the earliest date of disease response (CR or PR) until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
Will be assessed per RECIST 1.1.
The Kaplan-Meier (KM) technique will be used to obtain estimates of DOR.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From the earliest date of disease response (CR or PR) until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
|
Disease control
大体时间:Up to 4 years after completion of study treatment
|
Defined as achievement of CR, PR, or stable disease as a patient's best objective response to the study treatment, per RECIST v1.1.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
Up to 4 years after completion of study treatment
|
|
Progression free survival (PFS)
大体时间:From date of first dose of study treatment until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
The KM technique will be used to obtain estimates of PFS.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From date of first dose of study treatment until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
|
Overall survival (OS)
大体时间:From date of first dose of study treatment until the date of death from any cause, assessed up to 4 years after completion of study treatment
|
The KM technique will be used to obtain estimates of OS.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From date of first dose of study treatment until the date of death from any cause, assessed up to 4 years after completion of study treatment
|
|
Disease specific survival
大体时间:From date of first dose of study treatment until the date of death, assessed up to 4 years after completion of study treatment
|
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From date of first dose of study treatment until the date of death, assessed up to 4 years after completion of study treatment
|
|
Incidence of adverse events
大体时间:Up to 90 days years after completion of study treatment
|
Will include immune-related adverse events, treatment interruption and treatment discontinuation, and the use of immunosuppressive medications for toxicities.
|
Up to 90 days years after completion of study treatment
|
|
Accrual and by compliance with treatment timepoints
大体时间:Up to 4 years after completion of study treatment
|
Feasibility defined by accrual and by compliance with treatment timepoints in this unique setting.
|
Up to 4 years after completion of study treatment
|
合作者和调查者
调查人员
- 首席研究员:Shailender Bhatia, MD、Fred Hutch/University of Washington Cancer Consortium
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
- 泌尿生殖系统疾病
- 生殖器疾病
- 病理过程
- 泌尿生殖系统肿瘤
- 按部位分类的肿瘤
- 肿瘤
- 男性泌尿生殖系统疾病
- 肾脏疾病
- 泌尿系统疾病
- 女性泌尿生殖系统疾病
- 女性泌尿生殖系统疾病和妊娠并发症
- 肠道疾病
- 免疫系统疾病
- 感染
- 病毒病
- 呼吸道疾病
- 组织学类型的肿瘤
- 消化道肿瘤
- 消化系统肿瘤
- 消化系统疾病
- 肠胃疾病
- 肠道肿瘤
- 直肠疾病
- 子宫疾病
- 生殖器疾病,女性
- 肺部疾病
- 头颈肿瘤
- 肿瘤、腺体和上皮
- 腺癌
- 呼吸道肿瘤
- 胸部肿瘤
- 结肠疾病
- 肿瘤过程
- DNA 病毒感染
- 生殖器肿瘤,女性
- 皮肤病
- 淋巴系统疾病
- 淋巴增生性疾病
- 免疫增生性疾病
- 泌尿系肿瘤
- 癌
- 宫颈疾病
- 神经外胚层肿瘤
- 肿瘤、生殖细胞和胚胎
- 肿瘤,神经组织
- 淋巴瘤
- 肾脏肿瘤
- 癌,支气管癌
- 支气管肿瘤
- 子宫肿瘤
- 神经内分泌肿瘤
- 肉瘤
- 肿瘤、结缔组织和软组织
- 疱疹病毒科感染
- 肿瘤病毒感染
- 痣和黑色素瘤
- 皮肤肿瘤
- 肿瘤、血管组织
- 癌,鳞状细胞
- 多瘤病毒感染
- 肿瘤,基底细胞
- 癌,神经内分泌
- 病理状况、体征和症状
- 皮肤和结缔组织疾病
- 半身和淋巴疾病
- 头颈部鳞状细胞癌
- 肺肿瘤
- 结直肠肿瘤
- 肿瘤转移
- 癌,肾细胞
- 癌,非小细胞肺癌
- 宫颈肿瘤
- 黑色素瘤
- 霍奇金病
- 卡波西肉瘤
- 癌,移行细胞
- 癌,基底细胞
- 癌,默克尔细胞
- 透明细胞转移性肾细胞癌
- 氨基酸,肽和蛋白质
- 蛋白质
- 调查技术
- 临床实验室技术
- 诊断技术和程序
- 诊断
- 抗体,单克隆,人源化
- 抗体,单克隆
- 抗体
- 免疫球蛋白
- 免疫蛋白
- 血蛋白
- 血清球蛋白
- 球蛋白
- 化学技术,分析
- 频谱分析
- 纳武单抗
- 标本处理
- 磁共振光谱
其他研究编号
- RG1125119
- NCI-2026-01874 (注册表标识符:CTRP (Clinical Trial Reporting Program))
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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