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Study identifier: NCT06649474 Synced from ClinicalTrials.gov · July 29, 2026
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Evaluation, in Humans, of the Correlation Between Hepatotoxicity, Neurotoxicity Induced by Oxaliplatin, and Blood Levels of HMGB1

Condition: Pancreatic Cancer · Resectable Pancreatic Adenocarcinoma · Adenocarcinoma  ·  Sponsor: University Hospital, Clermont-Ferrand

PhaseNA
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Oesogastric and pancreatic adenocarcinomas are poor-prognosis cancers. Incidence of pancreatic cancer drastically increases to such an extent that it will become the second cause of cancer's mortality by 2030. A major challenge is to optimize the therapies for localized setting, when oxaliplatin-based chemotherapy is the standard, before and after surgical excision. Because in 50% of cases oxaliplatin triggers a grade 2-3 sinusoidal obstruction syndrome (SOS) which increases post-operative morbidity, decreases histological response to chemotherapy, increases tumor recurrence, and aggravates the risk of chemotherapy-induced peripheral neuropathy (CIPN). There is an urgent need to better understand the biological processes involved in SOS, in order to prevent and treat it without stopping or reducing oxaliplatin administration. The biological link between oxaliplatin and SOS has not been described, but recent murine experiments argue for HMGB1 to be the mediator released after exposure to oxaliplatin and inducing SOS, and thereafter CIPN. To date, no biomarker is established between murine and patient analyses, and the release of HMGB1 after oxaliplatin treatment and its effect on hepatic parenchyma is not described in patients. Investigators hypothesized is that HMGB1 would also been increased in patients after oxaliplatin treatment, and correlated to the development of SOS and CIPN. If confirmed, personalized treatment will be possible to target this pathway. Therefore, in…

This description comes directly from the study's public registry record.

Talk to the study team

Marine JARY, MD  ·  +33 4 73 75 05 08  ·  mjary@chu-clermontferrand.fr

Brigitte GILLET  ·  bgillet@chu-clermontferrand.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU Estaing de Clermont-FerrandClermont-Ferrand, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06649474