A Pilot Study to Evaluate the Safety and Efficacy of Oral Treprostinil in the Treatment of Calcinosis in Patients With Systemic Sclerosis
A Pilot Study to Evaluate the Safety and Efficacy of Oral Treprostinil in the Treatment of Calcinosis in Patients With Systemic Sclerosis
This is a prospective open-label trial that will enroll 12 patients with systemic sclerosis (SSc) and at least one calcinotic lesion of the hands that is palpable on physical examination and also measureable on hand radiographs, at one single center. Each subject will receive treprostinil orally for 12 months, and follow-up evaluations will be performed every 3 months. Our main objective is to determine whether oral treprostinil is safe, and effective in reducing calcinosis in patients with SSc. We hypothesize that calcinosis is a result of microvascular injury and ischemic damage, and that therefore treprostinil may be beneficial in the treatment of calcinosis in patients with SSc.
Background:
Calcinosis cutis is the deposition of calcium in the skin and subcutaneous tissues. It is a common and potentially debilitating manifestation of systemic sclerosis (SSc), affecting almost one quarter of these patients. Several studies have found an association between calcinosis and vascular manifestations of SSc including digital ulcers (DU), and acro-osteolysis. The investigators confirmed this in a retrospective multi-center international cohort study of 5280 patients with SSc where DUs were the strongest predictor of calcinosis in multivariate analysis (OR 3.7, 95%CI 2.6-5.3, p<0.0001).
Treprostinil delivered by continuous subcutaneous infusion was effective in both the healing and prevention of DU in patients with SSc in an open-label, single-center clinical trial of 5 (of 12) patients who were able to tolerate the medication. A study of 148 subjects with DU showed that the administration of oral treprostinil up to 16 mg twice daily for 20 weeks was associated with a small but statistically insignificant reduction in net ulcer burden in comparison to placebo. Additionally, preliminary observations in the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma (PHAROS) registry have found that two patients with SSc-PAH and calcinosis treated with subcutaneous treprostinil for PAH experienced approximately 50% radiographic improvement in their calcinosis lesions after 6 months of therapy.
The investigators developed and validated a novel radiographic scoring system to assess the severity of calcinosis affecting the hands of patients with SSc that accounts for area coverage, density, and anatomic location. This scoring system is feasible and was found to have excellent intra- and inter-rater reliability with intra-class correlation coefficients (ICC) of .93 (.89-.97) and .89 (.86-.92), respectively.
Given that calcinosis is a frequent, debilitating complication of SSc associated with digital vascular ischemia with no effective therapies, a clinical trial, using novel outcome measures, testing the safety and efficacy of a powerful vasodilator for the treatment of calcinosis is warranted.
Primary/Secondary objectives:
Our main objective is to conduct an open-label proof-of-concept study with the primary and secondary endpoints entered elsewhere.
Hypothesis:
The investigators hypothesize that calcinosis is a result of microvascular injury and ischemic damage, and that therefore treprostinil may be beneficial in the treatment of calcinosis in patients with SSc.
Study design:
This prospective open-label trial will enroll 12 patients with SSc and at least one calcinotic lesion of the hands that is palpable on physical examination and also measureable on hand radiographs. Each subject will undergo a screening evaluation 4 weeks before treatment with the study drug is initiated. Each subject will receive treprostinil 0.125 mg TID orally, which will be increased by 0.125 mg TID every 3 to 4 days as tolerated. Follow-up evaluations will be performed every 3 months over a 12-month period of time.
Study population:
The population for this study will consist of adult SSc patients with evidence of at least one calcinotic lesion of the hands that is palpable on physical examination and also measureable on hand radiographs. Inclusion and exclusion criteria have been entered elsewhere.
Description of the treatment:
United Therapeutics will provide treprostinil labeled for investigational use. The Sponsor/Investigator of the trial will ensure maintenance of complete and accurate records of the receipt, dispensation, and disposal or return of all trial drug in accordance with Title 21 Code of Federal Regulations (C.F.R.), Part 312.57 and 312.62 and United Therapeutics requirements.
Treprostinil Treprostinil (Orenitram) is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension (WHO Group 1) to improve exercise capacity. The molecular formula is C23H34O5C4H11NO2, and its molecular weight is 495.65. Orenitram is an extended release osmotic tablet for oral administration, and it is formulated as the diolamine salt of treprostinil, a tricyclic benzindene analogue of prostacyclin. It is available in the following four strengths: 0.125 mg (white tablet imprinted with UT 0.125), 0.25 mg (green tablet imprinted with UT 0.25), 1 mg (yellow tablet imprinted with UT 1), and 2.5 mg (pink tablet imprinted with UT 2.5). The formulations also contain xylitol, maltodextrin, sodium lauryl sulfate, magnesium stearate, cellulose acetate, triethyl citrate, polyvinyl alcohol, titanium dioxide, polyethylene glycol, and talc. In addition tablets may contain colorants FD&C Blue 2, iron oxide yellow, and iron oxide red. The imprinting ink contains shellac glaze, ethanol, isopropyl alcohol USP, iron oxide black, n-butyl alcohol, propylene glycol, and ammonium hydroxide.
Mechanism of Action The major pharmacologic actions of treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds, inhibition of platelet aggregation, and inhibition of smooth muscle cell proliferation.
Storage Treprostinil must be stored at 25°C (77°F); excursions 15°C to 30°C (59°F to 86°F). For further details, see the Investigator Brochure and the Orenitram Package Insert.
Dosage and Administration Initiate treprostinil at 0.125 mg TID (every 8 ± 2 h), with dose escalation of an additional 0.125 mg TID every 3 to 4 days as tolerated. No dose changes will be allowed for 5 days before the month 12 visit. Give with food, swallow tablets whole, and use only intact tablets; do not crush, split, or chew. The maximum dose, dose escalation or titration will be done at the Investigator's discretion based upon individual subject tolerability. Patients with mild hepatic impairment (Child Pugh Class A) should initiate treprostinil at 0.125 mg TID, and increment at 0.125 mg TID every 6 to 8 days.[8]
Criteria for Treatment Discontinuation
Treatment will be discontinued in the following circumstances:
Criteria for Stopping Rules The study may be stopped at any time if, in the opinion of the Investigator and / or Sponsor, continuation of the study represents a serious medical risk to the subjects. This may include, but is not limited to, the presence of serious, life-threatening, or fatal adverse events or adverse events that are unacceptable in nature, severity, or frequency. The Sponsor reserves the right to discontinue the study for any reason at any time.
Estimated duration: 12 months
Time and events schedule and description of assessments:
What will happen at each visit?
Screening Visit (1 month prior to treatment):
Baseline Visit (0 month):
At 3 months visit:
At 6 months visit:
At 9 months visit:
At 12 months visit:
Description of assessments:
Medical history including SSc: Significant past or present illnesses, current prescription or nonprescription medications (including vitamins and herbal products), and history of allergies or idiosyncratic responses to drugs should be noted.
Physical examination: A complete physical examination will be conducted by a physician at Screening, 6 months, and at end of study. Any significant changes to the subject's medical condition, physical examination, and concomitant medications should be documented throughout the course of the study. Any untoward medical experience should be recorded as an adverse event.
Examination of calcinosis and digital ulcers: Investigator will perform a thorough clinical examination looking for calcinotic deposits at each visit. The investigators will use case report forms with picture images of the hands to record calcinosis and digital ulcers at each evaluation. The investigators will define digital ulcer as an area with visually discernable depth and a loss of continuity of epithelial coverage in the volar aspect of the finger and distal from the proximal interphalangeal joints, which could be denuded (active) or covered by a scab or necrotic tissue (indeterminate). At each visit, the status of each digital ulcer will be rated as "A," a current active digital ulcer, "H", a completely healed ulcer, or "I," an ulcer with indeterminate status, as previously defined.
Vital Signs: Systolic and diastolic blood pressure, heart rate, respiratory rate, and temperature (°C) will be measured prior to assessments and after sitting for 5 minutes at screening, baseline, 6 months, and 12 months. Vital signs should also be assessed in the case of abnormal clinical signs and symptoms.
Electrocardiogram (ECG): Twelve-lead ECGs will be recorded after at least 5 minutes rest in the semi-recumbent position at screening and at the end of the study at 12 months. Recordings should include lead II as a rhythm strip and contain at least 5 QRS complexes. ECG parameters collected (after at least 5 minutes rest) include heart rate, and PR interval, QT interval, QRS duration and any clinically significant abnormalities.
Laboratory tests: Blood and urine samples for the measurement and evaluation of CBC, CMP, and urinalysis (UA) will be collected at screening, 6 months and at the end of the study, and analyzed at Stanford laboratory.
Urine pregnancy test: urine beta-HCG will be measured in all female in reproductive age at all visits.
Radiological examination of calcinosis: Patients will have plain radiographs of the hands at baseline and at 1 year.
Scleroderma Health Assessment Questionnaire (SHAQ): The SHAQ is a patient self-administered instrument, which has been previously validated in SSc and demonstrates meaningful clinical changes in the course of the disease over time. It is comprised of the HAQ-DI, a self-administered 20-question instrument that assesses a patient's level of functional ability and five scleroderma visual analogue scale (VAS) measurements to evaluate symptoms specific to SSc.
Cochin Hand Function Scale (CHFS): CHFS is a questionnaire derived from 18 validated questions to assess functional disability and handicap due to hand involvement in rheumatoid arthritis. Each answer is scored on a scale of 0 (no difficulty) to 5 (impossible to do), with a maximum score of 90. A higher score indicates worse disability or handicap. The CHFS has been demonstrated as a reliable and valid assessment of hand function at the activity level in persons with SSc.
Mawdsley Calcinosis Questionnaire: The content of this questionnaire is patient-generated and includes 17 questions related to the impact of calcinosis rated from 0 (no limitation) to 10 (worst limitation possible).
The Medical Outcomes Study 36-Item Short Form Health Survey (SF-36): The SF-36 is one of the most widely used instruments to assess quality of life in patients with systemic illnesses. It is a self-administered questionnaire covering eight areas: physical function, physical role, bodily pain, general health, vitality, social function, emotional role, and mental health. For each area, the score ranges from 0 (poorer health status) to 100 (better health status).
Patient and Physician global assessments: Patients and physicians will each independently rate the severity of calcinosis on a 10 cm VAS. The term "severity" will be used to measure the extent of disease activity and associated disability or discomfort the patient experiences during the indicated time period.
Raynaud's Condition Score (RCS): The investigators will measure changes in Raynaud's phenomenon (RP) by using the RCS, a self-assessment of RP activity using a 0-10 ordinal scale. The RCS incorporates the cumulative daily frequency, duration, severity, and impact of RP attacks.
Modified Rodnan Skin Score (mRSS): The mRSS measures skin tightness and is the sum of scores from 17 surface anatomic areas (fingers, hands, forearms, arms, feet, legs, and thighs bilaterally, and face, chest, and abdomen singly) rated on a 0-3 scale (0=normal skin; 1=mild thickness; 2=moderate thickness; 3=severe thickness with inability to pinch the skin into a fold). The skin score will be the sum of the individual skin assessment scores and ranges from 0 (best possible outcome) to 51 (worst possible outcome).
Skin biopsies: The investigators will collect two side-by-side skin samples to assess for vascular changes on histopathology and gene expression changes following treatment with treprostinil: one at baseline and one at the end of the study. This part of the study will be optional for participating patients. Skin biopsies will be obtained from a standard site on the forearm (extensor surface of forearm approximately 10 cm proximal to the olecranon, which is chosen for its uniform involvement in patients with SSc). Two adjacent 5 mm punch biopsies (taken full thickness to subcutaneous fat) will be harvested from the site. This involves selecting an area to biopsy and wiping the skin with alcohol. Next, 1-2 cc of lidocaine with 1:100,000 epinephrine is introduced into the skin using a 30G needle. Two punch biopsies will then be taken and processed as described in appendix I. Next, the wound will be sutured with 1-2 4.0 nylon sutures. Wounds will be dressed with polysporin and a bandage. Verbal wound care instructions will be given. The first biopsy will be bisected: one half will be flash frozen in liquid nitrogen and half will be embedded in paraffin. The second biopsy will also be bisected: one half will be placed in RNA later, and the other half will be placed in a cryo-tube.
Research blood: The investigators will collect serum and peripheral blood samples to assess changes in vascular and SSc-associated biomarkers following treatment with treprostinil. Blood samples for the assessment of biomarkers will be drawn at baseline, 3 months, and end of study visit. Please see appendix for a complete list of biomarkers.
SPY: The SPY Near-Infrared Perfusion Assessment System (distributed by LifeCell Corp., Branchburg, N.J.; manufactured by Novadaq Technologies Inc., Richmond, BC, Canada) is an imaging technology that utilizes indocyanine green (ICG), and allows real-time visual assessment of superficial blood flow.
XtremeCT II scan: The latest-generation high-resolution peripheral quantitative computed tomography (HR-pQCT) XtremeCT II scan is a novel technology with dramatically improved spatial resolution. It is able to define the cortical and trabecular surfaces of the bones in a three-dimensional fashion, and therefore provides information on bone microarchitecture as well as bone density. The XtremeCT II machine at Stanford University is one of 10 in the United States.
Safety: During the study, the primary assessment of safety will be changes in vital signs, clinical laboratory parameters, EKG, and the development of adverse events.
Safety monitoring and reporting
Definitions:
Adverse Event (AE): An AE is any untoward medical experience occurring to a subject during a clinical trial whether or not it is related to the study drug. An AE may include an intercurrent illness, injury, or any other concomitant impairment of the subject's health, as well as abnormal laboratory findings if deemed to have clinical significance. AEs may also include worsening of an existing symptom or condition or post-treatment events that occur as a result of protocol-mandated procedures.
Severe Adverse Event (SAE): A SAE is an AE occurring at any dose that results in any of the following outcomes:
In addition, important medical events that may not result in death, be life-threatening, or require hospitalization may be considered serious when, based upon appropriate medical judgment, they may jeopardize the subject and require medical / surgical intervention to prevent one of the outcomes listed above. Examples of such medical events include allergic bronchospasm requiring intensive treatment in an emergency room or at home, blood dyscrasias or convulsions that do not result in hospitalization, or the development of drug dependency or drug abuse. Life threatening means that the subject was, in the view of the Investigator, at immediate risk of death from the event as it occurred. It does not mean that the event, had it occurred in a more severe form, might have caused death.
Reporting Responsibilities:
In the event of an adverse event, the first concern will be for the safety of the patients.
Investigators are required to collect and document all adverse events (AEs) and non-related serious adverse events (SAEs). All SAEs, regardless of expectedness or causality, must be reported to the Sponsor by fax (+ 1 919-313-1297 or other appropriate number) within 24 hours of awareness. A completed SAE report form along with any relevant hospital records and autopsy reports should be faxed to the Drug Safety Department at United Therapeutics Corporation. A follow-up SAE report form must be forwarded to the Drug Safety Department at United Therapeutics Corporation within 48 hours of the receipt of any new / updated information. The Investigator must also promptly notify their Investigational Review Board (IRB) or Ethics Committee (EC) of the SAE, including any follow-up information, in accordance with applicable national regulations and guidelines set forth by the IRB or EC. All documents related to AEs (serious, non serious, related, or not) will be readily available for review, should the need arise.
An AE or SAE occurring during the study must be documented in the subject's source documents and on the appropriate CRF page. Information relating to the AE such as onset and cessation date and times, intensity, seriousness, relationship to study drug, and outcome is also to be documented in the CRF. Where possible, AEs should be recorded using standard medical terminology. If several signs or symptoms are clearly related to a medically defined diagnosis or syndrome, the diagnosis or syndrome should be recorded on the CRF page, not the individual signs and symptoms.
All AEs should be followed until either resolution (or return to normal or baseline values), until they are judged by the Investigator to no longer be clinically significant, or for at least 4 weeks if the AE extends beyond the final visit. All SAEs that occur during the study will be followed until resolution, death, or the subject is lost to follow-up even if they are ongoing more than 4 weeks after completion of the final visit. Supplemental measurements and / or evaluations may be necessary to investigate fully the nature and / or causality of an AE or SAE. This may include additional laboratory tests, diagnostic procedures, or consultation with other healthcare professionals. CRF pages should be updated.
Statistical Considerations
Statistical analysis:
Descriptive statistics and frequency distributions of all variables of interest will be reported as proportions (%) for categorical variables and as mean ± standard deviation or median (range) for continuous variables. Baseline to 12 month differences and 95% confidence intervals will be calculated for scored outcomes (x-ray score, MRSS, physician's global assessment by VAS, and quality of life measurements). For the primary efficacy endpoint, mean change and standard deviation in calcinosis burden assessed by radiograph from baseline to 12-month visit, the investigators will use Student's t-test. The mean rate of change of calcinosis in radiograph will be calculated with the following formula: (Year 1 XR score - Baseline XR score)/time. XR score is defined as: sum of scores for 22 weighted areas affecting each hand: %area coverage (0-100) X density (1-3) X weight for each area.
Sample size calculation:
The investigators will need 9 paired radiographs (9 patients) at 1-year to provide >80% power to detect a mean change in x-ray score of 12.0 (equivalent to a minimally significant change in score of 25%) with a SD of 8.2 with moderate correlation r=0.5 using a two-sided test at alpha 0.05 level. The investigators estimate a 15% dropout rate based on prior clinical trials. Hence, the total number of subjects needed to obtain 9/0.85 subjects who complete the study is 11 subjects. Also, due to the small sample size, the investigators plan to use Wilcoxon signed rank test to analyze the effects. Thus, the investigators anticipate losing about 10% of power due to using a non-parametric test. As a result, the sample size is further adjusted to 11/0.9 = 12. Statistical significance will be defined as p ≤ 0.05.
Inclusion Criteria:
Exclusion Criteria: