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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2500114545 |
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最近更新日期: Date of Last Refreshed on: |
2025-12-15 10:19:56 |
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注册时间: Date of Registration: |
2025-12-15 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
放疗联合尼妥珠单抗对比单纯放疗治疗铂类不耐受局部晚期头颈部鳞状细胞癌的临床研究 |
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Public title: |
Radiotherapy combined with nimotuzumab versus radiotherapy alone in patients with platinum-intolerant locally advanced head and neck squamous cell carcinoma |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
放疗联合尼妥珠单抗对比单纯放疗治疗铂类不耐受局部晚期头颈部鳞状细胞癌患者的开放标签、前瞻性、随机对照、Ⅲ期、国际多中心临床研究 |
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Scientific title: |
An open-label, prospective, randomized, phase III, international multicenter clinical trial of radiotherapy plus nimotuzumab versus radiotherapy alone in patients with platinum-intolerant locally advanced head and neck squamous cell carcinoma |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
胡漫 |
研究负责人: |
于金明 胡漫 |
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Applicant: |
Hu Man |
Study leader: |
Yu Jinming/Hu Man |
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申请注册联系人电话: Applicant telephone: |
+86 158 0669 8606 |
研究负责人电话:
Study leader's |
+86 158 0669 8606 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
hu5770@sina.com |
研究负责人电子邮件: Study leader's E-mail: |
hu5770@sina.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
山东省济南市济兖路440号 |
研究负责人通讯地址: |
山东省济南市济兖路440号 |
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Applicant address: |
440 Jiyan Road, Jinan, Shandong |
Study leader's address: |
440 Jiyan Road, Jinan, Shandong |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
山东第一医科大学附属肿瘤医院 |
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Applicant's institution: |
Shandong First Medical University Affiliated Cancer Hospital |
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研究负责人所在单位: |
山东第一医科大学附属肿瘤医院 |
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Affiliation of the Leader: |
Shandong First Medical University Affiliated Cancer Hospital |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
SDZLEC2025-360-02 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
山东第一医科大学附属肿瘤医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Cancer Hospital Affiliated to Shandong First Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-11-27 00:00:00 | ||
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伦理委员会联系人: |
宋现让 |
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Contact Name of the ethic committee: |
Song Xianrang |
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伦理委员会联系地址: |
山东省济南市济兖路440号 |
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Contact Address of the ethic committee: |
440 Jiyan Road, Jinan, Shandong |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 531 6762 6929 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
山东第一医科大学附属肿瘤医院 |
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Primary sponsor: |
Shandong First Medical University Affiliated Cancer Hospital |
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研究实施负责(组长)单位地址: |
山东省济南市济兖路440号 |
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Primary sponsor's address: |
440 Jiyan Road, Jinan, Shandong |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
百泰生物药业有限公司提供尼妥珠单抗药物支持 |
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Source(s) of funding: |
Nimotuzumab drug support provided by Biotech Pharmaceutical Co., Ltd |
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研究疾病: |
头颈部鳞癌 |
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Target disease: |
Squamous cell carcinoma of head and neck |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
III期临床试验 | ||||||||||||||||||||||
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Study phase: |
3 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
探讨放疗联合尼妥珠单抗治疗铂类不耐受局部晚期头颈部鳞状细胞癌的有效性和安全性。 |
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Objectives of Study: |
To evaluate the efficacy and safety of radiotherapy combined with nimotuzumab in platinum?ineligible patients with locoregionally advanced head and neck squamous cell carcinoma. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.年龄≥18周岁; 2.经过病理组织学确诊的Ⅲ-ⅣB期(按照AJCC第八版分期)头颈部鳞癌(包括口腔癌、口咽癌、下咽癌、喉癌); 3.不适宜手术的患者(定义为:患者因身体状况、T3-4N0-3M0或T1-2N2-3M0或医学原因不可手术;肿瘤达不到R0切除); 4.适合以根治为目的放疗治疗; 5.患者具有以下不适合顺铂化疗的原因之一: (1)年龄≥65岁且研究者评估不耐受化疗; (2)ECOG PS 评分:>2分(若(2)存在,则不参照标准7)); (3)肾功能障碍(肌酐清除率 <50ml/min)(若(3)存在,则不参照标准11)); (4)严重的耳鸣或听力功能下降(需要助听器或听力检测显示连续两个频率出现 25分贝及以上的偏移); (5)>1 级的周围神经病变; (6)因心功能障碍或其他合并症(研究者判断)。 6.尽可能提供肿瘤组织进行EGFR检测,口咽癌尽可能提供肿瘤组织进行HPV/P16检测(既往已检测过则不必再测); 7.ECOG PS评分0-2或KPS评分≥80分; 8.根据RECIST 1.1版评价标准,至少具有一处可测量病灶; 9.预计生存时间≥6个月; 10.血液学指标基本正常:白细胞计数≥4×10^9/L;中性粒细胞绝对计数≥1.5×10^9/L;血小板≥100×10^9/L;血红蛋白≥90 g/L; 11.肾功能基本正常:血清肌酐≤1.5×ULN或肌酐清除率(CrCl)≥ 60 mL/min(使用Cockcroft-Gault公式): 女性CrCl=(140-年龄)×体重(kg)×0.85 / (72×Scr mg/dl) 男性CrCl=(140-年龄)×体重(kg)×1.00 / (72×Scr mg/dl) 12.肝功能基本正常:血清总胆红素≤1.5×ULN; 谷草转氨酶(AST)≤2.5×ULN;谷丙转氨酶(ALT)≤2.5×ULN; 13.受试者自愿加入本研究,并签署书面知情同意书,而且能够遵守方案规定的访视及相关程序。 |
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Inclusion criteria |
1. Age >=18 years. 2. Histologically confirmed stage III–IVB (AJCC 8th edition) head and neck squamous cell carcinoma (including cancers of the oral cavity, oropharynx, hypopharynx, and larynx). 3. Unsuitable for surgical treatment (defined as: due to patient condition or tumor factors [T3–4 N0–3 M0, or T1–2 N2–3 M0] or medical reasons, surgery is not feasible; or an R0 resection is not achievable). 4. Suitable for definitive radiotherapy with curative intent. 5. At least one of the following reasons for being unsuitable for cisplatin?based chemotherapy: (1) Age >=65 years and, in the investigator’s judgment, unable to tolerate chemotherapy; (2) ECOG Performance Status >2 (if this criterion is met, the ECOG criterion listed below may be waived); (3) Renal dysfunction: creatinine clearance (CrCl) <50 mL/min (Cockcroft–Gault) (if this criterion is met, the renal function criterion listed below may be waived); (4) Severe tinnitus or hearing loss (requires a hearing aid or audiometry shows >=25 dB loss at two consecutive frequencies); (5) Peripheral neuropathy > Grade 1; (6) Inability to receive intravenous hydration (e.g., due to cardiac dysfunction) or other comorbidities, per investigator’s judgment. 6. Provide tumor tissue, whenever possible, for EGFR testing; for oropharyngeal cancer, provide tissue for HPV/p16 testing if feasible (no need to retest if previously tested). 7. ECOG Performance Status 0–1 (or Karnofsky Performance Status ≥80). 8. At least one measurable lesion per RECIST 1.1. 9. Expected survival >=6 months. 10. Adequate hematologic function: WBC >=4×10^9/L; absolute neutrophil count >=1.5×10^9/L; platelets >=100×10^9/L; hemoglobin >=90 g/L. 11. Adequate renal function: serum creatinine <=1.5×ULN or CrCl >=60 mL/min (Cockcroft–Gault): – Female CrCl = (140 – age) × weight (kg) × 0.85 / (72 × S_cr [mg/dL]) – Male CrCl = (140 – age) × weight (kg) × 1.00 / (72 × S_cr [mg/dL]) 12. Adequate liver function: total bilirubin <=1.5×ULN; AST <=2.5×ULN; ALT <=2.5×ULN. 13. Voluntary participation: signed written informed consent and ability to comply with visits and procedures. |
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排除标准: |
1.入组前4 周内接受过PD-1抑制剂、EGFR单抗、EGFR-TKI、抗血管生成药物; 2.筛选前30天内参加过其它干预性临床试验; 3.有其他恶性肿瘤史者(已治愈的皮肤基底细胞癌除外); 4.原发性免疫缺陷病史; 5.存在控制不佳的并发疾病(如心衰、严重的肺部疾病、严重的肝病、精神疾病等); 6.已知感染HIV病毒或活动性病毒性肝炎或结核; 7.在首次服用试验药物前90天内进行重大外科手术或计划手术; 8.对本方案中使用药物或其成分过敏者; 9.研究者认为不适宜参加本研究者; 10.不愿参加本研究或无法签署知情同意书者; 11.给药30天内接种活疫苗。 |
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Exclusion criteria: |
1. Receipt of a PD?1 inhibitor, EGFR monoclonal antibody, EGFR?TKI, or anti?angiogenic agent within 4 weeks prior to enrollment. 2. Participation in another interventional clinical trial within 30 days prior to screening. 3. History of other malignancy (except cured basal cell carcinoma of the skin). 4. History of primary immunodeficiency. 5. Uncontrolled comorbid conditions (e.g., congestive heart failure, severe pulmonary disease, severe liver disease, psychiatric illness). 6. Known HIV infection, or active viral hepatitis or active tuberculosis. 7. Major surgery within 90 days before first study treatment, or planned surgery during the study. 8. Known allergy to nimotuzumab or its excipients. 9. Deemed unsuitable to participate by the investigator. 10. Unwilling or unable to sign informed consent. 11. Receipt of a live vaccine within 30 days before first dose. |
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研究实施时间: Study execute time: |
从 From 2025-09-01 00:00:00至 To 2029-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-12-15 00:00:00 至 To 2029-08-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
中央随机系统(IWRS),区组随机化,分层因素:原发部位及N分期。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Interactive Web Response System (IWRS), block randomization, stratified factors: primary location and N stage. |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
开放标签,研究者与受试者均知晓治疗分组。 |
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Blinding: |
This is an open-label study – neither investigators nor subjects are blinded to treatment. |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
否No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
本研究采用纸质CRF与EDC并行管理。研究者按访视在CRF/EDC录入数据,数据管理按《GCP》与数据管理计划执行;EDC具备角色权限、审计追踪、加密传输、逻辑核查与质控规则。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
This study uses paper CRF and EDC parallel management. The researchers entered data in crf/edc according to the visit, and the data management was implemented according to GCP and data management plan; EDC has role authority, audit trail, encrypted transmission, logic verification and quality control rules. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |