Overview

A Randomised Placebo-Controlled Study of Use of GnRHa During Chemotherapy for Fertility Protection of Young Women With Cancer

Status:
Not yet recruiting
Trial end date:
2032-01-31
Target enrollment:
0
Participant gender:
Female
Summary
Many cytotoxic drugs may harm the fertility of young women treated for cancer. The aim of the study is to investigate if the Gonadotropin-Releasing Hormone agonist (GnRHa) during cancer treatment can preserve the fertility of young female cancer subjects. Approximately 300 women with newly diagnosed breast cancer and up to 200 women with newly diagnosed lymphoma, acute leukemias or sarcomas will be recruited before start of cancer treatment. The patients will be randomised in between treatment with triptorelin (experimental) or placebo (control) intramuscularly a 1:1 ratio during chemotherapy. The injections may be given once monthly or once three months depending on type of chemotherapy given. Randomisation and study drug is blinded, neither investigator, research nurse nor patient will know if it is active drug or placebo. The only person who knows is the nurse preparing the injection. Patients will be followed up to 5 years after end of treatment with physical examinations, vital signs, biochemical markers, bone mineral density exams, ultrasound for antral follicle counts and ovarian doppler flow, concomitant medications, adverse events and quality of life questionnaires.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Kenny Rodriguez-Wallberg
Treatments:
Triptorelin Pamoate
Criteria
Inclusion Criteria:

- Signed informed consent

- Breast cancer or acute leukemias, lymphomas (Hodgkin and non-Hodgkin) or sarcomas
(osteo, soft tissue and Ewing) confirmed by histology and assigned for
diseace-specific chemotheraphy

- Confirmed menarche

- ECOG performance status 0-1

- Adequate bone marrow, renal, hepatic and cardiac functions and absence of other
uncontrolled medical or psychiatric disorders

Exclusion Criteria:

- Demonstrated premature ovarian failure at time of randomization according to clinical
or biochemical data

- Previous or planned bilateral oophorectomy

- Pregnancy or breastfeeding at time of start of chemotherapy

- Other malignancy diagnosed within the last five years

- Uncontrolled hypertension, heart, liver, kidney related or other uncontrolled medical
or psychiatric disorders including previous or current diagnosis of anorexia

- Known osteoporosis

- Known low platelet count with increased bleeding risk or refractory thrombocytopenia
in subjects with acute leukemias

- Known or suspected allergy against triptorelin

- Direct radiation of the gonads previous or planned (TBI allowed)

- Mental inability, reluctance or language difficulties that result in difficulty
understanding the meaning of study participation