Personalized Timing of Interval Debulking Surgery in Advanced Ovarian Cancer
报名条件（概要）
- 年龄：18 Years – 不限
- 性别：女性
- 健康志愿者：不接受
完整入排标准请以官方页面为准。
开展国家/地区
China、Hong Kong
药品与企业信息
(i) Patients with KELIM =\>1 will receive radiological assessment and undergo internal debulking surgery if the disease is operable. (ii) Patients with KELIM \<1 will have alternative management, such as addition of bevacizumab or changing to dose-dense chemotherapy, and defer the interval debulking surgery
Neoadjuvant chemotherapy
Interval debulking surgery
研发企业
试验官方登记的主要申办方；研究机构申办时会显示相应机构名称。
生产企业
公开药品批准资料或正式说明书暂未提供明确的生产企业信息。
合作机构
- Queen Mary Hospital, Hong Kong研究机构/其他
- United Christian Hospital研究机构/其他
- Pamela Youde Nethersole Eastern Hospital研究机构/其他
- The University of Hong Kong-Shenzhen Hospital研究机构/其他
- Sun Yat-Sen University Cancer Center研究机构/其他
研发企业与生产企业可能不是同一家。研究阶段药品可能尚未公布生产企业；生产企业仅取自美国上市原研药说明书所列企业（不含仿制药），不作推测；仅在其他国家上市的药品暂无法显示。
研究简介（原文）
About 70% of epithelial ovarian cancer patients are diagnosed at advanced stage. When primary optimal surgery is not possible, neoadjuvant chemotherapy will followed by interval debulking surgery is one treatment option. However, there is no consensus on the optimal timing of the surgery. CA125 is a well-known tumor marker in ovarian cancer. Its kinetic change has been proven to correlate with the patients' response to chemotherapy and chance of optimal resection. This study aims to utilize the kinetic change of CA125 to customize the timing of surgery for individual patients and compare this with the standard clinical practice.
适应症
主动联系研究团队
总联系人（申办方／研究总部）
- Lesley Lau, MPhillsk382@hku.hk+852 22554265
- Iris Tangiristwk@hku.hk+852 22554265
中国／港澳台研究中心
- Sun Yat-sen University Cancer CenterGuangzhou，China
- The University of Hong Kong - Shenzhen HospitalShenzhen，China
- Pamela Youde Nethersole Eastern HospitalPamela YChai Wan，Hong Kong
- Queen Mary Hospital, Department of Clinical OncologyHong Kong，Hong Kong
- The University of Hong Kong, Department of Obstetrics and GynaecologyHong Kong，Hong Kong
- United Christian HospitalKwun Tong，Hong Kong
问自己是否符合条件、如何预筛
我的病情档案
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英文版（发给研究团队）
Dear Study Team, I am a patient in China and I am interested in participating in your clinical trial: Study Title: Personalized Timing of Interval Debulking Surgery in Advanced Ovarian Cancer ClinicalTrials.gov Identifier: NCT07023484 Sponsor: The University of Hong Kong Investigational product: KELIM, Carboplatin plus Paclitaxel, Interval debulking surgery About me: - Age: (please fill in) - Sex: (please fill in) - Confirmed diagnosis and stage: (please fill in) - Biomarkers / genetic testing: not available - Prior and current treatments: (please fill in) - Performance status (ECOG): not assessed - Current location: China - Travel ability: (please fill in) Could you please let me know: 1. Whether I might be eligible for this study; 2. Which site would be closest and most practical for me, and whether remote pre-screening is possible; 3. What documents (medical records, pathology or imaging reports, recent labs) I should prepare for pre-screening. I can provide English translations of my medical records. Thank you very much for your time and help. Kind regards, (your name) (your email / phone with country code)
中文对照（供您核对）
尊敬的研究团队： 我是一位来自中国的患者，希望咨询参加以下临床试验的可能： 研究名称：Personalized Timing of Interval Debulking Surgery in Advanced Ovarian Cancer 试验编号：NCT07023484 申办方：The University of Hong Kong 研究药物：KELIM、Carboplatin plus Paclitaxel、Interval debulking surgery 我的基本情况： - 年龄：（请填写） - 性别：（请填写） - 确诊疾病与分期：（请填写） - 基因／标志物检测：暂无 - 既往及当前治疗：（请填写） - 体能状态（ECOG）：未评估 - 目前所在城市：中国 - 可前往范围：（请填写） 想请教三个问题： 1. 我是否可能符合本研究的入组标准？ 2. 哪个中心对我最方便可行？能否远程预筛？ 3. 预筛需要准备哪些资料（病历、病理、影像、近期化验）？ 我可以提供英文翻译版病历。感谢您的时间与帮助。 顺祝安康 （您的姓名） （您的邮箱／带国际区号的电话）
提示：请与主治医生一起发信——由医生署名的申请，回复率远高于患者单独发信。首封邮件不要附身份证号等敏感信息。研究团队通常在 3–10 个工作日内回复，两周无回音可礼貌追问一次。
下一步怎么做？
- 把本页信息带给您的主治医生，评估是否适合参加。
- 点击下方按钮打开官方注册页，查看研究中心联系方式。
- 直接联系研究团队咨询报名事宜（通常有中文同声翻译服务可协助沟通）。