Genetic Factors of the Desmopressin Response in Carriers of Hemophilia A

Factor VIII Deficiency Clinical Trial

— GIDEHAC  

Official title:

Study of Genetic Factors Influencing the Factor VIII Response to Desmopressin in Carriers of Hemophilia A: the GIDEHAC Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06020456
• Other study ID #: 2023_GIDEHAC_01
• Status: Completed
• Start date: January 1, 2022
• Est. completion date: April 1, 2023

Study information

• Verified date: August 2023
• Source: Groupe Maladies hémorragiques de Bretagne
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Hemophilia A (HA) is a rare X-linked bleeding disorder caused by a deficiency in factor VIII (FVIII) affecting 1/5,000 males1. Carriers of HA are females carrying the pathogenic variant responsible for the familial HA at a heterozygous status. About 30% of HA carriers have low FVIII levels and can therefore have abnormal bleeding symptoms2,3. Such as males with moderate/mild HA, bleeding can be treated or prevented with either FVIII concentrates or desmopressin4,5. This drug acts as a vasopressin type 2-receptor (V2R) agonist that causes endothelial cells to rapidly secrete von Willebrand factor (VWF) and FVIII from Weibel-Palade bodies into the bloodstream6,7. However, the mechanism of action of post-DDAVP FVIII increase remains poorly understood in hemophilia A. One advantage of DDAVP is that it increases the level of endogenous FVIII, thus avoiding the need for potentially immunogenic exogenous FVIII. It is also cheaper than FVIII concentrates. Finally, it is more widely available in pharmacies in all hospitals with emergency rooms and surgical facilities.

The FVIII response profile to DDAVP in carriers appears quite similar to that seen in men with mild/moderate HA8-11. A post-DDAVP increase in the FVIII level of 2-4 fold the basal level is usually observed. This FVIII response presents an important inter-individual variation making it necessary to carry out a therapeutic test before its use for the anti-hemorrhagic treatment. The basal FVIII level logically conditions the intensity of the post-DDAVP FVIII peak. However, other factors influencing the post-DDAVP FVIII response are very likely. Unfortunately, few series describing the FVIII response to DDAVP in HA carriers have been reported to date and they included too small numbers of patients to precisely analyze the factors of variation in the post-DDAVP FVIII pharmacokinetics (PK). Candy et al did not find any difference depending on the severity of the pathogenic variants for HA or on the age11. However, this study was carried out in a cohort including only 17 patients, therefore too small for a reliable statistical analysis.

The GIDEHAC study (Genetic Influence of Desmopressin Efficacy in Hemophilia A Carriers) is a French study with the following objectives: the description of the post-DDAVP FVIII PK in a large retrospective cohort of HA carriers, the research of patients-related factors influencing this FVIII PK, and the building of predictive population- and Bayesian-based models.

Description:

The GIDEHAC study is a French observational, retrospective, and multicentric study performed in carriers of hemophilia A of any age who have received the intravenous desmopressin in their French Hemophilia Treatment Centers (HTC).

Objectives of the GIDEHAC study:

• Description of the post-desmopressin (DDAVP) FVIII pharmacokinetics (PK) in a large retrospective cohort of patients with mild/moderate HA,

• Research of patients-related factors influencing this FVIII PK,

• Building of predictive population- and Bayesian-based models

Inclusion criteria:

• Females at any ages with a confirmed diagnosis of HA carriers based on the F8 gene analysis,

• Patients having received DDAVP during the last 10 years that was associated with dosages of FVIII before and just after DDAVP,

• Factor VIII levels measurements realized at least 2 times during the therapeutic test, just before the DDAVP infusion and 30 or 60 minutes after.

Exclusion criteria:

• Patients with an anti-factor VIII inhibitor,

• Refusal to participate in the study,

• Unable to understand the study's French letter of non-opposition and information.

Description of the DDAVP therapeutic tests:

The procedure of the DDAVP therapeutic test was identical for all investigator centers as recommended by international and French guidelines. DDAVP was so always administered intravenously at a dose of 0.3-0.4 μg.kg-1 diluted in 50 mL of saline solution over 30 minutes. The required hemostatic parameters are FVIII levels before and at least 30 or 60 minutes after the DDAVP infusion. Subsequent FVIII measurements performed at T2h, T4h and T6h after the infusion are also recorded during the test.

Collected data:

All data collected in this study were issued from the medical files at the moment of the DDAVP therapeutic test. They include:

• FVIII activity levels measured with a one-stage clotting assay from plasmas collected in 0.109 M sodium citrate (fresh or stored at -80°C). These FVIII levels were measured just before and after the DDAVP infusion (until 24 hours if available),

• The pathogenic variant of the F8 gene responsible for the familial HA,

• Blood group,

• DDAVP doses,

• Von Willebrand factor levels during the DDAVP test,

• Age,

• Weight,

• FVIII levels measured during pregnancies,

• The degree of familial link if relatives are included in this study.

Pharmacokinetic analyses The following FVIII and VWF pharmacokinetic parameters are calculated using a compartmental approach with non-linear models at mixed effect (MONOLIX software, v2021, Lixsoft): basal FVIII and post-DDAVP FVIII peak (highest level measured after DDAVP administration), FVIII recovery (recFVIII = peak FVIII / basal FVIII), FVIII half-life (FVIII T1/2), FVIII clearance, FVIII area under the curve (FVIII AUC), and duration with FVIII ≥0.5 and 0.8 IU.dL-1.

Scores measuring the FVIII response to DDAVP

For qualitative assessment of the biological response to DDAVP, criteria previously reported by Stoof et al were used:

• The absolute response was either "complete" (peak FVIII ≥0.5 IU.mL-1), "partial" (FVIII ≥0.3 - <0.5 IU.mL-1) or "null" (FVIII <0.3 IU.mL-1).

• The relative response was defined as "complete" (recFVIII >3), "partial" (recFVIII ≥2 - <3) or "null" (recFVIII <2).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 361
• Est. completion date: April 1, 2023
• Est. primary completion date: January 1, 2023
• Gender: Female
• Age group: 2 Years to 80 Years

Eligibility

Inclusion Criteria:

• Females at any ages with a formal diagnosis of HA carriers based on the F8 genetics,

• Patients having received DDAVP during the last 10 years that was associated with dosages of FVIII before and just after DDAVP,

• Factor VIII levels measurements realized at least 2 times during the therapeutic test, just before the DDAVP infusion and 30 or 60 minutes after.

Exclusion Criteria:

• Patients with an anti-factor VIII inhibitor,

• Refusal to participate in the study,

• Unable to understand the study's French letter of non-opposition and information

Related Conditions & MeSH terms

• Desmopressin
• Factor VIII Deficiency
• Hemophilia A

Intervention

Drug:
• Desmopressin
For the 2 groups, all patients have received an intravenous DDAVP 0,3-0,4 µg/Kg infusion associated with pre/post-desmopressin measurements of plasma FVIII levels

Locations

Country	Name	City	State
France	University hospital of Bordeaux	Bordeaux
France	University hospital of Brest	Brest
France	Hospices civils de Lyon	Bron
France	University hospital of Dijon	Dijon
France	University hospital of Bicêtre	Le Kremlin-Bicêtre
France	University hospital of Lille	Lille
France	Assistance publique hôpitaux de Marseille	Marseille
France	University hospital of Montpellier	Montpellier
France	University hospital of Nancy	Nancy
France	University hospital of Nantes	Nantes
France	University hospital of Rennes	Rennes
France	University hospital of Saint Etienne	Saint-Étienne

Sponsors (1)

Lead Sponsor	Collaborator
Groupe Maladies hémorragiques de Bretagne

Country where clinical trial is conducted

France, 

References & Publications (10)

Casonato A, Dannhauser D, Pontara E, Bertomoro A, Orazi B, Santarossa L, Zerbinati P, Girolami A. DDAVP infusion in haemophilia A carriers: different behaviour of plasma factor VIII and von Willebrand factor. Blood Coagul Fibrinolysis. 1996 Jul;7(5):549-53. — View Citation

Hews-Girard J, Rydz N, Lee A, Goodyear MD, Poon MC. Desmopressin in non-severe haemophilia A: Test-response and clinical outcomes in a single Canadian centre review. Haemophilia. 2018 Sep;24(5):720-725. doi: 10.1111/hae.13586. Epub 2018 Jul 13. — View Citation

Kaufmann JE, Oksche A, Wollheim CB, Gunther G, Rosenthal W, Vischer UM. Vasopressin-induced von Willebrand factor secretion from endothelial cells involves V2 receptors and cAMP. J Clin Invest. 2000 Jul;106(1):107-16. doi: 10.1172/JCI9516. — View Citation

Kaufmann JE, Vischer UM. Cellular mechanisms of the hemostatic effects of desmopressin (DDAVP). J Thromb Haemost. 2003 Apr;1(4):682-9. doi: 10.1046/j.1538-7836.2003.00190.x. — View Citation

Kobrinsky NL, Watson CM, Cheang MS, Bishop AJ. Improved hemophilia A carrier detection by DDAVP stimulation of factor VIII. J Pediatr. 1984 May;104(5):718-24. doi: 10.1016/s0022-3476(84)80951-8. — View Citation

Leissinger C, Carcao M, Gill JC, Journeycake J, Singleton T, Valentino L. Desmopressin (DDAVP) in the management of patients with congenital bleeding disorders. Haemophilia. 2014 Mar;20(2):158-67. doi: 10.1111/hae.12254. Epub 2013 Aug 12. — View Citation

Mannucci PM, Vicente V, Alberca I, Sacchi E, Longo G, Harris AS, Lindquist A. Intravenous and subcutaneous administration of desmopressin (DDAVP) to hemophiliacs: pharmacokinetics and factor VIII responses. Thromb Haemost. 1987 Dec 18;58(4):1037-9. — View Citation

Plug I, Mauser-Bunschoten EP, Brocker-Vriends AH, van Amstel HK, van der Bom JG, van Diemen-Homan JE, Willemse J, Rosendaal FR. Bleeding in carriers of hemophilia. Blood. 2006 Jul 1;108(1):52-6. doi: 10.1182/blood-2005-09-3879. Epub 2006 Mar 21. — View Citation

Seaman CD, Xavier F, Ragni MV. Hemophilia A (Factor VIII Deficiency). Hematol Oncol Clin North Am. 2021 Dec;35(6):1117-1129. doi: 10.1016/j.hoc.2021.07.006. Epub 2021 Aug 10. — View Citation

van Galen KPM, d'Oiron R, James P, Abdul-Kadir R, Kouides PA, Kulkarni R, Mahlangu JN, Othman M, Peyvandi F, Rotellini D, Winikoff R, Sidonio RF. A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH. J Thromb Haemost. 2021 Aug;19(8):1883-1887. doi: 10.1111/jth.15397. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparison of the post-DDAVP FVIII peak in patients of the group "Null variants" vs "No Null variants"	Factor VIII levels measured with a chronometric one stage-assay 30 or 60 minutes after the DDAVP infusion	FVIII levels 30-60 minutes after the DDAVP infusion
Primary	Comparison of the post-DDAVP FVIII recovery in patients of the group "Null variants" vs "No Null variants"	Factor VIII levels measured with a chronometric one stage-assay before (basal FVIII) the DDAVP infusion and 30 or 60 minutes after (FVIII peak). The FVIII recovery = ratio FVIII peak / basal FVIII	FVIII levels before and 30-60 minutes after the DDAVP infusion
Primary	Comparison of the post-DDAVP FVIII clearance in patients of the group "Null variants" vs "No Null variants"	Factor VIII levels measured with a chronometric one stage-assay before and after DDAVP until 24h post-infusion	Factor VIII levels were measured until 24 hours after the desmopressin infusion
Primary	Comparison of the post-DDAVP FVIII area under the curve (AUC) in patients of the group "Null variants" vs "No Null variants"	Factor VIII levels measured with a chronometric one stage-assay before and after DDAVP until 24h post-infusion	Factor VIII levels were measured until 24 hours after the desmopressin infusion
Primary	Comparison of the post-DDAVP duration with FVIII normalized above 0.5 IU.dL-1 in patients of the group "Null variants" vs "No Null variants"	Factor VIII levels measured with a chronometric one stage-assay before and after DDAVP until 24h post-infusion	Factor VIII levels were measured until 24 hours after the desmopressin infusion
Primary	Comparison of the post-DDAVP duration with FVIII normalized above 0.8 IU.dL-1 in patients of the group "Null variants" vs "No Null variants"	Factor VIII levels measured with a chronometric one stage-assay before and after DDAVP until 24h post-infusion	Factor VIII levels were measured until 24 hours after the desmopressin infusion
Secondary	Influence of the age on the post-DDAVP FVIII peak	factor VIII levels measured with a chronometric one stage-assay 30 or 60 minutes after the DDAVP infusion	FVIII levels 30-60 minutes after the DDAVP infusion
Secondary	Influence of the age on the post-DDAVP FVIII recovery	Factor VIII levels measured with a chronometric one stage-assay before (basal FVIII) the DDAVP infusion and 30 or 60 minutes after (FVIII peak). The FVIII recovery = ratio FVIII peak / basal FVIII	FVIII levels before and 30-60 minutes after the DDAVP infusion
Secondary	influence of the age on the post-DDAVP FVIII area under the curve (AUC)	Factor VIII levels measured with a chronometric one stage-assay before (basal FVIII) the DDAVP infusion and 30 or 60 minutes after (FVIII peak). The FVIII recovery = ratio FVIII peak / basal FVIII	Factor VIII levels were measured until 24 hours after the desmopressin infusion
Secondary	influence of the age on the post-DDAVP duration with FVIII normalized above 0.5 IU.dL-1	factor VIII levels measured with a chronometric one stage-assay before and after DDAVP until 24h post-infusion	Factor VIII levels were measured until 24 hours after the desmopressin infusion
Secondary	influence of the age on the post-DDAVP duration with FVIII normalized above 0.8 IU.dL-1	factor VIII levels measured with a chronometric one stage-assay before and after DDAVP until 24h post-infusion	Factor VIII levels were measured until 24 hours after the desmopressin infusion