Treatment of metastatic breast cancer with somatostatin analogues--a meta-analysis
Somatostatin analogues appear to have antiproliferative effects in breast cancer by inhibiting various hormones. Several small phase 1 and 2 clinical trails have evaluated the efficacy of somatostatin analogues, but the results are varied. The purpose of this study was to use the technique of meta-a...
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Veröffentlicht in: | Annals of surgical oncology 2001-04, Vol.8 (3), p.227-233 |
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creator | Dolan, J T Miltenburg, D M Granchi, T S Miller, 3rd, C C Brunicardi, F C |
description | Somatostatin analogues appear to have antiproliferative effects in breast cancer by inhibiting various hormones. Several small phase 1 and 2 clinical trails have evaluated the efficacy of somatostatin analogues, but the results are varied. The purpose of this study was to use the technique of meta-analysis to determine the effect of somatostatin analogues on tumor response, toxicity, and serum hormone levels in women with metastatic breast cancer.
All published and unpublished trials were reviewed. Meta-analysis was preformed by best linear unbiased estimate regression with observations weighted inversely to their variance. Significance was considered at P < .05.
Fourteen studies (N = 210) were included. Positive tumor response was reported in 87 patients (41.4%). Mean duration of response was 3.9 months. Response was best when somatostatin analogues were given as first-line therapy (69.5% versus 28.5%, P < .006) and in patients with < or =2 metastases (45.0% versus 5.6%, P = .3). Mild side effects occurred in 47 of 185 patients (25.4%). Therapy was associated with a decrease in serum insulin-like growth factor (IGF-1) and an increase in growth hormone.
In patients with metastatic breast cancer, treatment with somatostatin analogues was associated with a tumor response of over 40% with few side effects. Best results were achieved when somatostatin analogues were given as first-line therapy. |
doi_str_mv | 10.1007/s10434-001-0227-x |
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All published and unpublished trials were reviewed. Meta-analysis was preformed by best linear unbiased estimate regression with observations weighted inversely to their variance. Significance was considered at P < .05.
Fourteen studies (N = 210) were included. Positive tumor response was reported in 87 patients (41.4%). Mean duration of response was 3.9 months. Response was best when somatostatin analogues were given as first-line therapy (69.5% versus 28.5%, P < .006) and in patients with < or =2 metastases (45.0% versus 5.6%, P = .3). Mild side effects occurred in 47 of 185 patients (25.4%). Therapy was associated with a decrease in serum insulin-like growth factor (IGF-1) and an increase in growth hormone.
In patients with metastatic breast cancer, treatment with somatostatin analogues was associated with a tumor response of over 40% with few side effects. Best results were achieved when somatostatin analogues were given as first-line therapy.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1007/s10434-001-0227-x</identifier><identifier>PMID: 11314939</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Antineoplastic Agents, Hormonal - adverse effects ; Antineoplastic Agents, Hormonal - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Female ; Humans ; Insulin-Like Growth Factor I - drug effects ; Octreotide - adverse effects ; Octreotide - analogs & derivatives ; Octreotide - therapeutic use ; Peptides, Cyclic - adverse effects ; Peptides, Cyclic - therapeutic use ; Somatostatin - adverse effects ; Somatostatin - analogs & derivatives ; Somatostatin - therapeutic use ; Time Factors ; Treatment Outcome</subject><ispartof>Annals of surgical oncology, 2001-04, Vol.8 (3), p.227-233</ispartof><rights>The Society of Surgical Oncology, Inc. 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c256t-fc36e46e26712c15249219cf61726e82749bec69adc81806e7921b6f2befd7243</citedby><cites>FETCH-LOGICAL-c256t-fc36e46e26712c15249219cf61726e82749bec69adc81806e7921b6f2befd7243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11314939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dolan, J T</creatorcontrib><creatorcontrib>Miltenburg, D M</creatorcontrib><creatorcontrib>Granchi, T S</creatorcontrib><creatorcontrib>Miller, 3rd, C C</creatorcontrib><creatorcontrib>Brunicardi, F C</creatorcontrib><title>Treatment of metastatic breast cancer with somatostatin analogues--a meta-analysis</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><description>Somatostatin analogues appear to have antiproliferative effects in breast cancer by inhibiting various hormones. Several small phase 1 and 2 clinical trails have evaluated the efficacy of somatostatin analogues, but the results are varied. The purpose of this study was to use the technique of meta-analysis to determine the effect of somatostatin analogues on tumor response, toxicity, and serum hormone levels in women with metastatic breast cancer.
All published and unpublished trials were reviewed. Meta-analysis was preformed by best linear unbiased estimate regression with observations weighted inversely to their variance. Significance was considered at P < .05.
Fourteen studies (N = 210) were included. Positive tumor response was reported in 87 patients (41.4%). Mean duration of response was 3.9 months. Response was best when somatostatin analogues were given as first-line therapy (69.5% versus 28.5%, P < .006) and in patients with < or =2 metastases (45.0% versus 5.6%, P = .3). Mild side effects occurred in 47 of 185 patients (25.4%). Therapy was associated with a decrease in serum insulin-like growth factor (IGF-1) and an increase in growth hormone.
In patients with metastatic breast cancer, treatment with somatostatin analogues was associated with a tumor response of over 40% with few side effects. Best results were achieved when somatostatin analogues were given as first-line therapy.</description><subject>Antineoplastic Agents, Hormonal - adverse effects</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Insulin-Like Growth Factor I - drug effects</subject><subject>Octreotide - adverse effects</subject><subject>Octreotide - analogs & derivatives</subject><subject>Octreotide - therapeutic use</subject><subject>Peptides, Cyclic - adverse effects</subject><subject>Peptides, Cyclic - therapeutic use</subject><subject>Somatostatin - adverse effects</subject><subject>Somatostatin - analogs & derivatives</subject><subject>Somatostatin - therapeutic use</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpFkFtLAzEQhYMotlZ_gC8SfI9mkmyy-yjFGxQEqc8hmya6pbupSYr235tewKcZzpwzHD6EroHeAaXqPgEVXBBKgVDGFPk9QWOoiiJkDadlp7ImDZPVCF2ktCw-xWl1jkYAHETDmzF6n0dncu-GjIPHvcsmZZM7i9uip4ytGayL-KfLXziF3uSwvw_YDGYVPjcuEWL2ObJTtqlLl-jMm1VyV8c5QR9Pj_PpC5m9Pb9OH2bEskpm4i2XTkjHpAJmoWKiYdBYL0Ex6WqmRNM6KxuzsDXUVDpV7q30rHV-oZjgE3R7-LuO4bsUyXoZNrGUSLrA4EJRAcUEB5ONIaXovF7Hrjdxq4HqHUR9gKgLHL2DqH9L5ub4eNP2bvGfOFLjf_OkbRg</recordid><startdate>200104</startdate><enddate>200104</enddate><creator>Dolan, J T</creator><creator>Miltenburg, D M</creator><creator>Granchi, T S</creator><creator>Miller, 3rd, C C</creator><creator>Brunicardi, F C</creator><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200104</creationdate><title>Treatment of metastatic breast cancer with somatostatin analogues--a meta-analysis</title><author>Dolan, J T ; 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Several small phase 1 and 2 clinical trails have evaluated the efficacy of somatostatin analogues, but the results are varied. The purpose of this study was to use the technique of meta-analysis to determine the effect of somatostatin analogues on tumor response, toxicity, and serum hormone levels in women with metastatic breast cancer.
All published and unpublished trials were reviewed. Meta-analysis was preformed by best linear unbiased estimate regression with observations weighted inversely to their variance. Significance was considered at P < .05.
Fourteen studies (N = 210) were included. Positive tumor response was reported in 87 patients (41.4%). Mean duration of response was 3.9 months. Response was best when somatostatin analogues were given as first-line therapy (69.5% versus 28.5%, P < .006) and in patients with < or =2 metastases (45.0% versus 5.6%, P = .3). Mild side effects occurred in 47 of 185 patients (25.4%). Therapy was associated with a decrease in serum insulin-like growth factor (IGF-1) and an increase in growth hormone.
In patients with metastatic breast cancer, treatment with somatostatin analogues was associated with a tumor response of over 40% with few side effects. Best results were achieved when somatostatin analogues were given as first-line therapy.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>11314939</pmid><doi>10.1007/s10434-001-0227-x</doi><tpages>7</tpages></addata></record> |
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subjects | Antineoplastic Agents, Hormonal - adverse effects Antineoplastic Agents, Hormonal - therapeutic use Antineoplastic Combined Chemotherapy Protocols - therapeutic use Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - pathology Female Humans Insulin-Like Growth Factor I - drug effects Octreotide - adverse effects Octreotide - analogs & derivatives Octreotide - therapeutic use Peptides, Cyclic - adverse effects Peptides, Cyclic - therapeutic use Somatostatin - adverse effects Somatostatin - analogs & derivatives Somatostatin - therapeutic use Time Factors Treatment Outcome |
title | Treatment of metastatic breast cancer with somatostatin analogues--a meta-analysis |
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