Sparing of Organs at Risk in High Dose Rate Brachytherapy
Prospective Study on the Sparing of Organs at Risk in High Dose Rate Brachytherapy for Cervix Cancer
Cervix carcinoma is a common malignancy. Radiation therapy still remains a major treatment for patients with carcinoma cervix. Conventional treatment with radiation therapy includes a combination of external beam radiation therapy and intracavitary treatment. Low dose rate intracavitary brachytherapy treatment is already well studied. But high dose rate brachytherapy is a relatively new alternative.
In brachytherapy, major developments have been made in the integration of 3D imaging and computerized 3D treatment planning. Medical imaging improvements allowed for better definition of tumoral volumes and organs at risk.
The GYN GEC-ESTRO published recommendations on the 3D imaging for better characterization of these volumes. Improvements in CT-SCan and lately in RMN had lead to a better definition of volums of interest (tumor and his extensions and organs at risk : bladder, rectum, sigmoidis, small bowels). RMN is the imaging standard in the evaluation of tumoral extension in cervix cancer. However its use is not easy in many brachytherapy departments.
This study will evaluate the feasibility and sparing of organs at risk for high dose rate brachytherapy if volume delineation is done at each of the two sessions performed with 3D RMN.
調査の概要
状態
詳細な説明
After 60 Gy are delivered with Intensity Modulated Radiation Therapy (IMRT), the brachytherapy in high dose rate will deliver 15 Gy to the CTVhr (high risk CTV) in two sessions.
A clinical examination and an RMN are performed at the end of the external radiation to evaluate the residual tumoral volume. Two HDR brachytherapy sessions are then performed.
During the first session, a CT-Scan and an RMN will be performed after the fletcher application. A second CT-Scan will be performed during the second treatment session to create new volumes and to improve organs at risk sparing.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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-
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Lille、フランス、59020
- Centre Oscar Lambret
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
Patients with indication of HDR brachytherapy in cervix carcinoma of stage IB to II.
After realization of external radiation therapy done (60 Gy in IMRT)
説明
Inclusion Criteria:
- Cervix carcinoma stage Ib to IV (FIGO)
- OMS < 2
- Tomography by positron emission and/or chirurgical staging before the external radiotherapy
- RMN before the starting of treatment and at the end af external radiotherapy
- Patient information
- Validation of the indication af high dose rate brachytherapy
- External radiation therapy (60 Gy with IMRT)
Exclusion Criteria:
- No external radiation therapy
- Surgery in the 4 weeks before before the inclusion
- Prior pelvic radiation therapy
- intestinal inflammatory disease or active pathology
- active infection or severe pathology didn't allow the treatment
- Prior carcinoma in the last 5 years (except cutaneous carcinoma or in situ carcinoma)
- Inclusion in another clinical trial
研究計画
研究はどのように設計されていますか?
デザインの詳細
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Evaluation of the sparing of organs at risk with a delineation at each session and the CTVhr volume modification
時間枠:At 8 weeks of external radiotherapy
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To record the irradiated volumes modifications of each OAR at each session and the CTV volume modification.
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At 8 weeks of external radiotherapy
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Evaluation of medical imaging with CT-Scan and RMN for cervix cancer
時間枠:At 8 weeks of external radiotherapy
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|
At 8 weeks of external radiotherapy
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協力者と研究者
スポンサー
捜査官
- スタディディレクター:Philippe Nickers, MD, PhD、Centre Oscar Lambret
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- BRACHY-HDR
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