Abstract

The most widely accepted treatment for cutaneous angiosarcoma (CAS) is wide local excision and postoperative radiation to decrease the risk of recurrence. Positive surgical margins and large tumors (T2, >5 cm) are known to be associated with poor prognosis. Moreover, T2 tumors are known to be associated with positive surgical margins. According to previous reports, the majority of CAS patients in Japan had T2 tumors, whereas less than half of the patients in the studies from western countries did so. Consequently, the reported 5-year overall survival of Japanese CAS patients without distant metastasis was only 9%, lower than that for stage-IV melanoma. For patients with T2 tumors, management of subclinical metastasis should be considered when planning the initial treatment. Several attempts to control subclinical metastasis have been reported, such as using adjuvant/neoadjuvant chemotherapy in addition to conventional surgery plus radiation. Unfortunately, those attempts did not show any clinical benefit. Besides surgery, new chemotherapeutic approaches for advanced CAS have been introduced in the past couple of decades, such as paclitaxel and docetaxel. We proposed the use of chemoradiotherapy (CRT) using taxanes instead of surgery plus radiation for patients with T2 tumors without distant metastasis and showed a high response ratio with prolonged survival. However, this prolonged survival was seen only in patients who received maintenance chemotherapy after CRT, indicating that continuous chemotherapy is mandatory to control subclinical residual tumors. With the recent development of targeted drugs for cancer, many potential drugs for CAS are now available. Given that CAS expresses a high level of vascular endothelial growth factor (VEGF) receptor, drugs that target VEGF signaling pathways such as anti-VEGF monoclonal antibody and tyrosine kinase inhibitors are also promising, and several successful treatments have been reported. Besides targeted drugs, several new cytotoxic anticancer drugs such as eribulin or trabectedin have also been shown to be effective for advanced sarcoma. However, most of the clinical trials did not include a sufficient number of CAS patients. Therefore, clinical trials focusing only on CAS should be performed to evaluate the effectiveness of these new drugs.

Highlights

  • According to the Surveillance, Epidemiology, and End Results Program database, the number of patients with sarcoma recorded between 2010 and 2014 was only 1/100 of the number of patients with carcinoma in the same period

  • Complete removal of the tumor was believed to be essential, as it is for other sarcomas [4, 5], some reports have suggested that wide-margin surgery will not deliver favorable results [6, 7]

  • A Japanese retrospective study of cutaneous angiosarcoma (CAS) [49] revealed that the median overall survival of patients with non-metastatic localized CAS who received surgery was less than 20 months, but this finding was not surprising because we have reported a similar dismal outcome (13.5 months) [19]

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Summary

BACKGROUND

According to the Surveillance, Epidemiology, and End Results Program database, the number of patients with sarcoma recorded between 2010 and 2014 was only 1/100 of the number of patients with carcinoma in the same period. A study by Sinnamon et al [32] of 821 angiosarcomas included 211 cases of primary CAS in the head and neck In their cohort, all cases of metastatic disease were excluded and all the patients received surgical treatment. All cases of metastatic disease were excluded and all the patients received surgical treatment They scored the following factors and classified the risk from low (total score 0–1), intermediate (total score 2–3), and high (total score 4–7): age > 70 as 1, black ethnicity as 1, histologic tumor grade 3 as 1, tumor size 3–7 cm as 1, tumor size larger than 7 cm as 2, microscopic residual tumor as 1, and macroscopic residual tumor as 2. Lahat et al [53] reported 32 of 44 cases of locally recurrent angiosarcoma treated with surgery, 70% of which achieved complete removal of the recurrent tumor, with a 5-year overall survival of 44%. Pooled analysis of 11 clinical trials for angiosarcoma from all sites Young et al [58]

25 Response ratio
Findings
35–66 Gy MD: 56 Gy 48–80 Gy MD
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