宫颈癌与子宫内膜癌晚期放疗毒性反应:术后调强放疗/近距离放疗研究
宫颈癌和子宫内膜癌术后需调强放疗和/或近距离放疗的晚期胃肠道及泌尿生殖系统毒性评估
宫颈癌是全球女性中第四常见的癌症,在印度则是第二常见的癌症。 在印度,2018年至2020年间,宫颈癌病例从2018年到2020年激增了26,985例。 宫颈癌的治疗取决于临床分期。 早期宫颈癌(IB1-IIA期)的治疗包括放化疗或手术+/-辅助(CT)RT,若适用则加阴道近距离放疗。 辅助治疗的选择依赖于识别特定的风险因素。 满足Sedlis中危标准的患者,仅需盆腔放疗;而满足Peter's高危标准的患者,则需辅助放化疗。 这种基于风险的方法有助于为患者个体化定制辅助治疗方案。
印度报告了16,413例子宫内膜癌新发病例和6,385例死亡,死亡率为0.73%。 子宫内膜癌的主要治疗方法是全腹子宫切除术加双侧输卵管卵巢切除术(TAH-BSO)。 辅助治疗取决于根据ESGO/ESTRO/ESP指南通过基于分子的风险分层确定的风险分层组。 辅助治疗包括放疗、化疗和近距离放疗。
为减轻急性和晚期毒性负担,采用了先进的体外放射技术,如图像引导调强放疗(IG IMRT)。 与3DCRT技术相比,IG IMRT已显示出在长期生存者中降低晚期毒性的潜力。 自2020年1月起,我们机构(孟买塔塔纪念中心)已将常规IG-IMRT(图像引导调强放疗)纳入宫颈癌和子宫内膜癌的治疗中。 然而,尚未对实施后的治疗结果和潜在毒性进行评估。 这项回顾性观察性研究旨在评估IG-IMRT的临床应用。
本研究的主要目标是审计2020年1月至2023年6月期间接受辅助IMRT(伴或不伴化疗)的女性患者中,≥II级胃肠道和泌尿生殖系统毒性的3年发生率。
研究概览
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Supriya Chopra
- 电话号码:5113 02227405000
- 邮箱:supriyasastri@gmail.com
学习地点
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Maharashtra
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Mumbai、Maharashtra、印度、400012
- 招聘中
- Tata Memorial Center
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接触:
- Supriya sastri (Chopra), MD
- 电话号码:5113 022-68735000
- 邮箱:supriyasastri@gmail.com
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首席研究员:
- Supriya Sastri (Chopra), MD
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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
取样方法
研究人群
描述
纳入标准:
- 诊断时年龄超过18岁的患者。
- 所有经组织学确诊为宫颈癌或子宫内膜癌的患者。
- 仅纳入在TMH/ACTREC接受过调强放射治疗和/或近距离放射治疗作为辅助(化疗)放疗的患者。
- 可获得随访信息的患者。
排除标准:
- 治疗信息不完整的患者。
- 术后有残留病灶的患者。
- 因术后复发而接受治疗的患者。
- 失访的患者。
- 患有免疫抑制性疾病的患者。
学习计划
研究是如何设计的?
设计细节
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 |
|---|---|---|
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≥II级胃肠道及泌尿生殖道毒性的3年发生率
大体时间:3年
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审核2020年1月至2023年12月期间接受辅助调强放射治疗(联合或不联合化疗)的宫颈癌和子宫内膜癌女性患者中≥II级胃肠道与泌尿生殖系统毒性的3年发生率
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3年
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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报告接受辅助放射治疗患者的急性毒性反应
大体时间:3年
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报告从治疗完成至3年内接受辅助放疗患者的急性毒性
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3年
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分别评估宫颈癌和子宫内膜癌的无病生存期和总生存期。
大体时间:3年
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评估从治疗完成至3年期间的3年无病生存率和总生存率(分别针对宫颈癌和子宫内膜癌)
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3年
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评估局部区域控制
大体时间:3年
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评估从治疗完成至3年期间的3年局部区域控制率
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3年
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报告用于预测晚期II-IV级胃肠道和泌尿生殖系统毒性的剂量-体积参数
大体时间:3年
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报告剂量-体积参数,用于预测治疗完成后至3年内II-IV级晚期胃肠道和泌尿生殖系统毒性
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3年
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比较正在进行的和已完成的机构术后调强放射治疗试验结果
大体时间:3年
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比较从治疗完成到3年期间,正在进行的和已完成的机构术后IMRT试验的结果
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3年
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合作者和调查者
出版物和有用的链接
一般刊物
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研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
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
其他研究编号
- 4454
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
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