Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma
Background: In the National Cancer Institute of Canada Clinical Trials Group/Eastern Cooperative Oncology Group HD.6 trial, progression-free survival was better in patients randomized to therapy that included radiation, compared to doxorubicin (Adriamycin®), bleomycin, vinblastine and dacarbazine (A...
Gespeichert in:
Veröffentlicht in: | Annals of oncology 2007-10, Vol.18 (10), p.1680-1684 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1684 |
---|---|
container_issue | 10 |
container_start_page | 1680 |
container_title | Annals of oncology |
container_volume | 18 |
creator | Macdonald, D. A. Ding, K. Gospodarowicz, M. K. Wells, W. A. Pearcey, R. G. Connors, J. M. Winter, J. N. Horning, S. J. Djurfeldt, M. S. Shepherd, L. E. Meyer, R. M. |
description | Background: In the National Cancer Institute of Canada Clinical Trials Group/Eastern Cooperative Oncology Group HD.6 trial, progression-free survival was better in patients randomized to therapy that included radiation, compared to doxorubicin (Adriamycin®), bleomycin, vinblastine and dacarbazine (ABVD) alone. We now evaluate patterns of progression and subsequent outcomes of patients with progression. Patients and methods: After a median of 4.2 years, 33 patients have progressed. Two radiation oncologists determined whether sites of progression were confined within radiation fields. Freedom from second progression (FF2P) and freedom from second progression or death (FF2P/D) were compared. Results: Reviewers agreed for the extended (kappa = 0.87) and involved field (kappa = 1.0) analyses. Progression after ABVD alone was more frequently confined within both the extended (20/23 vs. 3/10; P = 0.002) and involved fields (16/23 vs. 2/10; P = 0.02). There was no difference in FF2P between groups [5-year estimate 99% (radiation) versus 96% (ABVD alone)] [hazard ratio (HR) = 3.14, 95% confidence interval (CI) 0.63–15.6; P = 0.14]; the 5-year estimates of FF2P/D were 94% in each group (HR = 1.04, 95% CI 0.41–2.63; P = 0.93). Conclusion: Treatment that includes radiation reduces the risk of progressive Hodgkin lymphoma in sites that receive this therapy, but we are unable to detect differences in FF2P or FF2P/D. |
doi_str_mv | 10.1093/annonc/mdm287 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68299837</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/annonc/mdm287</oup_id><sourcerecordid>68299837</sourcerecordid><originalsourceid>FETCH-LOGICAL-c489t-1fc11cf577534e839f821dc34544d0577a954f59d3107d1c4ea7f663b41930383</originalsourceid><addsrcrecordid>eNqF0UtrFTEUB_Agir29unQrQbC4GZvXZCbLWh9XKNiFinQT0jxu084k0ySD1g_g5zaXuVhw01XI4cdJzvkD8AKjtxgJeqxCiEEfj2YkffcIrHDLRdMjhh-DFRKENl1L2QE4zPkaIcQFEU_BAe56xhHuVuDPuSrFppBhdND4bFW2cEpxm2zOPgaogoFxLjqONkNf7zDVUhz9b2tgSV4NsNhcfNjCk3ff30M1xGChiwlOqngbSoY_fbmCgx99sabJRW0t3ESzvandhrtxuoqjegaeODVk-3x_rsG3jx--nm6asy-fPp-enDWa9aI02GmMtWu73VC2p8L1BBtNWcuYQbWsRMtcKwzFqDNYM6s6xzm9ZFhQRHu6BkdL3zri7Vz_LUeftR0GFWycs-Q9EaKn3YOQ1GViLHbw1X_wOs4p1CEkFpwzRgWvqFmQTjHnZJ2ckh9VupMYyV2McolRLjFW_3LfdL4crbnX-9wqeL0HKms1uJqJ9vneCYIJqktagzeLi_P04Jv7P_pc7K9_WKUbyTvatXLz40IyQjEj5xcS0b9Jl8SY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>196644396</pqid></control><display><type>article</type><title>Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Macdonald, D. A. ; Ding, K. ; Gospodarowicz, M. K. ; Wells, W. A. ; Pearcey, R. G. ; Connors, J. M. ; Winter, J. N. ; Horning, S. J. ; Djurfeldt, M. S. ; Shepherd, L. E. ; Meyer, R. M.</creator><creatorcontrib>Macdonald, D. A. ; Ding, K. ; Gospodarowicz, M. K. ; Wells, W. A. ; Pearcey, R. G. ; Connors, J. M. ; Winter, J. N. ; Horning, S. J. ; Djurfeldt, M. S. ; Shepherd, L. E. ; Meyer, R. M.</creatorcontrib><description>Background: In the National Cancer Institute of Canada Clinical Trials Group/Eastern Cooperative Oncology Group HD.6 trial, progression-free survival was better in patients randomized to therapy that included radiation, compared to doxorubicin (Adriamycin®), bleomycin, vinblastine and dacarbazine (ABVD) alone. We now evaluate patterns of progression and subsequent outcomes of patients with progression. Patients and methods: After a median of 4.2 years, 33 patients have progressed. Two radiation oncologists determined whether sites of progression were confined within radiation fields. Freedom from second progression (FF2P) and freedom from second progression or death (FF2P/D) were compared. Results: Reviewers agreed for the extended (kappa = 0.87) and involved field (kappa = 1.0) analyses. Progression after ABVD alone was more frequently confined within both the extended (20/23 vs. 3/10; P = 0.002) and involved fields (16/23 vs. 2/10; P = 0.02). There was no difference in FF2P between groups [5-year estimate 99% (radiation) versus 96% (ABVD alone)] [hazard ratio (HR) = 3.14, 95% confidence interval (CI) 0.63–15.6; P = 0.14]; the 5-year estimates of FF2P/D were 94% in each group (HR = 1.04, 95% CI 0.41–2.63; P = 0.93). Conclusion: Treatment that includes radiation reduces the risk of progressive Hodgkin lymphoma in sites that receive this therapy, but we are unable to detect differences in FF2P or FF2P/D.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1093/annonc/mdm287</identifier><identifier>PMID: 17846017</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Bleomycin - therapeutic use ; chemotherapy ; Dacarbazine - therapeutic use ; Disease Progression ; Doxorubicin - therapeutic use ; Hematologic and hematopoietic diseases ; Hodgkin ; Hodgkin Disease - drug therapy ; Hodgkin Disease - mortality ; Hodgkin Disease - pathology ; Humans ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; limited-stage ; Medical sciences ; Neoplasm Staging ; Pharmacology. Drug treatments ; relapse ; Treatment Outcome ; Vinblastine - therapeutic use</subject><ispartof>Annals of oncology, 2007-10, Vol.18 (10), p.1680-1684</ispartof><rights>2007 European Society for Medical Oncology 2007</rights><rights>2007 INIST-CNRS</rights><rights>2007 European Society for Medical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-1fc11cf577534e839f821dc34544d0577a954f59d3107d1c4ea7f663b41930383</citedby><cites>FETCH-LOGICAL-c489t-1fc11cf577534e839f821dc34544d0577a954f59d3107d1c4ea7f663b41930383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19212075$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17846017$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Macdonald, D. A.</creatorcontrib><creatorcontrib>Ding, K.</creatorcontrib><creatorcontrib>Gospodarowicz, M. K.</creatorcontrib><creatorcontrib>Wells, W. A.</creatorcontrib><creatorcontrib>Pearcey, R. G.</creatorcontrib><creatorcontrib>Connors, J. M.</creatorcontrib><creatorcontrib>Winter, J. N.</creatorcontrib><creatorcontrib>Horning, S. J.</creatorcontrib><creatorcontrib>Djurfeldt, M. S.</creatorcontrib><creatorcontrib>Shepherd, L. E.</creatorcontrib><creatorcontrib>Meyer, R. M.</creatorcontrib><title>Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>Background: In the National Cancer Institute of Canada Clinical Trials Group/Eastern Cooperative Oncology Group HD.6 trial, progression-free survival was better in patients randomized to therapy that included radiation, compared to doxorubicin (Adriamycin®), bleomycin, vinblastine and dacarbazine (ABVD) alone. We now evaluate patterns of progression and subsequent outcomes of patients with progression. Patients and methods: After a median of 4.2 years, 33 patients have progressed. Two radiation oncologists determined whether sites of progression were confined within radiation fields. Freedom from second progression (FF2P) and freedom from second progression or death (FF2P/D) were compared. Results: Reviewers agreed for the extended (kappa = 0.87) and involved field (kappa = 1.0) analyses. Progression after ABVD alone was more frequently confined within both the extended (20/23 vs. 3/10; P = 0.002) and involved fields (16/23 vs. 2/10; P = 0.02). There was no difference in FF2P between groups [5-year estimate 99% (radiation) versus 96% (ABVD alone)] [hazard ratio (HR) = 3.14, 95% confidence interval (CI) 0.63–15.6; P = 0.14]; the 5-year estimates of FF2P/D were 94% in each group (HR = 1.04, 95% CI 0.41–2.63; P = 0.93). Conclusion: Treatment that includes radiation reduces the risk of progressive Hodgkin lymphoma in sites that receive this therapy, but we are unable to detect differences in FF2P or FF2P/D.</description><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bleomycin - therapeutic use</subject><subject>chemotherapy</subject><subject>Dacarbazine - therapeutic use</subject><subject>Disease Progression</subject><subject>Doxorubicin - therapeutic use</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hodgkin</subject><subject>Hodgkin Disease - drug therapy</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - pathology</subject><subject>Humans</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>limited-stage</subject><subject>Medical sciences</subject><subject>Neoplasm Staging</subject><subject>Pharmacology. Drug treatments</subject><subject>relapse</subject><subject>Treatment Outcome</subject><subject>Vinblastine - therapeutic use</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UtrFTEUB_Agir29unQrQbC4GZvXZCbLWh9XKNiFinQT0jxu084k0ySD1g_g5zaXuVhw01XI4cdJzvkD8AKjtxgJeqxCiEEfj2YkffcIrHDLRdMjhh-DFRKENl1L2QE4zPkaIcQFEU_BAe56xhHuVuDPuSrFppBhdND4bFW2cEpxm2zOPgaogoFxLjqONkNf7zDVUhz9b2tgSV4NsNhcfNjCk3ff30M1xGChiwlOqngbSoY_fbmCgx99sabJRW0t3ESzvandhrtxuoqjegaeODVk-3x_rsG3jx--nm6asy-fPp-enDWa9aI02GmMtWu73VC2p8L1BBtNWcuYQbWsRMtcKwzFqDNYM6s6xzm9ZFhQRHu6BkdL3zri7Vz_LUeftR0GFWycs-Q9EaKn3YOQ1GViLHbw1X_wOs4p1CEkFpwzRgWvqFmQTjHnZJ2ckh9VupMYyV2McolRLjFW_3LfdL4crbnX-9wqeL0HKms1uJqJ9vneCYIJqktagzeLi_P04Jv7P_pc7K9_WKUbyTvatXLz40IyQjEj5xcS0b9Jl8SY</recordid><startdate>20071001</startdate><enddate>20071001</enddate><creator>Macdonald, D. A.</creator><creator>Ding, K.</creator><creator>Gospodarowicz, M. K.</creator><creator>Wells, W. A.</creator><creator>Pearcey, R. G.</creator><creator>Connors, J. M.</creator><creator>Winter, J. N.</creator><creator>Horning, S. J.</creator><creator>Djurfeldt, M. S.</creator><creator>Shepherd, L. E.</creator><creator>Meyer, R. M.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20071001</creationdate><title>Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma</title><author>Macdonald, D. A. ; Ding, K. ; Gospodarowicz, M. K. ; Wells, W. A. ; Pearcey, R. G. ; Connors, J. M. ; Winter, J. N. ; Horning, S. J. ; Djurfeldt, M. S. ; Shepherd, L. E. ; Meyer, R. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-1fc11cf577534e839f821dc34544d0577a954f59d3107d1c4ea7f663b41930383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bleomycin - therapeutic use</topic><topic>chemotherapy</topic><topic>Dacarbazine - therapeutic use</topic><topic>Disease Progression</topic><topic>Doxorubicin - therapeutic use</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hodgkin</topic><topic>Hodgkin Disease - drug therapy</topic><topic>Hodgkin Disease - mortality</topic><topic>Hodgkin Disease - pathology</topic><topic>Humans</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>limited-stage</topic><topic>Medical sciences</topic><topic>Neoplasm Staging</topic><topic>Pharmacology. Drug treatments</topic><topic>relapse</topic><topic>Treatment Outcome</topic><topic>Vinblastine - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Macdonald, D. A.</creatorcontrib><creatorcontrib>Ding, K.</creatorcontrib><creatorcontrib>Gospodarowicz, M. K.</creatorcontrib><creatorcontrib>Wells, W. A.</creatorcontrib><creatorcontrib>Pearcey, R. G.</creatorcontrib><creatorcontrib>Connors, J. M.</creatorcontrib><creatorcontrib>Winter, J. N.</creatorcontrib><creatorcontrib>Horning, S. J.</creatorcontrib><creatorcontrib>Djurfeldt, M. S.</creatorcontrib><creatorcontrib>Shepherd, L. E.</creatorcontrib><creatorcontrib>Meyer, R. M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Macdonald, D. A.</au><au>Ding, K.</au><au>Gospodarowicz, M. K.</au><au>Wells, W. A.</au><au>Pearcey, R. G.</au><au>Connors, J. M.</au><au>Winter, J. N.</au><au>Horning, S. J.</au><au>Djurfeldt, M. S.</au><au>Shepherd, L. E.</au><au>Meyer, R. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>2007-10-01</date><risdate>2007</risdate><volume>18</volume><issue>10</issue><spage>1680</spage><epage>1684</epage><pages>1680-1684</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>Background: In the National Cancer Institute of Canada Clinical Trials Group/Eastern Cooperative Oncology Group HD.6 trial, progression-free survival was better in patients randomized to therapy that included radiation, compared to doxorubicin (Adriamycin®), bleomycin, vinblastine and dacarbazine (ABVD) alone. We now evaluate patterns of progression and subsequent outcomes of patients with progression. Patients and methods: After a median of 4.2 years, 33 patients have progressed. Two radiation oncologists determined whether sites of progression were confined within radiation fields. Freedom from second progression (FF2P) and freedom from second progression or death (FF2P/D) were compared. Results: Reviewers agreed for the extended (kappa = 0.87) and involved field (kappa = 1.0) analyses. Progression after ABVD alone was more frequently confined within both the extended (20/23 vs. 3/10; P = 0.002) and involved fields (16/23 vs. 2/10; P = 0.02). There was no difference in FF2P between groups [5-year estimate 99% (radiation) versus 96% (ABVD alone)] [hazard ratio (HR) = 3.14, 95% confidence interval (CI) 0.63–15.6; P = 0.14]; the 5-year estimates of FF2P/D were 94% in each group (HR = 1.04, 95% CI 0.41–2.63; P = 0.93). Conclusion: Treatment that includes radiation reduces the risk of progressive Hodgkin lymphoma in sites that receive this therapy, but we are unable to detect differences in FF2P or FF2P/D.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>17846017</pmid><doi>10.1093/annonc/mdm287</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0923-7534 |
ispartof | Annals of oncology, 2007-10, Vol.18 (10), p.1680-1684 |
issn | 0923-7534 1569-8041 |
language | eng |
recordid | cdi_proquest_miscellaneous_68299837 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Antineoplastic agents Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Bleomycin - therapeutic use chemotherapy Dacarbazine - therapeutic use Disease Progression Doxorubicin - therapeutic use Hematologic and hematopoietic diseases Hodgkin Hodgkin Disease - drug therapy Hodgkin Disease - mortality Hodgkin Disease - pathology Humans Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis limited-stage Medical sciences Neoplasm Staging Pharmacology. Drug treatments relapse Treatment Outcome Vinblastine - therapeutic use |
title | Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T20%3A29%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Patterns%20of%20disease%20progression%20and%20outcomes%20in%20a%20randomized%20trial%20testing%20ABVD%20alone%20for%20patients%20with%20limited-stage%20Hodgkin%20lymphoma&rft.jtitle=Annals%20of%20oncology&rft.au=Macdonald,%20D.%20A.&rft.date=2007-10-01&rft.volume=18&rft.issue=10&rft.spage=1680&rft.epage=1684&rft.pages=1680-1684&rft.issn=0923-7534&rft.eissn=1569-8041&rft_id=info:doi/10.1093/annonc/mdm287&rft_dat=%3Cproquest_cross%3E68299837%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=196644396&rft_id=info:pmid/17846017&rft_oup_id=10.1093/annonc/mdm287&rfr_iscdi=true |