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NCT07393633Completed

Assessing Whole-body Metabolism in Gynecologic Cancers in Response to a Single Chemotherapy Cycle and/ or Immunotherapy

Source: ClinicalTrials.gov · Last updated 10 Feb 2026

Brief summary (registry, in English)

It is well established that cancer cells have fundamentally altered metabolism, which contributes to tumorigenicity and malignancy. For years, research findings supported that the universal property of all cancer cells was to increase glycolytic flux for anaerobic glycolysis (i.e., Warburg effect), which was accepted as the dominant pathway for energy metabolism. Fortunately, by understanding these changes in cellular metabolism multiple new approaches to cancer therapy, focused on reprogramming the energy metabolism of the cell. Recently, further investigation in the field found that cancer cells exhibit multiple alterations in metabolic pathways, not only glycolysis. Alterations in lipid metabolism in cancer cells have recently been recognized as potential targets for therapeutic interventions due to its role in cellular proliferation, energy storage, and the generation of signaling molecules. Numerous cancer types can rely on lipids as an energy source, increasing fatty acid synthesis and degradation to promote proliferation and metastasis. Several therapeutic agents utilized in gynecologic malignancies impact lipid metabolism. The objective of the proposed study will be to determine the impact of cancer directed therapy on the lipid metabolism of non-malignant tissues. No study to date has assessed whole-body lipid metabolism in patients undergoing chemotherapy (i.e. cytotoxic chemotherapy and/or immunotherapy). These novel findings will provide crucial knowledge about the dysregulation of whole-body metabolism in patients receiving chemotherapy for treatment of gynecologic cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
43 (actual)
First submitted
30 Jan 2026
Start date
1 Aug 2024
Primary completion date
4 Apr 2025
Lead sponsor
University of Tennessee Graduate School of Medicine
NCT number
NCT07393633

What you commit to

  • Study type: Observational
  • Participants enrolled: 43
  • From 1 Aug 2024 to the primary completion date, 4 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Received inpatient medical intervention for adverse effects of chemotherapy.

Other illness

  • Circumstances and/or medical condition that would limit compliance with study requirements and protocol, as determined by the principal investigators.

Other

  • Inability to provide voluntary informed consent.

Who the study is looking for

  • Women
  • Age \>18 years
  • Biopsy confirmed gynecologic cancer.
  • Scheduled to or currently undergoing infusion therapy.
  • Receiving cytotoxic chemotherapy or immunotherapy.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Tennessee Medical Center
Coordinator of this site? Confirm its status
KnoxvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.