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Published in: BMC Cancer 1/2019

Open Access 01-12-2019 | Tyrosine Kinase Inhibitors | Case report

Treatment of consistent BRAF/HRAS gene mutation and MYC amplification radiation-induced abdominal wall angiosarcoma with low-dose apatinib: a case report

Authors: Jieshan Guan, Zhijie Luo, Zhiwei Xiao, Yubin Xie, Lizhu Lin

Published in: BMC Cancer | Issue 1/2019

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Abstract

Background

An extremely rare condition, radiation-induced angiosarcoma is characterized by a poor prognosis, high recurrence rate and lack of effective treatment. Herein, we present a case report of a 48-year-old female patient with radiation-induced abdominal wall angiosarcoma who showed a dramatic response to low-dose apatinib.

Case presentation

The patient, who was diagnosed with cervical squamous cell carcinoma 20 years ago, had received radiotherapy and chemotherapy after operation. Angiosarcomas of the abdominal wall appeared 9 years later. After repeated surgical operations and intravenous chemotherapy for the angiosarcomas, the patient developed tumor recurrence and pulmonary metastasis. The abdominal wall tumors showed repeated rupture and bleeding, with poor wound healing. On evaluation, laboratory findings detected the negative serum tumor markers CEA, CA 125, CA 15–3 and CA 19–9. Imaging showed multiple subcutaneous nodules and masses in the abdominal wall, accompanied by suspected small subpleural nodule at the lower lobe of the right lung. Immunohistochemistry of previous surgical pathology indicated that CD31, ERG and Vim were positive. The result of whole exome sequencing suggested the mutations of BRAF and HRAS, and the amplification of MYC. Based on the above results, the patient was clinically diagnosed with radiation-induced angiosarcoma of the abdominal wall with pulmonary metastasis. The patient was treated with low-dose apatinib and rejected reoperation or chemotherapy.

Results

At the 6-month follow-up visit, the abdominal wall lesions that had previously ruptured stopped bleeding and showed significant shrinkage. Imaging showed that most of the abdominal wall lesions had partially regressed, and some of the lesions on the abdominal wall and the suspected lesion of subpleural nodule at the lower lobe of the right lung had disappeared.

Conclusions

We described this case and reviewed the literature on radiation-related angiosarcoma. Importantly, this case suggests that apatinib may be an effective and sensitive treatment for radiation-induced angiosarcoma even at the lowest dosage, without aggravating the bleeding of lesions.
Literature
1.
go back to reference Lu HJ, Chen PC, Yen CC, Hsiao FC, Tzeng CH, Ma H, Shiau CY, Chao TC. Refractory cutaneous angiosarcoma successfully treated with sunitinib. Br J Dermatol. 2013;169(1):204–6.CrossRef Lu HJ, Chen PC, Yen CC, Hsiao FC, Tzeng CH, Ma H, Shiau CY, Chao TC. Refractory cutaneous angiosarcoma successfully treated with sunitinib. Br J Dermatol. 2013;169(1):204–6.CrossRef
2.
go back to reference Tianhua G, Lei Z, Ning-En C, Samuel S, Maki RG, Antonescu CR. Consistent MYC and FLT4 gene amplification in radiation-induced angiosarcoma but not in other radiation-associated atypical vascular lesions. Genes Chromosom Cancer. 2011;50(1):25–33.CrossRef Tianhua G, Lei Z, Ning-En C, Samuel S, Maki RG, Antonescu CR. Consistent MYC and FLT4 gene amplification in radiation-induced angiosarcoma but not in other radiation-associated atypical vascular lesions. Genes Chromosom Cancer. 2011;50(1):25–33.CrossRef
3.
go back to reference Manner J, Bhohenberger R. MYC high level gene amplification is a distinctive feature of angiosarcomas after irradiation or chronic lymphedema. Am J Pathol. 2010;176(1):34–9.CrossRef Manner J, Bhohenberger R. MYC high level gene amplification is a distinctive feature of angiosarcomas after irradiation or chronic lymphedema. Am J Pathol. 2010;176(1):34–9.CrossRef
4.
go back to reference Paik HH, Komorowski R. Hemangiosarcoma of the abdominal wall following irradiation therapy of endometrial carcinoma. Am J Clin Pathol. 1976;66(5):810–4.CrossRef Paik HH, Komorowski R. Hemangiosarcoma of the abdominal wall following irradiation therapy of endometrial carcinoma. Am J Clin Pathol. 1976;66(5):810–4.CrossRef
5.
go back to reference Zhao D, Hou H, Zhang X. Progress in the treatment of solid tumors with apatinib: a systematic review. Oncotargets Ther. 2018;11:4137–47.CrossRef Zhao D, Hou H, Zhang X. Progress in the treatment of solid tumors with apatinib: a systematic review. Oncotargets Ther. 2018;11:4137–47.CrossRef
6.
go back to reference Rao P, Lahat G, Arnold C, Gavino AC, Lahat S, Hornick JL, Lev D, Lazar AJ. Angiosarcoma: a tissue microarray study with diagnostic implications. Am J Dermatopathol. 2013;35(4):432–7.CrossRef Rao P, Lahat G, Arnold C, Gavino AC, Lahat S, Hornick JL, Lev D, Lazar AJ. Angiosarcoma: a tissue microarray study with diagnostic implications. Am J Dermatopathol. 2013;35(4):432–7.CrossRef
7.
go back to reference Paral KM, Gordana R, Thomas K. MYCAmplification in Angiosarcoma arising from an Arteriovenous graft site. Case Rep Pathol. 2015;2015(1):537297.PubMedPubMedCentral Paral KM, Gordana R, Thomas K. MYCAmplification in Angiosarcoma arising from an Arteriovenous graft site. Case Rep Pathol. 2015;2015(1):537297.PubMedPubMedCentral
8.
go back to reference Harker D, Jennings M, Mcdonough P, Mauskar M, Savory S, Hosler GA, Vandergriff T. MYC amplification in angiosarcomas arising in the setting of chronic lymphedema of morbid obesity. J Cutan Pathol. 2016;44(1):15–9.CrossRef Harker D, Jennings M, Mcdonough P, Mauskar M, Savory S, Hosler GA, Vandergriff T. MYC amplification in angiosarcomas arising in the setting of chronic lymphedema of morbid obesity. J Cutan Pathol. 2016;44(1):15–9.CrossRef
9.
go back to reference Udager AM, Ishikawa MK, Lucas DR, Mchugh JB, Patel RM. MYC immunohistochemistry in angiosarcoma and atypical vascular lesions: practical considerations based on a single institutional experience. Pathology. 2016;48(7):697–704.CrossRef Udager AM, Ishikawa MK, Lucas DR, Mchugh JB, Patel RM. MYC immunohistochemistry in angiosarcoma and atypical vascular lesions: practical considerations based on a single institutional experience. Pathology. 2016;48(7):697–704.CrossRef
10.
go back to reference Antonescu CR, Akihiko Y, Tianhuo G, Ning-En C, Lei Z, Agaram NP, Li-Xuan Q, Brennan MF, Samuel S, Maki RG. KDR activating mutations in human angiosarcomas are sensitive to specific kinase inhibitors. Cancer Res. 2009;69(18):7175.CrossRef Antonescu CR, Akihiko Y, Tianhuo G, Ning-En C, Lei Z, Agaram NP, Li-Xuan Q, Brennan MF, Samuel S, Maki RG. KDR activating mutations in human angiosarcomas are sensitive to specific kinase inhibitors. Cancer Res. 2009;69(18):7175.CrossRef
11.
go back to reference Ono S, Tanioka M, Fujisawa A, Tanizaki H, Miyachi Y, Matsumura Y. Angiosarcoma of the scalp successfully treated with a single therapy of Sorafenib. Arch Dermatol. 2012;148(6):683.CrossRef Ono S, Tanioka M, Fujisawa A, Tanizaki H, Miyachi Y, Matsumura Y. Angiosarcoma of the scalp successfully treated with a single therapy of Sorafenib. Arch Dermatol. 2012;148(6):683.CrossRef
12.
go back to reference Ji G, Hong L, Yang P. Successful treatment of angiosarcoma of the scalp with apatinib: a case report. Oncotargets Ther. 2016;9(1):4989–92.CrossRef Ji G, Hong L, Yang P. Successful treatment of angiosarcoma of the scalp with apatinib: a case report. Oncotargets Ther. 2016;9(1):4989–92.CrossRef
13.
go back to reference Yang L, Liu L, Han B, Han W, Zhao M. Apatinib treatment for KIT- and KDR-amplified angiosarcoma: a case report. BMC Cancer. 2018;18(1):618.CrossRef Yang L, Liu L, Han B, Han W, Zhao M. Apatinib treatment for KIT- and KDR-amplified angiosarcoma: a case report. BMC Cancer. 2018;18(1):618.CrossRef
14.
go back to reference Geng R, Li J. Apatinib for the treatment of gastric cancer. Expert Opin Pharmacother. 2015;16(1):117–22.CrossRef Geng R, Li J. Apatinib for the treatment of gastric cancer. Expert Opin Pharmacother. 2015;16(1):117–22.CrossRef
15.
go back to reference Li F, Liao Z, Zhao J, Zhao G, Li X, Du X, Yang Y, Yang J. Efficacy and safety of Apatinib in stage IV sarcomas: experience of a major sarcoma center in China. Oncotarget. 2017;8(38):64471–80.PubMedPubMedCentral Li F, Liao Z, Zhao J, Zhao G, Li X, Du X, Yang Y, Yang J. Efficacy and safety of Apatinib in stage IV sarcomas: experience of a major sarcoma center in China. Oncotarget. 2017;8(38):64471–80.PubMedPubMedCentral
16.
go back to reference Fan M, Hu X, Zhang J, Wang Z, Zhang Q. Abstract P1–08-26: Hypertension and phosphorylated vascular endothelial growth factor receptor 2 are potential independent predictive factors for progession-free survival in apatinib-treated advanced breast cancer. Cancer Res. 2013;73:P1–08-26-P01–08-26.CrossRef Fan M, Hu X, Zhang J, Wang Z, Zhang Q. Abstract P1–08-26: Hypertension and phosphorylated vascular endothelial growth factor receptor 2 are potential independent predictive factors for progession-free survival in apatinib-treated advanced breast cancer. Cancer Res. 2013;73:P1–08-26-P01–08-26.CrossRef
17.
go back to reference Hu XC, Zhang J, Xu BH, Jiang ZF, Tong ZS, Zhang QY, Wang XJ, Feng JF, Pang DM, Fan MH. BP40 multicenter phase ii study of APATINIB, a novel inhibitor of VEGFR, in heavily pretreated patients with metastatic triple negative breast cancer. Breast. 2014;135(8):1961–9. Hu XC, Zhang J, Xu BH, Jiang ZF, Tong ZS, Zhang QY, Wang XJ, Feng JF, Pang DM, Fan MH. BP40 multicenter phase ii study of APATINIB, a novel inhibitor of VEGFR, in heavily pretreated patients with metastatic triple negative breast cancer. Breast. 2014;135(8):1961–9.
18.
go back to reference Li J, Qin S, Xu J, Xiong J, Wu C, Bai Y, Liu W, Tong J, Liu Y, Xu R. O-0029phase III study of apatinib in advanced gastric cancer: a randomized, double-blind, placebo-controlled trial. J Clin Oncol. 2014;25(suppl 2):ii117. Li J, Qin S, Xu J, Xiong J, Wu C, Bai Y, Liu W, Tong J, Liu Y, Xu R. O-0029phase III study of apatinib in advanced gastric cancer: a randomized, double-blind, placebo-controlled trial. J Clin Oncol. 2014;25(suppl 2):ii117.
19.
go back to reference Gou M, Si H, Zhang Y, Qian N, Wang Z, Shi W, Dai G. Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study. Sci Rep. 2018;8(1):4602.CrossRef Gou M, Si H, Zhang Y, Qian N, Wang Z, Shi W, Dai G. Efficacy and safety of apatinib in patients with previously treated metastatic colorectal cancer: a real-world retrospective study. Sci Rep. 2018;8(1):4602.CrossRef
20.
go back to reference Yizhou SU, Taiyu J, Hong WU, Pharmacy DO: Analysis of hypertension adverse reaction caused by apatinib. Chin J Clin Ration Drug Use 2018. Yizhou SU, Taiyu J, Hong WU, Pharmacy DO: Analysis of hypertension adverse reaction caused by apatinib. Chin J Clin Ration Drug Use 2018.
21.
go back to reference Tajima S, Mochizuki R, Sugimura H, Hoshi S. Radiation-induced breast Angiosarcoma with a confirmative feature of c-MYC amplification. Jpn J Clin Oncol. 2014;44(7):702–3.CrossRef Tajima S, Mochizuki R, Sugimura H, Hoshi S. Radiation-induced breast Angiosarcoma with a confirmative feature of c-MYC amplification. Jpn J Clin Oncol. 2014;44(7):702–3.CrossRef
22.
go back to reference Tian S, Quan H, Xie C, Guo H, Lü F, Xu Y, Li J, Lou L. YN968D1 is a novel and selective inhibitor of vascular endothelial growth factor receptor-2 tyrosine kinase with potent activity in vitro and in vivo. Cancer Sci. 2011;102(7):1374–80.CrossRef Tian S, Quan H, Xie C, Guo H, Lü F, Xu Y, Li J, Lou L. YN968D1 is a novel and selective inhibitor of vascular endothelial growth factor receptor-2 tyrosine kinase with potent activity in vitro and in vivo. Cancer Sci. 2011;102(7):1374–80.CrossRef
23.
go back to reference Cong L, Shen J, Ying J, Fang X, Wang X, Fu Z, Peng L. Case report of aKIT-mutated melanoma patient with an excellent response to apatinib and temozolomide combination therapy. Oncotargets Ther. 2017;10:4553–7.CrossRef Cong L, Shen J, Ying J, Fang X, Wang X, Fu Z, Peng L. Case report of aKIT-mutated melanoma patient with an excellent response to apatinib and temozolomide combination therapy. Oncotargets Ther. 2017;10:4553–7.CrossRef
Metadata
Title
Treatment of consistent BRAF/HRAS gene mutation and MYC amplification radiation-induced abdominal wall angiosarcoma with low-dose apatinib: a case report
Authors
Jieshan Guan
Zhijie Luo
Zhiwei Xiao
Yubin Xie
Lizhu Lin
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2019
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-019-6351-4

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