小さな腎腫瘍と原発性および二次性肝腫瘍の治療のためのマイクロ波焼灼療法
小さな腎腫瘍と原発性および二次性肝新生物の治療のためのマイクロ波熱アブレーションを受けている患者の短期、中期、および長期の臨床成績の回顧的および展望的分析
The goal of this observational study is to collect data on efficacy and safety of microwave ablation (MWA) used to treat subjects with primary and secondary liver malignancies and renal malignancies. The main question it aims to evaluate the short, medium and long-term clinical course of patients treated with MWA.
Participants will not alter their normal clinical and therapeutic practice, due to the observational nature of the study, and all data regarding microwave treatments will be collected (including demographic data). follow their normal clinical and therapeutic path
調査の概要
詳細な説明
Observational, retrospective and prospective, monocentric study. The objective is to evaluate the short, medium and long-term clinical course of patients undergoing microwave ablation (MWA) for small renal tumors and primary and secondary liver neoplasms. Evaluation of clinical efficacy (progression free survival),safety and technical outcome of microwave ablation as well as clinical outcome of the procedure will be evaluated.At the end of the follow-up periods, the data collected will be compared with those available in the literature on MWA, cryoablation (CA), radiofrequency ablation (RFA) and surgical resection.
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前：Francesco De Cobelli, MD
- 電話番号：+390226432529
- メール：decobelli.francesco@hsr.it
研究連絡先のバックアップ
- 名前：Stephanie Steidler, PhD
- 電話番号：+3926432529
- メール：steidler.stephanie@hsr.it
研究場所
-
-
-
Milan、イタリア、20153
- 募集
- IRCCS Ospedale San Raffaele
-
コンタクト：
- Francesco De Cobelli
- メール：decobelli.francesco@hsr.it
-
コンタクト：
- Stephanie Steidler, PhD
- 電話番号：+390226432529
- メール：steidler.stephanie@hsr.it
-
副調査官：
- Paolo Marra, MD
-
副調査官：
- Michele Colombo, MD
-
-
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
Subjects with indication of laparoscopic or percutaneous ablation of primary or secondary liver tumors and small primary kidney tumors (according to ESMO guidelines).
All patients will follow their normal therapeutic procedure and no examination will be added to what is already provided for in the normal management of patients suffering from these diseases.
説明
Inclusion Criteria:
- > 18 years with primary or secondary liver tumors or small kidney tumors that are not candidates for surgery or cannot be radically resected by surgery alone
- Primary liver cancer: up to three liver nodules ≤ 3 cm
- Secondary hepatic tumours: up to nodules ≤ 3 cm provided that the objective is complete hepatic clearance Renal tumours: single or multiple (von Hippel Lindau syndrome), < 4 cm
Exclusion Criteria:
- pregnant women
- non-manageable coagulopathies
- Extended extrahepatic or extrarenal disease
- for liver ablation: presence of bilio-digestive anastomosis
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
- 観測モデル：COHORT
- 時間の展望：CROSS_SECTIONAL
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
Small Renal Tumors
Subjects with small renal tumors (SRT) ad described by current ESMO (European Society for Medical Oncology) guidelines who are candidates for MWA |
Thermal ablation |
|
Primary and Secondary Liver cancer
Primary liver tumors: subjects who are candidates for MWA with nodules ≤ 3 cm Liver metastases: subjects who are candidates for MWA with nodules less than ≤ 3 cm |
Thermal ablation |
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 |
|---|---|---|
|
Local Tumor Progression Free Survival
時間枠：From date of ablation until death from any cause; evaluated up to 5 years
|
Based on imaging evidence of tumor reccurence at site of ablation (within 5mm of ablation margins) |
From date of ablation until death from any cause; evaluated up to 5 years
|
|
Time to Local Progression
時間枠：From date of ablation until death from any cause; evaluated up to 5 years
|
Time from ablation to imaging evidence of tumor reccurence at site of ablation (within 5mm of ablation margins) |
From date of ablation until death from any cause; evaluated up to 5 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Survival (OS)
時間枠：From date of ablation until death from any cause; evaluated up to 5 years
|
From date of ablation until death for any cause |
From date of ablation until death from any cause; evaluated up to 5 years
|
|
Progression Free Survival (PFS)
時間枠：From date of ablation until death from any cause; evaluated up to 5 years
|
From date of ablation until any documented evidence of tumor progression at any site |
From date of ablation until death from any cause; evaluated up to 5 years
|
|
Organ specific Progression Free Survival (PFS)
時間枠：From date of ablation until death from any cause; evaluated up to 5 years
|
From date of ablation until any documented evidence of tumor progression at the ablated organ (including reccurence at ablation site) |
From date of ablation until death from any cause; evaluated up to 5 years
|
協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
- De Cobelli F, Marra P, Ratti F, Ambrosi A, Colombo M, Damascelli A, Sallemi C, Gusmini S, Salvioni M, Diana P, Cipriani F, Venturini M, Aldrighetti L, Del Maschio A. Microwave ablation of liver malignancies: comparison of effects and early outcomes of percutaneous and intraoperative approaches with different liver conditions : New advances in interventional oncology: state of the art. Med Oncol. 2017 Apr;34(4):49. doi: 10.1007/s12032-017-0903-8. Epub 2017 Feb 20.
- di Gaeta E, Olivieri M, Savi A, Magnani P, Canevari C, Gusmini S, Palumbo D, Guazzarotti G, Augello L, Calabrese F, Steidler S, Cipriani F, Rimini M, Casadei-Gardini A, Aldrighetti L, Chiti A, De Cobelli F. Radioembolization for Hepatocellular Carcinoma: a Comparison on Dual-phase Cone-beam CT, Contrast-enhanced CT (CECT) and 99mTc-macroaggregated albumin-SPECT/CT in predicting final distribution volumes and dosimetry of the post-embolization 90Y PET/CT. Radiol Med. 2025 Apr;130(4):474-485. doi: 10.1007/s11547-024-01946-0. Epub 2024 Dec 20.
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
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 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- MWA-01
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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