Effects and safety of triamcinolone acetonide-controlled common therapy in keloid treatment: a Bayesian network meta-analysis
Authors Zhang Z, Cheng L, Wang R, Cen Y, Li Z
Received 12 January 2018
Accepted for publication 7 March 2018
Published 29 May 2018 Volume 2018:14 Pages 973—980
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 3
Editor who approved publication: Professor Deyun Wang
Zhenyu Zhang,1 Lihui Cheng,2 Ru Wang,1 Ying Cen,1 Zhengyong Li1
1Department of Aesthetic Plastic and Burn Surgery, West China Hospital, Sichuan University, Chengdu, People’s Republic of China; 2Department of Pancreatic Surgery, West China Hospital, Sichuan University, Chengdu, People’s Republic of China
Background: Triamcinolone acetonide (TAC) is used frequently in the treatment of keloid scars, but has presented controversial results. In this study, we aim to evaluate the effectiveness of TAC compared with other common therapies used in keloid treatment.
Methods: MEDLINE, Embase, Web of Science and the Cochrane Library databases were searched until January 2018. Key data were extracted from eligible randomized controlled trials. Both pairwise and network meta-analyses were conducted for synthesizing data from eligible studies.
Results: Ten randomized controlled trials were included in this meta-analysis. The relative risk of keloids associated with seven adjuvants was analyzed, including placebo, pulsed dye laser (PDL), 5-fluorouracil (5-FU), silicone, verapamil, TAC+5-FU and TAC+5-FU+PDL. Patients treated with the following adjuvants appeared to not have significantly reduced risk of keloid in relation to those treated with TAC: placebo (OR=1.86, 95% CI 1.12–2.61), PDL (OR=1.32, 95% CI 0.53–3.30), 5-FU (OR=1.13, 95% CI 0.48–2.68), silicone (OR=1.28, 95% CI 0.59–2.78), verapamil (OR=1.86, 95% CI 0.67–5.14), TAC+5-FU (OR=0.77, 95% CI 0.38–1.58) and TAC+5-FU+PDL (OR=0.80, 95% CI 0.16–4.03). The surface under the cumulative ranking curve values for each adjuvant were as follows: TAC, 59.9%; placebo, 17.4%; PDL, 46.3%; 5-FU, 48.9%; silicone, 56.2%; verapamil, 84.7%; TAC+5-FU, 68.5% and TAC+5-FU+PDL, 18.1%.
Conclusion: There were no differences between the efficacy of TAC and other common therapies in keloid treatment. TAC also acts as an effective alternative modality in the prevention and treatment of keloids. Incorporating adjuvants particularly verapamil appeared to be significantly associated with a decreased risk of keloids.
Keywords: keloid, triamcinolone acetonide, randomized controlled trial, network meta-analysis
Keloids are caused by the uncontrolled deposition of collagen and glycosaminoglycans around the wounds on the dermal dermis of the skin.1 During wound healing, the balance between the anabolic and catabolic effects of collagen is destroyed due to various causes forming a pathological scar.2,3 Keloids are caused by the proliferation of fibrogenic cells and the formation of large extracellular matrix, and their development is characterized by excessive collagen synthesis and deposition.4 Keloids can bring psychological and physical pain to patients from the aspect of appearance and body function. In severe cases, keloids even affect the self-confidence of patients leading to inferiority complex.4 Therefore, in the burn trauma, plastic surgery and dermatology department, keloid is the focus of high clinical attention. Although drugs and treatments are currently available for keloids, there are enormous challenges in their prevention and treatment, and there is no satisfactory universal treatment for all keloids.5
Corticosteroids are highly bioactive substances secreted by the adrenal cortex through tissue fluid and blood, which play a powerful role in physiological regulation.6 Most of them are hormones, such as glucocorticosteroids and sex hormones. They have anti-inflammatory, anti-allergy, antidrug, anti-nuclear fission and other effects, and their role is strong and lasting.7–9 Corticosteroids are most commonly used as injections in the early stage of the maturation phase, and intralesional injection of the corticosteroid triamcinolone acetonide (TAC) is one of the first-line treatment modalities for keloid treatment.10
The use of TAC in keloid treatment is commonplace. Wong et al found TAC therapy reduces the incidence of keloids among patients.11 However, the efficacy of TAC has not been compared with other common therapies efficacious in treating keloids. Therefore, to determine the efficacy and safety of TAC in keloid treatment compared to other common therapies, we conducted a network meta-analysis based on randomized controlled trials.
Eligible studies were systematically searched in MEDLINE, Embase, Web of Science and the Cochrane Library databases until January 2018 with keywords including “Keloid” [MeSH] OR “Acne Keloid” [MeSH] OR “Hypertrophic” [MeSH] OR “Scar” [MeSH] AND “triamcinolone acetonide” [MeSH] OR “Corticosteroids” [MeSH] OR “steroids” [MeSH] AND “Randomized Controlled Trial” [MeSH].
The studies that met the following inclusion criteria were included in the meta-analysis: (1) the study must have included keloid patients; (2) the relationship between TAC and keloid must have been studied; and (3) the study must be a randomized controlled trial.
We conducted a network meta-analysis (Bayesian approach) which included both direct and indirect evidence in the network. Adjuvants were ranked based on the surface under the cumulative ranking curve (SUCRA) values. One adjuvant is more preferable than the other if it has a larger SUCRA value. Small study effects or publication bias were visually inspected using the funnel plots.
Literature search results
A total of 1,005 studies from MEDLINE, 1,127 studies from Embase and 1,074 studies from Web of Science were selected. After removing duplicates, 1,066 studies were identified. After reviewing their titles and abstracts, 1,029 citations were excluded. The remaining 37 citations were assessed in more detail for eligibility by reading the full text. Among them, one study was excluded due to no relevant outcome measure, 11 studies were excluded due to insufficient network connections and eight studies were excluded due to lack of detailed information. Finally, 10 studies were used for the final data synthesis.12–21 The flowchart of literature search is presented in Figure 1, and the risk of bias of eight studies included in this meta-analysis is summarized in Figure 2. The characteristics of the included studies are shown in Table 1, with the pattern of evidence within the network displayed in Figure 3.
Figure 1 Flow diagram of the study selection process.
Figure 2 Risk of bias of the included randomized controlled trials (judgments about each risk-of-bias item for each included study: +, low risk; −, high risk; ?, unclear risk).
Table 1 Characteristics of included studies
Results of pairwise meta-analysis
Table 2 displays the results produced by pairwise meta-analysis. Patients treated with the following seven adjuvants appeared to not have significantly reduced risk of keloids in relation to those treated with TAC: placebo (OR=1.86, 95% CI 1.12–2.61), pulsed dye laser (PDL; OR=1.32, 95% CI 0.53–3.30), 5-fluorouracil (5-FU; OR=1.13, 95% CI 0.48–2.68), silicone (OR=1.28, 95% CI 0.59–2.78), verapamil (OR=1.86, 95% CI 0.67–5.14), TAC+5-FU (OR=0.77, 95% CI 0.38–1.58) and TAC+5-FU+PDL (OR=0.80, 95% CI 0.16–4.03). Patients treated with the following adjuvants appeared to have a significantly reduced risk of keloids in relation to those treated with placebo: PDL (OR=0.34, 95% CI 0.27–0.43), 5-FU (OR=0.37, 95% CI 0.26–0.52), silicone (OR=0.40, 95% CI 0.29–0.54) and TAC+5-FU (OR=0.49, 95% CI 0.28–0.85). Moreover, there was no significant heterogeneity among studies for the abovementioned significant results (P-heterogeneity>0.05 and I2<50%).
Table 2 Summary ORs of TAC and heterogeneity for each direct comparison
Table 3 displays the results produced by network meta-analysis. Patients treated with the following seven adjuvants appeared to have a significantly reduced risk of keloids in relation to those treated with placebo: TAC (OR=0.08, 95% CI 0.00–0.18), PDL (OR=0.30, 95% CI 0.06–0.55), 5-FU (OR=0.32, 95% CI 0.05–0.78), silicone (OR=0.20, 95% CI 0.01–0.40), verapamil (OR=0.23, 95% CI 0.01–0.46), TAC+5-FU (OR=0.12, 95% CI 0.01–0.24) and TAC+5-FU+PDL (OR=0.46, 95% CI 0.27–0.77).
Table 3 Network meta-analysis comparisons
The corresponding SUCRA values are presented in Figure 4. The adjuvants were ranked based on SUCRA values as follows: TAC, 59.9%; placebo, 17.4%; PDL, 46.3%; 5-FU, 48.9%; silicone, 56.2%; verapamil, 84.7%; TAC+5-FU, 68.5%; and TAC+5-FU+PDL, 18.1%. Incorporating adjuvants particularly verapamil appeared to be significantly associated with a decreased risk of keloids.
The result of the comparison-adjusted funnel plots did not reveal any evidence of apparent asymmetry (Figure 5). No significant publication bias was observed.
Objective and reliable clinical evaluation methods and prevention and control measures for scars are still a hot issue. Most of the scar treatments have achieved good results in the past 20 years, but few have been supported by prospective surveys in the control group, and some of them even lack safety data. Many new therapies have shown early effects in small-sample trials, but these effects have not been confirmed with long-term follow-up and large samples. In recent years, the understanding of wound healing and scar formation has deepened. The accumulation of a great deal of clinical experience in scar treatment, and the research and application of new preparations and new treatment methods, especially the emerging technologies, have subverted some traditional treatment concepts and thus require the establishment of safe and effective standardized scar management protocols that can be used in routine clinical practice to guide clinical treatment.22–24 The mechanism of scar formation is not fully understood, but the relevant cognitive exploration in micro and macro aspects is ongoing. The whole process of scar formation involves not only micro cells (fibroblasts, myofibroblasts, mast cells, neutrophils, etc.) but also cytokines (transforming growth factor beta, tumor necrosis factor alpha, vascular endothelial growth factor, etc.), extracellular matrix components (collagen metabolism and arrangement of arrhythmia, the change in glycosaminoglycan interactions) and organization space structure (space regulation network of repair cells formed between the three dimensions).25,26 Surgical procedures are not the best choice for keloid management as the recurrence rate is high. As alternatives to the use of corticosteroids, chemotherapeutic agents, verapamil, silicone gel tablets and cryotherapy have become important, particularly in patients with high recurrence rates after surgery.10 Khansa et al performed a meta-analysis and showed silicone gel, PDL, TAC and 5-FU had high efficacy in improving keloids.27 However, which common therapy was the most effective in improving keloids was unknown.
This network meta-analysis attempted to evaluate the effectiveness of TAC compared with other common therapies used in keloid treatment. Our analysis suggests that verapamil is potentially more preferable than other adjuvants. Verapamil has been used as a coronary dilator since 1962. In the recent years, it has been used for the treatment of hypertension, angina, arrhythmia, cerebrovascular disease, finger vasospasm, abdominal pain, esophageal delaying, migraine and pulmonary hypertension and to prevent preterm birth. In 1997, Dong et al first reported the treatment of keloids with calcium channel blocker verapamil, which immediately attracted the attention of clinicians.28 After 1997, attempts have been made to identify and treat keloid patients with verapamil. Verapamil has been shown to increase procollagenase synthesis in normal cultured fibroblasts. It also leads to the depolymerization of actin, cell conformation change and cell apoptosis, and ultimately leads to the reduction of fibrous tissue formation.29 Boggio et al confirmed 50 μM verapamil was effective in wound healing, and it can also avoid the development of keloids and hypertrophic scars after plastic surgery.30
As suggested by the SUCRA ranking scheme, TAC+5-FU was ranked behind verapamil. 5-FU is an anti-pyrimidine drug. It has to be enzymatically converted to 5-fluorodeoxyuridine nucleotides and exhibits antitumor activity.31,32 The action of this enzyme may also transfer one carbon unit of leucovorin to deoxyuridine nucleotide monophosphate for the synthesis of thymidine monoacid. At the same time, it also shows some inhibitory effect on the synthesis of RNA.31 Shin et al found 5-FU was more effective than TAC in keloid treatment after surgical excision.33
This meta-analysis also has some limitations. The test result of the corticosteroid therapy showed statistical heterogeneity was limited in randomized controlled trials, and limited evidence of a dose-dependent association between corticosteroids therapy and keloids, which provides limited confidence in the findings. Second, there is no record of keloid patients treated in a standardized manner, which leads to the difference between the trials; therefore, these results should be interpreted with caution. Third, study durations were short in these randomized controlled trials, and patients included in these trials may be different from real life. Fourth, these findings may not be generalizable to a specific group of patients because randomized controlled trials tend to exclude participants.
Our findings underscore the notion that any common therapy compared with TAC did not reduce keloid risk. Verapamil is potentially the most preferable adjuvant in keloid treatment. In the future, large-scale trials must be performed to validate the risk identified in the current meta-analysis.
This study was supported by the Sichuan Science and Technology Department Applied Basic Research Project (grant no. 2017JY0335) and (grant no.2017JY0250).
The authors report no conflicts of interest in this work.
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