Cardiac sequelae of doxorubicin and paclitaxel as induction chemotherapy prior to high-dose chemotherapy and peripheral blood progenitor cell transplantation in women with high-risk primary or metastatic breast cancer
Doxorubicin plus paclitaxel has been shown to be an active regimen for metastatic breast cancer and is now frequently used as adjuvant therapy for high-risk primary breast cancer. Initial studies reported a higher than expected rate of cardiac toxicity with this regimen. We studied 105 patients with...
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Veröffentlicht in: | Bone marrow transplantation (Basingstoke) 2000-05, Vol.25 (10), p.1047-1052 |
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description | Doxorubicin plus paclitaxel has been shown to be an active regimen for metastatic breast cancer and is now frequently used as adjuvant therapy for high-risk primary breast cancer. Initial studies reported a higher than expected rate of cardiac toxicity with this regimen. We studied 105 patients with either high-risk primary breast cancer or metastatic breast cancer who were treated with doxorubicin (60 mg/m2) and 3-h infusions of paclitaxel (175 mg/m2) cycled every 3 weeks. Patients received three cycles of chemotherapy for high-risk primary or four cycles for metastatic disease. Patients then proceeded to high-dose chemotherapy (HDC) (STAMP I cyclophosphamide, cisplatin and carmustine) and peripheral blood progenitor cell transplantation (PBPCT). Patients underwent radionuclide multi-gated angiograms (MUGA) before and following induction chemotherapy and following HDC. During induction chemotherapy 40 (38%) of the patients had a reduction in left ventricular ejection fraction (LVEF). Fourteen had a decrease of 20% or greater and two were mildly symptomatic from CHF. There was additional reduction in the LVEF after HDC with a median value for LVEF of 59% (range, 20-78%). During HDC 10 patients developed clinical signs of congestive heart failure (CHF). Five patients responded to diuretic therapy and did not require any additional treatment. Four patients responded to vasodilation and/or digoxin with improvement in cardiac function. A clinically significant decrease in cardiac function was found in a small number of patients after induction chemotherapy and HDC with PBPCT. The majority of the patients tolerated this regimen without problems. Although there was a decline in LVEF as measured by radionuclide MUGA this did not prevent the majority of patients from proceeding with HDC. Bone Marrow Transplantation (2000). |
doi_str_mv | 10.1038/sj.bmt.1702394 |
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Initial studies reported a higher than expected rate of cardiac toxicity with this regimen. We studied 105 patients with either high-risk primary breast cancer or metastatic breast cancer who were treated with doxorubicin (60 mg/m2) and 3-h infusions of paclitaxel (175 mg/m2) cycled every 3 weeks. Patients received three cycles of chemotherapy for high-risk primary or four cycles for metastatic disease. Patients then proceeded to high-dose chemotherapy (HDC) (STAMP I cyclophosphamide, cisplatin and carmustine) and peripheral blood progenitor cell transplantation (PBPCT). Patients underwent radionuclide multi-gated angiograms (MUGA) before and following induction chemotherapy and following HDC. During induction chemotherapy 40 (38%) of the patients had a reduction in left ventricular ejection fraction (LVEF). Fourteen had a decrease of 20% or greater and two were mildly symptomatic from CHF. There was additional reduction in the LVEF after HDC with a median value for LVEF of 59% (range, 20-78%). During HDC 10 patients developed clinical signs of congestive heart failure (CHF). Five patients responded to diuretic therapy and did not require any additional treatment. Four patients responded to vasodilation and/or digoxin with improvement in cardiac function. A clinically significant decrease in cardiac function was found in a small number of patients after induction chemotherapy and HDC with PBPCT. The majority of the patients tolerated this regimen without problems. Although there was a decline in LVEF as measured by radionuclide MUGA this did not prevent the majority of patients from proceeding with HDC. Bone Marrow Transplantation (2000).</description><identifier>ISSN: 0268-3369</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/sj.bmt.1702394</identifier><identifier>PMID: 10828864</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject><![CDATA[Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Blood ; Bone marrow ; Bone marrow transplantation ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - radiotherapy ; Breast Neoplasms - therapy ; Cancer therapies ; Cardiac function ; Carmustine - administration & dosage ; Cells (biology) ; Chemotherapy ; Cisplatin ; Cisplatin - administration & dosage ; Combined Modality Therapy ; Complications ; Congestive heart failure ; Cyclophosphamide ; Cyclophosphamide - administration & dosage ; Digoxin ; Diuretics ; Doxorubicin ; Doxorubicin - administration & dosage ; Doxorubicin - adverse effects ; Drug Synergism ; Female ; Health risks ; Heart Failure - chemically induced ; Heart rate ; Hematopoietic Stem Cell Transplantation ; Hemopoiesis ; Humans ; Metastases ; Metastasis ; Middle Aged ; Neoplasm Metastasis ; Paclitaxel ; Paclitaxel - administration & dosage ; Paclitaxel - adverse effects ; Patients ; Peripheral blood ; Progenitor cells ; Radioisotopes ; Radiotherapy - adverse effects ; Risk ; Stem cell transplantation ; Stroke Volume ; Toxicity ; Transplantation ; Treatment Outcome ; Vasodilation ; Ventricle ; Ventricular Dysfunction, Left - chemically induced ; Ventricular Dysfunction, Left - etiology]]></subject><ispartof>Bone marrow transplantation (Basingstoke), 2000-05, Vol.25 (10), p.1047-1052</ispartof><rights>Copyright Nature Publishing Group May 2000</rights><rights>Macmillan Publishers Limited 2000.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-c86a32665bd3d23471ace0e0a96e80cefb2c206c8ac725069325a0acc55d0d113</citedby><cites>FETCH-LOGICAL-c348t-c86a32665bd3d23471ace0e0a96e80cefb2c206c8ac725069325a0acc55d0d113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10828864$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Klein, J L</creatorcontrib><creatorcontrib>Rey, P M</creatorcontrib><creatorcontrib>Dansey, R D</creatorcontrib><creatorcontrib>Karanes, C</creatorcontrib><creatorcontrib>Du, W</creatorcontrib><creatorcontrib>Abella, E</creatorcontrib><creatorcontrib>Cassells, L</creatorcontrib><creatorcontrib>Hamm, C</creatorcontrib><creatorcontrib>Peters, W P</creatorcontrib><creatorcontrib>Baynes, R D</creatorcontrib><title>Cardiac sequelae of doxorubicin and paclitaxel as induction chemotherapy prior to high-dose chemotherapy and peripheral blood progenitor cell transplantation in women with high-risk primary or metastatic breast cancer</title><title>Bone marrow transplantation (Basingstoke)</title><addtitle>Bone Marrow Transplant</addtitle><description>Doxorubicin plus paclitaxel has been shown to be an active regimen for metastatic breast cancer and is now frequently used as adjuvant therapy for high-risk primary breast cancer. Initial studies reported a higher than expected rate of cardiac toxicity with this regimen. We studied 105 patients with either high-risk primary breast cancer or metastatic breast cancer who were treated with doxorubicin (60 mg/m2) and 3-h infusions of paclitaxel (175 mg/m2) cycled every 3 weeks. Patients received three cycles of chemotherapy for high-risk primary or four cycles for metastatic disease. Patients then proceeded to high-dose chemotherapy (HDC) (STAMP I cyclophosphamide, cisplatin and carmustine) and peripheral blood progenitor cell transplantation (PBPCT). Patients underwent radionuclide multi-gated angiograms (MUGA) before and following induction chemotherapy and following HDC. During induction chemotherapy 40 (38%) of the patients had a reduction in left ventricular ejection fraction (LVEF). Fourteen had a decrease of 20% or greater and two were mildly symptomatic from CHF. 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Bone Marrow Transplantation (2000).</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Blood</subject><subject>Bone marrow</subject><subject>Bone marrow transplantation</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - radiotherapy</subject><subject>Breast Neoplasms - therapy</subject><subject>Cancer therapies</subject><subject>Cardiac function</subject><subject>Carmustine - administration & dosage</subject><subject>Cells (biology)</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Cisplatin - administration & dosage</subject><subject>Combined Modality Therapy</subject><subject>Complications</subject><subject>Congestive 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Klein, J L</au><au>Rey, P M</au><au>Dansey, R D</au><au>Karanes, C</au><au>Du, W</au><au>Abella, E</au><au>Cassells, L</au><au>Hamm, C</au><au>Peters, W P</au><au>Baynes, R D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiac sequelae of doxorubicin and paclitaxel as induction chemotherapy prior to high-dose chemotherapy and peripheral blood progenitor cell transplantation in women with high-risk primary or metastatic breast cancer</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><addtitle>Bone Marrow Transplant</addtitle><date>2000-05-01</date><risdate>2000</risdate><volume>25</volume><issue>10</issue><spage>1047</spage><epage>1052</epage><pages>1047-1052</pages><issn>0268-3369</issn><eissn>1476-5365</eissn><abstract>Doxorubicin plus paclitaxel has been shown to be an active regimen for metastatic breast cancer and is now frequently used as adjuvant therapy for high-risk primary breast cancer. Initial studies reported a higher than expected rate of cardiac toxicity with this regimen. We studied 105 patients with either high-risk primary breast cancer or metastatic breast cancer who were treated with doxorubicin (60 mg/m2) and 3-h infusions of paclitaxel (175 mg/m2) cycled every 3 weeks. Patients received three cycles of chemotherapy for high-risk primary or four cycles for metastatic disease. Patients then proceeded to high-dose chemotherapy (HDC) (STAMP I cyclophosphamide, cisplatin and carmustine) and peripheral blood progenitor cell transplantation (PBPCT). Patients underwent radionuclide multi-gated angiograms (MUGA) before and following induction chemotherapy and following HDC. During induction chemotherapy 40 (38%) of the patients had a reduction in left ventricular ejection fraction (LVEF). Fourteen had a decrease of 20% or greater and two were mildly symptomatic from CHF. There was additional reduction in the LVEF after HDC with a median value for LVEF of 59% (range, 20-78%). During HDC 10 patients developed clinical signs of congestive heart failure (CHF). Five patients responded to diuretic therapy and did not require any additional treatment. Four patients responded to vasodilation and/or digoxin with improvement in cardiac function. A clinically significant decrease in cardiac function was found in a small number of patients after induction chemotherapy and HDC with PBPCT. The majority of the patients tolerated this regimen without problems. Although there was a decline in LVEF as measured by radionuclide MUGA this did not prevent the majority of patients from proceeding with HDC. Bone Marrow Transplantation (2000).</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>10828864</pmid><doi>10.1038/sj.bmt.1702394</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Blood Bone marrow Bone marrow transplantation Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - radiotherapy Breast Neoplasms - therapy Cancer therapies Cardiac function Carmustine - administration & dosage Cells (biology) Chemotherapy Cisplatin Cisplatin - administration & dosage Combined Modality Therapy Complications Congestive heart failure Cyclophosphamide Cyclophosphamide - administration & dosage Digoxin Diuretics Doxorubicin Doxorubicin - administration & dosage Doxorubicin - adverse effects Drug Synergism Female Health risks Heart Failure - chemically induced Heart rate Hematopoietic Stem Cell Transplantation Hemopoiesis Humans Metastases Metastasis Middle Aged Neoplasm Metastasis Paclitaxel Paclitaxel - administration & dosage Paclitaxel - adverse effects Patients Peripheral blood Progenitor cells Radioisotopes Radiotherapy - adverse effects Risk Stem cell transplantation Stroke Volume Toxicity Transplantation Treatment Outcome Vasodilation Ventricle Ventricular Dysfunction, Left - chemically induced Ventricular Dysfunction, Left - etiology |
title | Cardiac sequelae of doxorubicin and paclitaxel as induction chemotherapy prior to high-dose chemotherapy and peripheral blood progenitor cell transplantation in women with high-risk primary or metastatic breast cancer |
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