Abstract
Keywords
Introduction
Hemangiomas are common benign vascular tumorsoccurring in 5% to 10% of neonates and approximately in 10% of children older than 1 year. Hemangiomais are morefrequently in females, particularly with low birth weight (1, 2). Hemangioma may be present at birth but it is generally recognized a few weeks after birth.The most common form of hemangioma is cutaneous;however organs like the brain, lungs, intestinal tract, liver, orbit, and airway may be involved.Hemangioma may lead to complications like ulceration, infection, hemorrhage, and scarring.More than 80% of cases will undergo spontaneous involution but some of them will become problematic and need medical interventions(3).According to the location and size of hemangioma, the appropriate treatment is chosen. Corticosteroids, interferon alfa, and vincristine have been extensively used for complicated and refractory hemangiomas, albeit these medical treatments are associated with variable responses and safety concerns exist about them(4-7). An old β-adrenergic antagonist, propranolol,hasrecently gained prominence in the treatment of infantilehemangioma (8). Propranolol-induced vasoconstriction immediately impacts hemangioma and causes size of hemangioma to decrease (9). At present, there is a paucity of data aboutinitiation and duration of treatment, range of age,target dose, and formulation of propranolol for treating pediatric hemangioma. This was the aim of our study. Here we report the efficacy of propranolol for pediatric hemangioma in a 6month treatment period.
Methods
Trial design
The study was conducted as a randomized, open label, crossover trial in Amir Kabir Hospital, Arak, Iran. The local Ethics Committee approved the study and written informed consent was taken from parents. The study was conducted in accord with the European directive 2001/20/EC. The registration number of this trial corresponding to the Iranian Registry of Clinical Trials was IRCT2015011920715N1. Thirty seven children younger than 15 years old who had skin hemangiomawith surface area of bigger than 35 cm2were included in the study. Patients were randomly assigned to either propranolol or no treatment for 24 weeks followed by a 1-week washout period before they crossed over to the next phase which lasted 24 weeks. Patients were given oral propranolol 2 mg/Kg/day (Abidi, Tehran, Iran) divided into twice daily doses for 6 months. Propranolol was tapered in the last month of treatment. The exclusion criteria were diabetes, asthma, overt heart failure, hypersensitivity, severe sinus bradycardia, deep visceral hemangioma, pheochromocytoma, and cardiogenic shock.
Efficacy assessment
The patients were evaluated at baseline, day 3, day 7 and then every month. Outcome for hemangioma improvement or worsening including size, color, swelling, redness and thickening were assessed and recorded by blinded pediatricians at each visit.
Safety assessment
Ateach visit, physical examination, and assessment of vital signs were done by blinded pediatricians. Untoward effects of propranolol including hypotension, bradycardia, hypoglycemia, and bronchospasm were closely monitored. Parents were informed not to discontinue the drug without physician advice and they were trained about serious side effects of propranolol.
Data analysis
The Data are shown in mean ± SD. The Analyses were done using t test and x2.P < 0.05 was considered as statistical significance. The Analyses were carried out using SPSS software version 19.0, Chicago, USA.
Results
Baseline characteristics
Of the 37 patients who had been assessed for eligibility, 5 patients did not enter the randomized treatment. A total of 32 patients were studied between September 2014 and September 2015. Patients flow through the study is presented in Figure 1. Clinical characteristics of study subjects are shown in Table 1. The mean age was 39.6 ± 4.4 months with an excess of girls (68 %vs32 %). There was no significant difference in gender between two groups. In 18 cases (56 %) hemangioma was present in the head and neck, 10 cases (31%) in the trunk and 4 cases (12.5%) in the extremities. No patient had multiple hemangioma. Patients had no previous medical treatments for hemangioma.
Baseline characteristics of patients
| value | Characteristic |
|---|---|
| 39.6 ± 4.4 | Age (months) |
| 62± 6.2 | DBP (mmHg) |
| 27 ± 4.2 | Respiratory rate (breaths/min) |
| 115 ± 1.3 | Heart rate (beats/min) |
Efficacy
In the first phase, at baseline, there was no significant difference in hemangioma size between observation and treatment groups. As shown in Figure 2, after 1 month of treatment, a significantdecrease was present in hemangioma size (30 cm2vs 16 cm2, p < 0.01). At other intervals,significant differences were present between observation and treatment groups (p < 0.05).
In the second phase, as shown in Figure 3, a significant difference was seen in the 7thmonth of treatment between two groups (p< 0.05). In spite of decrease in hemangioma size, no significant difference was seen in other intervals. In the 1st month of treatment, a significant difference was noted in range of age; children who were in 0 to 5 years of age had quicker response compared to children who were in 5 to 15 years of age (14.3 ± 3.7 vs 26.4 ± 1.3 (cm2), p < 0.01). Seven (22 %) patients did not respond to the treatment. No case of regrowth was seen during treatment and within a-6 month follow-up.
Safety
None of the cases in two groups had any side effects related to propranolol therapy during one year of treatment and observation.
Discussion
To the best our knowledge, this is the first randomized, and cross over trial on propranolol effects for treating hemangioma in children up to 15 years old. Our findings suggest that oral dose of propranolol, 2 mg/Kg, is associated with decrease in size of hemangiomas. At this dose, no case of regrowth was seen during treatment and within 6 months of follow-up. In addition, no adverse effect of propranolol therapy was observed. Our results correspond to previously published data and confirm in particular the efficacy of propranolol. Notably, we have studied children with age of 1 month to 15 years. Due to lack of high-quality randomized and controlled studies, current recommendations are not evidence-based. In the study by Goswamy, propranolol was effective during the first months of treatment but a reproliferation was seen during the drug therapy (10).Schiestl showed in his work that 10 months use of oral propranolol was effective to reduce size of hemangioma in children aged from 1.5 to 9.1 months. In contrast to our work, 2 regrowth cases were reported during treatment (11). A work by Labreze showed that 6 months treatment with 3 mg propranolol oral solution is effective in infants 1 to 5 months of age. He reported propranolol related side effects like bradycardia and hypotension. In addition, 11% of the study subjects needed additional treatments (12). A similar investigation with smaller sample size by Hogeling proved efficacy of propranolol solution in children with ages from 9 weeks to 5 years. A few cases of bronchiolitis and respiratory infections were reported in his work (13). Furthermore, the study by Bertrand demonstrated efficacy of propranolol versus prednisone in children with 3.5 months of age. It is of note that the sample size was too small. The study showed that propranolol was associated with good or excellent response compared to prednisone which was associated with mild to moderate response (14).Compared to those investigations, different age range was used in our study. In the current work, children who were younger than 5 years had quicker response than patients who were between 5 to 15 years. This difference has not been reported elsewhere. It is not known with certainty that how propranolol could affect young children more quickly. In our study, 7 (22%) children did not respond to the treatment; however, some reports have shown full response to propranolol therapy. In the present study, no hemangioma regrowth was observed during six months follow-up. In the studies by Chik and Xiao, relative hemangioma recurrence was observed in several cases, which required further treatments (15, 16). It is noteworthy that none of our patients showed any serious complications related to propranolol during2 phases of the study. Side effects such as hypotension, bradycardia, shortness of breath, and lethargy have been reported in several investigations (17-19).Mechanism of action of propranolol in treatment of hemangiom has been extensively investigated. In the study by Hadashick, it has been shown that infantile hemangiomas have a large amount of beta 2 receptors (20). Support for this finding, comes from Wong’s work which revealed presence of both beta 1 and beta 2 receptors in hemangiomas (21). Propranolol blocks beta 1 and beta 2 and reduces the blood supply of the lesions. This effect is responsible for discoloration and softening of hemangiomas. In addition, inhibition of angiogensis and induction of apoptosis are other proposed mechanisms of action of propranolol for treatment of hemangioma. Angiotensin II has a pivotal role in hemangioma. It can upregulate factors that are necessary for proliferation and angiogenesis of the lesions; on the other hand, it can up regulate anti apopototic factors (22). Propranolol ability to suppress levels of rennin, may partially explain other modes of actions. In addition, propranolol can reduce levels of matrix metalloproteinase-9which is an important enzyme for angiogenesis (23). The exact mechanism of action of propranolol in hemangioma remains to be properly addressed.
Conclusion
This trial suggests that propranolol at dose of 2 mg/Kg/day is beneficial in treating pediatric hemangioma with an acceptable safety profile.
Study limitations
The present study has a number of limitations that should be acknowledged. As this was a single-arm study, further investigations with a randomized control study are necessary. In addition, due to a small number of patients in our study, efficacy and safety of propranolol should be tested in large and high-quality randomized control trials.
Conflict of Interest
None.
References
-
1.
G Joseph M, Kliegman R, Stanton B, Geme J, Schor N, Behrman R. Nelson text book of pediatrics. Philadelphia: Saunders; 2011.
-
2.
MarlerJJ, Mulliken JB. Current management of hemangiomas andvascular malformations. Clin. Plast. Surg. 2005;32:99-116. [PubMed ID: 15636768].
-
3.
Restrepo R, Palani R, Cervantes LF, Duarte AM, Amjad I, Altman NR. Hemangiomas revisited: the useful, the unusual and the new Part 2: endangering hemangiomas and treatment. Pediatr. Radiol. 2011;41:905-15. [PubMed ID: 21607598].
-
4.
Pienaar C, Graham R, Geldenhys S, Hudson D. Intralesionalbleomycin for the treatment of hemangiomas. Plast.Reconstr.Surg. 2006;117:221-6. [PubMed ID: 16404271].
-
5.
Roganovic J. An update on the treatment of high-risk haemangiomas in infants. Eur. J. Pediatr. Surg. 2007;17:147. [PubMed ID: 17503313].
-
6.
Enjolras O, Riche M, Merland J, Escande P. Management of alarming hemangiomas in infancy: a review of 25 cases. Pediatrics. 1990;85:491-8. [PubMed ID: 2097998].
-
7.
Bertrand J, McCuaig C, Dubois J, Hatami A, Ondreichak S, Powell J. Propranolol versus prednisone in the treatmentof infantile hemangiomas: a retrospective comparative study. Pediatr. Dermatol. 2011;28:649-54. [PubMed ID: 21995756].
-
8.
Lawley L, Siegfried E, Todd J. Propranolol treatmentfor hemangioma of infancy: risks and recommendations. Pediatr. Dermatol. 2009;26:610-4. [PubMed ID: 19840322].
-
9.
Pavlakovic H, Kietz S, Lauerer P, Zutt M, Lakomek M. Hyperkalemia complicating propranolol treatment of an infantile hemangioma. Pediatrics. 2010;126:1589-93.
-
10.
Goswamy J, Rothera MP, Bruce IA. Failure of propranolol in the treatment of childhood haemangiomas of the head and neck. J. Laryngol. Otol. 2011;125:1164-72. [PubMed ID: 21846414].
-
11.
Schiestl C, Neuhaus K, Zoller S, Subotic U, Forster-Kuebler I, Michels R, Micheal R, Balmer C, Weibel L. Efficacy and safety of propranolol as first-line treatment for infantile hemangiomas. Eur. J. Pediatr. 2011;170:493-501. [PubMed ID: 20936416].
-
12.
Léauté-Labrèze C, Hoeger P, Mazereeuw-Hautier J, Guibaud L, Baselga E, Posiunas G, Phillips RJ, Caceres H, Lopez Gutierrez JC, Ballona R, Friedlander SF, Powell J, Perek D, Metz B, Barbarot S, Maruani A, Szalai ZZ, Krol A, Boccara O, Foelster-Holst R, Febrer Bosch MI, Su J, Buckova H, Torrelo A, Cambazard F, Grantzow R, Wargon O, Wyrzykowski D, Roessler J, Bernabeu-Wittel J, Valencia AM, Przewratil P, Glick S, Pope E, Birchall N, Benjamin L, Mancini AJ, Vabres P, Souteyrand P, Frieden IJ, Berul CI, Mehta CR, Prey S, Boralevi F, Morgan CC, Heritier S, Delarue A, Voisard JJ. A randomized, Controlled trial of oral propranolol in infantile hemangioma. N. Engl. J. Med. 2015;372:735-46. [PubMed ID: 25693013].
-
13.
Hogeling M, Adams S, Wargon O. A randomized controlled trial of propranolol for infantile hemangiomas. Pediatrics. 2011;128:e259-66. [PubMed ID: 21788220].
-
14.
Bertrand J, McCuaig C, Dubois J, Hatami A, Ondrejchak S, Powell J. Propranolol versus prednisone in the treatment of infantile hemangiomas: a retrospective comparative study. Pediatr. Dermatol. 2011;28:649-54. [PubMed ID: 21995756].
-
15.
ChikKK, LukCK, Chan HB, Tan HY. Use of propranolol in infantile haemangioma among Chinese children. Hong Kong Med. J. 2010;16:341-6. [PubMed ID: 20889997].
-
16.
Xiao Q, Li Q, Zhang B, Yu W. Propranolol therapy of infantile hemangiomas: efficacy, adverse effects, and recurrence. Pediatr. Surg. Int. 2013;29:575-8. [PubMed ID: 23519547].
-
17.
Sans V, Roque E, Berge J, Grenier N. Propranolol for severe infantile hemangiomas. Pediatrics. 2009;124:423-31.
-
18.
Sharma V, Fraulin F, DumestreD3, Walker L, Harrop A. Beta-blockers for the treatment of problematic hemangiomas. Can. J. Plast. Surg. 2013;21:23-8. [PubMed ID: 24431932].
-
19.
CausséS, Aubert H, Saint-Jean M, Puzenat E, Bursztejn AC, Eschard C, Mahé E, Maruani A, Mazereeuw-Hautier J, Dreyfus I, Miquel J, Chiaverini C, Boccara O, Hadj-Rabia S, Stalder JF, Barbarot S; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Propranolol-resistant infantile haemangiomas. Br. J. Dermatol. 2013;169:125-9. [PubMed ID: 23659587].
-
20.
Hadaschik E, Scheiba N, Engstner M, Flux K. High levels of b2-adrenoceptors are expressed in infantile capillary hemangiomas and may mediate the therapeutic effect ofpropranolol. J. Cutan. Pathol. 2012;39:881-3. [PubMed ID: 22764832].
-
21.
Wong A, Hardy KL, Kitajewski AM, Shawber CJ, KitajewskiJK, Wu JK. Propranolol accelerates adipogenesis in hemangioma stem cells and causes apoptosis of hemangioma endothelial cells. Plast. Reconstr. Surg. 2012;130:1012-21. [PubMed ID: 23096601].
-
22.
Arneja JS. Pharmacologic therapies for infantile hemangioma: is there a rational basis? Plast. Reconstr. Surg. 2012;129:724-5.
-
23.
Thaivalappil S, Bauman N, Saieg A, Movius E, Brown KJ, Preciado D. Propranolol mediated attenuation of MMP-9 excretion in infants with hemangiomas. JAMAOtolaryngol. Head Neck. Surg. 2013;139:1026-31.