A Study Comparing Whole-Body Heat Treatment Plus Systemic Therapy to Systemic Therapy Alone, for Advanced Pancreatic Cancer (MATTERS-2)
A Multi-Centric, Randomized, Pivotal Study, Evaluating Efficacy and Safety of Whole-Body Hyperthermia Alongside Standard Systemic Anticancer Therapy in Patients With Metastatic Pancreatic Cancer After Failure of First Line Treatment.
Pancreatic ductal adenocarcinoma (PDAC) is associated with poor prognosis and limited treatment options following failure of first-line therapy. Whole-body hyperthermia (WBHT) is a non-invasive treatment approach that raises the body's core temperature under controlled conditions and may enhance the effects of anticancer therapies through multiple biological mechanisms, including improved drug delivery, modulation of the immune response, and increased sensitivity to treatment.
The MATTERS-2 study is a multicentre, randomized clinical trial designed to evaluate the efficacy and safety of WBHT in combination with standard systemic anticancer therapy in patients with metastatic PDAC after failure of first-line treatment. Participants will receive either standard systemic therapy alone or standard systemic therapy combined with WBHT.
The primary objective of the study is to determine whether the addition of WBHT improves clinical outcomes compared with standard therapy alone in terms of overall survival (OS) while maintaining safety. Secondary objectives include other clinical outcomes such as progression-free survival (PFS), disease control rate (DCR) and objective response rate (ORR). Further, quality of life assessments (QoL) and exploratory biomarker analyses will also be performed.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ2
- フェーズ 3
連絡先と場所
研究連絡先
研究連絡先
- 名前:John-Paul Bogers, Prof. Dr.
- 電話番号:+32 474296669
- メール:john-paul.bogers@elmedix.com
研究場所
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Madrid
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Madrid、Madrid、スペイン、28050
- Hospital Universitario HM Sanchinarro (HM CIOCC)
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主任研究者:
- Antonio Cubillo, Dr.
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Navarre
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Pamplona、Navarre、スペイン、31008
- Clinica Universidad de Navarra
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主任研究者:
- Mariano Ponz, Dr.
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Antwerpen
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Antwerp、Antwerpen、ベルギー、2650
- Universitair Ziekenhuis Antwerpen (UZA)
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主任研究者:
- Timon Vandamme, Prof. Dr.
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Oost-Vlaanderen
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Ghent、Oost-Vlaanderen、ベルギー、9000
- Algemeen Ziekenhuis Maria Middelares (AZ MM)
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主任研究者:
- Vincent Bouderez, Dr.
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-
参加基準
適格基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Subjects at least 18 years of age at time of signing the informed consent
- Subjects with metastatic pancreatic adenocarcinoma (PDAC) confirmed by histology
- Measurable disease per RECIST 1.1
- Subjects previously treated with chemotherapy in first line for metastatic disease
- ECOG performance status ≤ 1
- Height ≤ 2,00 m, BMI maximal 40 or positive fitting session
- Adequate liver structure (accessible metastasis-free and functional liver parenchyma) allowing stable liver sensor positioning without unacceptable risks of bleeding and perforation, based on echographic assessment (or any imaging modality)
Adequate bone marrow function defined as
- white blood cell count ≥ 2000/µl
- neutrophils ≥ 1500 cells/μL
- platelets ≥ 100 x 109/L
- hemoglobin ≥ 9 g/dl (female) and ≥10 g/dl (male) documented
Adequate coagulation defined as
- PT (%) ≥ 70%
- aPTT ≤ ULN
Adequate liver function defined as
- Transaminases (AST, ALT) ≤ 2.5 x ULN or ≤ 5.0 in presence of liver metastasis
- bilirubin ≤ 2 x ULN
- Adequate renal function defined as calculated eGFR ≥ 60 mL/min (CKD-EPI equation)
- Normal ionogram
- Effective contraception for both male and female subjects if applicable. Women of childbearing potential must have a negative pregnancy test at screening visit.
- Written informed consent must be given according to good clinical practice and national/local regulations.
Exclusion Criteria:
- Pregnant or breastfeeding women
- Presence of brain metastasis (known or suspected)
- Other malignant diseases in the medical history during the last 5 years (exceptions: carcinoma in situ of the cervix or adequately treated basal cell carcinoma of the skin)
- Serious medical risk factors involving any of the major organ systems, including high cardiovascular risk defined as recent major cardiovascular events (such as myocardial infarction or stroke), clinically relevant heart failure due to structural or mechanical cardiac abnormalities (e.g., valvular disease or myocardial dysfunction), and clinically significant arrhythmias.
- Pathology that would interfere with the placement of the bladder catheter
- Clinically significant pulmonary disease which might interfere with mechanical ventilation
- History of autonomic dysfunction (due to the influence on skin blood flow)
- History of malignant hyperthermia
- History of untreated endocrine pathology (e.g. diabetes type II, hyper- or hypothyroidism).
- Primary untreated diabetes type I not related to the oncological condition (due to vascular complications).
- Known allergies to drugs that will be used during the trial (e.g. anesthetic, analgesic, chemotherapy)
- Active infections not controlled by medication
- Presence of clinically significant ascites and/or decompensated cirrhosis/portal hypertension
- Severe, non-healing wounds, ulcers or bone fractures
- Organ allografts requiring immunosuppressive therapy
- Implants that are not compatible with temperature changes
- (History of) clinically significant (investigator decision) psychiatric disorder and/or psychosocial disorder that may interfere with adequate compliance to the protocol or signature of the informed consent
- Other clinically significant disease which could impair the subject's ability to participate in the study according to the investigator's opinion
- Participation in another clinical trial 2 weeks prior to the randomization
- Biological therapy during the 2 weeks prior to the randomization
- Radiotherapy up to 2 weeks prior to the randomization
- Major surgery up to 6 weeks prior to the randomization (port-a-cath placement is minor)
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
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
アクティブコンパレータ:Control group
Participants receive standard-of-care systemic treatment as indicated for metastatic pancreatic ductal adenocarcinoma (mPDAC, stage IV) after failure of the first-line treatment.
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Standard-of-care systemic therapy for patients with metastatic pancreatic ductal adenocarcinoma (mPDAC, stage IV) after failure of first-line treatment.
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実験的:Whole-body hyperthermia treatment (WBHT) group
Participants will receive whole-body hyperthermia (WBHT) alongside their indicated standard-of-care systemic treatment.
|
Standard-of-care systemic therapy for patients with metastatic pancreatic ductal adenocarcinoma (mPDAC, stage IV) after failure of first-line treatment.
Initially every 2 weeks, until a total of 3 treatments is reached.
Thereafter every 4 weeks.
The treatment will raise the body temperature to 41,50 °C for a total of 4 hours.
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall survival (OS)
時間枠:From randomization until death from any cause, assessed up to study completion (primary analysis triggered upon occurrence of 66 death events), an (expected) average of 12 months
|
To compare Overall Survival (OS) between WBHT + standard-of-care (SoC) and SoC treatment group
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From randomization until death from any cause, assessed up to study completion (primary analysis triggered upon occurrence of 66 death events), an (expected) average of 12 months
|
|
Safety and tolerability of WBHT + SoC and SoC alone
時間枠:From moment of enrollment (ICF signature) up to End of Treatment visit, an (expected) average of 10 months
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Incidence of Adverse Events (AE), Serious Adverse Events (SAE), treatment-related AE/SAE and Adverse Device Effects (ADE).
They will be reported from moment of enrollment (ICF signature) up to End of Treatment visit and will be assessed for seriousness, severity and relationship to the device and to WBHT treatment.
|
From moment of enrollment (ICF signature) up to End of Treatment visit, an (expected) average of 10 months
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Progression-free survival (PFS)
時間枠:Up to time of progression, death or study discontinuation; an (expected) average of 8 months
|
To compare Progression-Free Survival (PFS) between WBHT +SoC and SoC treatment group based on RECIST 1.1.
criteria.
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Up to time of progression, death or study discontinuation; an (expected) average of 8 months
|
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Disease control rate (DCR)
時間枠:Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
To compare Disease Control Rate (DCR) between WBHT +SoC and SoC treatment group based on RECIST 1.1 criteria.
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Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
|
Objective response rate (ORR)
時間枠:Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
To compare Objective Response Rate (ORR) between WBHT +SoC and SoC treatment group based on RECIST 1.1 criteria and further described with duration of response (DOR) and time to response (TTR).
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Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
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Quality of Life assessments (EORTC-QLQ-C30 version 3)
時間枠:Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
Quality of Life (QoL) according to EORTC-QLQ-C30 version 3 scoring changes from baseline (at 4-weeks, 8-weeks and End of Treatment)
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Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
|
Quality of Life assessments (QLQ Pan 26)
時間枠:Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
Quality of Life (QoL) according to QLQ Pan 26 scoring changes from baseline (at 4-weeks, 8-weeks and End of Treatment)
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Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
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Evolution of CA19-9
時間枠:Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
To evaluate CA19-9 changes from baseline in WBHT +SoC and SoC treatment groups (at 4-weeks, 8-weeks and End of Treatment)
|
Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
その他の成果指標
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Exploratory analyses
時間枠:Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
To explore potential biomarkers and molecular correlates through the analysis of blood and tumor tissue samples.
|
Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
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
その他の研究ID番号
- CIV-26-06-058215
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
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