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

  • STATUS
    Recruiting
  • participants needed
    90
  • sponsor
    Oslo University Hospital
Updated on 19 February 2024
cancer
diabetes
blood transfusion
renal function
serum pregnancy test
neutrophil count
squamous cell carcinoma
adenocarcinoma
chemoradiotherapy
carcinoma
hypoxia
metformin
hydronephrosis
renal function test
adenosquamous carcinoma
nephrostomy
cervical neoplasm
cervical cancer
cisplatin

Summary

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.

Details
Condition Cervical Cancer, Cervical Cancer, Uterine Cancer, Uterine Cancer
Age 18years - 100years
Treatment Metformin, Cisplatin
Clinical Study IdentifierNCT04275713
SponsorOslo University Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

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
Known diabetes mellitus
Currently taking Metformin or any other antidiabetic drugs (sulfonylureas, thiazolidinediones, insulin)
History of allergic reaction attributed to compounds of similar chemical or biologic composition to metformin
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
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)
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
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