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Vol 14, No 6 (2018)
Review paper
Published online: 2019-03-15
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Clear cell sarcoma

Anna M. Czarnecka12, Paweł Sobczuk13, Marcin Zdzienicki1, Mateusz Spałek4, Monika Dudzisz-Śledź1, Piotr Rutkowski1
DOI: 10.5603/OCP.2018.0049
·
Oncol Clin Pract 2018;14(6):354-363.
Affiliations
  1. Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie Institute — Oncology Centre, Warsaw, Poland
  2. Department of Experimental Pharmacology, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland
  3. Department of Experimental and Clinical Physiology, Laboratory of Centre of Preclinical Research, Medical University of Warsaw, Poland
  4. Radiotherapy Department, Maria Sklodowska-Curie Institute — Oncology Centre, Warsaw, Poland

open access

Vol 14, No 6 (2018)
REVIEW ARTICLES
Published online: 2019-03-15

Abstract

Clear cell sarcoma (CCS), also referred as to melanoma of soft tissues, is a rare malignant tumour of soft tissues. This tumour harbors the characteristic features of soft tissue sarcoma (STS) and is a slowly growing, painless tumour, which then acquires an aggressive course. CCS is characterized by a translocation t(12; 22)(q13; q12), which in addition to the diagnostic implications may be important for targeted treatment in the future. CCS occurs mainly on the limbs, most often shin (in feet and ankle area) in the tendons and aponeurosis, often at a young age. CCS is characterized by high potential to develop metastases in regional lymph nodes (about 30% of cases). In the diagnostic process one should consider performing a sentinel node biopsy with possible subsequent radical lymphadenectomy in the case of metastases detection. Treatment of localized disease is limited to radical local excision with complementary radiotherapy. Due to the resistance to classical chemotherapy and the presence of characteristic molecular abnormalities, trials of molecular targeted therapies in this group of cancers are ongoing. In clinical trials, MET inhibitors, tyrosine kinase inhibitors (TKI) — sunitinib and pazopanib were evaluated. CCS was also one of the subtypes of tumours evaluated in the CREATE clinical trial with crizotinib.

Abstract

Clear cell sarcoma (CCS), also referred as to melanoma of soft tissues, is a rare malignant tumour of soft tissues. This tumour harbors the characteristic features of soft tissue sarcoma (STS) and is a slowly growing, painless tumour, which then acquires an aggressive course. CCS is characterized by a translocation t(12; 22)(q13; q12), which in addition to the diagnostic implications may be important for targeted treatment in the future. CCS occurs mainly on the limbs, most often shin (in feet and ankle area) in the tendons and aponeurosis, often at a young age. CCS is characterized by high potential to develop metastases in regional lymph nodes (about 30% of cases). In the diagnostic process one should consider performing a sentinel node biopsy with possible subsequent radical lymphadenectomy in the case of metastases detection. Treatment of localized disease is limited to radical local excision with complementary radiotherapy. Due to the resistance to classical chemotherapy and the presence of characteristic molecular abnormalities, trials of molecular targeted therapies in this group of cancers are ongoing. In clinical trials, MET inhibitors, tyrosine kinase inhibitors (TKI) — sunitinib and pazopanib were evaluated. CCS was also one of the subtypes of tumours evaluated in the CREATE clinical trial with crizotinib.

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Keywords

clear cell sarcoma; crizotinib; sentinel node biopsy; sarcoma; translocation

About this article
Title

Clear cell sarcoma

Journal

Oncology in Clinical Practice

Issue

Vol 14, No 6 (2018)

Article type

Review paper

Pages

354-363

Published online

2019-03-15

Page views

2317

Article views/downloads

1941

DOI

10.5603/OCP.2018.0049

Bibliographic record

Oncol Clin Pract 2018;14(6):354-363.

Keywords

clear cell sarcoma
crizotinib
sentinel node biopsy
sarcoma
translocation

Authors

Anna M. Czarnecka
Paweł Sobczuk
Marcin Zdzienicki
Mateusz Spałek
Monika Dudzisz-Śledź
Piotr Rutkowski

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