Role of application of tadalafil 5 mg once-daily (≥6 months) in men with erectile dysfunction from six randomized controlled trials
Review Article

Role of application of tadalafil 5 mg once-daily (≥6 months) in men with erectile dysfunction from six randomized controlled trials

Jiajia Ma1#, Zi Liu1,2#, Jitao Wu1, Zhongbao Zhou1, 2, Xuebao Zhang1, Yuanshan Cui1, Chunhua Lin1

1Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China; 2Binzhou Medical University, Yantai, China

Contributions: (I) Conception and design: C Lin, Y Cui, Z Liu, J Ma; (II) Administrative support: C Lin, Y Cui; (III) Provision of study material or patients: C Lin, Y Cui, Z Liu, J Ma; (IV) Collection and assembly of data: Y Cui, X Zhang, J Wu, Z Liu; (V) Data analysis and interpretation: Z Liu, J Ma, X Zhang, Z Zhou; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

#These authors contributed equally to this work.

Correspondence to: Yuanshan Cui, MD, PhD; Chunhua Lin, MD, PhD. Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, NO. 20 East Yuhuangding Road, Yantai, China. Email: 1260042585@qq.com; Linchunhua1980@163.com.

Abstract: This meta-analysis was performed to assess the efficacy and safety of taking tadalafil 5 mg once-daily for at least 6 months in the treatment of erectile dysfunction (ED). Based on databases: MEDLINE, EMBASE and Cochrane Controlled Trials Register, this analysis was performed to collect randomized controlled trials (RCTs) of tadalafil 5mg once-daily in treating ED over 6 months. Reviewers also investigated the references of each literature. The meta-analysis covered a total of 1,596 patients in six RCTs. The tadalafil group performed a better effect in terms of the international index of erectile function-erectile function (IIEF) domain (P=0.005) for the treatment of ED compared with the placebo group. Safety assessments including discontinuations due to adverse events (AEs) (P=0.31) and treatment-emergent AEs (P=0.06) indicated that the tadalafil group had a better tolerate. The analysis elucidates that the dose of 5 mg per day of tadalafil showed a good effect after the treatment of at least 6 months relative to the control group with fewer side effects.

Keywords: Randomized controlled trial; Tadalafil; erectile dysfunction (ED); once-daily


Submitted Dec 30, 2019. Accepted for publication Apr 27, 2020.

doi: 10.21037/tau-19-809


Introduction

Erectile dysfunction (ED) is defined as the inability to achieve and maintain an erection sufficient for satisfactory sexual intercourse (1). Although ED is not life-threatening, it is closely related to the patient’s quality of life, sexual relationship and family stability (2). It is also an early warning sign of many physical diseases, such as stroke, tumors, Parkinson’s disease, and spinal cord disease, etc. (3). Estimates suggest that ED affects approximately 150 million men worldwide, and the rates of ED are expected to double by the year 2025 (4,5). In view of the current trend, the research and treatment of ED is very important and meaningful. A number of therapeutic options are available to treat men with ED. Of these, oral phosphodiesterase type 5 (PDE5) inhibitors are recommended as a first line of therapy (6-8).

Tadalafil can be absorbed rapidly and possesses a longer half-life of 17.5 hours than other PDE5 inhibitor (9,10). The prolonged half-life of tadalafil and effective steady-state serum concentration makes it ideally suited for daily dosing (11,12). Although PDE5 inhibitors are easy to use, men should take these oral agents when they wish to engage in sexual activity, and therefore, they should remain temporally linked to treatment. For some patients and their partners, planning sexual activity around drug intake is troublesome. The concept of daily administration of PDE5 inhibitors was also established to provide an alternative treatment option that is closer to a natural sexual life.

Several clinical studies have evaluated the safety and efficacy of tadalafil dosed once daily in patients with ED. Compared with taking on demand, it can eliminate the embarrassment of taking medication before intercourse, increase male confidence, avoid psychological barriers between husband and wife, especially for patients with severe ED. In patients with ED, tadalafil 2.5 and 5 mg administered once daily for 12 weeks were well tolerated and significantly improved erectile function compared with placebo (13). Although tadalafil has been shown to be safe and well tolerated when taken on demand for up to 2 years (14), long-term safety and efficacy data for tadalafil dosed once daily has rarely been reported.

This analysis was to assess the efficacy and safety of taking tadalafil 5 mg once-daily for at least 6 months in the treatment of ED, which may resolve some of the current debate over use of the drug. We present the following article in accordance with the PRISMA reporting checklist (available at http://dx.doi.org/10.21037/tau-19-809).


Methods

Search strategy

With Embase (2003 to Jun 2019), MEDLINE (2003 to Jun 2019), and Cochrane Central Register of Controlled Trials, we undertook a retrieval to examine published randomized controlled trials (RCTs), which investigated long-term tadalafil (5 mg once-daily) for ED at least 6 months of treatment. The searching terms were following: “ED”, “tadalafil”, “once-daily”, “long-term” and “RCT”. Additionally, we screened the retrieved references for each article.

Inclusion criteria and trial selection

The met criteria of RCTs: (I) tadalafil (5 mg once-daily) in treating ED; (II) accurate data could be analyzed; (III) the study can be accessed. If the same study is published in a different journal, we will include the latest one. However, if the same group of researchers conducts multiple different trials on a group of subjects, we will include each study. A flow chart was used to show the selection process of the study (Figure 1).

Figure 1 A flow diagram of the study selection process. RCT, randomized controlled trial.

Quality assessment

We used the Jadad scale to determine the quality of the retrieved RCTs (15). The methodological quality of each study was assessed based on how patients were assigned to the various departments of the study, the concealment of the distribution procedure, blinding, and data loss due to wear and tear. Then, according to the plan published in the Cochrane Handbook for Systematic Reviews of Interventions v.5.1.0 (16), the studies were then classified qualitatively. Each article is evaluated and assigned according to three quality classification criteria: (I) meting all quality criteria: low risk of bias; (II) partially met or ambiguous: moderate risk of bias; or (III) rarely met or not involved: high risk of bias. All authors participated in the RCTs quality assessment and resolved the differences through discussion.

Data extraction

This systematic review and meta-analysis was not required ethical approval. All six articles included were obtained from open databases. The following details from individual studies: (I) regimen patients received; (II) design of study and size of sample; (III) name of the RCT; (IV) the study of country; (V) total international index of erectile function (IIEF) domain, international index of erectile function questionnaire intercourse satisfaction (IIEF-IS) domain, IIEF overall satisfaction (IIEF-OS) domain, question 3 (IIEF-5 Q3) and question 4 (IIEF-5 Q4), IIEF sexual encounter profile (SEP) question 2 (SEP2), question 3 (SEP3), question 4 (SEP4), question 5 (SEP5), treatment-emergent adverse events (AEs), headache, back pain, dyspepsia and discontinuations due to AEs. It should be noted that both IIEF-5 and IIEF-EF belong to the IIEF category, so we choose the IIEF domain as an indicator.

Statistical analysis and meta-analysis

The meta-analysis of comparable data was carried out using RevMan v.5.1.0 (Cochrane Collaboration, Oxford, UK). We used a fixed-effect and random-effects model to estimate the mean difference (MD) of continuous data and the odds ratio (OR) of the categorical results, with a corresponding 95% confidence interval (CI) (17). When the analysis results showed that the P value was >0.05, the study was considered to be homogeneous, we would use fixed-effect model. Otherwise, the random effect model was chosen to analyze the data.


Results

Characteristics of the individual studies

The study retrieved 113 articles. Based on the above inclusion criteria, after reading the titles and abstracts of these articles, 74 studies were deleted. Thirty-three articles lack valid data. Finally, six articles (18-23) were included in the study to access the long-term (≥6 months) effect of tadalafil (5 mg once-daily) in treating male with ED (Figure 1). Table 1 showed the characteristics of each trail.

Table 1
Table 1 The details of individual study
Full table

Quality of the individual studies

All six trials were randomized controlled studies, both of which addressed randomized and double-blind processes. All studies included adequate patients (Table 2). All of the study has a reasonable assessment for the quality of each trail.

Table 2
Table 2 Quality assessment of individual study
Full table

Efficacy

IIEF domain

Six RCTs with 1,596 participants (Figure 2) were identified. Based on our analysis, the random-effects estimate of MD=3.09, and 95% CI: 0.92–5.26 (P=0.005). The result shows that long-term tadalafil 5mg once-daily showed greater increases in the IIEF domain compared with control group.

Figure 2 Forest plots showing changes in the IIEF domain. CI, confidence interval; IV, inverse variance; MH, mantel haenszel; SD, standard deviation.

IIEF-IS

Figure 3 shows the results of the change in the IIEF-IS. The random-effects estimate of the MD=1.42, 95% CI: 0.04–2.80 (P=0.04). The result shows that experimental group showed greater increases in the IIEF-IS domain compared with control group.

Figure 3 Forest plots showing changes in (A) IIEF-IS, (B) IIEF-OS, (C) IIEF-5 Q3 and (D) IIEF-5 Q4. CI, confidence interval; IV, inverse variance; MH, mantel haenszel; SD, standard deviation.

IIEF-OS

Three RCTs met the inclusion criteria (Figure 3). The fixed-effects estimate of the MD=0.96, 95% CI: 0.19–1.72 (P=0.01). The result shows that experimental group showed greater increases in the IIEF-OS domain compared with control group.

IIEF-5 Q3

Three studies failed to report the data. Three RCTs, representing 979 participants were identified (Figure 3). Heterogeneity test indicated P=0.69, the random effect model was selected for statistical analysis. The forest plots showed the SD=0.90 and 95% CI: 0.85–0.95 (P<0.00001). The result shows that experimental group showed greater improvement in the IIEF-5 Q3 compared with control group.

IIEF-5 Q4

Three RCTs including 979 participants were identified (Figure 3). No heterogeneity was found among the trials in our analysis (Figure 3), the fixed-effects model was chosen for the statistical analysis. The pooled estimate of MD was 0.66, and the 95% CI was 0.58–0.74 (P<0.00001). Our meta-analysis suggests that experimental group showed greater improvement in the IIEF-5 Q4 compared with control group.

SEP2, SEP3, SEP4 and SEP5

Two RCTs including 471 participants were identified (Figure 4). Based on our analysis, we concluded that (I) the pooled estimate of odds ratio (OR) of the SEP2 was 3.53, and the 95% CI was 1.01–12.40 (P=0.05); (II) the OR of the SEP3 was 2.93, and the 95% CI was 1.14–7.53 (P=0.03); (III) the OR of the SEP4 was 2.87, and the 95% CI was 1.80–4.58 (P<0.00001); (IV) the OR of the SEP5 was 2.98, and 95% CI was 1.85-4.81 (P<0.00001). Our meta-analysis suggests that the experimental group showed greater improvement in the SEP 3, SEP 4 and SEP 5 in comparison with placebo.

Figure 4 Forest plots showing (A) SEP2, (B) SEP3, (C) SEP4 and (D) SEP5. CI, confidence interval; MH, mantel haenszel; SD, standard deviation.

Safety

Treatment-emergent AEs (TEAEs)

Six RCTs with 1,596 participants reported the TEAEs data (Figure 5). We adopted the fixed-effects model (The pooled OR 1.25, 95% CI: 0.99–1.58, P=0.06). The results showed no difference in the incidence of TEARs between the two groups.

Figure 5 Forest plots showing changes in (A) treatment-emergent AEs, (B) headache, (C) back pain, (D) dyspepsia and (E) discontinuation due to AEs. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Discontinuation due to AEs

Six RCTs with 1,596 participants were included. The random-effects estimate of the MD=1.29, 95% CI: 0.79–2.09 (P=0.31). In terms of the incidence of discontinuation due to AEs, the result showed that tadalafil and placebo are similar.

Headache, back pain and dyspepsia

Six RCTs including 1,596 participants were involved in the analysis for headache. The pooled estimate of the OR was 1.46, and the 95% CI was 0.85 to 2.51 (P=0.17). Three RCTs included data on back pain (OR 2.24; 95% CI: 1.09–4.62; P=0.03), and 4 RCTs included data on dyspepsia (OR 1.82; 95% CI: 1.01–3.26; P=0.05). These results indicate that there is no significant difference between the two groups in terms of headache, back pain and indigestion (Figure 5).


Discussion

ED is a common disease that affects men worldwide and is associated with increased age, underlying cardiovascular, neurological, psychological, and even some urology surgery (24). Male sexual arousal is a complex process that involves the brain, hormones, emotions, nerves, muscles and blood vessels. ED can result from a problem with any of these (25,26). In addition, reconstructive radical prostatectomy (NSRP) has become the main treatment for localized prostate cancer, and ED is a common sequela of NSRP (27,28). PDE5 is a phosphodiesterase that is cGMP specific and highly expressed in corpus cavernosum smooth muscle cells. PDE5 inhibitors enhance erectile function by maintaining adequate cGMP levels in the corpus cavernosum and supplying vascular smooth muscle cells during sexual stimulation, increasing the expansion of the cavernous sinus (29,30). PDE5 inhibitor therapies, which include tadalafil, sildenafil and vardenafil, have provided nonaggressive, productive and well-tolerated treatments for ED (31).

The fact that tadalafil is effective in treating ED once a day has been confirmed or a consensus has been established. So, the effectiveness of long-term use of tadalafil is also certain, as evidenced by our research. Our study suggests that long-term tadalafil 5mg once- daily is efficacious for ED patients over 6 months. Patients take orally tadalafil 5 mg once-daily showed greater improvement in the IIEF domain. Long-term low-dose tadalafil is one of the first-line treatments for repairing damaged vascular endothelium and promoting long-term improvement of erectile function (32). Our present study also confirmed this point. What is worth mentioning is that in the early stages of treatment, low-dose tadalafil cannot achieve sufficient erectile stiffness as fast and clearly as sildenafil (33). For most ED patients seeking treatment, rapid and satisfactory sexual intercourse erection hardness is the key to success. Sildenafil has a quick onset of action of 30 min after the initial dose, a duration of action of 4–6 h and a maximum duration of 12 h (34). Therefore, sildenafil in early treatment may be necessary. However, it may lead to higher costs, the uncertainty of the agreement and possible side effects.

Recent global trends indicate that drug expenditures have become a major financial burden for ED patients due to the increasing use of PDE5 inhibitors. Cost analysis showed that the direct cost of tadalafil was higher than that of sildenafil (35). ED was not life-threatening and there was no physical pain, so patients were willing to pay for treatment, which also proved the value of tadalafil. Therefore, the economics of the long-term once-daily tadalafil is a potential problem that deserves further discussion.

The meta-analysis involved a total of 1,596 patients in six publications. The long-term tadalafil once-daily group perform a better in terms of the international index of erectile function-erectile function (IIEF) domain (P=0.005) for the treatment of ED compared with the placebo group. Safety assessments including discontinuations due to adverse events (AEs) (P=0.31) and treatment-emergent AEs (P=0.06) indicated that the long-term tadalafil group had a better tolerate. The analysis elucidates that tadalafil 5mg once-daily showed a good effect after the treatment of at least 6 months relative to the control group with fewer side effects.

Among these TEAEs, generally in the diagnosis of investigators adverse events related to drugs studied are back pain, dyspepsia, myalgia and headache. In laboratory parameters, vital signs or electrocardiogram readings no clinically significant changes were observed for patients in all of the six RCTs. Safety assessments including discontinuations due to AEs (P=0.31) and treatment-emergent AEs (P=0.06) indicated that the long-term tadalafil group had a better tolerate. There were no deaths or serious adverse events in the six studies, and most of the adverse events were well-tolerated. The effectiveness of tadalafil in the treatment of ED has been proven, and the focus of our analysis is primarily on the safety of long-term use of tadalafil, which has not been well studied and confirmed before.

PDE5 has been found to have relatively high expression in only a few limited tissues, such as the corpus cavernosum, the reproductive system of the pulmonary blood vessels and smooth muscle, platelets and visceral smooth muscle (36,37). Therefore, the most common side effects of tadalafil are headache, flushing, dyspepsia, nasal congestion, conjunctivitis and hypotension, which are also common to PDE5 inhibitors, but these side effects are usually transient and reversible (38-40).

From a scientific and daily clinical practice perspective, the results of this analysis are very important and may provide some treatment recommendations for ED patients and may resolve some of the current debate over use of the drug. In addition, unpublished research data is not included in the analysis and these factors may lead to bias. Individual nature of study design, patient inclusion and exclusion criteria and eventual patient demographics including severity may also led to bias. In addition, it is worth mentioning that the cost of drugs is a factor that cannot be ignored, especially for those patients who need to take drugs for a long time but have to bear the cost, which is a considerable financial burden. Therefore, we hope that more effective studies and long-term data will be included in our analysis in the future, so as to better prove the effectiveness and safety of long-term tadalafil 5 mg once-daily in treating ED.


Conclusions

The analysis elucidates that tadalafil 5 mg once-daily showed a good effect after the treatment of at least 6 months relative to the control group with fewer side effects.


Acknowledgments

Funding: None.


Footnote

Reporting Checklist: The authors have completed the PRISMA checklist. Available at http://dx.doi.org/10.21037/tau-19-809

Conflict of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau-19-809). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


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Cite this article as: Ma J, Liu Z, Wu J, Zhou Z, Zhang X, Cui Y, Lin C. Role of application of tadalafil 5 mg once-daily (≥6 months) in men with erectile dysfunction from six randomized controlled trials. Transl Androl Urol 2020;9(3):1405-1414. doi: 10.21037/tau-19-809