Protocol - Population-based Pharmacokinetic Study Using Chromogenic Substrate Assay - Extended Half-life Factor VIII Products

Description

This protocol provides instructions and guidance for collecting and processing samples for coagulation testing, performing a population-based pharmacokinetic study using the chromogenic substrate assay, and interpreting pharmacokinetic results in response to infusion of extended half-life Factor VIII products. Because there are many comparable assays for performing the chromogenic substrate assay, the protocol also provides basic guidelines to aid comparability among different studies.

Specific Instructions

The PhenX Hemophilia Inhibitor Research Working Group (WG) notes that these measures are intended for use in observational and interventional trials but are not sufficient to define hemophilia phenotypes when used in isolation.

The WG recommends that when measuring inhibitor recovery in non-severe patients, endogenous factor should be measured by the same assay that was optimized prior to inhibitor development.

The WG recommends that Factor VIII and IX assays, either by one-stage clotting factor or chromogenic substrate methodology, should be performed by a laboratory that is College American Pathologists (CAP) accredited or Clinical Laboratory Improvement Amendments of 1998 (CLIA) certified. For multi-center clinical trials, the use of a central laboratory is strongly encouraged.

The WG notes that in comparison to the one-stage clotting factor assay, the chromogenic substrate assay demonstrates less variation by reagents, thus enabling cross-laboratory comparisons.

Availability

Available

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Protocol

Population-based Pharmacokinetic Study Using Chromogenic Substrate Assay - Extended Half-life Factor VIII Products

Sample Collection

The PhenX Hemophilia Inhibitors Working Group (WG) recommends that investigators follow the sample collection procedures outlined in Lippi et al. (2012) to ensure quality specimens for coagulation testing. These recommendations include basic criteria for venipuncture (e.g., proper patient identification, use of correct techniques, appropriate devices and needles) as well as additional guidance for critical parameters which can affect the outcome of clot-based tests. These critical parameters include prevention of prolonged venous stasis, collection of nonhemolyzed samples, order of blood draw, and appropriate filling and mixing of collection tubes.

Additionally, the WG highlights that blood should be collected by direct venipuncture into 3.2% sodium citrate tubes and filled within 11% of fill line. A second tube should be collected. A discard tube should be drawn if using a winged butterfly collection system.

Sample Processing

The WG recommends that investigators follow the sample collection procedures outlined in Adcock Funk et al. (2012). The procedures include that:

unprocessed or processed sodium citrate samples remain capped and at room temperature until testing,
samples should not be refrigerated or stored on ice or in an ice bath,
samples should be transported vertically, and
processed samples should not be agitated during transportation to avoid remixing of components.

Additionally, samples can be transported and stored as:

unprocessed sodium citrate whole blood samples,
whole blood samples centrifuged and maintained in sodium citrate tubes, or
plasma processed by centrifugation and aliquoted into a second tube.

Ideally, whole blood samples should be processed to platelet poor plasma (PPP) within 1 hour of collection and assayed within 4 hours of collection.

If centrifuging samples, the centrifuge should be validated so that post-centrifuged samples contain less than 10,000 platelets/microliter. Centrifuged and processed plasma can be stored at -20^o C for 2 weeks and should be transferred to < -70^o C for longer storage, including shipment.

Extended Half-life Factor VIII Products: Chromogenic Substrate Assay

The WG notes that there are a number of different assays and instruments that are appropriate to perform the chromogenic substrate assay. Once an assay is chosen for a particular study, the WG recommends that no changes in the protocol be made over the course of the study. Because results can vary with the instrumentation and reagents, the WG recommends that the investigator record the make and manufacturer of equipment, the repeatability and coefficients of variation for the assay, and the reagents used.

Extended Half-life Factor VIII Products: Population-based Pharmacokinetic Study

The WG recommends that investigators follow parameters outlined by the International Society on Thrombosis and Haemostasis Subcommittee on Factor VIII, Factor VIII and Rare Coagulation Disorders (Iorio et al., 2017). These parameters include taking two to three measurements at least 12 hours apart in the after a routine dose of the extended half-life product (i.e., no washout period and no standardized dose) at the following timepoints:

4-8 hours after infusion;
16-28 hours after infusion; and
40-60 hours after infusion.

In addition, investigators should take a sample 60-84 hours after infusion.

Extended Half-life Factor VIII Products: Population-based Pharmacokinetics Model

Investigators should use a "robust" population pharmacokinetics model, such as WAPPS-Hemo or PKFit.

Personnel and Training Required

Phlebotomist

Equipment Needs

Laboratory with the ability to perform the chromogenic substrate assay.

Requirements

Requirement Category	Required
Major equipment	No
Specialized training	No
Specialized requirements for biospecimen collection	Yes
Average time of greater than 15 minutes in an unaffected individual	Yes

Mode of Administration

Bioassay

Lifestage

Toddler, Child, Adolescent, Adult

Participants

Any age

Selection Rationale

The PhenX Hemophilia Inhibitors Working Group selected the recommendations from Lippi et al. (2012) and Adcock Funk et al. (2012) as the best standardized methodology for collecting and processing samples for coagulation testing. The International Society on Thrombosis and Haemostasis (Iorio et al., 2017) provides recommended parameters for consistent implementation of the pharmacokinetic study.

Language

English

Standards

Standard	Name	ID	Source

Derived Variables

None

Process and Review

Not applicable.

Protocol Name from Source

Iorio et al. Estimating and interpreting the pharmacokinetic profiles of individual patients with hemophilia A or B using a population pharmacokinetic approach: Communication from the SSC of the ISTH. J Thromb Haemost, 2017

Source

Adcock Funk, D. M., Lippi, G., & Favaloro, E. J. (2012). Quality standards for sample processing, transportation, and storage in hemostasis testing. Seminars in Thrombosis and Hemostasis, 38(6), 576-585.

Iorio, A., Blanchette, V., Blatny, J., Collins, P., Fischer, K., & Neufeld, E. (2017). Estimating and interpreting the pharmacokinetic profiles of individual patients with hemophilia A or B using a population pharmacokinetic approach: Communication from the SSC of the ISTH. Journal of Thrombosis and Haemostasis, 15(12), 2461-2465.

Lippi, G., Salvagno, G. L., Montagnana, M., Lima-Oliveira, G., Guidi, G. C., & Favaloro, E. J. (2012). Quality standards for sample collection in coagulation testing. Seminars in Thrombosis and Hemostasis, 38(6), 565-575.

General References

lvarez-Romn, M. T., Fernandez-Bello, I., de la Corte-Rodrguez, H., Hernndez-Moreno, A. L., Martn-Salces, M., Butta-Coll, N., Rivas-Pollmar, M. I., Rivas-Muoz, S., & Jimnez-Yuste, V. (2017). Experience of tailoring prophylaxis using factor VIII pharmacokinetic parameters estimated with myPKFiT in patients with severe haemophilia A without inhibitors. Haemophilia, 23(1), e50-e54.

Blanchette, V. S., Key, N. S., Ljung, L. R., Manco-Johnson, M. J., van den Berg, H. M., & Srivastava, A.; Subcommittee on Factor VIII, Factor VIII and Rare Coagulation Disorders of the Scientific and Standardization Committee of the International Society on Thrombosis and Hemostasis. (2014). Definitions in hemophilia: Communication from the SSC of the ISTH. Journal of Thrombosis and Haemostasis, 12(11), 1935-1939.

Hay, C. R., & DiMichele, D. M.; International Immune Tolerance Study. (2012). The principal results of the International Immune Tolerance Study: A randomized dose comparison. Blood, 119(6), 1335-1344.

Iorio, A., Edginton, A.N., Blanchette, V., Blatny, J., Boban, A., Cnossen, M., Collins, P., Croteau, S.E., Fischer, K., Hart, D.P., Ito, S., Korth-Bradley, J., Lethagen, S., Lillicrap, D., Makris, M., Matht, R., Morfini, M., Neufeld, E.J., Spears, J. (2018). Performing and interpreting individual pharmacokinetic profiles in patients with Hemophilia A or B: Rationale and general considerations. Research and Practice in Thrombosis and Haemostasis, 2(3), 535-548.

Iorio, A., Keepanasseril, A., Foster, G., Navarro-Ruan, T., McEneny-King, A., Edginton, A. N., & Thabane, L.; WAPPS-Hemo Co-investigator Network. (2016). Development of a Web-Accessible Population Pharmacokinetic Service-Hemophilia (WAPPS-Hemo): Study protocol. JMIR Research Protocols, 5(4), e239.

Kitchen, S., Kershaw, G., & Tiefenbacher, S. (2016). Recombinant to modified factor VIII and factor VIII Chromogenic and one-stage assays issues. Haemophilia, 22(Suppl. 5), 72-77.

Lee, M., Morfini, M., Schulman, S., & Ingerslev, J.; Factor VIII/Factor VIII Scientific and Standardization Committee of the International Society for Thrombosis and Haemostasis. (2001). Scientific and Standardization Committee communication. The design and analysis of pharmacokinetic studies of coagulation factors. https://www.isth.org/members/group_content_view.asp?group=100348&id=159244. Retrieved August 30, 2018.

Peyvandi, F., Oldenburg, J., & Friedman, K. D. (2006). A critical appraisal of one-stage and chromogenic assays of factor VIII activity. Journal of Thrombosis and Haemostasis, 14(2), 248-261.

Teichman, J., Chaudhry, H. R., & Sholzberg, M. (2018). Novel assays in the coagulation laboratory: A clinical and laboratory perspective. Transfusion and Apheresis Science, 57(4), 480-484.

Protocol ID

911204

Variables

Export Variables

Variable Name	Variable ID	Variable Description	dbGaP Mapping
PX911204_Factor_Eight_Population_Chromogenic_Extended_One_Stage_Clotting_Factor_Assay_Changes
	PX911204030100	Were any changes made in the protocol over more the course of the study? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_One_Stage_Clotting_Factor_Assay_Record
	PX911204030200	Were the make and manufacturer of equipment, more repeatability and coefficients of variation for the assay, and the reagents used recorded? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Model
	PX911204050000	Was a robust population pharmacokinetics more model, such as WAPPS-Hemo or PKFit, used? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Study
	PX911204040100	Were the parameters outlined by the more International Society on Thrombosis and Haemostasis Subcommittee on Factor VIII, Factor VIII and Rare Coagulation Disorders (Iorio et al., 2017) followed? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Study_After_Infusion_Hours_16
	PX911204040400	Was Factor VIII activity tested 16-28 hours more after infusion? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Study_After_Infusion_Hours_4
	PX911204040300	Was Factor VIII activity tested 4-8 hour more after infusion? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Study_After_Infusion_Hours_40
	PX911204040500	Was Factor VIII activity tested 40-60 hours more after infusion? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Study_After_Infusion_Hours_60
	PX911204040600	Was Factor VIII activity tested 60-84 hours more after infusion? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Pharmacokinetic_Study_Infusion_Baseline
	PX911204040200	Was Factor VIII activity tested before more infusion (baseline)? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection
	PX911204010100	Were the sample collection procedures more outlined in Lippi et al. (2012) followed? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Blood_Draw
	PX911204010400	Was the order of blood draw recorded?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Nonhemolyzed
	PX911204010300	Were nonhemolyzed samples collected?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Tubes
	PX911204010500	Were collection tubes filled and mixed as more outlined in Lippi et al. (2012)? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Tubes_Discard
	PX911204011000	Was a discard tube drawn?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Tubes_Filled
	PX911204010700	Were the tubes filled within 11% of the fill line?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Tubes_Second
	PX911204010800	Was a second tube collected?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Tubes_Winged
	PX911204010900	Was a winged butterfly collection system used?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Venipuncture
	PX911204010600	Was blood collected by direct venipuncture more into 3.2% sodium citrate tubes? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Collection_Venous_Statsis
	PX911204010200	Were steps taken to prevent prolonged venous more stasis? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing
	PX911204020100	Were the sample collection and processing more procedures outlined in Adcock Funk et al. (2012) followed? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Agitation
	PX911204020500	Were samples agitated during transportation?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Assayed
	PX911204021000	Were samples assayed within 4 hours of collection?	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Centrifuge_Validated
	PX911204021100	Was the centrifuge validated so that process more results in less than 10,000 platelets/microliter show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Deep_Freeze
	PX911204021300	Was the sample transferred to <= -70 C, more including shipment? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Frozen
	PX911204021200	Was the sample frozen immediately and stored more at -20 C for at most 2 weeks? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Platelet_Poor_Plasma
	PX911204020900	Were samples processed to platelet poor more plasma (PPP) within 1 hour of collection? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Refrigerated
	PX911204020300	Were samples refrigerated or stored on ice more or in an ice bath? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Sodium_Citrate
	PX911204020200	Did unprocessed or processed sodium citrate more samples remain capped and at room temperature until testing? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Storage_Plasma
	PX911204020800	Were samples stored as plasma processed by more centrifugation and aliquoting into a second tube? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Storage_Unprocessed
	PX911204020600	Were samples stored as unprocessed sodium more citrate whole blood samples? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Storage_Whole_Blood
	PX911204020700	Were samples stored as whole blood samples more centrifuged and maintained in sodium citrate tubes? show less	N/A
PX911204_Factor_Eight_Population_Chromogenic_Extended_Sample_Processing_Transportation
	PX911204020400	Were samples transported vertically?	N/A

Hemophilia Inhibitor

Measure Name

Response to Factor VIII Infusion - Population-based Pharmacokinetic Study

Release Date

May 7, 2019

Definition

A series of plasma Factor VIII activity determinations in blood samples are obtained immediately prior to, and at timepoints after, infusion of FVIII concentrate.

Purpose

The results of the population-based pharmacokinetic study (i.e., initial recovery and half-life) can be used to guide prophylactic dosage of standard and extended half-life Factor VIII products in hemophiliacs who do not have FVIII inhibitors.

Keywords

Hemophilia inhibitors, Factor VIII, FVIII, hemophilia A, inhibitors, pharmacokinetic study, population pharmacokinetic study, popPK, prophylaxis, half-life, recovery

Measure Protocols

Protocol ID	Protocol Name
911201	Population-based Pharmacokinetic Study Using One-stage Clotting Factor Assay - Standard Half-life Factor VIII Products
911202	Population-based Pharmacokinetic Study Using One-stage Clotting Factor Assay - Extended Half-life Factor VIII Products
911203	Population-based Pharmacokinetic Study Using Chromogenic Substrate Assay - Standard Half-life Factor VIII Products
911204	Population-based Pharmacokinetic Study Using Chromogenic Substrate Assay - Extended Half-life Factor VIII Products

Publications

There are no publications listed for this protocol.