Mirabegron as adjuvant treatment for patients with interstitial cystitis/bladder pain syndrome.
Interstitial cystitis (IC), or bladder pain syndrome (BPS), is a chronic disease characterized by suprapubic pain related to bladder filling, coupled with additional symptoms, including increased urinary frequency or urgency, without proven urinary infection or obvious pathology (1-3). The symptoms typically associated with IC often overlap with other gynecologic and urologic conditions, including overactive bladder (OAB), which is characterized by urinary urgency, with without urge urinary incontinence, usually with frequency and nocturia but no pain. (4) Patients diagnosed with IC/BPS comprise a diverse group of patients with varied clinical phenotypes (5-7) and the presence of various other co-morbid chronic pain and symptom-based syndromes has been widely reported. (8-10) The heterogeneity of this patient population suggests that IC/BPS, instead of existing as one diagnosable entity is more likely a combination of etiologies with a varied pathogenesis and symptom patterns. Given its diverse clinical phenotype, appropriately managing these patients' symptoms has historically been difficult and the current goals of treatment are largely based on symptomatic relief. At present, a number of treatments are available for IC/BPS which includes conservative measures, oral medical therapy, intravesical drug instillation, hydrodistention, neuromodulation, and surgical therapy. (11) Although several therapies have been shown to help the symptoms of IC/BPS in clinical trials, multimodal therapy may be the most effective approach in dealing with the range of IC symptoms. (12)
One of the more common and bothersome symptoms in the IC/BPS population is that of urinary urgency (13). As urgency is considered to be the characteristic symptom of overactive bladder, its presence often confounds and delays the diagnosis and treatment of IC/BPS. Given the reports of qualitative differences in the urgency experienced by IC/BPS patients compared to OAB patients (14-15), the pathophysiology behind this symptoms development may not be similar. Although, anticholinergics are well established as pharmacotherapy for reducing OAB symptoms (16) classic anticholinergic and bladder antispasmodics have shown not to be efficacious in regards to these symptoms in the IC/BPS population (17-18)
The novel bladder antispasmodics, mirabegron, targets an alternative pathway to achieve control of urinary storage dysfunction. Recent advances in the understanding of the physiopathology of OAB have identified three subtypes of b-adrenoceptor (b1, b2, and b3) in the detrusor muscle and urothelium (19-21) of which b3-adrenoceptors predominate. The stimulation of the b3 subtype is thought to be the main subtype responsible for mediating relaxation of the detrusor in humans. Mirabegron is the first b3-adrenoceptor agonist to enter clinical practice, and has been approved for the treatment of symptoms of OAB including urinary frequency, urgency and urge incontinence. As mirabegron has been shown to be successful in treating the urgency and frequency symptoms in patients with OAB, it may also provide a potential efficacious treatment for the IC/BPS patient population. To our knowledge, the use of mirabegron has yet to be reported in this specific population. Our objective was to provide preliminary real life clinical practice data of effectiveness outcomes of mirabegron in patients with IC/BPS.
Participants and study design
The current report is a prospective evaluation of IC/BPS patients treated at a single outpatient clinic in a real life clinical practice setting. This study was an open-label design where the patients were not blinded to treatment. Clinical features of our patients included chronic (for at least 6 months) pelvic pain, pressure, or discomfort, perceived to be related to the urinary bladder accompanied by at least one other urinary symptom, such as persistent urge to void or frequency. Patients fulfilled the recent IC/BPS definition in the AUA (11) guidelines.
Exclusion criteria included vesical and urethral pathologies (urinary tract infection, neurogenic bladder, urethral diverticula, bladder or urethral cancer, urinary stones, urge/stress incontinence, pelvic prolapses) or nonurological pathologies (vaginitis, uterine, vaginal or cervical cancers, endometriosis) not related to IC/BPS, or previous/current treatment with mirabegron prior to enrollment.
Patients with IC/BPS with bothersome storage symptoms that did not respond to an anticholinergic trial were offered mirabegron 25 mg daily as add on therapy. Patients continued on standard therapy as prescribed. As part of the clinic protocol, all patients underwent standard assessment which includes history and physical exam and completion of validated questionnaires before and after any treatment intervention. Prospective data was collected as part of our ongoing IRB approved quality assurance audit process. Patients were de-identified before inclusion in this protocol data base.
Patients were re-assessed at the time of their routine clinic appointments and participants underwent standardized clinic repeat assessment and completion of IC/BPS questionnaires.
Demographics and self-reported symptom history
Demographics, self-reported symptom history (including duration of IC/BPS symptoms) and concurrent medications were collected as standard clinic routine.
Condition-specific symptom questionnaires
IC/BPS specific symptoms were evaluated by the validated ICSI (Interstitial Cystitis Symptom Index), ICPI (Interstitial Cystitis Problem Index) (23), PUF (Pelvic Pain and Urgency/Frequency Patient Symptom Scale) (24), NRS pain, NRS urgency, NRS frequency scores. These instruments are routinely collected before and after any treatment change. Pre and post treatment questionnaires were analyzed and reported with a global score. In addition, questions corresponding to specific symptom parameters (pain, urinary urgency, urinary frequency) were identified and scores pre and post treatment were assessed.
Statistical analysis was completed using Microsoft Excel 2010 Data Analysis package and R--version 3.3.1. All questionnaire scores collected at first post-treatment visit was compared to mean baseline scores using a Wilcoxon ranked-sign test assuming unequal variances. All results were regarded as statistically significant at a p value of 0.05.
Twenty-eight patients completed standardized clinic questionnaires before and after mirabegron add-on treatment was initiated. Of the twenty-eight patients, five were prescribed but did not take mirabegron and were excluded from final analysis. Patient demographics for the 23 IC/BPS patients are depicted in Table 1. Patients were predominantly female (n=22, 95.7%) and caucasian (n=22, 95.7%) with a mean age of 49.0 years. Standard duration between pre and post treatment assessments was 6.9 months. Of the patients who had information available regarding length of symptom duration (n=15), the average IC/BPS patient had experienced symptoms 10.5 months prior to mirabegron treatment.
Concurrent therapy of BPS/IC patients pre- and post-treatment
Table 2 lists the concomitant treatments of patients for their IC/BPS symptoms during mirabegron treatment period. All patients (n=23) enrolled in the study were taking first and second line treatment recommendations as outline by AUA guidelines. Of note, one patient stopped intravesical lidocaine and another initiated botox injections during the course of the study.
Mirabegron was well tolerated by the IC/BPS patient population. All patients who initiated mirabegron therapy remained compliant on the medication during the course of the study. Of the twenty-three patients enrolled, 4 patients noted adverse effects believed by patient to be caused by mirabegron treatment. One patient noted increase in blood pressure, another reported headaches, and two noted increased difficulty voiding.
Global and symptom specific questionnaire scores pre- and post-treatment
Table 3 lists the pre and post treatment total score of the questionnaires. There was no significant difference in total scores of ICSI, ICPI, PUF of patients pre and post treatment with mirabegron. When subcategorizing the PUF questionnaire to symptom score and bother score, no statistically significant difference was identified following treatment.
In terms of discrete symptoms measures (Table 4), there was a statistically significant improvement in urgency measures gathered from the ICSI questionnaire (p= 0.0102). No statistically significant difference was seen in the pain (p=0.9823) and frequency (p=0.9293) domains of the questionnaires.
In recent large Phase III clinical trials, mirabegron has demonstrated significant efficacy over placebo in treating the symptoms of OAB, including micturition frequency, urgency incontinence, and urgency (25-26). Given IC/BPS similar overlying symptomatology with OAB in terms of urgency related symptoms, we hypothesized that mirabegron may also play a role in treating that subset of symptoms in the IC/BPS population. The analysis of our prospectively collected real life clinical practice data from a single centre IC/BPS patient population shows that mirabegron may improve urgency symptoms in patients with IC/BPS however, showed no significant improvement in frequency or pain symptoms. Furthermore, no significant improvement was noted in the total scores of the disease specific ICSI, ICPI, and PUF questionnaires.
Although the symptoms of urgency and frequency are described by both OAB and IC populations, there may be a qualitative difference in the way these symptoms are experienced. IC/BPS patients may experience a more constant urge to void as opposed to the ICS definition of a "compelling need to urinate which, is difficult to postpone." (52,53) The prototypical OAB patients urge to void is driven to prevent episodes of incontinence however in the IC/BPS population, patients void to stop or to relieve pain. Overall the patients perceive some improvement in urgency not corroborated by the specific urgency associated questions. As mirabegron is primarily targeted at motor relaxation of the detrusor muscle and not bladder sensation, this may explain mirabegron's efficacy at treating the urgency in the OAB population compared to the IC/BPS subgroup and therefore the limited benefit seen in this study.
Pain and discomfort is also a significant symptom in IC/BPS. However, our knowledge of the afferent mechanisms that determine perceptions of lower urinary tract symptoms is limited. It is known that afferent sensory receptors of the urothelium of the bladder communicate with the central nervous system via finely mylenated a-delta fibers and unmylenated c-fibers. A-delta fibers sense bladder filling and tension within the bladder wall whereas C fibers transmit discomfort or pain in response to excessive stretching of the bladder wall. A study performed by Aizawa et al. (27) found that mirabegron can inhibit bladder afferent activity of A[delta]-fibers and c-fibers in a dose dependent fashion. Via inhibition of these afferent pain fibers, it was anticipated that mirabegron may decrease the sensation of pain associated with IC/BPS. Despite this, we were not able to show any significant reduction in pain following mirabegron administration. It is conceivable that pain reduction by other IC/BPS treatments could potentiate the benefits in terms of urgency improvement, but our analysis was not powered to show such an effect.
The findings of this study must be interpreted in the context of real life clinical setting rather than a prospective clinical trial design. Given then real world design, this study was not without limitations which include the limited sample size and subsequent low power. Furthermore, as this was a real world evaluation, patients were enrolled were on concurrent medications in addition to starting mirabegron therapy as well as unblinded to treatment. The effect of synergistic treatment with mirabegron is difficult to ascertain given the heterogeneity in treatment baseline. Furthermore our patient population has previously been assessed and optimally treated prior to starting mirabegron as an add-on. Perhaps mirabegron may more effective in newly diagnosed IC/BPS patients with early storage symptoms and mild pain.
Given the results of our current observations, we cannot recommend a large double blind placebo-controlled clinical trial to assess the efficacy of mirabegron as a monotherapy and it would be difficult to design a study evaluating it as an add-on or adjuvant treatment. That being said, it seems reasonable to consider initiating mirabegron as an adjuvant treatment in patients who continue to have bothersome urgency despite standard IC/BPS therapy.
Our study was the first evaluation of daily low-dose mirabegron therapy for IC/BPS. Despite the limitations of this analysis, the outcomes suggest that mirabegron currently plays a limited role for the treatment of urgency but not the pain associated with IC/BPS.
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Michael Di Lena; Victoria Tolls; Kerri-Lynn Kelly; J. Curtis Nickel
Department of Urology, Queen's University, Kingston, ON, Canada
Cite as: Can Urol Assoc J 2017 Dec. 22; Epub ahead of print. http://dx.doi.org/10.5489/cuaj.4325
Published online December 22, 2017
Figures and Tables
Table 1. Patient demographics (n=23) Mean SD Median IQR Age 48.96 [+ or -] 13.5 49 20.5 Symptom duration (months) 10.47 [+ or -] 10.8 5 13.5 Months between visits 6.9 [+ or -] 4.0 6 3.5 Sex Female 22 95.6% Male 1 4.4% Race Caucasian 22 95.6% Other 1 4.4% IQR: interquartile range; SD: standard deviation. Table 2. Ongoing therapy of IC/BPS patients during mirabegron treatment (n=23) Therapy n % Diet modifications 19 82.6 Antidepressants 8 34.8 Pentosan polysulfate 8 34.8 Pelvic floor physiotherapy 4 17.4 Massage/yoga 3 13.0 Psychotherapy pain program 2 8.7 Gabapentinoids 2 8.7 Pyridium 2 8.7 Lidocaine (1) 1 4.3 Sodium citrate 1 4.3 Botox injections (2) 1 4.3 (1) Started after mirabegron administration. (2) Stopped prior to completion of study. Table 3. Total scores before and after mirabegron treatment (n=23) Before treatment Median IQR ICSI total 12 6 Total scores ICPI total 10 3.5 PUF total 18 6 Symptom score total PUF 13 4.5 Bother score total PUF 6 3 After treatment p Median IQR ICSI total 12 5.5 0.554 Total scores ICPI total 10 5 0.313 PUF total 19 8.5 0.991 Symptom score total PUF 12 5.5 0.834 Bother score total PUF 6 3 0.894 ICPI: Interstitial Cystitis Problem Index; ICSI: Interstitial Cystitis Symptom Index; IQR: interquartile range; PUF: Pelvic Pain and Urgency /Frequency Patient Symptom Scale. Table 4. Symptom-specific scores before and after mirabegron treatment (n=23) Before treatment Median IQR Pain Pain NRS 6 3.5 Frequency Frequency NRS 7 3.5 Urinate less than 2 hours after coid 4 2 ICSI Frequent urination day ICPI 3 0.5 Bathroom count per day PUF 2 2 Urgency Urgency NRS 7 2 Urinate with no warning ICSI 4 1.5 Need urinate little warning ICPI 3 1 Urgency rating PUF 2 1.5 After p treatment Median IQR Pain 6 4 0.9823 Frequency 7 3.5 0.9293 4 3 0.8615 3 2 0.7897 2 1.5 0.5336 Urgency 5 3 0.0717 2 3 0.0102 2 2 0.6209 1 2 0.6541 ICPI: Interstitial Cystitis Problem Index; ICSI: Interstitial Cystitis Symptom Index; IQR: interquartile range; PUF: Pelvic Pain and Urgency /Frequency Patient Symptom Scale.
Please Note: Illustration(s) are not available due to copyright restrictions.
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|Title Annotation:||Original Research|
|Author:||di Lena, Michael; Tolls, Victoria; Kelly, Kerri-Lynn; Nickel, J. Curtis|
|Publication:||Canadian Urological Association Journal (CUAJ)|
|Date:||Mar 1, 2018|
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