Surgical treatment outcomes of primary hepatic sarcomas: A single-center experience

BACKGROUND Primary hepatic sarcoma is a rare tumor originated from mesenchymal tissue. There are various pathologic types of primary hepatic sarcoma and the treatment outcome of this tumor was usually disappointing. Unlike hepatocellular carcinoma, outcome of primary hepatic sarcoma is not well-known due to it’s rarity. However, with development of medical technology, surgical treatment may lead to better survival. AIM To investigate the surgical outcomes of primary hepatic sarcoma, we gathered and analyzed the cases of a single institute. METHODS From August 2001 to September 2016, a total of nine patients were surgically treated for primary hepatic sarcoma after exclusion of cases with open and closure, early loss to follow-up and sarcomatoid hepatocellular carcinoma and sarcomatoid cholangiocellular carcinoma. Baseline characteristics, tumor characteristics such as tumor pathology, size and number, surgical and adjuvant treatments were reviewed. Tumor recurrence, and patient survival were analyzed with retrospective approach. RESULTS The enrolled participants included five patients with angiosarcoma and four patients with undifferentiated sarcoma. All patients experienced tumor recurrence at a median of 52 post-operative days. Only two patients survived and the 5-year survival rate was 29.6%. One patient with angiosarcoma who received central hepatectomy for primary tumor and received radiofrequency ablation for recurrent tumor still lives for 11 years. One patient with undifferentiated sarcoma received Rt. lobectomy for primary tumor followed by chemotherapy and radiation therapy still lives around 30 mo even though she got additional operation for recurrent tumor. Two patients who received living donor liver transplantation due to angiosarcoma died. Only adjuvant therapy was associated with survival gain (P = 0.002). CONCLUSION Patients with primary hepatic sarcoma may gain survival benefit with surgical resection followed by adjuvant therapy, even though the outcome remains relatively poor.

[1]  W. Koizumi,et al.  Undifferentiated Embryonal Sarcoma of the Liver Identified after the Initial Diagnosis of a Hepatic Cyst , 2020, Internal medicine.

[2]  Yanming Zhou,et al.  Long‐term survival outcomes of undifferentiated embryonal sarcoma of the liver: a pooled analysis of 308 patients , 2020, ANZ journal of surgery.

[3]  P. Chu,et al.  Primary liver sarcomas in the modern era: Resection or transplantation? , 2018, Journal of surgical oncology.

[4]  Yixin Zeng,et al.  Successful treatment with pazopanib plus PD-1 inhibitor and RAK cells for advanced primary hepatic angiosarcoma: a case report , 2018, BMC Cancer.

[5]  F. Motoi,et al.  A case of adult undifferentiated embryonal sarcoma of the liver successfully treated with right trisectionectomy: a case report , 2017, Surgical Case Reports.

[6]  How-Ran Guo,et al.  Hepatic Angiosarcoma May Have Fair Survival Nowadays , 2015, Medicine.

[7]  X. Ren,et al.  Primary hepatic angiosarcoma and potential treatment options , 2014, Journal of gastroenterology and hepatology.

[8]  G. Tiao,et al.  Multimodal therapy including liver transplantation for hepatic undifferentiated embryonal sarcoma , 2014, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

[9]  T. Garrington,et al.  Undifferentiated Sarcoma of the Liver: A Single Institution Experience Using a Uniform Treatment Approach , 2012, Journal of pediatric hematology/oncology.

[10]  K. Sung,et al.  Primary hepatic angiosarcoma: imaging findings and palliative treatment with transcatheter arterial chemoembolization or embolization. , 2009, Clinical radiology.

[11]  C. Poremba,et al.  Long-term survival after surgery for primary hepatic sarcoma in adults. , 2009, Archives of surgery.

[12]  Y. N. Park,et al.  Clinical features and treatment outcomes of advanced stage primary hepatic angiosarcoma. , 2009, Annals of oncology : official journal of the European Society for Medical Oncology.

[13]  P. Lenz,et al.  Undifferentiated embryonal sarcoma of the liver in adults , 2008, Cancer.

[14]  M. Guiney,et al.  Hepatic Angiosarcoma Presenting as an Acute Intraabdominal Hemorrhage Treated with Transarterial Chemoembolization , 2007, Sarcoma.

[15]  M. D'Angelica,et al.  Management of primary liver sarcomas , 2007, Cancer.

[16]  D H Leung,et al.  Analysis of prognostic factors in 1,041 patients with localized soft tissue sarcomas of the extremities. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[17]  B. Portmann,et al.  Hepatic sarcomas in adults: a review of 25 cases. , 1987, Gut.

[18]  K. Ishak,et al.  HEPATIC ANGIOSARCOMA ASSOCIATED WITH ANDROGENIC-ANABOLIC STEROIDS , 1979, The Lancet.

[19]  K. Ishak,et al.  Undifferentiated (embryonal) sarcoma of the liver. Report of 31 cases , 1978, Cancer.