Combined cytostatic chemotherapy of advanced non-small-cell bronchial carcinoma with doxorubicin and ifosfamide
Fifty-three patients with inoperable non-small cell bronchial carcinoma were treated at four-weekly intervals with two cytostatic drugs, doxorubicin (50 mg/m2 on day 1) and ifosfamide (2000 mg/m2 on days 1-3). To avoid urotoxicity of ifosfamide, mesna, a uroprotective drug, was additionally given in...
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Veröffentlicht in: | Deutsche medizinische Wochenschrift 1983-05, Vol.108 (21), p.810 |
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description | Fifty-three patients with inoperable non-small cell bronchial carcinoma were treated at four-weekly intervals with two cytostatic drugs, doxorubicin (50 mg/m2 on day 1) and ifosfamide (2000 mg/m2 on days 1-3). To avoid urotoxicity of ifosfamide, mesna, a uroprotective drug, was additionally given intravenously at a dose of three times 400 mg/m2 on days 1-3. All diagnoses had been histologically and/or cytologically confirmed. Adenocarcinoma was present in 22, large-cell undifferentiated carcinoma in 18, and squamous-cell carcinoma in 13. Distant metastases were present in 46, seven had a regionally localized tumour growth. There were one complete and 20 partial remissions (response rate 40%). Among a further 19 patients temporary growth arrest was registered. The remissions occurred in seven with adenocarcinoma, nine with large-cell carcinoma and five with squamous-cell carcinoma. Median remission was 8.3 months, mean survival time 10.5 months. Patients without response survived a mean of 5.5 months, patients with tumour progression for 1.3 months (Kaplan-Meier method). Most prominent among side-effects were cardiotoxicity and infection during the leukopenic phase. Urotoxicity was minor, due to treatment with mesna. The results suggest that doxorubicin and ifosfamide in combination can be considered an effective means, with acceptable toxicity, of treating advanced non-small cell bronchial carcinoma. |
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To avoid urotoxicity of ifosfamide, mesna, a uroprotective drug, was additionally given intravenously at a dose of three times 400 mg/m2 on days 1-3. All diagnoses had been histologically and/or cytologically confirmed. Adenocarcinoma was present in 22, large-cell undifferentiated carcinoma in 18, and squamous-cell carcinoma in 13. Distant metastases were present in 46, seven had a regionally localized tumour growth. There were one complete and 20 partial remissions (response rate 40%). Among a further 19 patients temporary growth arrest was registered. The remissions occurred in seven with adenocarcinoma, nine with large-cell carcinoma and five with squamous-cell carcinoma. Median remission was 8.3 months, mean survival time 10.5 months. Patients without response survived a mean of 5.5 months, patients with tumour progression for 1.3 months (Kaplan-Meier method). Most prominent among side-effects were cardiotoxicity and infection during the leukopenic phase. Urotoxicity was minor, due to treatment with mesna. The results suggest that doxorubicin and ifosfamide in combination can be considered an effective means, with acceptable toxicity, of treating advanced non-small cell bronchial carcinoma.</description><identifier>ISSN: 0012-0472</identifier><identifier>PMID: 6851871</identifier><language>ger</language><publisher>Germany</publisher><subject>Adenocarcinoma - drug therapy ; Adenocarcinoma - pathology ; Adult ; Aged ; Carcinoma - drug therapy ; Carcinoma - pathology ; Carcinoma, Bronchogenic - drug therapy ; Carcinoma, Bronchogenic - pathology ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - pathology ; Cyclophosphamide - analogs & derivatives ; Doxorubicin - adverse effects ; Doxorubicin - therapeutic use ; Drug Therapy, Combination ; Female ; Humans ; Ifosfamide - adverse effects ; Ifosfamide - therapeutic use ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Male ; Middle Aged ; Neoplasm Metastasis</subject><ispartof>Deutsche medizinische Wochenschrift, 1983-05, Vol.108 (21), p.810</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6851871$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matthiessen, W</creatorcontrib><creatorcontrib>Stempinski, E</creatorcontrib><creatorcontrib>Göbel, D</creatorcontrib><creatorcontrib>Thalmann, U</creatorcontrib><title>Combined cytostatic chemotherapy of advanced non-small-cell bronchial carcinoma with doxorubicin and ifosfamide</title><title>Deutsche medizinische Wochenschrift</title><addtitle>Dtsch Med Wochenschr</addtitle><description>Fifty-three patients with inoperable non-small cell bronchial carcinoma were treated at four-weekly intervals with two cytostatic drugs, doxorubicin (50 mg/m2 on day 1) and ifosfamide (2000 mg/m2 on days 1-3). To avoid urotoxicity of ifosfamide, mesna, a uroprotective drug, was additionally given intravenously at a dose of three times 400 mg/m2 on days 1-3. All diagnoses had been histologically and/or cytologically confirmed. Adenocarcinoma was present in 22, large-cell undifferentiated carcinoma in 18, and squamous-cell carcinoma in 13. Distant metastases were present in 46, seven had a regionally localized tumour growth. There were one complete and 20 partial remissions (response rate 40%). Among a further 19 patients temporary growth arrest was registered. The remissions occurred in seven with adenocarcinoma, nine with large-cell carcinoma and five with squamous-cell carcinoma. Median remission was 8.3 months, mean survival time 10.5 months. Patients without response survived a mean of 5.5 months, patients with tumour progression for 1.3 months (Kaplan-Meier method). Most prominent among side-effects were cardiotoxicity and infection during the leukopenic phase. Urotoxicity was minor, due to treatment with mesna. The results suggest that doxorubicin and ifosfamide in combination can be considered an effective means, with acceptable toxicity, of treating advanced non-small cell bronchial carcinoma.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Carcinoma - drug therapy</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma, Bronchogenic - drug therapy</subject><subject>Carcinoma, Bronchogenic - pathology</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cyclophosphamide - analogs & derivatives</subject><subject>Doxorubicin - adverse effects</subject><subject>Doxorubicin - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Humans</subject><subject>Ifosfamide - adverse effects</subject><subject>Ifosfamide - therapeutic use</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><issn>0012-0472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotj8tqwzAURLVoSdO0n1DQDwgky5bsZTF9QSCb7MP1lYRVLMlITtv8fV2a1XCGw8DckC3nomK81tUduS_l8w87WW_IRrWNaLXYktSnMPhoDcXLksoCi0eKow1pGW2G-UKTo2C-IOLqxBRZCTBNDO000SGniKOHiSJk9DEFoN9-GalJPymfB792FKKh3qXiIHhjH8itg6nYx2vuyPH15di_s_3h7aN_3rO5kYKpzrba6qGFCi22oKVwSktnHBfOroZSq4BoXG1QOKFEXdeGV9p1vOFSyR15-p-dz0Ow5jRnHyBfTtff8hfaDlXK</recordid><startdate>19830527</startdate><enddate>19830527</enddate><creator>Matthiessen, W</creator><creator>Stempinski, E</creator><creator>Göbel, D</creator><creator>Thalmann, U</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19830527</creationdate><title>Combined cytostatic chemotherapy of advanced non-small-cell bronchial carcinoma with doxorubicin and ifosfamide</title><author>Matthiessen, W ; Stempinski, E ; Göbel, D ; Thalmann, U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p531-69e87e7b8a2cec8a731f673fdf01fe53166e87ccdf4dc1f161444d027f9050363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>ger</language><creationdate>1983</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Carcinoma - drug therapy</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma, Bronchogenic - drug therapy</topic><topic>Carcinoma, Bronchogenic - pathology</topic><topic>Carcinoma, Squamous Cell - drug therapy</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cyclophosphamide - analogs & derivatives</topic><topic>Doxorubicin - adverse effects</topic><topic>Doxorubicin - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Humans</topic><topic>Ifosfamide - adverse effects</topic><topic>Ifosfamide - therapeutic use</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Metastasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matthiessen, W</creatorcontrib><creatorcontrib>Stempinski, E</creatorcontrib><creatorcontrib>Göbel, D</creatorcontrib><creatorcontrib>Thalmann, U</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Deutsche medizinische Wochenschrift</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matthiessen, W</au><au>Stempinski, E</au><au>Göbel, D</au><au>Thalmann, U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined cytostatic chemotherapy of advanced non-small-cell bronchial carcinoma with doxorubicin and ifosfamide</atitle><jtitle>Deutsche medizinische Wochenschrift</jtitle><addtitle>Dtsch Med Wochenschr</addtitle><date>1983-05-27</date><risdate>1983</risdate><volume>108</volume><issue>21</issue><spage>810</spage><pages>810-</pages><issn>0012-0472</issn><abstract>Fifty-three patients with inoperable non-small cell bronchial carcinoma were treated at four-weekly intervals with two cytostatic drugs, doxorubicin (50 mg/m2 on day 1) and ifosfamide (2000 mg/m2 on days 1-3). To avoid urotoxicity of ifosfamide, mesna, a uroprotective drug, was additionally given intravenously at a dose of three times 400 mg/m2 on days 1-3. All diagnoses had been histologically and/or cytologically confirmed. Adenocarcinoma was present in 22, large-cell undifferentiated carcinoma in 18, and squamous-cell carcinoma in 13. Distant metastases were present in 46, seven had a regionally localized tumour growth. There were one complete and 20 partial remissions (response rate 40%). Among a further 19 patients temporary growth arrest was registered. The remissions occurred in seven with adenocarcinoma, nine with large-cell carcinoma and five with squamous-cell carcinoma. Median remission was 8.3 months, mean survival time 10.5 months. Patients without response survived a mean of 5.5 months, patients with tumour progression for 1.3 months (Kaplan-Meier method). Most prominent among side-effects were cardiotoxicity and infection during the leukopenic phase. Urotoxicity was minor, due to treatment with mesna. The results suggest that doxorubicin and ifosfamide in combination can be considered an effective means, with acceptable toxicity, of treating advanced non-small cell bronchial carcinoma.</abstract><cop>Germany</cop><pmid>6851871</pmid></addata></record> |
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subjects | Adenocarcinoma - drug therapy Adenocarcinoma - pathology Adult Aged Carcinoma - drug therapy Carcinoma - pathology Carcinoma, Bronchogenic - drug therapy Carcinoma, Bronchogenic - pathology Carcinoma, Squamous Cell - drug therapy Carcinoma, Squamous Cell - pathology Cyclophosphamide - analogs & derivatives Doxorubicin - adverse effects Doxorubicin - therapeutic use Drug Therapy, Combination Female Humans Ifosfamide - adverse effects Ifosfamide - therapeutic use Lung Neoplasms - drug therapy Lung Neoplasms - pathology Male Middle Aged Neoplasm Metastasis |
title | Combined cytostatic chemotherapy of advanced non-small-cell bronchial carcinoma with doxorubicin and ifosfamide |
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