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Ovarian tissue cryopreserved for fertility preservation from patients with Ewing or other sarcomas appear to have no tumour cell contamination
Abstract Aim The chemotherapy required to treat patients with sarcoma may as a side-effect induce infertility in girls and young women. If these patients have ovarian cortical tissue cryopreserved prior to chemotherapy, they may, if necessary, have the tissue transplanted and restore their fertility...
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Published in: | European journal of cancer (1990) 2013-05, Vol.49 (8), p.1932-1938 |
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container_end_page | 1938 |
container_issue | 8 |
container_start_page | 1932 |
container_title | European journal of cancer (1990) |
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creator | Greve, Tine Wielenga, Vera Timmermans Grauslund, Morten Sørensen, Nils Christiansen, Dorte Bang Rosendahl, Mikkel Yding Andersen, Claus |
description | Abstract Aim The chemotherapy required to treat patients with sarcoma may as a side-effect induce infertility in girls and young women. If these patients have ovarian cortical tissue cryopreserved prior to chemotherapy, they may, if necessary, have the tissue transplanted and restore their fertility. The aim of this study was to evaluate the risk of residual cancer cells in the ovarian cortex intended for transplantation. Patients and methods Ovarian tissue stored for fertility preservation from 16 surviving patients diagnosed with sarcoma (nine with Ewing sarcomas, four with osteosarcomas, two with synovial sarcomas and one with chondrosarcoma) was evaluated for the presence of malignant cells by histology and by transplantation to immunodeficient mice for 20 weeks. A fraction of the tissue from patients with Ewing sarcoma was also evaluated for the presence of the molecular marker EWS-FLI1 by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The transplant itself and selected murine organs were analysed for the presence of malignant cells by histology. Results All the mice accommodated the human tissue for 20 weeks of transplantation period with none of the mice developing any sign of cancer. In no instance were any cancer cells detected by histology or RT-qPCR. Conclusion Ovarian tissue from patients with sarcoma appears to be without metastatic malignant cells in numbers that allow detection. Although the actual pieces of ovarian tissue used for transplantation remain unchecked, the current data indicate that the procedure is safe at least in patients that survive the sarcoma disease. |
doi_str_mv | 10.1016/j.ejca.2013.01.032 |
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If these patients have ovarian cortical tissue cryopreserved prior to chemotherapy, they may, if necessary, have the tissue transplanted and restore their fertility. The aim of this study was to evaluate the risk of residual cancer cells in the ovarian cortex intended for transplantation. Patients and methods Ovarian tissue stored for fertility preservation from 16 surviving patients diagnosed with sarcoma (nine with Ewing sarcomas, four with osteosarcomas, two with synovial sarcomas and one with chondrosarcoma) was evaluated for the presence of malignant cells by histology and by transplantation to immunodeficient mice for 20 weeks. A fraction of the tissue from patients with Ewing sarcoma was also evaluated for the presence of the molecular marker EWS-FLI1 by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The transplant itself and selected murine organs were analysed for the presence of malignant cells by histology. Results All the mice accommodated the human tissue for 20 weeks of transplantation period with none of the mice developing any sign of cancer. In no instance were any cancer cells detected by histology or RT-qPCR. Conclusion Ovarian tissue from patients with sarcoma appears to be without metastatic malignant cells in numbers that allow detection. Although the actual pieces of ovarian tissue used for transplantation remain unchecked, the current data indicate that the procedure is safe at least in patients that survive the sarcoma disease.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2013.01.032</identifier><identifier>PMID: 23452988</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Animals ; Biological and medical sciences ; Child ; Cryopreservation ; Cryopreservation - methods ; Female ; Fertility preservation ; Fertility Preservation - methods ; Hematology, Oncology and Palliative Medicine ; Humans ; Medical sciences ; Mice ; Mice, Inbred Strains ; Mice, Nude ; Micrometastatic disease ; Molecular markers ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Oncogene Proteins, Fusion - genetics ; Ovarian metastases ; Ovary ; Ovary - metabolism ; Ovary - transplantation ; Pharmacology. Drug treatments ; Proto-Oncogene Protein c-fli-1 - genetics ; Reproducibility of Results ; Reverse Transcriptase Polymerase Chain Reaction ; RNA-Binding Protein EWS - genetics ; Sarcoma ; Sarcoma - diagnosis ; Sarcoma - genetics ; Sarcoma, Ewing - diagnosis ; Sarcoma, Ewing - genetics ; Time Factors ; Transplantation, Heterologous ; Tumors</subject><ispartof>European journal of cancer (1990), 2013-05, Vol.49 (8), p.1932-1938</ispartof><rights>Elsevier Ltd</rights><rights>2013 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-367354dc55b6cf59a06ec75f23a5946c9ed1b530206142509e6f61176bf68e5b3</citedby><cites>FETCH-LOGICAL-c474t-367354dc55b6cf59a06ec75f23a5946c9ed1b530206142509e6f61176bf68e5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27285865$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23452988$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Greve, Tine</creatorcontrib><creatorcontrib>Wielenga, Vera Timmermans</creatorcontrib><creatorcontrib>Grauslund, Morten</creatorcontrib><creatorcontrib>Sørensen, Nils</creatorcontrib><creatorcontrib>Christiansen, Dorte Bang</creatorcontrib><creatorcontrib>Rosendahl, Mikkel</creatorcontrib><creatorcontrib>Yding Andersen, Claus</creatorcontrib><title>Ovarian tissue cryopreserved for fertility preservation from patients with Ewing or other sarcomas appear to have no tumour cell contamination</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Abstract Aim The chemotherapy required to treat patients with sarcoma may as a side-effect induce infertility in girls and young women. If these patients have ovarian cortical tissue cryopreserved prior to chemotherapy, they may, if necessary, have the tissue transplanted and restore their fertility. The aim of this study was to evaluate the risk of residual cancer cells in the ovarian cortex intended for transplantation. Patients and methods Ovarian tissue stored for fertility preservation from 16 surviving patients diagnosed with sarcoma (nine with Ewing sarcomas, four with osteosarcomas, two with synovial sarcomas and one with chondrosarcoma) was evaluated for the presence of malignant cells by histology and by transplantation to immunodeficient mice for 20 weeks. A fraction of the tissue from patients with Ewing sarcoma was also evaluated for the presence of the molecular marker EWS-FLI1 by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The transplant itself and selected murine organs were analysed for the presence of malignant cells by histology. Results All the mice accommodated the human tissue for 20 weeks of transplantation period with none of the mice developing any sign of cancer. In no instance were any cancer cells detected by histology or RT-qPCR. Conclusion Ovarian tissue from patients with sarcoma appears to be without metastatic malignant cells in numbers that allow detection. Although the actual pieces of ovarian tissue used for transplantation remain unchecked, the current data indicate that the procedure is safe at least in patients that survive the sarcoma disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Cryopreservation</subject><subject>Cryopreservation - methods</subject><subject>Female</subject><subject>Fertility preservation</subject><subject>Fertility Preservation - methods</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Mice, Nude</subject><subject>Micrometastatic disease</subject><subject>Molecular markers</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Oncogene Proteins, Fusion - genetics</subject><subject>Ovarian metastases</subject><subject>Ovary</subject><subject>Ovary - metabolism</subject><subject>Ovary - transplantation</subject><subject>Pharmacology. Drug treatments</subject><subject>Proto-Oncogene Protein c-fli-1 - genetics</subject><subject>Reproducibility of Results</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA-Binding Protein EWS - genetics</subject><subject>Sarcoma</subject><subject>Sarcoma - diagnosis</subject><subject>Sarcoma - genetics</subject><subject>Sarcoma, Ewing - diagnosis</subject><subject>Sarcoma, Ewing - genetics</subject><subject>Time Factors</subject><subject>Transplantation, Heterologous</subject><subject>Tumors</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkt-K1DAUh4so7rj6Al5IbgRvZjxJmrQFEWRZ_8DCXqjXIU1PndQ2qUk6y7yEz2zqjApe6FVC-M4vh_OdonhKYUeBypfDDgejdwwo3wHdAWf3ig2tq2YLtWD3iw00otnWUDYXxaMYBwCo6hIeFheMl4I1db0pvt8edLDakWRjXJCYcPRzwIjhgB3pfSA9hmRHm47k_K6T9Y70wU9kznd0KZI7m_bk-s66LySX-LTHQKIOxk86Ej3PqANJnuz1AYnzJC2TXwIxOI7EeJf0ZN3P2MfFg16PEZ-cz8vi89vrT1fvtze37z5cvbnZmrIq05bLiouyM0K00vSi0SDRVKJnXIumlKbBjraCAwNJSyagQdlLSivZ9rJG0fLL4sUpdw7-24IxqcnGtR3t0C9RUUFlJXiZR_tflJc5WuYjo-yEmuBjDNirOdhJh6OioFZlalCrMrUqU0BVVpaLnp3zl3bC7nfJL0cZeH4GdDR67IN2xsY_XMVqUUuRuVcnDvPgDhaDiibbMdjZgCapztt_9_H6r3IzWmfzj1_xiHHIwlxWoqiKTIH6uC7XuluUA1CQNf8BHWDLjA</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Greve, Tine</creator><creator>Wielenga, Vera Timmermans</creator><creator>Grauslund, Morten</creator><creator>Sørensen, Nils</creator><creator>Christiansen, Dorte Bang</creator><creator>Rosendahl, Mikkel</creator><creator>Yding Andersen, Claus</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope><scope>7TV</scope><scope>C1K</scope></search><sort><creationdate>20130501</creationdate><title>Ovarian tissue cryopreserved for fertility preservation from patients with Ewing or other sarcomas appear to have no tumour cell contamination</title><author>Greve, Tine ; Wielenga, Vera Timmermans ; Grauslund, Morten ; Sørensen, Nils ; Christiansen, Dorte Bang ; Rosendahl, Mikkel ; Yding Andersen, Claus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-367354dc55b6cf59a06ec75f23a5946c9ed1b530206142509e6f61176bf68e5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Cryopreservation</topic><topic>Cryopreservation - methods</topic><topic>Female</topic><topic>Fertility preservation</topic><topic>Fertility Preservation - methods</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Mice, Nude</topic><topic>Micrometastatic disease</topic><topic>Molecular markers</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Oncogene Proteins, Fusion - genetics</topic><topic>Ovarian metastases</topic><topic>Ovary</topic><topic>Ovary - metabolism</topic><topic>Ovary - transplantation</topic><topic>Pharmacology. Drug treatments</topic><topic>Proto-Oncogene Protein c-fli-1 - genetics</topic><topic>Reproducibility of Results</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA-Binding Protein EWS - genetics</topic><topic>Sarcoma</topic><topic>Sarcoma - diagnosis</topic><topic>Sarcoma - genetics</topic><topic>Sarcoma, Ewing - diagnosis</topic><topic>Sarcoma, Ewing - genetics</topic><topic>Time Factors</topic><topic>Transplantation, Heterologous</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Greve, Tine</creatorcontrib><creatorcontrib>Wielenga, Vera Timmermans</creatorcontrib><creatorcontrib>Grauslund, Morten</creatorcontrib><creatorcontrib>Sørensen, Nils</creatorcontrib><creatorcontrib>Christiansen, Dorte Bang</creatorcontrib><creatorcontrib>Rosendahl, Mikkel</creatorcontrib><creatorcontrib>Yding Andersen, Claus</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Pollution Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Greve, Tine</au><au>Wielenga, Vera Timmermans</au><au>Grauslund, Morten</au><au>Sørensen, Nils</au><au>Christiansen, Dorte Bang</au><au>Rosendahl, Mikkel</au><au>Yding Andersen, Claus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ovarian tissue cryopreserved for fertility preservation from patients with Ewing or other sarcomas appear to have no tumour cell contamination</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2013-05-01</date><risdate>2013</risdate><volume>49</volume><issue>8</issue><spage>1932</spage><epage>1938</epage><pages>1932-1938</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Abstract Aim The chemotherapy required to treat patients with sarcoma may as a side-effect induce infertility in girls and young women. If these patients have ovarian cortical tissue cryopreserved prior to chemotherapy, they may, if necessary, have the tissue transplanted and restore their fertility. The aim of this study was to evaluate the risk of residual cancer cells in the ovarian cortex intended for transplantation. Patients and methods Ovarian tissue stored for fertility preservation from 16 surviving patients diagnosed with sarcoma (nine with Ewing sarcomas, four with osteosarcomas, two with synovial sarcomas and one with chondrosarcoma) was evaluated for the presence of malignant cells by histology and by transplantation to immunodeficient mice for 20 weeks. A fraction of the tissue from patients with Ewing sarcoma was also evaluated for the presence of the molecular marker EWS-FLI1 by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The transplant itself and selected murine organs were analysed for the presence of malignant cells by histology. Results All the mice accommodated the human tissue for 20 weeks of transplantation period with none of the mice developing any sign of cancer. In no instance were any cancer cells detected by histology or RT-qPCR. Conclusion Ovarian tissue from patients with sarcoma appears to be without metastatic malignant cells in numbers that allow detection. Although the actual pieces of ovarian tissue used for transplantation remain unchecked, the current data indicate that the procedure is safe at least in patients that survive the sarcoma disease.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>23452988</pmid><doi>10.1016/j.ejca.2013.01.032</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Animals Biological and medical sciences Child Cryopreservation Cryopreservation - methods Female Fertility preservation Fertility Preservation - methods Hematology, Oncology and Palliative Medicine Humans Medical sciences Mice Mice, Inbred Strains Mice, Nude Micrometastatic disease Molecular markers Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Oncogene Proteins, Fusion - genetics Ovarian metastases Ovary Ovary - metabolism Ovary - transplantation Pharmacology. Drug treatments Proto-Oncogene Protein c-fli-1 - genetics Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction RNA-Binding Protein EWS - genetics Sarcoma Sarcoma - diagnosis Sarcoma - genetics Sarcoma, Ewing - diagnosis Sarcoma, Ewing - genetics Time Factors Transplantation, Heterologous Tumors |
title | Ovarian tissue cryopreserved for fertility preservation from patients with Ewing or other sarcomas appear to have no tumour cell contamination |
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