Набор скоро начнётся NCT07711067

A Study Comparing Whole-Body Heat Treatment Plus Systemic Therapy to Systemic Therapy Alone, for Advanced Pancreatic Cancer

Фаза II / Фаза III С лечением Pancreatic Ductal Adenocarcinoma (mPDAC) Metastatic Pancreatic Ductal Adenocarcinoma (PDAC)

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают: В протоколе указаны: Whole-body hyperthermia, Standard-of-Care Systemic therapy.
Кому может быть актуально: Состояния в реестре: Pancreatic Ductal Adenocarcinoma (mPDAC), Metastatic Pancreatic Ductal Adenocarcinoma (PDAC). Базовые параметры: от 18 лет · Все.
Что важно проверить: Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится: Бельгия, Испания
Следующий шаг: Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

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.

Обзор

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.

Вмешательства

Устройство Whole-body hyperthermia
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.
Препарат Standard-of-Care Systemic therapy
Standard-of-care systemic therapy for patients with metastatic pancreatic ductal adenocarcinoma (mPDAC, stage IV) after failure of first-line treatment.

Первичные конечные точки

Overall survival (OS) [Срок оценки: 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 [Срок оценки: From moment of enrollment (ICF signature) up to End of Treatment visit, an (expected) average of 10 months]

Вторичные конечные точки (6)

Progression-free survival (PFS) [Срок оценки: Up to time of progression, death or study discontinuation; an (expected) average of 8 months]
Disease control rate (DCR) [Срок оценки: Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months]
Objective response rate (ORR) [Срок оценки: Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months]
Quality of Life assessments (EORTC-QLQ-C30 version 3) [Срок оценки: Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months]
Quality of Life assessments (QLQ Pan 26) [Срок оценки: Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months]
Evolution of CA19-9 [Срок оценки: Until death, end of treatment visit or study discontinuation; an (expected) average of 10 months]

Критерии участия

Критерии включения

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.

Критерии исключения

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)