The protein C pathway: implications for the design of the RESPOND study
© BioMed Central Ltd 2007
Published: 19 December 2007
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© BioMed Central Ltd 2007
Published: 19 December 2007
The predictive value of plasma protein C level in sepsis has been demonstrated in a number of studies in which depressed protein C levels were associated with increased likelihood of negative outcome. Data from the PROWESS (Recombinant Human Activated Protein C Worldwide Evaluation in Severe Sepsis) trial indicate that administration of drotrecogin alfa (activated; DrotAA) leads to an increase in endogenous protein C levels in severe sepsis patients. In a group as heterogeneous as sepsis patients, the currently approved dose and duration of administration (24 μg/kg per hour for 96 hours) might not be optimal in some individuals. The RESPOND (Research Evaluating Serial Protein C levels in severe sepsis patients ON Drotrecogin alfa [activated]) trial is a phase II study being conducted to explore the use of endogenous protein C level as both a biomarker and a steering parameter for administration of DrotAA. Eligible patients will receive DrotAA either at the normal, currently approved dose and duration of administration ('standard therapy') or at a higher dose with variable infusion duration or variable infusion duration only ('alternative therapy'). The duration of DrotAA infusion in the alternative therapy arm depends on the individual response in terms of sustained increase in endogenous protein C. The ultimate aims of this and potential following studies are as follows: to establish serial plasma protein C measurement as a biomarker that will aid in the identification of severe sepsis patients who are most likely to benefit from DrotAA therapy, to enable adjustment of DrotAA therapy in individual patients (specifically, the possibility to use a higher dose and to adjust the infusion duration), and to provide guidance to the clinician regarding whether the patient is responding to DrotAA.
That there is an association between sepsis and activation of the coagulation system has been known for nearly 40 years . Microbial toxins and inflammatory cytokines released into the systemic circulation initiate a cascade of events that results in widespread inflammation, endothelial injury and microvascular thrombosis [2, 3]. Endogenous protein C, a vitamin K dependent glycoprotein that is synthesized by the liver, plays an important role in the maintenance of haemostasis and modulation of inflammation under normal conditions [4, 5]. Protein C circulates in the blood in zymogen form (inactivated form) at a concentration of approximately 4 μg/ml. Currently, various methods, reagents and equipment exist to measure protein C in the laboratory or even at the bedside in the intensive care unit (ICU). In general, these methods can be subdivided into those that are based on measuring the functional activity of the protein (%) and antigenic methods, which measure the amount of protein available (μg/ml).
Protein C is converted to activated protein C (APC) by thrombin-thrombomodulin complexes. APC inactivates coagulation factors Va and VIIIa, thereby inhibiting further thrombin generation. Moreover, by inhibiting plasminogen activator inhibitor-1, APC is indirectly profibrinolytic. In addition to its role as an anticoagulant, a number of anti-inflammatory effects and anti-apoptotic properties have been described . Recent research indicates that inhibition of neutrophil chemotaxis and a role in maintaining endothelial integrity are other important effects of APC. Direct cytoprotective effects of APC have been reported to be mediated by intracellular signalling, initiated by binding of APC to its receptor (the endothelial protein C receptor), which appears to be mediated by interaction with an adjacent protease-activated receptor or by indirect activation of the sphingosine 1-phosphate pathway [7, 8].
Protein C is rapidly depleted in severe sepsis because of consumption, degradation by elastase and a reduced synthesis by the liver. With the reduction in protein C zymogen, the hypercoagulable condition and hyper-inflammatory response in sepsis is not counterbalanced, which leads to organ dysfunction and death in approximately 20% to 40% of cases.
Drotrecogin alfa (activated; DrotAA) is a recombinant version of endogenous human APC. The PROWESS (Recombinant Human Activated Protein C Worldwide Evaluation in Severe Sepsis) trial established that DrotAA (Xigris®, Eli Lilly and Company, Indianapolis, IN, USA) is an effective treatment for adult patients with severe sepsis when it is infused at 24 μg/kg per hour for 96 hours , which is the currently licensed regimen. Thus far, the compound has been evaluated in more than 9,000 patients enrolled in clinical trials. Studies have considered the following issues: safety (ENHANCE [Extended Evaluation of Recombinant Human Activated Protein C, drotrecogin alfa (activated)] study ), use in patients who are less severely ill than the licensed indication (ADDRESS [Administration of Drotrecogin Alfa (Activated) in Early Stage Severe Sepsis] study ), paediatric use (RESOLVE [Researching severe Sepsis and Organ dysfunction in children: a global perspective] study ), interaction with prophylactic heparin (XPRESS [Xigris and Prophylactic Heparin Evaluation in Severe Sepsis] study ), and prolonged administration (EXTEND [Efficacy and Safety of Extended Drotrecogin Alfa (Activated) Therapy in Patients With Persistent Requirement for Vasopressor Support After 96 Hour Infusion With Commercial Drotrecogin Alfa (Activated)] ).
No biomarker has yet been established that can guide the clinical use of DrotAA. The identification of severe sepsis patients most likely to benefit from this drug is based mainly on clinical parameters. The phase II study RESPOND (Research Evaluating Serial Protein C levels in severe sepsis patients ON Drotrecogin alfa [activated])  aims to evaluate the use of endogenous protein C level as a biomarker to guide treatment with DrotAA.
Abnormalities in coagulation parameters are commonly observed in patients with severe sepsis and have been associated with higher mortality. These include reductions of the major natural anticoagulants antithrombin III, tissue factor pathway inhibitor and protein C. Studies have shown that more than 80% of patients with severe sepsis had a baseline protein C level below the lower limit of normal [9, 16–18]. Plasma protein C levels decrease early in patients who develop severe sepsis, often before clinical symptoms appear, and these levels remain low, gradually rising in patients who recover and survive [18–21].
Numerous reports have examined the predictive value of plasma protein C levels in sepsis. These reports confirm the association between depressed protein C levels and the increased likelihood of negative outcomes in sepsis, including time on a ventilator, time in the ICU, development of shock and increased mortality [17, 19, 22–33]. Protein C levels less than approximately half the lower limit of normal are associated with a much greater risk for death [19, 29]. In a recent multivariable analysis with ICU mortality as the dependent variable , a minimum protein C concentration of less than 45% was identified as an independent risk factor in surgical ICU patients.
Data from previous studies of DrotAA also show a strong association between very low protein C levels and mortality in patients with severe sepsis. In the placebo arm of PROWESS  no difference in mortality was identified between patients with normal protein C levels (>80% functional activity in the assay used) at baseline and those with moderate protein C deficiency (41% to 80% activity). In the former group, mortality was 5.7% at day 4 and 26.7% at day 28, and in the latter group the corresponding percentages were 5.5% and 24.9%, respectively. However, patients who presented with severe protein C deficiency (activity levels half the lower limit of normal or less [≤40%]) had a markedly higher mortality both at day 4 (20%) and at day 28 (41.8%).
It is important to note that the activity assay utilized to measure protein C (the inactive zymogen) in the above studies is not subject to significant interference by therapeutic DrotAA (specifically, the assay reflects native endogenous protein C and not infusion of APC).
In PROWESS  the observed relative risk reduction in patients with protein C deficiency at baseline (≤80%) was 20%, whereas that in patients with normal protein C levels at baseline (>80%) was 42%. There was no statistically significant treatment-by-subgroup interaction observed based on subgroups defined by baseline protein C deficiency status (P = 0.3338). This suggested that there was a treatment benefit associated with DrotAA administration in severe sepsis, irrespective of baseline protein C level. In an attempt to gain a better understanding of these findings, the changes in protein C levels from baseline to the end of study drug infusion were analyzed.
RESPOND, a phase II double blind study aiming to recruit 488 patients, is the first step toward exploring the use of endogenous protein C level as a biomarker to guide the administration (both dosage and duration) of DrotAA. The study is organized into three periods: pretreatment, treatment and post-treatment. To be eligible for inclusion in the study, patients must have multiple organ dysfunction and protein C deficiency (protein C level less than the lower limit of normal). Protein C levels will be measured at each investigative site using a point-of-care immunoassay or a standard laboratory analyzer using an activity-based diagnostic kit.
The pretreatment period starts with the onset of multiple organ dysfunction (two or more sepsis-induced organ dysfunctions). After the onset of the second sepsis-induced organ dysfunction, a maximum of 24 hours is allowed to assess patient eligibility for inclusion in the study, obtain informed consent, perform baseline evaluations and determine patient treatment assignment. No more than 36 hours can elapse between the onset of the first sepsis-induced organ dysfunction and the start of the treatment period.
The treatment period begins with a common therapy lead-in, in which all patients will receive DrotAA at a dose of 24 μg/kg per hour for 24 hours. The rationale for this is underpinned by the observations from PROWESS that approximately one-third of patients who had severe protein C deficiency at baseline were no longer severely deficient after 24 hours of DrotAA therapy, and that approximately one-quarter of patients who were not severely deficient at baseline were deficient at 24 hours, despite DrotAA treatment. This allows an initial assessment of response to standard dose therapy (24 μg/kg per hour DrotAA).
After the 24-hour lead-in period, patients will receive the treatment that they were randomly assigned to (at baseline), either standard or alternative therapy. The alternative therapy received will depend on whether the patient's protein C level at the end of the lead-in period is less or greater than half the lower limit of normal, as demonstrated in Figure 1.
All patients assigned to standard therapy will receive an additional 72-hour infusion of DrotAA 24 μg/kg per hour (for a total infusion duration of 96 hours).
Patients assigned to receive alternative therapy of variable duration (the alternative therapy-variable duration arm), who have moderate protein C deficiency at the end of the lead-in period, will receive DrotAA 24 μg/kg per hour for an additional 24 to 144 hours. The treatment will be continued until two consecutive protein C levels are greater than or equal to the lower limit of normal, or the patient has received DrotAA for a total infusion duration of 168 hours. Based on results from PROWESS, this group of patients is anticipated to have a relatively low risk for early death (6.3% at day 5 and 20.0% at day 28, Figure 5), and therefore they will only be exposed to variable duration of DrotAA infusion and not a higher dose.
Patients assigned to alternative therapy at higher dose and of variable duration (the alternative therapy-higher dose/variable duration arm), who have severe protein C deficiency at the end of the lead-in period, will receive a variable duration of DrotAA infusion (as described above for the alternative therapy-variable duration arm) and a higher dose of DrotAA (30 μg/kg per hour up to 48 μg/kg per hour). Based on results from PROWESS this group is anticipated to have a relatively high risk for early death (18.8% at day 5 and 33.6% at day 28, Figure 5), and therefore this group will be exposed to both higher doses and a variable duration of DrotAA infusion.
Each patient's infusion will be administered at a single infusion rate. A data monitoring committee will review safety data from the lower dose groups before enrolling patients in the next higher dose group. Figure 6 illustrates the different arms of the trial after completion of the common lead-in period, and shows the outcomes of corresponding PROWESS patients, indicating lower mortality among patients in whom protein C levels normalized by the end of the infusion period.
RESPOND seeks to demonstrate that 'alternative therapy' results in a greater increase in protein C levels than 'standard therapy' and, importantly, to provide appropriate safety and efficacy data to determine the most appropriate aspects of alternative therapy to incorporate into possible future studies. If RESPOND is successful, then a larger phase 3 study will be required to demonstrate whether improved protein C levels resulting from alternative therapy are also associated with statistically significant mortality reductions as compared with standard therapy. The ultimate aim of RESPOND and potential following studies is to establish serial plasma protein C measurements as a biomarker that will aid in the identification of those patients with severe sepsis who are most likely to benefit from DrotAA, that will enable adjustment of DrotAA therapy to the needs of individual patients (specifically, the possibility to use a higher dose and to adjust the infusion duration), and that will provide guidance to the clinician regarding whether the patient is responding to DrotAA therapy.
The future of medicine might be individualized therapy based on biomarkers or gene profiles. Until then, RESPOND represents the first step toward tailored sepsis treatment.
activated protein C
drotrecogin alfa (activated)
intensive care unit.
This article is part of Critical Care Volume 11 Supplement 5: Severe sepsis and drotrecogin alfa (activated). The full contents of the supplement are available online at http://ccforum.com/supplements/11/S5. Publication of the supplement has been sponsored by Eli Lilly and Company.