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NCT04275713CompletedPhase 2

Altered Tumor Oxygenation by Metformin, a Potential Step in Overcoming Radiotherapy Resistance in LACC

Altered Tumor Oxygenation by Metformin, a Potential Step in Overcoming Radiotherapy Resistance in Locally Advanced Cervical Cancer.

Source: ClinicalTrials.gov · Last updated 20 Jan 2025

Brief summary (registry, in English)

Poor tumor oxygenation (hypoxia) is an established negative prognostic and predictive factor in locally advanced cervical cancer (LACC). Hypoxia-modifying measures implemented in the clinic are lacking. Metformin is a well-known, well-tolerated and low-cost drug used for decades in the treatment of type 2- diabetes. Recent studies suggest an improved tumor oxygenation by metformin potentially improving radiotherapy response and patient outcome. This study is a randomized, phase II, open label study in patients with LACC where patients are randomized to standard cisplatin-based chemoradiotherapy +/- Metformin. Metformin will be started one week prior to the start of chemoradiotherapy, and will be continued throughout the entire radiation treatment. Tumor oxygenation will be evaluated by gene signatures and MRI- parameters.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
41 (actual)
First submitted
12 Feb 2020
Start date
22 May 2020
Primary completion date
11 Jun 2024
Lead sponsor
Oslo University Hospital
NCT number
NCT04275713

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 41
  • From 22 May 2020 to the primary completion date, 11 Jun 2024
  • 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

  • Evidence of distant metastasis. Suspicious paraaortic lymph nodes below the renal vessel are allowed if they are covered by the radiation field
  • Patients who have received other cancer treatments for their cervical cancer
  • Patients who receive other experimental drugs
  • Currently taking Metformin or any other antidiabetic drugs (sulfonylureas, thiazolidinediones, insulin)
  • Uncontrolled intercurrent somatic illness including, but not limited to, ongoing or active serious infections, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, myocardial infarction within 6 months and cerebrovascular disease with previous stroke
  • Already on medication with increased risk of lactic acidosis
  • Patients who are pregnant or breastfeeding are excluded due to risk of teratogenic and abortifacient effects of radiotherapy and cisplatin, and the potential risk of adverse effect of nursing infants

Other illness

  • Known diabetes mellitus
  • History of allergic reaction attributed to compounds of similar chemical or biologic composition to metformin
  • Any condition associated with increased risk of metformin- induced lactic acidosis (congestive heart failure defined as New York Heart Association (NYHA) class III or IV functional status, history of acidosis of any kind)

Lab values

  • Contraindications such as
    • Hypersensitivity to the active substance or to any of the excipients listed Section 6.1.
    • Severe renal failure (GFR \<30 ml / min).
    • Acute conditions leading to the risk of renal impairment, eg: dehydration, severe infectious conditions, shock.
    • Disease that can cause tissue hypoxia (especially acute illness or exacerbation of chronic illness), such as: acute decompensated heart failure, lung failure, recent heart attack, shock.
    • Liver failure, acute alcohol intoxication, alcoholism.

Who the study is looking for

  • Histologically confirmed cervical cancer (squamous cell carcinoma, adenocarcinoma and adenosquamous carcinoma)
    • Planned for radical chemoradiotherapy
    • Over 18 years
    • Speaks and understands Norwegian
    • ECOG 0-1
    • Cervical tumor available for biopsy by gynecological examination
    • Hemoglobin ≥ 9 g/dL (blood transfusions are allowed)
    • Leukocytes ≥ 3,5 x 10\^9/L 18
    • Absolute neutrophil count ≥ 1,5 x 10\^9/L
    • Platelets ≥ 100 x 10\^9/L
    • Total bilirubin ≤ 25 umol/L
    • AST/ALT ≤ 2,5 x institutional upper limit
    • Creatinine ≤ 90 or creatinine clearance ≥ 60 ml/min/1.73m2 Patients with elevated creatinine secondary to hydronephrosis may be eligible if renal function returns to normal after inserting an internal stent or nephrostomy
    • Women of childbearing potential (WOCBP) should have a negative highly sensitive serum pregnancy test within 72 hours prior to receiving the first dose of study medication.

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
Oslo University Hospital
Coordinator of this site? Confirm its status
OsloNorwayUnknown status

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