A phase I/II trial of recombinant human granulocyte-macrophage colony-stimulating factor in the intensification of cisplatin and cyclophosphamide chemotherapy for advanced ovarian cancer
A pilot study was undertaken in eight patients to assess the feasibility of recombinant human granulocyte-macrophage colony-stimulating factor (rH GM-CSF) support to intensify standard chemotherapy for advanced ovarian cancer using a shortened 15 day treatment interval. Only four patients completed...
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Veröffentlicht in: | British journal of cancer 1994-03, Vol.69 (3), p.537-540 |
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description | A pilot study was undertaken in eight patients to assess the feasibility of recombinant human granulocyte-macrophage colony-stimulating factor (rH GM-CSF) support to intensify standard chemotherapy for advanced ovarian cancer using a shortened 15 day treatment interval. Only four patients completed the course of six cycles of cisplatin 75 mg m-2 and cyclophosphamide 750 mg m-2 with rH GM-CSF, 3-5 micrograms kg-1 day-1, days 3-14, but one of these suffered a toxic death on study. Another died of disease progression. There were two episodes of life-threatening infection (WHO grade 4), and three patients were withdrawn because of various rH GM-CSF-related problems. Although potentially affording some patients the hypothetical benefits of dose intensification, as well as the possible attraction of a shorter duration of chemotherapy, this regimen is not without problems. |
doi_str_mv | 10.1038/bjc.1994.97 |
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J ; STANLEY, A ; EARL, H. M ; BLACKLEDGE, G. R. P</creator><creatorcontrib>KEHOE, S ; POOLE, C. J ; STANLEY, A ; EARL, H. M ; BLACKLEDGE, G. R. P</creatorcontrib><description>A pilot study was undertaken in eight patients to assess the feasibility of recombinant human granulocyte-macrophage colony-stimulating factor (rH GM-CSF) support to intensify standard chemotherapy for advanced ovarian cancer using a shortened 15 day treatment interval. Only four patients completed the course of six cycles of cisplatin 75 mg m-2 and cyclophosphamide 750 mg m-2 with rH GM-CSF, 3-5 micrograms kg-1 day-1, days 3-14, but one of these suffered a toxic death on study. Another died of disease progression. There were two episodes of life-threatening infection (WHO grade 4), and three patients were withdrawn because of various rH GM-CSF-related problems. Although potentially affording some patients the hypothetical benefits of dose intensification, as well as the possible attraction of a shorter duration of chemotherapy, this regimen is not without problems.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1994.97</identifier><identifier>PMID: 8123484</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>Adenocarcinoma - drug therapy ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adenocarcinoma, Mucinous - drug therapy ; Adenocarcinoma, Mucinous - mortality ; Adenocarcinoma, Mucinous - pathology ; Adult ; Aged ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Cisplatin - administration & dosage ; Cisplatin - adverse effects ; Combined treatments (chemotherapy of immunotherapy associated with an other treatment) ; Cyclophosphamide - administration & dosage ; Cyclophosphamide - adverse effects ; Feasibility Studies ; Female ; Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use ; Granulocyte-Macrophage Colony-Stimulating Factor - toxicity ; Humans ; Medical sciences ; Middle Aged ; Neoplasm Staging ; Ovarian Neoplasms - drug therapy ; Ovarian Neoplasms - mortality ; Ovarian Neoplasms - pathology ; Pharmacology. 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J</creatorcontrib><creatorcontrib>STANLEY, A</creatorcontrib><creatorcontrib>EARL, H. M</creatorcontrib><creatorcontrib>BLACKLEDGE, G. R. P</creatorcontrib><title>A phase I/II trial of recombinant human granulocyte-macrophage colony-stimulating factor in the intensification of cisplatin and cyclophosphamide chemotherapy for advanced ovarian cancer</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><description>A pilot study was undertaken in eight patients to assess the feasibility of recombinant human granulocyte-macrophage colony-stimulating factor (rH GM-CSF) support to intensify standard chemotherapy for advanced ovarian cancer using a shortened 15 day treatment interval. Only four patients completed the course of six cycles of cisplatin 75 mg m-2 and cyclophosphamide 750 mg m-2 with rH GM-CSF, 3-5 micrograms kg-1 day-1, days 3-14, but one of these suffered a toxic death on study. Another died of disease progression. There were two episodes of life-threatening infection (WHO grade 4), and three patients were withdrawn because of various rH GM-CSF-related problems. Although potentially affording some patients the hypothetical benefits of dose intensification, as well as the possible attraction of a shorter duration of chemotherapy, this regimen is not without problems.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma, Mucinous - drug therapy</subject><subject>Adenocarcinoma, Mucinous - mortality</subject><subject>Adenocarcinoma, Mucinous - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cisplatin - administration & dosage</subject><subject>Cisplatin - adverse effects</subject><subject>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Cyclophosphamide - adverse effects</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - toxicity</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Ovarian Neoplasms - drug therapy</subject><subject>Ovarian Neoplasms - mortality</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Pharmacology. Drug treatments</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>Recombinant Proteins - toxicity</subject><subject>Survival Rate</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1r3DAQhk1pSTdpTz2X6lByKd5I_pJ8CYTQj4VAL7mLsSytFWxpK8kL_mv9dR13l6W9aBDvO88M82bZB0a3jJbirntRW9a21bblr7INq8siZ6Lgr7MNpZTntC3o2-w6xhf8tlTwq-xKsKKsRLXJfj-QwwBRk93dbkdSsDASb0jQyk-ddeASGeYJHNkHcPPo1ZJ0PoEKHtv2mig_erfkMdlpHiFZtycGVPKBWEfSoLEk7aI1VqHq3QpXNh7-egm4nqhFjQjzEYGT7RE56Mlja4DDQgySoD-CU7on_gi4oCNq_YZ32RsDY9Tvz_Ume_729fnxR_708_vu8eEpV1VDUw68E0JwVUNlCmEobYQxTPRF0wGjXDOmypq2AqhmLXQcH04LTnvVGVr15U12f8Ie5m7SvdIuBRjlIdgJwiI9WPm_4uwg9_4oWdsIUXIE3J4Bwf-adUxyslHpcQSn_RwlawSr6rpA45eTEa8bY9DmMoRRuSYtMWm5Ji3bFfvx370u3nO0qH8-6xAVjAbzw8NfbGXLRUUbtH062RykOeiLjqPWSTjoD-dZwmQ</recordid><startdate>19940301</startdate><enddate>19940301</enddate><creator>KEHOE, S</creator><creator>POOLE, C. 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Drug treatments</topic><topic>Recombinant Proteins - therapeutic use</topic><topic>Recombinant Proteins - toxicity</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KEHOE, S</creatorcontrib><creatorcontrib>POOLE, C. J</creatorcontrib><creatorcontrib>STANLEY, A</creatorcontrib><creatorcontrib>EARL, H. M</creatorcontrib><creatorcontrib>BLACKLEDGE, G. R. 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P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A phase I/II trial of recombinant human granulocyte-macrophage colony-stimulating factor in the intensification of cisplatin and cyclophosphamide chemotherapy for advanced ovarian cancer</atitle><jtitle>British journal of cancer</jtitle><addtitle>Br J Cancer</addtitle><date>1994-03-01</date><risdate>1994</risdate><volume>69</volume><issue>3</issue><spage>537</spage><epage>540</epage><pages>537-540</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>A pilot study was undertaken in eight patients to assess the feasibility of recombinant human granulocyte-macrophage colony-stimulating factor (rH GM-CSF) support to intensify standard chemotherapy for advanced ovarian cancer using a shortened 15 day treatment interval. 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subjects | Adenocarcinoma - drug therapy Adenocarcinoma - mortality Adenocarcinoma - pathology Adenocarcinoma, Mucinous - drug therapy Adenocarcinoma, Mucinous - mortality Adenocarcinoma, Mucinous - pathology Adult Aged Antineoplastic agents Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Cisplatin - administration & dosage Cisplatin - adverse effects Combined treatments (chemotherapy of immunotherapy associated with an other treatment) Cyclophosphamide - administration & dosage Cyclophosphamide - adverse effects Feasibility Studies Female Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use Granulocyte-Macrophage Colony-Stimulating Factor - toxicity Humans Medical sciences Middle Aged Neoplasm Staging Ovarian Neoplasms - drug therapy Ovarian Neoplasms - mortality Ovarian Neoplasms - pathology Pharmacology. Drug treatments Recombinant Proteins - therapeutic use Recombinant Proteins - toxicity Survival Rate |
title | A phase I/II trial of recombinant human granulocyte-macrophage colony-stimulating factor in the intensification of cisplatin and cyclophosphamide chemotherapy for advanced ovarian cancer |
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