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ArticleCancer research communications2026

The MATTERS Trial: Safety and Tolerability of Whole-Body Hyperthermia at 41.50°C in Combination with Chemotherapy in Metastatic Cancer Patients.

Luigi Brancato, Ivana Gorbaslieva, Oleg Rudenko, Tine Logghe, Eke van Zwol, Gaëlle Boulet, Laurent Van den Bossche, Johan Van den Bossche, Marc Peeters, Thiery Chapelle and 6 more

Registry-linked trialAbstract read
In one paragraph

Article in Cancer research communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07564440 (Clinical and Biological Safety Study of the BTT Hyperthermia in Adult Subjects), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07564440 naenrolling by invitationnot on this map

Clinical and Biological Safety Study of the BTT Hyperthermia in Adult Subjects

TypeinterventionalSponsorMarc AbreuRan2026 to 2026Enrolled20ConditionsSafety StudyArmsHyperthermia
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Luigi Brancato *ElmediX NV, Leuven, Belgium.ORCID 0000-0002-3396-5445
Ivana Gorbaslieva *Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0003-2276-379X
Oleg RudenkoElmediX NV, Leuven, Belgium.ORCID 0000-0002-1295-3218
Tine LoggheElmediX NV, Leuven, Belgium.ORCID 0009-0002-0812-131X
Eke van ZwolElmediX NV, Leuven, Belgium.ORCID 0000-0002-3152-8903
Gaëlle BouletElmediX NV, Leuven, Belgium.ORCID 0009-0007-1295-6973
Laurent Van den BosscheElmediX NV, Leuven, Belgium.ORCID 0009-0000-2643-2790
Johan Van den BosscheElmediX NV, Leuven, Belgium.ORCID 0000-0002-5498-6368
Marc PeetersFaculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0003-4969-2303
Thiery ChapelleFaculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0002-6923-2278
Vera SaldienFaculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0002-5151-8999
Peter VueghsElmediX NV, Leuven, Belgium.ORCID 0000-0002-9421-037X
Timon VandammeFaculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0003-3701-5305
Rowan DankerluiFaculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0009-0004-3323-0651
Dirk YsebaertFaculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0002-3350-6994
Johannes BogersElmediX NV, Leuven, Belgium.ORCID 0000-0001-9107-132X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWhole-body hyperthermia (WBHT) is a promising therapy for advanced malignancies, including metastatic pancreatic ductal adenocarcinoma (PDAC). This first-in-human study evaluated the safety and tolerability of repeated WBHT sessions at 41.50°C for various treatment durations and in combination with standard-of-care chemotherapy regimens. PATIENTS AND

methodsTwelve patients with advanced solid tumors, primarily metastatic PDAC, completed the study. WBHT was administered using an innovative medical device (TempoCure, ElmediX) as monotherapy or with standard-of-care chemotherapy in escalating durations of 2, 4, and 6 hours, in four cohorts. Safety was assessed through adverse event (AE) monitoring, serious AE (SAE) reporting, and comprehensive clinical and laboratory evaluations up to a 10-week follow-up. Tolerability was evaluated according to whether patients were able to complete all planned WBHT cycles, with or without concomitant chemotherapy, without the need for dose modifications or treatment interruptions.

resultsThe WBHT treatment was well tolerated, with most patients completing scheduled treatments despite advanced disease. The most frequent AEs were fatigue, hypokalemia, nausea, and diarrhea. Initial decubitus ulcers led to improved patient handling protocols. No clear increase in AE or SAE incidence was associated with longer WBHT durations or chemotherapy combination. The trend toward fewer AEs in later treatments likely reflects a procedural learning curve.

conclusionsWBHT administered with the TempoCure system at 41.50°C for 2, 4, and 6 hours is safe and tolerable alone or in combination with chemotherapy, in patients with advanced cancer refractory to prior treatments. These findings support further investigation in upcoming randomized trials designed to evaluate efficacy in metastatic PDAC. SIGNIFICANCE: The MATTERS trial demonstrates that WBHT at 41.50°C, delivered with the TempoCure device, is a safe and well-tolerated treatment for advanced malignancies, particularly in patients with refractory metastatic PDAC. These findings support the integration of WBHT with standard chemotherapy regimens, paving the way for future efficacy trials aimed at improving therapeutic outcomes in challenging cancer populations.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalHyperthermia, InducedNeoplasmsPancreatic NeoplasmsAdultAgedCombined Modality TherapyFemaleHumansMaleMiddle AgedNeoplasm MetastasisTreatment Outcome

Identifiers

PMID41642747
PMCPMC12869149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.