Impact of the Inhibitors of Tyrosine Kinase on the Male Fertility

Chronic Myeloid Leukemia Clinical Trial

— GLIFERTI  

Official title:

Impact of the Inhibitors of Tyrosine Kinase on the Male Fertility

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01114087
• Other study ID #: P070131
• Status: Completed
• Phase: N/A
• First received: April 29, 2010
• Last updated: March 28, 2011
• Start date: October 2008
• Est. completion date: May 2009

Study information

• Verified date: January 2011
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

Evaluate the possible deleterious effects of tyrosine kinase inhibitors on sperm concentration, after 6 months of therapy, which corresponds to 2 cycles of spermatogenesis and on the sperm nuclear integrity. The main comparison criterion will be the mean difference in sperm concentration before and after the 6 month treatment.

Description:

Antityrosine - kinases, such as imatinib are presently the gold standard therapy of chronic myeloid leukaemia (CML), with complete cytogenetic responses being achieved in 70-90% of patients receiving the drug as first -line monotherapy. Imatinib selectively inhibits the hybrid oncogen BCR/ABL involved in the genesis of CML and other tyrosine kinases, such as c-kit and platelet derived growth factor receptor (PGDF-R), involved in malignant gastro intestinal stromal tumours (GIST) . Despite its good tolerance, in vivo animal studies have proved that imatinib induces teratogenesis and dose-related effect on spermatogenesis. In humans, few pregnancies involving male CML patients have been reported with one spontaneous abortion, one case of gut malrotation and 15 healthy children. However, in the absence of detailed and definite evidence of the lack of deleterious effect of imatinib on spermatogenesis and sperm nuclear integrity in humans, specific studies are warranted. Male patients (38) will be included in this study if they are 18 to 60 years old, presenting with chronic myeloid leukaemia or malignant GIST and receiving for the first time a treatment by imatinib, a tyrosin-kinase inhibitor, preceded or not by hydroxyurea therapy for less than one month. These patients should have signed the informed consent and be covered by the French social security system. In this open prospective study, each patient will be his own control. The effect of imatinib on the spermatogenesis will be evaluated by the concentration of spermatozoa before the beginning of the treatment and after 6 months of imatinib, representing 2 cycles of spermatogenesis. Patients will be recruited by the onco-haematologists (5 corresponding centres) and referred to the CECOS Tenon. A medical investigator will collect the informed consent and fill the study file. A classical sperm analysis, according to OMS, will be performed. A sample of the ejaculate will be fixed for further analysis of the percentage of sperm nuclei with fragmented DNA (TUNEL procedure). The rest of the semen will be frozen, packaged in straws and stored in liquid nitrogen to be used, if necessary, by the patient if an ART is mandatory to conceive a child.Another sperm recovery will be performed after a period of 6 months under the anti tyrosine-kinase (ATK) therapy and the same sperm analysis will be carried out and the results compared to the first evaluation, before ATK. The plasmatic concentration of imatinib will be determined, for each patient, the day of the second sperm recovery to check the efficiency of ATK administration.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2
• Est. completion date: May 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Men from 18 to 60 years old

• Patients recently diagnosed CML or GIST

• Patients for whom a treatment by an inhibitor of tyrosine kinase in monotherapy is prescribed

• Patients having signed the informed consent

• Patients with social security

Exclusion Criteria:

• Patients already subjected to a treatment potentially sterilizing

• Patients under supervision or guardianship

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Myeloid Leukemia
• Gastrointestinal Stromal Tumors
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive

Intervention

Drug:
• Imatinib treatment
Imatinib is a tyrosin-kinase inhibitor

Locations

Country	Name	City	State
France	Department of Biology of reproduction (TENON Hospital-APHP)	Paris

Sponsors (1)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Average difference of the concentration of spermatozoa in the ejaculate measured before treatment and after 6 months of treatment.		At the inclusion and M6 visits	No
Secondary	Analysis of the fragmentation of the spermatic DNA		At the inclusion and M6 visits	No
Secondary	Plasmatic concentration of the inhibitors of tyrosine kinase		At the inclusion and M6 visits	No