Patient and physician preferences for first‐line treatment of classical Hodgkin lymphoma in Germany, France and the United Kingdom

Summary First‐line treatments for classical Hodgkin lymphoma (HL) include ABVD (adriamycin, bleomycin, vinblastine, dacarbazine) and BEACOPPescalated (escalated dose bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone). To further improve overall outcomes, posit...

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Veröffentlicht in:British journal of haematology 2019-01, Vol.184 (2), p.202-214
Hauptverfasser: Bröckelmann, Paul J., McMullen, Suzanne, Wilson, J Ben, Mueller, Kerstin, Goring, Sarah, Stamatoullas, Aspasia, Zagadailov, Erin, Gautam, Ashish, Huebner, Dirk, Dalal, Mehul, Illidge, Tim
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container_end_page 214
container_issue 2
container_start_page 202
container_title British journal of haematology
container_volume 184
creator Bröckelmann, Paul J.
McMullen, Suzanne
Wilson, J Ben
Mueller, Kerstin
Goring, Sarah
Stamatoullas, Aspasia
Zagadailov, Erin
Gautam, Ashish
Huebner, Dirk
Dalal, Mehul
Illidge, Tim
description Summary First‐line treatments for classical Hodgkin lymphoma (HL) include ABVD (adriamycin, bleomycin, vinblastine, dacarbazine) and BEACOPPescalated (escalated dose bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone). To further improve overall outcomes, positron emission tomography‐driven strategies and ABVD or BEACOPP variants incorporating the antibody‐drug conjugate brentuximab vedotin (BV) or anti‐PD1 antibodies are under investigation in advanced‐stage patients. The present study aimed to elicit preferences for attributes associated with ABVD, BEACOPPescalated and BV‐AVD (BV, adriamycin, vinblastine and dacarbazine) among patients and physicians. Cross‐sectional online discrete choice experiments were administered to HL patients (n = 381) and haematologists/oncologists (n = 357) in France, Germany and the United Kingdom. Included attributes were progression‐free survival (PFS), overall survival (OS), and the risk of neuropathy, lung damage, infertility and hospitalisation due to adverse events. Whereas 5‐year PFS and OS were the most important treatment attributes to patients, the relative importance of each attribute and preference weights for each level varied among physicians according to the description of the hypothetical patient for whom treatment was recommended. PFS and OS most strongly influenced physicians’ recommendations when considering young female patients who did not want children or young male patients. Infertility was more important to physicians’ treatment decision than PFS when considering young women with unknown fertility preferences, whereas hospitalisations due to adverse events played the largest role in treatment decisions for older patients.
doi_str_mv 10.1111/bjh.15566
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To further improve overall outcomes, positron emission tomography‐driven strategies and ABVD or BEACOPP variants incorporating the antibody‐drug conjugate brentuximab vedotin (BV) or anti‐PD1 antibodies are under investigation in advanced‐stage patients. The present study aimed to elicit preferences for attributes associated with ABVD, BEACOPPescalated and BV‐AVD (BV, adriamycin, vinblastine and dacarbazine) among patients and physicians. Cross‐sectional online discrete choice experiments were administered to HL patients (n = 381) and haematologists/oncologists (n = 357) in France, Germany and the United Kingdom. Included attributes were progression‐free survival (PFS), overall survival (OS), and the risk of neuropathy, lung damage, infertility and hospitalisation due to adverse events. Whereas 5‐year PFS and OS were the most important treatment attributes to patients, the relative importance of each attribute and preference weights for each level varied among physicians according to the description of the hypothetical patient for whom treatment was recommended. PFS and OS most strongly influenced physicians’ recommendations when considering young female patients who did not want children or young male patients. 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To further improve overall outcomes, positron emission tomography‐driven strategies and ABVD or BEACOPP variants incorporating the antibody‐drug conjugate brentuximab vedotin (BV) or anti‐PD1 antibodies are under investigation in advanced‐stage patients. The present study aimed to elicit preferences for attributes associated with ABVD, BEACOPPescalated and BV‐AVD (BV, adriamycin, vinblastine and dacarbazine) among patients and physicians. Cross‐sectional online discrete choice experiments were administered to HL patients (n = 381) and haematologists/oncologists (n = 357) in France, Germany and the United Kingdom. Included attributes were progression‐free survival (PFS), overall survival (OS), and the risk of neuropathy, lung damage, infertility and hospitalisation due to adverse events. Whereas 5‐year PFS and OS were the most important treatment attributes to patients, the relative importance of each attribute and preference weights for each level varied among physicians according to the description of the hypothetical patient for whom treatment was recommended. PFS and OS most strongly influenced physicians’ recommendations when considering young female patients who did not want children or young male patients. Infertility was more important to physicians’ treatment decision than PFS when considering young women with unknown fertility preferences, whereas hospitalisations due to adverse events played the largest role in treatment decisions for older patients.</description><subject>ABVD</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>BEACOPP</subject><subject>Bleomycin</subject><subject>Bleomycin - administration &amp; dosage</subject><subject>Bleomycin - adverse effects</subject><subject>Children</subject><subject>Cross-Sectional Studies</subject><subject>Cyclophosphamide</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Cyclophosphamide - adverse effects</subject><subject>Dacarbazine</subject><subject>discrete choice experiment</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin - administration &amp; 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McMullen, Suzanne ; Wilson, J Ben ; Mueller, Kerstin ; Goring, Sarah ; Stamatoullas, Aspasia ; Zagadailov, Erin ; Gautam, Ashish ; Huebner, Dirk ; Dalal, Mehul ; Illidge, Tim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4436-8c7758b869954fa7b51aa815f3d543b67008e03fda506a6dc262b7603a34df4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>ABVD</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>BEACOPP</topic><topic>Bleomycin</topic><topic>Bleomycin - administration &amp; dosage</topic><topic>Bleomycin - adverse effects</topic><topic>Children</topic><topic>Cross-Sectional Studies</topic><topic>Cyclophosphamide</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>Cyclophosphamide - adverse effects</topic><topic>Dacarbazine</topic><topic>discrete choice experiment</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - administration &amp; 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dosage</topic><topic>Vinblastine - adverse effects</topic><topic>Vincristine</topic><topic>Vincristine - administration &amp; dosage</topic><topic>Vincristine - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bröckelmann, Paul J.</creatorcontrib><creatorcontrib>McMullen, Suzanne</creatorcontrib><creatorcontrib>Wilson, J Ben</creatorcontrib><creatorcontrib>Mueller, Kerstin</creatorcontrib><creatorcontrib>Goring, Sarah</creatorcontrib><creatorcontrib>Stamatoullas, Aspasia</creatorcontrib><creatorcontrib>Zagadailov, Erin</creatorcontrib><creatorcontrib>Gautam, Ashish</creatorcontrib><creatorcontrib>Huebner, Dirk</creatorcontrib><creatorcontrib>Dalal, Mehul</creatorcontrib><creatorcontrib>Illidge, Tim</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library (Open Access Collection)</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>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bröckelmann, Paul J.</au><au>McMullen, Suzanne</au><au>Wilson, J Ben</au><au>Mueller, Kerstin</au><au>Goring, Sarah</au><au>Stamatoullas, Aspasia</au><au>Zagadailov, Erin</au><au>Gautam, Ashish</au><au>Huebner, Dirk</au><au>Dalal, Mehul</au><au>Illidge, Tim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patient and physician preferences for first‐line treatment of classical Hodgkin lymphoma in Germany, France and the United Kingdom</atitle><jtitle>British journal of haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2019-01</date><risdate>2019</risdate><volume>184</volume><issue>2</issue><spage>202</spage><epage>214</epage><pages>202-214</pages><issn>0007-1048</issn><eissn>1365-2141</eissn><abstract>Summary First‐line treatments for classical Hodgkin lymphoma (HL) include ABVD (adriamycin, bleomycin, vinblastine, dacarbazine) and BEACOPPescalated (escalated dose bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone). To further improve overall outcomes, positron emission tomography‐driven strategies and ABVD or BEACOPP variants incorporating the antibody‐drug conjugate brentuximab vedotin (BV) or anti‐PD1 antibodies are under investigation in advanced‐stage patients. The present study aimed to elicit preferences for attributes associated with ABVD, BEACOPPescalated and BV‐AVD (BV, adriamycin, vinblastine and dacarbazine) among patients and physicians. Cross‐sectional online discrete choice experiments were administered to HL patients (n = 381) and haematologists/oncologists (n = 357) in France, Germany and the United Kingdom. Included attributes were progression‐free survival (PFS), overall survival (OS), and the risk of neuropathy, lung damage, infertility and hospitalisation due to adverse events. Whereas 5‐year PFS and OS were the most important treatment attributes to patients, the relative importance of each attribute and preference weights for each level varied among physicians according to the description of the hypothetical patient for whom treatment was recommended. PFS and OS most strongly influenced physicians’ recommendations when considering young female patients who did not want children or young male patients. Infertility was more important to physicians’ treatment decision than PFS when considering young women with unknown fertility preferences, whereas hospitalisations due to adverse events played the largest role in treatment decisions for older patients.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>30239982</pmid><doi>10.1111/bjh.15566</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-3315-4674</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Journals; Wiley Online Library (Open Access Collection)
subjects ABVD
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - adverse effects
BEACOPP
Bleomycin
Bleomycin - administration & dosage
Bleomycin - adverse effects
Children
Cross-Sectional Studies
Cyclophosphamide
Cyclophosphamide - administration & dosage
Cyclophosphamide - adverse effects
Dacarbazine
discrete choice experiment
Disease-Free Survival
Doxorubicin - administration & dosage
Doxorubicin - adverse effects
Etoposide
Female
Fertility
France - epidemiology
Germany - epidemiology
Haematological Malignancy
Hematology
Hodgkin Disease - drug therapy
Hodgkin Disease - mortality
Hodgkin lymphoma
Hodgkin's lymphoma
Humans
Infertility
Lungs
Lymphoma
Male
Medical personnel
Middle Aged
Monoclonal antibodies
Neuropathy
patient and physician preferences
Patient Preference
Patients
PD-1 protein
Physicians
Positron emission tomography
Practice Patterns, Physicians
Prednisone
Procarbazine
Procarbazine - administration & dosage
Procarbazine - adverse effects
Research Paper
Survival
Survival Rate
Targeted cancer therapy
United Kingdom - epidemiology
Vinblastine
Vinblastine - administration & dosage
Vinblastine - adverse effects
Vincristine
Vincristine - administration & dosage
Vincristine - adverse effects
title Patient and physician preferences for first‐line treatment of classical Hodgkin lymphoma in Germany, France and the United Kingdom
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