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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Veröffentlicht in:Pediatric blood & cancer 2020-11, Vol.67 (11), p.e28598-n/a
Hauptverfasser: Murawski, Maciej, Scheer, Monika, Leuschner, Ivo, Stefanowicz, Joanna, Bonar, Jolanta, Dembowska‐Bagińska, Bożenna, Kaliciński, Piotr, Koscielniak, Ewa, Czauderna, Piotr, Fuchs, Jörg
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container_issue 11
container_start_page e28598
container_title Pediatric blood & cancer
container_volume 67
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
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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 &amp; 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 &amp; 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. 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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. 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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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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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