Giant cell tumour of bone in the denosumab era
Abstract Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of num...
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description | Abstract Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated osteoclast-like giant cells, causing lacunar bone resorption. Preferential treatment is curettage with local adjuvants such as phenol, alcohol or liquid nitrogen. The remaining cavity may be filled with bone graft or polymethylmethacrylate (PMMA) bone cement; benefits of the latter are a lower risk of recurrence, possibility of direct weight bearing and early radiographic detection of recurrences. Reported recurrence rates are comparable for the different local adjuvants (27–31%). Factors increasing the local recurrence risk include soft tissue extension and anatomically difficult localisations such as the sacrum. When joint salvage is impossible, en-bloc resection and endoprosthetic joint replacement may be performed. Local tumour control on the one hand and maintenance of a functional native joint and quality of life on the other hand are the main pillars of surgical treatment for this disease. Current knowledge and development in the fields of imaging, functional biology and systemic therapy are forcing us into a paradigm shift from a purely surgical approach towards a multidisciplinary approach. Systemic therapy with denosumab (RANKL inhibitor) or zoledronic acid (bisphosphonates) blocks, respectively inhibits, bone resorption by osteoclast-like giant cells. After use of zoledronic acid, stabilisation of local and metastatic disease has been reported, although the level of evidence is low. Denosumab is more extensively studied in two prospective trials, and appears effective for the optimisation of surgical treatment. Denosumab should be considered in the standard multidisciplinary treatment of advanced GCTB (e.g. cortical destruction, soft tissue extension, joint involvement or sacral localisation) to facilitate surgery at a later stage, and thereby aiming at immediate local control. Even though several questions concerning optimal treatment dose, duration and interval and drug safety remain unanswered, denosumab is among the most effective drug therapies in oncology. |
doi_str_mv | 10.1016/j.ejca.2017.02.021 |
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Sander ; Blay, Jean-Yves ; Gelderblom, Hans</creator><creatorcontrib>van der Heijden, Lizz ; Dijkstra, P.D. Sander ; Blay, Jean-Yves ; Gelderblom, Hans</creatorcontrib><description>Abstract Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated osteoclast-like giant cells, causing lacunar bone resorption. Preferential treatment is curettage with local adjuvants such as phenol, alcohol or liquid nitrogen. The remaining cavity may be filled with bone graft or polymethylmethacrylate (PMMA) bone cement; benefits of the latter are a lower risk of recurrence, possibility of direct weight bearing and early radiographic detection of recurrences. Reported recurrence rates are comparable for the different local adjuvants (27–31%). Factors increasing the local recurrence risk include soft tissue extension and anatomically difficult localisations such as the sacrum. When joint salvage is impossible, en-bloc resection and endoprosthetic joint replacement may be performed. Local tumour control on the one hand and maintenance of a functional native joint and quality of life on the other hand are the main pillars of surgical treatment for this disease. Current knowledge and development in the fields of imaging, functional biology and systemic therapy are forcing us into a paradigm shift from a purely surgical approach towards a multidisciplinary approach. Systemic therapy with denosumab (RANKL inhibitor) or zoledronic acid (bisphosphonates) blocks, respectively inhibits, bone resorption by osteoclast-like giant cells. After use of zoledronic acid, stabilisation of local and metastatic disease has been reported, although the level of evidence is low. Denosumab is more extensively studied in two prospective trials, and appears effective for the optimisation of surgical treatment. Denosumab should be considered in the standard multidisciplinary treatment of advanced GCTB (e.g. cortical destruction, soft tissue extension, joint involvement or sacral localisation) to facilitate surgery at a later stage, and thereby aiming at immediate local control. Even though several questions concerning optimal treatment dose, duration and interval and drug safety remain unanswered, denosumab is among the most effective drug therapies in oncology.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2017.02.021</identifier><identifier>PMID: 28365529</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adjuvants ; Alcohols ; Antineoplastic Agents - therapeutic use ; Biocompatibility ; Biomedical materials ; Bisphosphonates ; Bone cancer ; Bone cements ; Bone Density Conservation Agents - therapeutic use ; Bone diseases ; Bone grafts ; Bone Neoplasms - drug therapy ; Bone Neoplasms - radiotherapy ; Bone Neoplasms - surgery ; Bone resorption ; Bone tumors ; Cells ; Clinical Trials, Phase II as Topic ; Combined Modality Therapy ; Curettage ; Denosumab ; Denosumab - therapeutic use ; Drug therapy ; Epiphysis ; Genes, Neoplasm - genetics ; Giant Cell Tumor of Bone - drug therapy ; Giant Cell Tumor of Bone - radiotherapy ; Giant Cell Tumor of Bone - surgery ; Giant cell tumour of bone ; Giant cells ; Grafting ; Hematology, Oncology and Palliative Medicine ; Humans ; Liquid nitrogen ; Medical treatment ; Metastases ; Monoclonal antibodies ; Mutation - genetics ; Nuclear engineering ; Nuclear safety ; Oncology ; Pharmacovigilance ; Phenols ; Polymethyl methacrylate ; Polymethylmethacrylate ; Postoperative Complications - etiology ; Prostheses ; Quality of life ; RANK ligand ; Sacrum ; Salvage ; Stromal cells ; Substitute bone ; Surgery ; Targeted cancer therapy ; Therapy ; TRANCE protein ; Tumors ; Zoledronic acid</subject><ispartof>European journal of cancer (1990), 2017-05, Vol.77, p.75-83</ispartof><rights>Elsevier Ltd</rights><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. May 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-2534bd17a2c71d16493e3f6a40d778540544a66c3c8295fa2b268b13470687883</citedby><cites>FETCH-LOGICAL-c439t-2534bd17a2c71d16493e3f6a40d778540544a66c3c8295fa2b268b13470687883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0959804917307876$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28365529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Heijden, Lizz</creatorcontrib><creatorcontrib>Dijkstra, P.D. Sander</creatorcontrib><creatorcontrib>Blay, Jean-Yves</creatorcontrib><creatorcontrib>Gelderblom, Hans</creatorcontrib><title>Giant cell tumour of bone in the denosumab era</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Abstract Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated osteoclast-like giant cells, causing lacunar bone resorption. Preferential treatment is curettage with local adjuvants such as phenol, alcohol or liquid nitrogen. The remaining cavity may be filled with bone graft or polymethylmethacrylate (PMMA) bone cement; benefits of the latter are a lower risk of recurrence, possibility of direct weight bearing and early radiographic detection of recurrences. Reported recurrence rates are comparable for the different local adjuvants (27–31%). Factors increasing the local recurrence risk include soft tissue extension and anatomically difficult localisations such as the sacrum. When joint salvage is impossible, en-bloc resection and endoprosthetic joint replacement may be performed. Local tumour control on the one hand and maintenance of a functional native joint and quality of life on the other hand are the main pillars of surgical treatment for this disease. Current knowledge and development in the fields of imaging, functional biology and systemic therapy are forcing us into a paradigm shift from a purely surgical approach towards a multidisciplinary approach. Systemic therapy with denosumab (RANKL inhibitor) or zoledronic acid (bisphosphonates) blocks, respectively inhibits, bone resorption by osteoclast-like giant cells. After use of zoledronic acid, stabilisation of local and metastatic disease has been reported, although the level of evidence is low. Denosumab is more extensively studied in two prospective trials, and appears effective for the optimisation of surgical treatment. Denosumab should be considered in the standard multidisciplinary treatment of advanced GCTB (e.g. cortical destruction, soft tissue extension, joint involvement or sacral localisation) to facilitate surgery at a later stage, and thereby aiming at immediate local control. Even though several questions concerning optimal treatment dose, duration and interval and drug safety remain unanswered, denosumab is among the most effective drug therapies in oncology.</description><subject>Adjuvants</subject><subject>Alcohols</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Bisphosphonates</subject><subject>Bone cancer</subject><subject>Bone cements</subject><subject>Bone Density Conservation Agents - therapeutic use</subject><subject>Bone diseases</subject><subject>Bone grafts</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - radiotherapy</subject><subject>Bone Neoplasms - surgery</subject><subject>Bone resorption</subject><subject>Bone tumors</subject><subject>Cells</subject><subject>Clinical Trials, Phase II as Topic</subject><subject>Combined Modality Therapy</subject><subject>Curettage</subject><subject>Denosumab</subject><subject>Denosumab - therapeutic use</subject><subject>Drug therapy</subject><subject>Epiphysis</subject><subject>Genes, Neoplasm - genetics</subject><subject>Giant Cell Tumor of Bone - drug therapy</subject><subject>Giant Cell Tumor of Bone - radiotherapy</subject><subject>Giant Cell Tumor of Bone - surgery</subject><subject>Giant cell tumour of bone</subject><subject>Giant cells</subject><subject>Grafting</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Liquid nitrogen</subject><subject>Medical treatment</subject><subject>Metastases</subject><subject>Monoclonal antibodies</subject><subject>Mutation - genetics</subject><subject>Nuclear engineering</subject><subject>Nuclear safety</subject><subject>Oncology</subject><subject>Pharmacovigilance</subject><subject>Phenols</subject><subject>Polymethyl methacrylate</subject><subject>Polymethylmethacrylate</subject><subject>Postoperative Complications - etiology</subject><subject>Prostheses</subject><subject>Quality of life</subject><subject>RANK ligand</subject><subject>Sacrum</subject><subject>Salvage</subject><subject>Stromal cells</subject><subject>Substitute bone</subject><subject>Surgery</subject><subject>Targeted cancer therapy</subject><subject>Therapy</subject><subject>TRANCE protein</subject><subject>Tumors</subject><subject>Zoledronic acid</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctq3jAQhUVpaf4kfYEugqGbbOyOLtYFSqGEXAqBLpKshSyPqVxfEskO5O0r8ydZZBEYmM13DjPnEPKVQkWByu99hb13FQOqKmB56Aeyo1qZEnTNPpIdmNqUGoQ5IIcp9QCgtIDP5IBpLuuamR2pLoOblsLjMBTLOs5rLOauaOYJizAVy18sWpzmtI6uKTC6Y_Kpc0PCL8_7iNxdnN-eXZXXfy5_n_26Lr3gZilZzUXTUuWYV7SlUhiOvJNOQKuUrgXUQjgpPfeambpzrGFSN5QLBVIrrfkROd373sf5YcW02DGk7Ug34bwmSzOjudF0Q7-9Qfv8xZSvsww45UoCY5lie8rHOaWInb2PYXTxyVKwW5q2t1uadkvTAstDs-jk2XptRmxfJS_xZeDHHsCcxWPAaJMPOHlsQ0S_2HYO7_v_fCP3Q5iCd8M_fML0-ge1KQvszdbnVidVPDepJP8PncGWKQ</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>van der Heijden, Lizz</creator><creator>Dijkstra, P.D. 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Sander ; Blay, Jean-Yves ; Gelderblom, Hans</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-2534bd17a2c71d16493e3f6a40d778540544a66c3c8295fa2b268b13470687883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adjuvants</topic><topic>Alcohols</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Bisphosphonates</topic><topic>Bone cancer</topic><topic>Bone cements</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Bone diseases</topic><topic>Bone grafts</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Bone Neoplasms - radiotherapy</topic><topic>Bone Neoplasms - surgery</topic><topic>Bone resorption</topic><topic>Bone tumors</topic><topic>Cells</topic><topic>Clinical Trials, Phase II as Topic</topic><topic>Combined Modality Therapy</topic><topic>Curettage</topic><topic>Denosumab</topic><topic>Denosumab - therapeutic use</topic><topic>Drug therapy</topic><topic>Epiphysis</topic><topic>Genes, Neoplasm - genetics</topic><topic>Giant Cell Tumor of Bone - drug therapy</topic><topic>Giant Cell Tumor of Bone - radiotherapy</topic><topic>Giant Cell Tumor of Bone - surgery</topic><topic>Giant cell tumour of bone</topic><topic>Giant cells</topic><topic>Grafting</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Liquid nitrogen</topic><topic>Medical treatment</topic><topic>Metastases</topic><topic>Monoclonal antibodies</topic><topic>Mutation - genetics</topic><topic>Nuclear engineering</topic><topic>Nuclear safety</topic><topic>Oncology</topic><topic>Pharmacovigilance</topic><topic>Phenols</topic><topic>Polymethyl methacrylate</topic><topic>Polymethylmethacrylate</topic><topic>Postoperative Complications - etiology</topic><topic>Prostheses</topic><topic>Quality of life</topic><topic>RANK ligand</topic><topic>Sacrum</topic><topic>Salvage</topic><topic>Stromal cells</topic><topic>Substitute bone</topic><topic>Surgery</topic><topic>Targeted cancer therapy</topic><topic>Therapy</topic><topic>TRANCE protein</topic><topic>Tumors</topic><topic>Zoledronic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Heijden, Lizz</creatorcontrib><creatorcontrib>Dijkstra, P.D. 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Sander</au><au>Blay, Jean-Yves</au><au>Gelderblom, Hans</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Giant cell tumour of bone in the denosumab era</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>77</volume><spage>75</spage><epage>83</epage><pages>75-83</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Abstract Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated osteoclast-like giant cells, causing lacunar bone resorption. Preferential treatment is curettage with local adjuvants such as phenol, alcohol or liquid nitrogen. The remaining cavity may be filled with bone graft or polymethylmethacrylate (PMMA) bone cement; benefits of the latter are a lower risk of recurrence, possibility of direct weight bearing and early radiographic detection of recurrences. Reported recurrence rates are comparable for the different local adjuvants (27–31%). Factors increasing the local recurrence risk include soft tissue extension and anatomically difficult localisations such as the sacrum. When joint salvage is impossible, en-bloc resection and endoprosthetic joint replacement may be performed. Local tumour control on the one hand and maintenance of a functional native joint and quality of life on the other hand are the main pillars of surgical treatment for this disease. Current knowledge and development in the fields of imaging, functional biology and systemic therapy are forcing us into a paradigm shift from a purely surgical approach towards a multidisciplinary approach. Systemic therapy with denosumab (RANKL inhibitor) or zoledronic acid (bisphosphonates) blocks, respectively inhibits, bone resorption by osteoclast-like giant cells. After use of zoledronic acid, stabilisation of local and metastatic disease has been reported, although the level of evidence is low. Denosumab is more extensively studied in two prospective trials, and appears effective for the optimisation of surgical treatment. Denosumab should be considered in the standard multidisciplinary treatment of advanced GCTB (e.g. cortical destruction, soft tissue extension, joint involvement or sacral localisation) to facilitate surgery at a later stage, and thereby aiming at immediate local control. Even though several questions concerning optimal treatment dose, duration and interval and drug safety remain unanswered, denosumab is among the most effective drug therapies in oncology.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28365529</pmid><doi>10.1016/j.ejca.2017.02.021</doi><tpages>9</tpages></addata></record> |
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subjects | Adjuvants Alcohols Antineoplastic Agents - therapeutic use Biocompatibility Biomedical materials Bisphosphonates Bone cancer Bone cements Bone Density Conservation Agents - therapeutic use Bone diseases Bone grafts Bone Neoplasms - drug therapy Bone Neoplasms - radiotherapy Bone Neoplasms - surgery Bone resorption Bone tumors Cells Clinical Trials, Phase II as Topic Combined Modality Therapy Curettage Denosumab Denosumab - therapeutic use Drug therapy Epiphysis Genes, Neoplasm - genetics Giant Cell Tumor of Bone - drug therapy Giant Cell Tumor of Bone - radiotherapy Giant Cell Tumor of Bone - surgery Giant cell tumour of bone Giant cells Grafting Hematology, Oncology and Palliative Medicine Humans Liquid nitrogen Medical treatment Metastases Monoclonal antibodies Mutation - genetics Nuclear engineering Nuclear safety Oncology Pharmacovigilance Phenols Polymethyl methacrylate Polymethylmethacrylate Postoperative Complications - etiology Prostheses Quality of life RANK ligand Sacrum Salvage Stromal cells Substitute bone Surgery Targeted cancer therapy Therapy TRANCE protein Tumors Zoledronic acid |
title | Giant cell tumour of bone in the denosumab era |
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