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Randomized phase II clinical trial of adriamycin, methotrexate, and actinomycin‐d in advanced measurable pancreatic carcinoma. A gastrointestinal tumor study group report
Sixty‐six patients with advanced pancreatic carcinoma were randomized to receive single agent chemotherapy with either adriamycin, methotrexate, or actinomycin‐D using conventional dose, route and schedule of administration. All patients had measurable lesions which were used for objective assessmen...
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Published in: | Cancer 1978-07, Vol.42 (1), p.19-22 |
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creator | Schein, Philip S. Lavin, Philip T. Moertel, Charles G. Frytak, Stephen Hahn, Richard G. O'Connell, Michael J. Reitemeier, Richard J. Rubin, Joseph Schutt, Allen J. Weiland, Louis H. Kalser, M. Barkin, J. Lessner, H. Mann‐Kaplan, R. Redlhammer, D. Silverman, M. Troner, M. Douglass, H. O. Milliron, S. Lokich, J. Brooks, J. Chaffe, J. Like, A. Zamcheck, N. Ramming, K. Bateman, J. Spiro, H. Livstone, E. Knowlton, A. |
description | Sixty‐six patients with advanced pancreatic carcinoma were randomized to receive single agent chemotherapy with either adriamycin, methotrexate, or actinomycin‐D using conventional dose, route and schedule of administration. All patients had measurable lesions which were used for objective assessment of response. For adriamycin, 2 of 25 patients (8%) evidenced a partial response (2 of 15 (13%) previously untreated patients). One of 25 patients treated with methotrexate and one of 28 who received actinomycin‐D responded. The duration of responses ranged from 43–64 days for those patients with no chemotherapy prior to study entry. The median survival of patients who received adriamycin as initial treatment was 12 weeks compared to 8 weeks for methotrexate and 6 weeks for actinomycin‐D therapy. |
doi_str_mv | 10.1002/1097-0142(197807)42:1<19::AID-CNCR2820420103>3.0.CO;2-4 |
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A gastrointestinal tumor study group report</title><source>EZB Electronic Journals Library</source><creator>Schein, Philip S. ; Lavin, Philip T. ; Moertel, Charles G. ; Frytak, Stephen ; Hahn, Richard G. ; O'Connell, Michael J. ; Reitemeier, Richard J. ; Rubin, Joseph ; Schutt, Allen J. ; Weiland, Louis H. ; Kalser, M. ; Barkin, J. ; Lessner, H. ; Mann‐Kaplan, R. ; Redlhammer, D. ; Silverman, M. ; Troner, M. ; Douglass, H. O. ; Milliron, S. ; Lokich, J. ; Brooks, J. ; Chaffe, J. ; Like, A. ; Zamcheck, N. ; Ramming, K. ; Bateman, J. ; Spiro, H. ; Livstone, E. ; Knowlton, A.</creator><creatorcontrib>Schein, Philip S. ; Lavin, Philip T. ; Moertel, Charles G. ; Frytak, Stephen ; Hahn, Richard G. ; O'Connell, Michael J. ; Reitemeier, Richard J. ; Rubin, Joseph ; Schutt, Allen J. ; Weiland, Louis H. ; Kalser, M. ; Barkin, J. ; Lessner, H. ; Mann‐Kaplan, R. ; Redlhammer, D. ; Silverman, M. ; Troner, M. ; Douglass, H. O. ; Milliron, S. ; Lokich, J. ; Brooks, J. ; Chaffe, J. ; Like, A. ; Zamcheck, N. ; Ramming, K. ; Bateman, J. ; Spiro, H. ; Livstone, E. ; Knowlton, A.</creatorcontrib><description>Sixty‐six patients with advanced pancreatic carcinoma were randomized to receive single agent chemotherapy with either adriamycin, methotrexate, or actinomycin‐D using conventional dose, route and schedule of administration. All patients had measurable lesions which were used for objective assessment of response. For adriamycin, 2 of 25 patients (8%) evidenced a partial response (2 of 15 (13%) previously untreated patients). One of 25 patients treated with methotrexate and one of 28 who received actinomycin‐D responded. The duration of responses ranged from 43–64 days for those patients with no chemotherapy prior to study entry. The median survival of patients who received adriamycin as initial treatment was 12 weeks compared to 8 weeks for methotrexate and 6 weeks for actinomycin‐D therapy.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(197807)42:1<19::AID-CNCR2820420103>3.0.CO;2-4</identifier><identifier>PMID: 352505</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Bone Marrow - drug effects ; Clinical Trials as Topic ; Dactinomycin - adverse effects ; Dactinomycin - therapeutic use ; Doxorubicin - adverse effects ; Doxorubicin - therapeutic use ; Drug Evaluation ; Female ; Humans ; Male ; Methotrexate - adverse effects ; Methotrexate - therapeutic use ; Middle Aged ; Pancreatic Neoplasms - drug therapy ; Remission, Spontaneous ; Time Factors</subject><ispartof>Cancer, 1978-07, Vol.42 (1), p.19-22</ispartof><rights>Copyright © 1978 American Cancer Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/352505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schein, Philip S.</creatorcontrib><creatorcontrib>Lavin, Philip T.</creatorcontrib><creatorcontrib>Moertel, Charles G.</creatorcontrib><creatorcontrib>Frytak, Stephen</creatorcontrib><creatorcontrib>Hahn, Richard G.</creatorcontrib><creatorcontrib>O'Connell, Michael J.</creatorcontrib><creatorcontrib>Reitemeier, Richard J.</creatorcontrib><creatorcontrib>Rubin, Joseph</creatorcontrib><creatorcontrib>Schutt, Allen J.</creatorcontrib><creatorcontrib>Weiland, Louis H.</creatorcontrib><creatorcontrib>Kalser, M.</creatorcontrib><creatorcontrib>Barkin, J.</creatorcontrib><creatorcontrib>Lessner, H.</creatorcontrib><creatorcontrib>Mann‐Kaplan, R.</creatorcontrib><creatorcontrib>Redlhammer, D.</creatorcontrib><creatorcontrib>Silverman, M.</creatorcontrib><creatorcontrib>Troner, M.</creatorcontrib><creatorcontrib>Douglass, H. O.</creatorcontrib><creatorcontrib>Milliron, S.</creatorcontrib><creatorcontrib>Lokich, J.</creatorcontrib><creatorcontrib>Brooks, J.</creatorcontrib><creatorcontrib>Chaffe, J.</creatorcontrib><creatorcontrib>Like, A.</creatorcontrib><creatorcontrib>Zamcheck, N.</creatorcontrib><creatorcontrib>Ramming, K.</creatorcontrib><creatorcontrib>Bateman, J.</creatorcontrib><creatorcontrib>Spiro, H.</creatorcontrib><creatorcontrib>Livstone, E.</creatorcontrib><creatorcontrib>Knowlton, A.</creatorcontrib><title>Randomized phase II clinical trial of adriamycin, methotrexate, and actinomycin‐d in advanced measurable pancreatic carcinoma. A gastrointestinal tumor study group report</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Sixty‐six patients with advanced pancreatic carcinoma were randomized to receive single agent chemotherapy with either adriamycin, methotrexate, or actinomycin‐D using conventional dose, route and schedule of administration. All patients had measurable lesions which were used for objective assessment of response. For adriamycin, 2 of 25 patients (8%) evidenced a partial response (2 of 15 (13%) previously untreated patients). One of 25 patients treated with methotrexate and one of 28 who received actinomycin‐D responded. The duration of responses ranged from 43–64 days for those patients with no chemotherapy prior to study entry. The median survival of patients who received adriamycin as initial treatment was 12 weeks compared to 8 weeks for methotrexate and 6 weeks for actinomycin‐D therapy.</description><subject>Adult</subject><subject>Aged</subject><subject>Bone Marrow - drug effects</subject><subject>Clinical Trials as Topic</subject><subject>Dactinomycin - adverse effects</subject><subject>Dactinomycin - therapeutic use</subject><subject>Doxorubicin - adverse effects</subject><subject>Doxorubicin - therapeutic use</subject><subject>Drug Evaluation</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Methotrexate - adverse effects</subject><subject>Methotrexate - therapeutic use</subject><subject>Middle Aged</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Remission, Spontaneous</subject><subject>Time Factors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><recordid>eNpdUdtu1DAUtBC3pfAHPPgRpGY5tpNNsiDQKrSwUsVKFUi8Wb6ctEa5yXFol6d-Ah_CV_VLcFhUCV7s8RnNWGeGkHcMlgyAv2JQ5gmwlL9gZV5A_jLla_aGlev1Zvs-qT5V57zgkHJgIN6KJSyr3WuepPfI4k55nywAoEiyVHx9TJ6M47f4zHkmHpGHIuMZZAvy61x1tm_dD7R0uFQj0u2WmsZ1zqiGBu_i2ddU2YjavXHdMW0xXPbB47UKeEyjnCoTXNf_oW9vflrquij4rjoTTVtU4-SVbpAOceJRBWeoUd7MErWkG3qhxuB71wUco8_87dT2no5hsnt64ftpoB6H3oen5EGtmhGf_b2PyJfTk8_Vx-Rs92Fbbc6SgTMmEltnRV5zxDLjrMgLgxyVjntrWOncrrIUdSpMAaK2uS11zUvMeQkro7MVohZH5PnBd5h0i1YO3rXK7-UhtEjrA33lGtzfsQzk3Jyc85dz_vLQnJxRxDIWJ_8tTgoJstpJLtP_GPEbVRuYCg</recordid><startdate>197807</startdate><enddate>197807</enddate><creator>Schein, Philip S.</creator><creator>Lavin, Philip T.</creator><creator>Moertel, Charles G.</creator><creator>Frytak, Stephen</creator><creator>Hahn, Richard G.</creator><creator>O'Connell, Michael J.</creator><creator>Reitemeier, Richard J.</creator><creator>Rubin, Joseph</creator><creator>Schutt, Allen J.</creator><creator>Weiland, Louis H.</creator><creator>Kalser, M.</creator><creator>Barkin, J.</creator><creator>Lessner, H.</creator><creator>Mann‐Kaplan, R.</creator><creator>Redlhammer, D.</creator><creator>Silverman, M.</creator><creator>Troner, M.</creator><creator>Douglass, H. 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O.</au><au>Milliron, S.</au><au>Lokich, J.</au><au>Brooks, J.</au><au>Chaffe, J.</au><au>Like, A.</au><au>Zamcheck, N.</au><au>Ramming, K.</au><au>Bateman, J.</au><au>Spiro, H.</au><au>Livstone, E.</au><au>Knowlton, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized phase II clinical trial of adriamycin, methotrexate, and actinomycin‐d in advanced measurable pancreatic carcinoma. A gastrointestinal tumor study group report</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1978-07</date><risdate>1978</risdate><volume>42</volume><issue>1</issue><spage>19</spage><epage>22</epage><pages>19-22</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>Sixty‐six patients with advanced pancreatic carcinoma were randomized to receive single agent chemotherapy with either adriamycin, methotrexate, or actinomycin‐D using conventional dose, route and schedule of administration. All patients had measurable lesions which were used for objective assessment of response. For adriamycin, 2 of 25 patients (8%) evidenced a partial response (2 of 15 (13%) previously untreated patients). One of 25 patients treated with methotrexate and one of 28 who received actinomycin‐D responded. The duration of responses ranged from 43–64 days for those patients with no chemotherapy prior to study entry. The median survival of patients who received adriamycin as initial treatment was 12 weeks compared to 8 weeks for methotrexate and 6 weeks for actinomycin‐D therapy.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>352505</pmid><doi>10.1002/1097-0142(197807)42:1<19::AID-CNCR2820420103>3.0.CO;2-4</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Aged Bone Marrow - drug effects Clinical Trials as Topic Dactinomycin - adverse effects Dactinomycin - therapeutic use Doxorubicin - adverse effects Doxorubicin - therapeutic use Drug Evaluation Female Humans Male Methotrexate - adverse effects Methotrexate - therapeutic use Middle Aged Pancreatic Neoplasms - drug therapy Remission, Spontaneous Time Factors |
title | Randomized phase II clinical trial of adriamycin, methotrexate, and actinomycin‐d in advanced measurable pancreatic carcinoma. A gastrointestinal tumor study group report |
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