EMBRAVE: IntErnational Observational Study on Primary Chemoradiotherapy and iMage-based Adaptive BRAchytherapy for Vaginal cancEr
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 300
- 试验地点
- 1
- 主要终点
- Local failure
研究概览
简要总结
The goal of this clinical study is to improve clinical outcomes of patients with vaginal cancer including vaginal recurrences who are treated with curative intent by primary radio(chemo)therapy and image-guided adaptive brachytherapy (IGABT).
Being an observational, prospective registration study, wherein neither an experimental treatment is compared to the standard treatment, nor groups of patients are compared.
The specific aims are:
- to develop evidence-based recommendations for curative intent treatment with primary radio(chemo)therapy and IGABT.
- to identify prognostic parameters for oncological outcomes, morbidity and quality of life.
The study aims to enroll at least 300 patients. Oncological events will be evaluated at 2 and 5 years of follow-up. Acute and late morbidity events will be evaluated at end of treatment, 2 and 5 years of follow-up.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •o Histologically proven primary vaginal cancer, vaginal carcinoma in situ (VAIN) or vaginal recurrence, per WHO classification.
- •Histological proven stage I-IVA primary vaginal cancer: squamous cell carcinoma, adenocarcinoma or adenosquamous carcinoma of the vagina, other epithelial carcinoma's and carcinoma in situ
- •Histological proven vaginal recurrence from any gynaecological cancer for whom curative treatment is envisioned that includes image guided adaptive brachytherapy according to the target concept.
- •Para-aortic lymph node metastasis below L1-L2 interspace are allowed
- •Macroscopic visible tumour present on MRI and/or gynaecological examination at diagnosis.
- •Planned IGABT treatment with MRI-guided adaptive brachytherapy (at least the 1st fraction contouring and planning on MRI; CT for later fractions is allowed):
- •External beam radio(chemo)therapy followed by IGABT
- •IGABT alone for stage I <2cm or carcinoma in situ
- •Treatment with curative intent
- •Written informed consent
排除标准
- •Primary vaginal cancers with involvement of the ostium of the cervix or vulva (these should be classified as cervical cancer or vulvar cancer, respectively)
- •Metastatic disease beyond para-aortic region L1-L2 interspace
- •Sarcomas and melanomas.
- •Treatment only by external beam radiotherapy without brachytherapy to boost the primary disease
- •Primary vaginal cancer: treatment by primary surgery or debulking surgery
- •Vaginal recurrences: treatment by primary surgery or debulking surgery
- •Treatment with neo-adjuvant chemotherapy followed by surgery
- •Treatment with radiotherapy followed by surgery
- •Previous pelvic or abdominal radiotherapy
- •Pregnancy
结局指标
主要结局
Local failure
时间窗: 2 and 5 years of follow-up
A new, recurrent or progressive residual tumor within the external beam low-risk clinical target volume (CTV-TLR).
Acute physician-assessed morbidity and patient reported outcomes
时间窗: End of Treatment
Physician-assessed (CTCAE v.5) and Patient Reported Outcome (EORTC C30, selected items of CX24, EN24 and VU34).
Late physician-assessed morbidity and patient reported outcomes
时间窗: 2 and 5 years of follow-up
Physician-assessed (CTCAE v.5) and Patient Reported Outcome (EORTC C30, selected items of CX24, EN24 and VU34).
次要结局
- Other oncological outcomes(2 and 5 years of follow-up)
研究者
Prof. Dr. Remi A. Nout
Prof. dr.
Erasmus Medical Center