Terlipressin is part of the new wave of HRS that focus on splanchnic vasoconstriction to reverse one of the initiating events in the pathologic cascade that results in HRS. I have been using the combination of octreotide and midodrine to exploit the same therapeutic target. I have had mixed results. I am not aware of any prior controlled trials of this therapeutic target.
- Age ≥18
- Liver disease
- Doubling of serum cr to ≥2.5 mg/dL in less than 2 weeks with no responce to stopping diuretics and giving plasma expansion
- Obstructive nephropathy
- Parenchymal renal disease (ATN, glomerular disease, interstitial nephritis)
- Use of renal toxic medications
- Uncontrolled bacterial infection
- Uncorrected fluid losses
- Liver disease due to factors which are also nephrotoxic (e.g. acetominophen)
- Severe cardiovascular disease (investigators discretion)
Primary end-point: percent of patiens with a serum Cr ≤1.5 on two measurements 48 hours apart without dialysis, death or recurrence of HRS.
- Change in serum Cr from baseline to day 14
- incidence of treatment failure (Cr ≥ baseline after day 7, dialysis, death)
- Combined incidence of treatment success and partial response (Cr decreased by >50% but not ≤ 1.5) without diqalysis or recurrence of HRS
- Survival [Yay!] at 60 days (though they did not show the results)
- Transplant-free survival at 60 days (though they did not show the results)
- Survival at 180 days
- Transplant-free survival at 180 days
They randomized 112 patients from 35 centers.
More patients in the terlipressin group had a Cr > 7, though the average creatinine was 3.96 in the experimental group and 3.85 in the control group.
The Table 1 did not have p values to allow you to compare differences between the two groups.
The primary outcomes were summarized in Table 2:
The primary outcome is the first line "Treatment success at day 14" and unfortunately they "Missed it by that much" with a p value of 0.093. The next line is HRS reversal which according to the article is the traditional definition of response to therapy in prior investigations of HRS. It is interesting that if the authors had used this "traditional" end-point we would be dancing in the streets about a positive therapy but since they selected a more stringent criteria of response (under pressure from the FDA?) they have a negative trial. The power analysis they provided states they predicted a 50% response rate for terlipressin and a 5% response for the placebo. They actually found a 25% response for terlipressin and 12.5% for placebo. So one cold look at this as an underpowered study because they did not meet the effectiveness they estimated in the power analysis.
The authors then provide an intriguing figure which shows that the patients who recovered in the placebo group, all recovered very early while the recoveries in the terlipressin group occurred through the period the drug was administered.
I believe the point was to show proof of efficacy, implying that the early spontaneous recoveries in the placebo group were due to misdiagnosis or lack of serious disease while the recovery of patients in the terlipressin's group increased with increasing duration of therapy. I find this fairly compelling.
One of the secondary outcomes was survival (Yay!). There was no difference in survival between the two groups.
Though I love investigators that have the cojones to look at survival, it is a little strange in HRS because the renal failure is secondary to another life threatening primary illness, liver failure. Even if the therapy is perfectly effective at reversing the renal failure, the long-term survival is dependent on getting a liver transplant or spontaneous recovery of the liver disease. One might argue that curing the renal failure would extend the life of the patient making a transplant more likely but since renal failure is a large component of the MELD score, curing the renal failure actually pushes patients down the list for a liver transplant. So in my mind, the lack of a survival benefit in the treatment of HRS is not nearly as damaging as it normally is.
My final conclusion is that though the study did nt reach scientific signifigance for its primary outcome it did demonstrate compelling evidence for positive biologic activity and since all of the alternative therapies have worse data I would use terlipressin if it was available. My guess though is this negative trial will mean that it will not be licensed and distributed in the U.S.