Australian experience of peptide receptor radionuclide therapy in lung neuroendocrine tumours

BACKGROUNDPeptide receptor radionuclide therapy (PRRT) is an approved treatment modality for gastroenteropancreatic neuroendocrine tumours (GEP NETs), Although Phase III randomised clinical trial data is not available for NETs of other site of origin, in practice, PRRT is used more widely in clinica...

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Veröffentlicht in:Oncotarget 2020-07, Vol.11 (27), p.2636-2646
Hauptverfasser: Lim, Lisi Elizabeth, Chan, David L., Thomas, David, Du, Yang, Tincknell, Gary, Kuchel, Anna, Davis, Alexander, Bailey, Dale L., Pavlakis, Nick, Cehic, Gabrielle, Macdonald, William, Wyld, David, Segelov, Eva
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container_end_page 2646
container_issue 27
container_start_page 2636
container_title Oncotarget
container_volume 11
creator Lim, Lisi Elizabeth
Chan, David L.
Thomas, David
Du, Yang
Tincknell, Gary
Kuchel, Anna
Davis, Alexander
Bailey, Dale L.
Pavlakis, Nick
Cehic, Gabrielle
Macdonald, William
Wyld, David
Segelov, Eva
description BACKGROUNDPeptide receptor radionuclide therapy (PRRT) is an approved treatment modality for gastroenteropancreatic neuroendocrine tumours (GEP NETs), Although Phase III randomised clinical trial data is not available for NETs of other site of origin, in practice, PRRT is used more widely in clinical practice, based on its mechanism of targeting the somatostatin receptor. Use of PRRT for lung (bronchial) NET, specifically typical and atypical carcinoid (TC, AC), has been reported only in small retrospective case series. This multicentre study adds to the evidence regarding utility of PRRT for lung NETs. MATERIALS AND METHODSA retrospective chart review of patients with TC and AC who received 177Lu-dotatate PRRT between January 2002 and June 2019 in six hospitals across Australia was undertaken. Data regarding demographics, efficacy and toxicity was evaluated at each site by the treating clinician. RESULTSForty-eight patients (32 AC, 15 TC, 1 unclassified) received a median of four 177Lu-dotatate treatments. There was a median of one prior line of systemic treatment (range: 0-3). The response rate to 177Lu-dotatate was 33%, with a median overall survival of 49 months (range of 3-91), at a median follow up of 33 months. This compares favourably with GEP NET. Overall toxicity was recorded as modest. CONCLUSIONS177Lu-dotatate PRRT in patients with lung NETs is used in real world practice, where it appears well-tolerated with some efficacy. Further evidence could be obtained through a global prospective clinical or registry trial.
doi_str_mv 10.18632/oncotarget.27659
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Use of PRRT for lung (bronchial) NET, specifically typical and atypical carcinoid (TC, AC), has been reported only in small retrospective case series. This multicentre study adds to the evidence regarding utility of PRRT for lung NETs. MATERIALS AND METHODSA retrospective chart review of patients with TC and AC who received 177Lu-dotatate PRRT between January 2002 and June 2019 in six hospitals across Australia was undertaken. Data regarding demographics, efficacy and toxicity was evaluated at each site by the treating clinician. RESULTSForty-eight patients (32 AC, 15 TC, 1 unclassified) received a median of four 177Lu-dotatate treatments. There was a median of one prior line of systemic treatment (range: 0-3). The response rate to 177Lu-dotatate was 33%, with a median overall survival of 49 months (range of 3-91), at a median follow up of 33 months. This compares favourably with GEP NET. Overall toxicity was recorded as modest. CONCLUSIONS177Lu-dotatate PRRT in patients with lung NETs is used in real world practice, where it appears well-tolerated with some efficacy. Further evidence could be obtained through a global prospective clinical or registry trial.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.27659</identifier><identifier>PMID: 32676165</identifier><language>eng</language><publisher>Impact Journals LLC</publisher><subject>Research Paper</subject><ispartof>Oncotarget, 2020-07, Vol.11 (27), p.2636-2646</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2919-5d3fd2f0f96dd19ec2ee12d41b8122300e6ff21c01d100c560403f7fe6b34f143</citedby><cites>FETCH-LOGICAL-c2919-5d3fd2f0f96dd19ec2ee12d41b8122300e6ff21c01d100c560403f7fe6b34f143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343632/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343632/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids></links><search><creatorcontrib>Lim, Lisi Elizabeth</creatorcontrib><creatorcontrib>Chan, David L.</creatorcontrib><creatorcontrib>Thomas, David</creatorcontrib><creatorcontrib>Du, Yang</creatorcontrib><creatorcontrib>Tincknell, Gary</creatorcontrib><creatorcontrib>Kuchel, Anna</creatorcontrib><creatorcontrib>Davis, Alexander</creatorcontrib><creatorcontrib>Bailey, Dale L.</creatorcontrib><creatorcontrib>Pavlakis, Nick</creatorcontrib><creatorcontrib>Cehic, Gabrielle</creatorcontrib><creatorcontrib>Macdonald, William</creatorcontrib><creatorcontrib>Wyld, David</creatorcontrib><creatorcontrib>Segelov, Eva</creatorcontrib><title>Australian experience of peptide receptor radionuclide therapy in lung neuroendocrine tumours</title><title>Oncotarget</title><description>BACKGROUNDPeptide receptor radionuclide therapy (PRRT) is an approved treatment modality for gastroenteropancreatic neuroendocrine tumours (GEP NETs), Although Phase III randomised clinical trial data is not available for NETs of other site of origin, in practice, PRRT is used more widely in clinical practice, based on its mechanism of targeting the somatostatin receptor. Use of PRRT for lung (bronchial) NET, specifically typical and atypical carcinoid (TC, AC), has been reported only in small retrospective case series. This multicentre study adds to the evidence regarding utility of PRRT for lung NETs. MATERIALS AND METHODSA retrospective chart review of patients with TC and AC who received 177Lu-dotatate PRRT between January 2002 and June 2019 in six hospitals across Australia was undertaken. Data regarding demographics, efficacy and toxicity was evaluated at each site by the treating clinician. RESULTSForty-eight patients (32 AC, 15 TC, 1 unclassified) received a median of four 177Lu-dotatate treatments. There was a median of one prior line of systemic treatment (range: 0-3). The response rate to 177Lu-dotatate was 33%, with a median overall survival of 49 months (range of 3-91), at a median follow up of 33 months. This compares favourably with GEP NET. Overall toxicity was recorded as modest. CONCLUSIONS177Lu-dotatate PRRT in patients with lung NETs is used in real world practice, where it appears well-tolerated with some efficacy. 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Use of PRRT for lung (bronchial) NET, specifically typical and atypical carcinoid (TC, AC), has been reported only in small retrospective case series. This multicentre study adds to the evidence regarding utility of PRRT for lung NETs. MATERIALS AND METHODSA retrospective chart review of patients with TC and AC who received 177Lu-dotatate PRRT between January 2002 and June 2019 in six hospitals across Australia was undertaken. Data regarding demographics, efficacy and toxicity was evaluated at each site by the treating clinician. RESULTSForty-eight patients (32 AC, 15 TC, 1 unclassified) received a median of four 177Lu-dotatate treatments. There was a median of one prior line of systemic treatment (range: 0-3). The response rate to 177Lu-dotatate was 33%, with a median overall survival of 49 months (range of 3-91), at a median follow up of 33 months. This compares favourably with GEP NET. Overall toxicity was recorded as modest. CONCLUSIONS177Lu-dotatate PRRT in patients with lung NETs is used in real world practice, where it appears well-tolerated with some efficacy. Further evidence could be obtained through a global prospective clinical or registry trial.</abstract><pub>Impact Journals LLC</pub><pmid>32676165</pmid><doi>10.18632/oncotarget.27659</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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title Australian experience of peptide receptor radionuclide therapy in lung neuroendocrine tumours
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