Undifferentiated sarcoma of the liver: Multicenter international experience of the Cooperative Soft‐Tissue Sarcoma Group and Polish Paediatric Solid Tumor Group
Background Undifferentiated embryonal sarcomas of the liver (UESL) are extremely rare and continue to pose a diagnostic and therapeutic challenge. The aim of the study was to present a multicenter experience of the German CWS and Polish PPSTG groups in the treatment of UESL in children. Procedure Tw...
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creator | Murawski, Maciej Scheer, Monika Leuschner, Ivo Stefanowicz, Joanna Bonar, Jolanta Dembowska‐Bagińska, Bożenna Kaliciński, Piotr Koscielniak, Ewa Czauderna, Piotr Fuchs, Jörg |
description | Background
Undifferentiated embryonal sarcomas of the liver (UESL) are extremely rare and continue to pose a diagnostic and therapeutic challenge. The aim of the study was to present a multicenter experience of the German CWS and Polish PPSTG groups in the treatment of UESL in children.
Procedure
Twenty‐five patients were treated according to the CWS‐96, CWS‐2002, and CYVADIC protocols. Distant metastases were observed in four cases (16%). In four cases, an initial disease presentation mimicked other entities. A pure cystic appearance of liver mass led to misdiagnosis of hydatid cyst in three cases. In one case, laparotomy was performed due to the signs of appendicitis, and bleeding from ruptured liver tumor was found. All these patients were finally diagnosed as UESL.
Results
Thirteen patients received preoperative chemotherapy. Partial response was observed in 10 cases. Tumor resection was performed in 20 patients (primary resections, 12; delayed resections–, 8). In five patients, the primary tumor never became operable. The macroscopically complete resection rate was 95% (19/20). Postoperative chemotherapy was given to 20 children. Local radiotherapy was used in three children. After a median follow‐up time of 136 months, 17 patients (68%) were alive with no evidence of disease. All children with unresectable tumor and three out of four patients with distant metastases died. The five‐year overall survival (OS) rate was 72%.
Conclusions
In summary, a complete tumor excision plays the central role in the treatment of UESL. A cystic presentation of the liver lesion on imaging does not exclude the diagnosis of malignant tumor. |
doi_str_mv | 10.1002/pbc.28598 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2427308276</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2427308276</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3538-1b482508831710276ddddec7db9638d8e26cbf4548ca2a5c97b8a3f6ed8da3503</originalsourceid><addsrcrecordid>eNp1kctO3DAUhi3UimsXvACy1A0sBnyJE4cdjCitRMVIHdaRY58IIycOdsJlxyPwDDxan6SeZmBRqV7Yx_Z3Pkv-Edqn5JgSwk76Wh8zKUq5gbapyMRMEFp8-qhJuYV2YrxLaE6E3ERbnBUkF5Ruo7ebztimgQDdYNUABkcVtG8V9g0ebgE7-wDhFP8c3WB1giBgu5o7NVjfKYfhqYdgodPw3jL3Ph2l-wfAv3wz_H55XdoYx7Rbuy-DH3usOoMX3tl4ixcKTHo-WJ06nDV4ObY-TNwe-twoF-HLet1FN98ulvPvs6vryx_zs6uZ5oLLGa0zyQSRktOCElbkJg3QhanLnEsjgeW6bjKRSa2YErosaql4k4ORRnFB-C46nLx98PcjxKFqbdTgnOrAj7FiGSs4kcmc0K__oHd-TF_iVlQmZCHzckUdTZQOPsYATdUH26rwXFFSrYKrUnDV3-ASe7A2jnUL5oN8TyoBJxPwaB08_99ULc7nk_IPqgSluQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2445878696</pqid></control><display><type>article</type><title>Undifferentiated sarcoma of the liver: Multicenter international experience of the Cooperative Soft‐Tissue Sarcoma Group and Polish Paediatric Solid Tumor Group</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Murawski, Maciej ; Scheer, Monika ; Leuschner, Ivo ; Stefanowicz, Joanna ; Bonar, Jolanta ; Dembowska‐Bagińska, Bożenna ; Kaliciński, Piotr ; Koscielniak, Ewa ; Czauderna, Piotr ; Fuchs, Jörg</creator><creatorcontrib>Murawski, Maciej ; Scheer, Monika ; Leuschner, Ivo ; Stefanowicz, Joanna ; Bonar, Jolanta ; Dembowska‐Bagińska, Bożenna ; Kaliciński, Piotr ; Koscielniak, Ewa ; Czauderna, Piotr ; Fuchs, Jörg</creatorcontrib><description>Background
Undifferentiated embryonal sarcomas of the liver (UESL) are extremely rare and continue to pose a diagnostic and therapeutic challenge. The aim of the study was to present a multicenter experience of the German CWS and Polish PPSTG groups in the treatment of UESL in children.
Procedure
Twenty‐five patients were treated according to the CWS‐96, CWS‐2002, and CYVADIC protocols. Distant metastases were observed in four cases (16%). In four cases, an initial disease presentation mimicked other entities. A pure cystic appearance of liver mass led to misdiagnosis of hydatid cyst in three cases. In one case, laparotomy was performed due to the signs of appendicitis, and bleeding from ruptured liver tumor was found. All these patients were finally diagnosed as UESL.
Results
Thirteen patients received preoperative chemotherapy. Partial response was observed in 10 cases. Tumor resection was performed in 20 patients (primary resections, 12; delayed resections–, 8). In five patients, the primary tumor never became operable. The macroscopically complete resection rate was 95% (19/20). Postoperative chemotherapy was given to 20 children. Local radiotherapy was used in three children. After a median follow‐up time of 136 months, 17 patients (68%) were alive with no evidence of disease. All children with unresectable tumor and three out of four patients with distant metastases died. The five‐year overall survival (OS) rate was 72%.
Conclusions
In summary, a complete tumor excision plays the central role in the treatment of UESL. A cystic presentation of the liver lesion on imaging does not exclude the diagnosis of malignant tumor.</description><identifier>ISSN: 1545-5009</identifier><identifier>EISSN: 1545-5017</identifier><identifier>DOI: 10.1002/pbc.28598</identifier><identifier>PMID: 32706511</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Adult ; Appendicitis ; Chemotherapy ; Child ; Child, Preschool ; Children ; Combined Modality Therapy ; Female ; Follow-Up Studies ; Hematology ; Humans ; Infant ; Liver ; Liver cancer ; Liver Neoplasms - diagnosis ; Liver Neoplasms - therapy ; liver sarcoma ; Male ; Metastases ; Metastasis ; Oncology ; pediatric liver tumor ; Pediatrics ; Poland ; Prognosis ; Radiation therapy ; Retrospective Studies ; Sarcoma ; Sarcoma - diagnosis ; Sarcoma - therapy ; Solid tumors ; Survival Rate ; undifferentiated embryonal sarcoma ; Young Adult</subject><ispartof>Pediatric blood & cancer, 2020-11, Vol.67 (11), p.e28598-n/a</ispartof><rights>2020 Wiley Periodicals LLC</rights><rights>2020 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-1b482508831710276ddddec7db9638d8e26cbf4548ca2a5c97b8a3f6ed8da3503</citedby><cites>FETCH-LOGICAL-c3538-1b482508831710276ddddec7db9638d8e26cbf4548ca2a5c97b8a3f6ed8da3503</cites><orcidid>0000-0003-1152-2659 ; 0000-0002-0665-6268 ; 0000-0001-8014-4263</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpbc.28598$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpbc.28598$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32706511$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murawski, Maciej</creatorcontrib><creatorcontrib>Scheer, Monika</creatorcontrib><creatorcontrib>Leuschner, Ivo</creatorcontrib><creatorcontrib>Stefanowicz, Joanna</creatorcontrib><creatorcontrib>Bonar, Jolanta</creatorcontrib><creatorcontrib>Dembowska‐Bagińska, Bożenna</creatorcontrib><creatorcontrib>Kaliciński, Piotr</creatorcontrib><creatorcontrib>Koscielniak, Ewa</creatorcontrib><creatorcontrib>Czauderna, Piotr</creatorcontrib><creatorcontrib>Fuchs, Jörg</creatorcontrib><title>Undifferentiated sarcoma of the liver: Multicenter international experience of the Cooperative Soft‐Tissue Sarcoma Group and Polish Paediatric Solid Tumor Group</title><title>Pediatric blood & cancer</title><addtitle>Pediatr Blood Cancer</addtitle><description>Background
Undifferentiated embryonal sarcomas of the liver (UESL) are extremely rare and continue to pose a diagnostic and therapeutic challenge. The aim of the study was to present a multicenter experience of the German CWS and Polish PPSTG groups in the treatment of UESL in children.
Procedure
Twenty‐five patients were treated according to the CWS‐96, CWS‐2002, and CYVADIC protocols. Distant metastases were observed in four cases (16%). In four cases, an initial disease presentation mimicked other entities. A pure cystic appearance of liver mass led to misdiagnosis of hydatid cyst in three cases. In one case, laparotomy was performed due to the signs of appendicitis, and bleeding from ruptured liver tumor was found. All these patients were finally diagnosed as UESL.
Results
Thirteen patients received preoperative chemotherapy. Partial response was observed in 10 cases. Tumor resection was performed in 20 patients (primary resections, 12; delayed resections–, 8). In five patients, the primary tumor never became operable. The macroscopically complete resection rate was 95% (19/20). Postoperative chemotherapy was given to 20 children. Local radiotherapy was used in three children. After a median follow‐up time of 136 months, 17 patients (68%) were alive with no evidence of disease. All children with unresectable tumor and three out of four patients with distant metastases died. The five‐year overall survival (OS) rate was 72%.
Conclusions
In summary, a complete tumor excision plays the central role in the treatment of UESL. A cystic presentation of the liver lesion on imaging does not exclude the diagnosis of malignant tumor.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Appendicitis</subject><subject>Chemotherapy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hematology</subject><subject>Humans</subject><subject>Infant</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - therapy</subject><subject>liver sarcoma</subject><subject>Male</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Oncology</subject><subject>pediatric liver tumor</subject><subject>Pediatrics</subject><subject>Poland</subject><subject>Prognosis</subject><subject>Radiation therapy</subject><subject>Retrospective Studies</subject><subject>Sarcoma</subject><subject>Sarcoma - diagnosis</subject><subject>Sarcoma - therapy</subject><subject>Solid tumors</subject><subject>Survival Rate</subject><subject>undifferentiated embryonal sarcoma</subject><subject>Young Adult</subject><issn>1545-5009</issn><issn>1545-5017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctO3DAUhi3UimsXvACy1A0sBnyJE4cdjCitRMVIHdaRY58IIycOdsJlxyPwDDxan6SeZmBRqV7Yx_Z3Pkv-Edqn5JgSwk76Wh8zKUq5gbapyMRMEFp8-qhJuYV2YrxLaE6E3ERbnBUkF5Ruo7ebztimgQDdYNUABkcVtG8V9g0ebgE7-wDhFP8c3WB1giBgu5o7NVjfKYfhqYdgodPw3jL3Ph2l-wfAv3wz_H55XdoYx7Rbuy-DH3usOoMX3tl4ixcKTHo-WJ06nDV4ObY-TNwe-twoF-HLet1FN98ulvPvs6vryx_zs6uZ5oLLGa0zyQSRktOCElbkJg3QhanLnEsjgeW6bjKRSa2YErosaql4k4ORRnFB-C46nLx98PcjxKFqbdTgnOrAj7FiGSs4kcmc0K__oHd-TF_iVlQmZCHzckUdTZQOPsYATdUH26rwXFFSrYKrUnDV3-ASe7A2jnUL5oN8TyoBJxPwaB08_99ULc7nk_IPqgSluQ</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Murawski, Maciej</creator><creator>Scheer, Monika</creator><creator>Leuschner, Ivo</creator><creator>Stefanowicz, Joanna</creator><creator>Bonar, Jolanta</creator><creator>Dembowska‐Bagińska, Bożenna</creator><creator>Kaliciński, Piotr</creator><creator>Koscielniak, Ewa</creator><creator>Czauderna, Piotr</creator><creator>Fuchs, Jörg</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1152-2659</orcidid><orcidid>https://orcid.org/0000-0002-0665-6268</orcidid><orcidid>https://orcid.org/0000-0001-8014-4263</orcidid></search><sort><creationdate>202011</creationdate><title>Undifferentiated sarcoma of the liver: Multicenter international experience of the Cooperative Soft‐Tissue Sarcoma Group and Polish Paediatric Solid Tumor Group</title><author>Murawski, Maciej ; Scheer, Monika ; Leuschner, Ivo ; Stefanowicz, Joanna ; Bonar, Jolanta ; Dembowska‐Bagińska, Bożenna ; Kaliciński, Piotr ; Koscielniak, Ewa ; Czauderna, Piotr ; Fuchs, Jörg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-1b482508831710276ddddec7db9638d8e26cbf4548ca2a5c97b8a3f6ed8da3503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Appendicitis</topic><topic>Chemotherapy</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hematology</topic><topic>Humans</topic><topic>Infant</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - therapy</topic><topic>liver sarcoma</topic><topic>Male</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Oncology</topic><topic>pediatric liver tumor</topic><topic>Pediatrics</topic><topic>Poland</topic><topic>Prognosis</topic><topic>Radiation therapy</topic><topic>Retrospective Studies</topic><topic>Sarcoma</topic><topic>Sarcoma - diagnosis</topic><topic>Sarcoma - therapy</topic><topic>Solid tumors</topic><topic>Survival Rate</topic><topic>undifferentiated embryonal sarcoma</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murawski, Maciej</creatorcontrib><creatorcontrib>Scheer, Monika</creatorcontrib><creatorcontrib>Leuschner, Ivo</creatorcontrib><creatorcontrib>Stefanowicz, Joanna</creatorcontrib><creatorcontrib>Bonar, Jolanta</creatorcontrib><creatorcontrib>Dembowska‐Bagińska, Bożenna</creatorcontrib><creatorcontrib>Kaliciński, Piotr</creatorcontrib><creatorcontrib>Koscielniak, Ewa</creatorcontrib><creatorcontrib>Czauderna, Piotr</creatorcontrib><creatorcontrib>Fuchs, Jörg</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric blood & cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murawski, Maciej</au><au>Scheer, Monika</au><au>Leuschner, Ivo</au><au>Stefanowicz, Joanna</au><au>Bonar, Jolanta</au><au>Dembowska‐Bagińska, Bożenna</au><au>Kaliciński, Piotr</au><au>Koscielniak, Ewa</au><au>Czauderna, Piotr</au><au>Fuchs, Jörg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Undifferentiated sarcoma of the liver: Multicenter international experience of the Cooperative Soft‐Tissue Sarcoma Group and Polish Paediatric Solid Tumor Group</atitle><jtitle>Pediatric blood & cancer</jtitle><addtitle>Pediatr Blood Cancer</addtitle><date>2020-11</date><risdate>2020</risdate><volume>67</volume><issue>11</issue><spage>e28598</spage><epage>n/a</epage><pages>e28598-n/a</pages><issn>1545-5009</issn><eissn>1545-5017</eissn><abstract>Background
Undifferentiated embryonal sarcomas of the liver (UESL) are extremely rare and continue to pose a diagnostic and therapeutic challenge. The aim of the study was to present a multicenter experience of the German CWS and Polish PPSTG groups in the treatment of UESL in children.
Procedure
Twenty‐five patients were treated according to the CWS‐96, CWS‐2002, and CYVADIC protocols. Distant metastases were observed in four cases (16%). In four cases, an initial disease presentation mimicked other entities. A pure cystic appearance of liver mass led to misdiagnosis of hydatid cyst in three cases. In one case, laparotomy was performed due to the signs of appendicitis, and bleeding from ruptured liver tumor was found. All these patients were finally diagnosed as UESL.
Results
Thirteen patients received preoperative chemotherapy. Partial response was observed in 10 cases. Tumor resection was performed in 20 patients (primary resections, 12; delayed resections–, 8). In five patients, the primary tumor never became operable. The macroscopically complete resection rate was 95% (19/20). Postoperative chemotherapy was given to 20 children. Local radiotherapy was used in three children. After a median follow‐up time of 136 months, 17 patients (68%) were alive with no evidence of disease. All children with unresectable tumor and three out of four patients with distant metastases died. The five‐year overall survival (OS) rate was 72%.
Conclusions
In summary, a complete tumor excision plays the central role in the treatment of UESL. A cystic presentation of the liver lesion on imaging does not exclude the diagnosis of malignant tumor.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32706511</pmid><doi>10.1002/pbc.28598</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1152-2659</orcidid><orcidid>https://orcid.org/0000-0002-0665-6268</orcidid><orcidid>https://orcid.org/0000-0001-8014-4263</orcidid></addata></record> |
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subjects | Adolescent Adult Appendicitis Chemotherapy Child Child, Preschool Children Combined Modality Therapy Female Follow-Up Studies Hematology Humans Infant Liver Liver cancer Liver Neoplasms - diagnosis Liver Neoplasms - therapy liver sarcoma Male Metastases Metastasis Oncology pediatric liver tumor Pediatrics Poland Prognosis Radiation therapy Retrospective Studies Sarcoma Sarcoma - diagnosis Sarcoma - therapy Solid tumors Survival Rate undifferentiated embryonal sarcoma Young Adult |
title | Undifferentiated sarcoma of the liver: Multicenter international experience of the Cooperative Soft‐Tissue Sarcoma Group and Polish Paediatric Solid Tumor Group |
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