The Potential for Metformin to Improve Tumor Oxygenation in Locally Advanced Cervix Cancer: A Phase II Randomized Trial

NCT02394652CompletedPHASE2INTERVENTIONAL

Summary

Key Facts

Lead Sponsor

University Health Network, Toronto

Enrollment

16

Start Date

2015-05-21

Completion Date

2021-01-12

Study Type

INTERVENTIONAL

Official Title

The Potential for Metformin to Improve Tumor Oxygenation in Locally Advanced Cervix Cancer: A Phase II Randomized Trial

Interventions

MetforminCisplatinFAZA

Conditions

Uterine Cervical NeoplasmsSquamous Cell CarcinomaAdenocarcinomaCarcinomaAdenosquamous

Eligibility

Age Range

18 Years+

Sex

FEMALE

Inclusion Criteria:

* Histologically confirmed squamous cell carcinoma, adenocarcinoma or adenosquamous carcinoma of the cervix, FIGO stage IB2-IVA
* Planned for radical radiotherapy and concurrent cisplatin chemotherapy.
* Able to receive weekly cisplatin.
* No prior anticancer treatment for cervical cancer
* ECOG 0 or 1
* Life expectancy of greater than 3 months.
* Normal organ and marrow function
* Able to take oral medications.
* Ability to understand and willing to sign the consent form
* Willing to undergo biopsies of cervical tumor.

Exclusion Criteria:

* Evidence of distant metastases
* Receiving any other investigational agents concurrently or within 4 weeks.
* Known diabetes mellitus.
* Currently taking metformin, sulfonylureas, thiazolidinediones or insulin.
* History of allergic reactions attributed to compounds of similar chemical or biologic composition to metformin or cisplatin.
* Any condition associated with increased risk of metformin-associated lactic acidosis
* Uncontrolled inter-current illness
* Pregnant women
* History of another invasive malignancy, except for non-melanoma skin cancer or tumors curatively treated with no evidence of disease for \>=5 years.
* Known HIV-positive
* History of bowel obstruction or malabsorption syndromes
* History of active clinically significant bleeding
* Contraindications to radiotherapy
* Taking drug disulfiram (antabuse).

Outcome Measures

Primary Outcomes

• Change in fractional hypoxic volume of the tumor on FAZA-PET scan before and after 1 week of metformin.

Time frame: About 7 days

Secondary Outcomes

Disease-free survival

Time frame: 2 years

Acute and late gastrointestinal and genitourinary toxicities following metformin and chemoradiation.

Time frame: 2 years

Effect of metformin on endogenous hypoxia and other markers.

Time frame: About 7 days

Biomarkers of response to metformin.

Time frame: 2 years

Locations

Tom Baker Cancer Centre, Calgary, Canada

Cross Cancer Institute, Edmonton, Canada

Princess Margaret Cancer Centre, Toronto, Canada

Hôpital Maisonneuve-Rosemont, Montreal, Canada

Centre Hospitalier De L'Université de Montréal, Montreal, Canada