Blood Res 2014; 49(3): 192-195  https://doi.org/10.5045/br.2014.49.3.192
Hereditary hemorrhagic telangiectasia treated with low dose intravenous bevacizumab
Jee Wan Wee, Young Woo Jeon, Jun Young Eun, Han Jo Kim, Sang Byung Bae, and Kyu Taek Lee*

Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Korea.

Correspondence to: Correspondence to Kyu Taek Lee, M.D. Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, 44, Suncheonhyang 4-gil, Dongnam-gu, Cheonan 330-930, Korea. Tel: +82-41-570-3667, Fax: +82-41-574-5762, khy1234@schmc.ac.kr
Received: August 27, 2012; Revised: December 12, 2012; Accepted: July 9, 2014; Published online: September 25, 2014.
© The Korean Journal of Hematology. All rights reserved.

cc This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder that leads to mucocutaneous telangiectasias, epistaxis, and gastrointestinal bleeding. Depending on the severity and manifestation of the disease, various therapeutic modalities have been used, from local bleeding control to surgery or concomitant drug therapy. Several articles under review have presented guidelines for treatment of HHT with bevacizumab as a direct anti-angiogenesis strategy. Still, neither the exact optimal dose nor the minimum effective dose of intravenous bevacizumab in patients with severe HHT has been reported. A 55-year-old man presented with long-standing epistaxis, recent melena, dizziness, and a three-generation family history of chronic epistaxis, anemia, and regular blood transfusions. Treatment with argon plasma coagulation (APC) for the gastrointestinal bleeding failed to raise hemoglobin levels, we considered using the bevacizumab. We report a patient with severe HHT, who was treated with low-dose bevacizumab (2 mg/kg) and improved substantially.

Keywords: Bevacizumab, Hereditary hemorrhagic telangiectasia, Low dose
INTRODUCTION

Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant inherited vascular dysplasia characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations [1, 2]. Patients with HHT experience repeated epistaxis and gastrointestinal bleeding with severe iron-deficiency anemia [1], and the organs that are usually affected are the lungs, liver, and brain [1]. The abnormal vessels of HHT are vulnerable to bleeding because of their inadequate vessel wall structure and high perfusion pressure [3]. The cellular mechanisms underlying the generation of HHT telangiectasia and arteriovenous malformations have been unraveled, with recent reports focusing on a defective response to angiogenic stimuli in various settings [2]. Serum concentrations of transforming growth factor beta (TGF-β), activin receptor-like kinase 1, and vascular endothelial growth factor (VEGF) are significantly higher in patients with HHT [3, 4]. TGF-β stimulates the production of VEGF, which plays a key role in angiogenesis [4]. Generally, a conventional dose (5-10 mg/kg) of bevacizumab is administered intravenously as a direct anti-angiogenesis strategy to treat patients with severe HHT, but the relative efficacy of lower-dose intravenous bevacizumab is not well known. We report a substantial effect of low-dose bevacizumab (2 mg/kg) in a patient with severe anemia due to HHT.

CASE REPORT

A 55-year-old man presented with long-standing epistaxis, recent melena, and dizziness. He had a three-generation family history of chronic epistaxis, anemia, and regular blood transfusions for 16 years (Fig. 1). Physical examinations showed mucocutaneous telangiectasias of the lips, tongue, finger tips, and lower eyelids (Fig. 2A), along with finger clubbing and pale conjunctivae. Initial laboratory findings were 6.0 g/dL hemoglobin (90 fL MCV, 27 pg MCH), 308×109/L platelets, 15.4% red blood cell distribution width, 6.4% reticulocytes, 25 µg/dL serum iron, and 13.17 ng/mL serum ferritin. Endoscopic gastroduodenoscopy (EGD) and colonoscopy were performed for the anemia workup, during which numerous telangiectasia of the total gastric mucosa with old blood clots and easy touch bleeding were observed (Fig. 2B). We treated the patient using an argon plasma coagulator (APC) (Fig. 2B), which successfully stopped the melena. During the hospitalization period, total 8 units of red blood cell were transfused. However, he was readmitted 1 month after discharge with dizziness and anemia because of repeated gastrointestinal bleeding. Repeated endoscopic treatment with APC of multiple gastric telangiectasias was performed. Concurrently, other bleeding foci were screened using a red blood cell nuclear scan, and radioactivity was detected in the stomach, jejunum, ileum, and upper small bowel areas on both dynamic and 24-h delayed images. We needed another 8 units of red blood cell transfusion to raise hemoglobin level. As treatment methods with oral iron and endoscopic APC both failed to raise hemoglobin levels, we considered using the anti-VEGF antibody, bevacizumab. The patient first refused bevacizumab treatment due to financial problems. It was only after several failures to control local bleeding with endoscopic APC that he finally agreed to the bevacizumab treatment. Standard regimens for HHT treatment using bevacizumab have not been established, and the minimum intravenous bevacizumab dosage is >5 mg/kg in almost all reported cases. We decided to administer low-dose intravenous bevacizumab (2 mg/kg) considering his financial status. The patient received four courses of intravenous bevacizumab, 2 mg/kg per course, every 3 weeks. Despite the low bevacizumab dosage, both hemoglobin and serum ferritin levels increased and maintained higher levels after treatment, and the frequency of red blood cell transfusions decreased beginning at the early phase of treatment (Fig. 3). He had been transfused with more than four units of packed red blood cells every 2 weeks before the bevacizumab treatment. After the low-dose intravascular bevacizumab administration, he did not need blood transfusions for 2 months. Follow-up EGD also demonstrated improvement in the numerous telangiectasias of the gastric mucosa (Fig. 2C). However, blood transfusions resumed after the fourth course of bevacizumab treatment. Nevertheless, the frequency of blood transfusions was reduced by half (every month), and epistaxis frequency per month decreased by 50% (Fig. 3). The patient could not continue treatment because of his financial status.

DISCUSSION

HHT is a familial disorder characterized by delicate, ecstatic vessels in the skin, mucous membranes, and viscera [5]. HHT is an autosomal dominant inherited disorder, in which small telangiectasias on the face represent an important cosmetic problem, and larger lesions lead to iron deficiency anemia due to chronic blood loss [6]. Early diagnosis of HHT is important to avoid complications from arteriovenous malformations, and proper clinical management of symptomatic as well as pre-symptomatic individuals is necessary [7]. Several studies that aimed to guide management practice have been published recently [2]. New data suggest surgery and cauterization for nosebleeds as a local bleeding control method [2]. Patients with HHT and gastrointestinal bleeding require numerous endoscopic examinations or surgical resections to prevent recurrent bleeding [8]. In addition, the number of required blood transfusions can be reduced by hormonal treatment (estrogen/progesterone preparations or danacrine) in patients with HHT and gastrointestinal bleeding [8]. However, this therapy is of limited applicability, particularly for male patients, as they often suffer from pronounced side effects such as gynecomastia, edema, and feminization [8].

Bevacizumab is a full-length recombinant humanized antibody active against all VEGF-A isoforms, which plays differing and non-overlapping roles in the induction and patterning of angiogenesis [9]. Bevacizumab is an anti-neoplastic agent and is commonly used to treat various cancers, including colorectal, lung, breast, and kidney cancers, as well as glioblastomas [9, 10, 11]. Common adverse effects of intravenous bevacizumab include bleeding or hemorrhage, hypertension, proteinuria, gastrointestinal symptoms such as abdominal pain or vomiting, and venous or arterial thromboembolic events [10]. According to the 2009 HHT guidelines, intravenous bevacizumab is another treatment option for patients with HHT [2]. Several reports of successful HHT treatment with intravenous bevacizumab have been published in Western countries [12]. However, the standard dosage of intravenous anti-VEGF regimens for severe HHT treatment has not been reported. In particular, the conventional (5-10 mg/kg) dose of intravenous bevacizumab that has been reported so far has not been applied to patients with gastrointestinal bleeding. In previous reports, at least 5 mg/kg intravenous bevacizumab was administered for initial and maintenance treatment [6, 13, 14].

Our patient had received countless blood transfusions due to recurrent anemia until June 2011. Although low-dose intravenous bevacizumab (2 mg/kg) was administered due to the patient's financial status, it reduced the frequency of blood transfusions required, even during the early phase of treatment. The patient had never experienced a period longer than 2 weeks without receiving a blood transfusion in the 16 years before bevacizumab administration, but he did not require a blood transfusion for 2 months after the bevacizumab therapy. Furthermore, he did not complain of any adverse effects during the bevacizumab treatment. However, his hemoglobin level began to decrease after the fourth course of bevacizumab treatment, and blood transfusions resumed. A relapse in epistaxis or mucocutaneous bleeding after bevacizumab treatment was reported by Bose et al. [4], likely due to the short half-life of bevacizumab (20 days) [11] with spontaneous regeneration of VEGF in its absence [3, 12]. Our results demonstrate that low-dose intravenous bevacizumab (2 mg/kg) was inadequate to maintain stable hemoglobin levels due to severe gastrointestinal bleeding in the long term. However, an early clinical effect was confirmed in our case. A few cases of treatment with low-dose (2-3 mg/kg) intravenous bevacizumab for severe epistaxis have been reported as initial treatments of <6 months' duration, but long-term data are lacking [15].

In our case, the commonly encountered skin and other side effects of a conventional dose of intravenous bevacizumab were minimal and tolerable. Low-dose intravenous bevacizumab was effective at the beginning of treatment. However, we could not find the optimal duration of the treatment because the present patient discontinued the treatment. This case suggests that the use of low dose (2-3 mg/kg) of intravenous bevacizumab can be effective for severe gastrointestinal bleeding of HHT.

Figures
Fig. 1.

Pedigree of the patient's family. Red box indicates those affected by hereditary hemorrhagic telangiectasia.


Fig. 2.

(A) The lips and tongue showed mucocutaneous telangiectasias. (B) Numerous telangiectasia lesions of the total gastric mucosa with old blood clots and easy touch bleeding patterns were observed by endoscopic gastroduodenoscopy (EGD). Argon plasma coagulation (APC) provided successful management. (C) Follow-up EGD showed improved telangiectasia of the gastric mucosa after bevacizumab therapy.


Fig. 3.

Hemoglobin and serum ferritin levels increased after administration of low-dose intravenous bevacizumab and were maintained. The frequency of red blood cell transfusions decreased. However, the hemoglobin level again decreased, and blood transfusions were required after the fourth bevacizumab cycle.


References
  1. Shovlin, CL, Guttmacher, AE, Buscarini, E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet, 2000;91;66-67.
    Pubmed
  2. Shovlin, CL. Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev, 2010;24;203-219.
    Pubmed
  3. Sadick, H, Riedel, F, Naim, R, et al. Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor-beta1 as well as high ALK1 tissue expression. Haematologica, 2005;90;818-828.
    Pubmed
  4. Bose, P, Holter, JL, Selby, GB. Bevacizumab in hereditary hemorrhagic telangiectasia. N Engl J Med, 2009;360;2143-2144.
    Pubmed
  5. Kim, YJ, Kim, IH, Moon, TH, et al. A case of hereditary hemorrhagic telangiectasia with pulmonary arteriovenous malformation. Korean J Med, 1996;50;571-575.
  6. Suppressa, P, Liso, A, Sabba, C. Low dose intravenous bevacizumab for the treatment of anaemia in hereditary haemorrhagic telangiectasia. Br J Haematol, 2011;152;365.
    Pubmed
  7. Richards-Yutz, J, Grant, K, Chao, EC, Walther, SE, Ganguly, A. Update on molecular diagnosis of hereditary hemorrhagic telangiectasia. Hum Genet, 2010;128;61-77.
    Pubmed
  8. Amanzada, A, Toppler, GJ, Cameron, S, Schworer, H, Ramadori, G. A case report of a patient with hereditary hemorrhagic telangiectasia treated successively with thalidomide and bevacizumab. Case Rep Oncol, 2010;3;463-470.
    Pubmed
  9. Loges, S, Roncal, C, Carmeliet, P. Development of targeted angiogenic medicine. J Thromb Haemost, 2009;7;21-33.
    Pubmed
  10. Cohen, MH, Gootenberg, J, Keegan, P, Pazdur, R. FDA drug approval summary: bevacizumab (Avastin) plus Carboplatin and Paclitaxel as first-line treatment of advanced/metastatic recurrent nonsquamous non-small cell lung cancer. Oncologist, 2007;12;713-718.
    Pubmed
  11. Lu, JF, Bruno, R, Eppler, S, Novotny, W, Lum, B, Gaudreault, J. Clinical pharmacokinetics of bevacizumab in patients with solid tumors. Cancer Chemother Pharmacol, 2008;62;779-786.
    Pubmed
  12. Brinkerhoff, BT, Poetker, DM, Choong, NW. Long-term therapy with bevacizumab in hereditary hemorrhagic telangiectasia. N Engl J Med, 2011;364;688-689.
    Pubmed
  13. Lazaraki, G, Akriviadis, E, Pilpilidis, I, Parisi, I, Tzilves, D, Tarpangos, A. Low dose of bevacizumab is safe and effective in preventing bleeding episodes in hereditary hemorrhagic telangiectasia. Am J Gastroenterol, 2011;106;2204-2206.
    Pubmed
  14. Fodstad, P, Dheyauldeen, S, Rinde, M, Bachmann-Harildstad, G. Anti-VEGF with 3-week intervals is effective on anemia in a patient with severe hereditary hemorrhagic telangiectasia. Ann Hematol, 2011;90;611-612.
    Pubmed
  15. Rohrmeier, C, Kuhnel, TS. Bevacizumab in therapy-refractory epistaxis: case report of low-dose antibody therapy for hereditary hemorrhagic telangiectasia. HNO, 2012;60;1003-1006.
    Pubmed


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