Long-Term Follow-Up of the Response-Adapted Intergroup EORTC/LYSA/FIL H10 Trial for Localized Hodgkin Lymphoma
JCO The primary analysis of the Early positron emission tomography (ePET) Response-Adapted Treatment in localized Hodgkin Lymphoma H10 Trial demonstrated that in ePET-negative patients, the risk of relapse increased when involved-node radiotherapy (INRT) was omitted and that in ePET-positive patient...
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creator | Federico, Massimo Fortpied, Catherine Stepanishyna, Yana Gotti, Manuel van der Maazen, Richard Cristinelli, Caterina Re, Alessandro Plattel, Wouter Lazarovici, Julien Merli, Francesco Specht, Lena Schiano de Colella, Jean-Marc Hutchings, Martin Versari, Annibale Edeline, Véronique Stamatoulas, Aspasia Girinsky, Theodore Ricardi, Umberto Aleman, Berthe Meulemans, Bart Tonino, Sanne Raemaekers, John André, Marc |
description | JCO
The primary analysis of the Early positron emission tomography (ePET) Response-Adapted Treatment in localized Hodgkin Lymphoma H10 Trial demonstrated that in ePET-negative patients, the risk of relapse increased when involved-node radiotherapy (INRT) was omitted and that in ePET-positive patients, switching from doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) to bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPesc) significantly improved 5-year progression-free survival (PFS). Here, we report the final results of a preplanned analysis at a 10-year follow-up. In the favorable (F) ePET-negative group, the 10-year PFS rates were 98.8% versus 85.4% (hazard ratio [HR], 13.2; 95% CI, 3.1 to 55.8;
value for noninferiority = .9735; difference test
< .0001) in favor of ABVD + INRT; in the unfavorable (U) ePET-negative group, the 10-year PFS rates were 91.4% and 86.5% (HR, 1.52; 95% CI, 0.84 to 2.75;
value for noninferiority = .8577; difference test
= .1628). In ePET-positive patients, the difference in terms of PFS between standard ABVD and intensified BEACOPPesc was no longer statistically significant (HR, 0.67; 95% CI, 0.37 to 1.20;
= .1777). In conclusion, the present long-term analysis confirms that in ePET-negative patients, the omission of INRT is associated with lower 10-year PFS. Instead, in ePET-positive patients, no significant difference between standard and experimental arms emerged although intensification with BEACOPPesc was safe, with no increase in late adverse events, namely, second malignancies. |
doi_str_mv | 10.1200/JCO.23.01745 |
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The primary analysis of the Early positron emission tomography (ePET) Response-Adapted Treatment in localized Hodgkin Lymphoma H10 Trial demonstrated that in ePET-negative patients, the risk of relapse increased when involved-node radiotherapy (INRT) was omitted and that in ePET-positive patients, switching from doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) to bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPesc) significantly improved 5-year progression-free survival (PFS). Here, we report the final results of a preplanned analysis at a 10-year follow-up. In the favorable (F) ePET-negative group, the 10-year PFS rates were 98.8% versus 85.4% (hazard ratio [HR], 13.2; 95% CI, 3.1 to 55.8;
value for noninferiority = .9735; difference test
< .0001) in favor of ABVD + INRT; in the unfavorable (U) ePET-negative group, the 10-year PFS rates were 91.4% and 86.5% (HR, 1.52; 95% CI, 0.84 to 2.75;
value for noninferiority = .8577; difference test
= .1628). In ePET-positive patients, the difference in terms of PFS between standard ABVD and intensified BEACOPPesc was no longer statistically significant (HR, 0.67; 95% CI, 0.37 to 1.20;
= .1777). In conclusion, the present long-term analysis confirms that in ePET-negative patients, the omission of INRT is associated with lower 10-year PFS. Instead, in ePET-positive patients, no significant difference between standard and experimental arms emerged although intensification with BEACOPPesc was safe, with no increase in late adverse events, namely, second malignancies.</description><identifier>ISSN: 0732-183X</identifier><identifier>ISSN: 1527-7755</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.23.01745</identifier><identifier>PMID: 37967311</identifier><language>eng</language><publisher>United States: Wolters Kluwer Health</publisher><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Bleomycin ; CLINICAL TRIAL UPDATES ; Dacarbazine ; Disease-Free Survival ; Doxorubicin ; Follow-Up Studies ; Hodgkin Disease - diagnostic imaging ; Hodgkin Disease - drug therapy ; Hodgkin Disease - pathology ; Humans ; Neoplasm Recurrence, Local - drug therapy ; Prednisone ; Procarbazine - adverse effects ; Vinblastine ; Vincristine</subject><ispartof>Journal of clinical oncology, 2024-01, Vol.42 (1), p.19-25</ispartof><rights>2023 by American Society of Clinical Oncology 2023 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-993491fb4dedf3271ea3e0206674a8e199700da981d1724dfaed47bfb13ff3043</citedby><cites>FETCH-LOGICAL-c385t-993491fb4dedf3271ea3e0206674a8e199700da981d1724dfaed47bfb13ff3043</cites><orcidid>0000-0002-9889-3796 ; 0000-0003-0360-9172 ; 0000-0003-2306-6590 ; 0000-0003-4406-7621 ; 0000-0003-3873-1741 ; 0000-0002-0979-7883 ; 0000-0002-8675-2435 ; 0000-0002-7884-193X ; 0000-0002-6902-2190 ; 0000-0001-9923-4808 ; 0000-0003-1156-6395 ; 0000-0001-7101-810X ; 0000-0001-7321-5254 ; 0000-0002-5757-3569 ; 0000-0001-9828-9460 ; 0009-0000-3496-7445</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37967311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Federico, Massimo</creatorcontrib><creatorcontrib>Fortpied, Catherine</creatorcontrib><creatorcontrib>Stepanishyna, Yana</creatorcontrib><creatorcontrib>Gotti, Manuel</creatorcontrib><creatorcontrib>van der Maazen, Richard</creatorcontrib><creatorcontrib>Cristinelli, Caterina</creatorcontrib><creatorcontrib>Re, Alessandro</creatorcontrib><creatorcontrib>Plattel, Wouter</creatorcontrib><creatorcontrib>Lazarovici, Julien</creatorcontrib><creatorcontrib>Merli, Francesco</creatorcontrib><creatorcontrib>Specht, Lena</creatorcontrib><creatorcontrib>Schiano de Colella, Jean-Marc</creatorcontrib><creatorcontrib>Hutchings, Martin</creatorcontrib><creatorcontrib>Versari, Annibale</creatorcontrib><creatorcontrib>Edeline, Véronique</creatorcontrib><creatorcontrib>Stamatoulas, Aspasia</creatorcontrib><creatorcontrib>Girinsky, Theodore</creatorcontrib><creatorcontrib>Ricardi, Umberto</creatorcontrib><creatorcontrib>Aleman, Berthe</creatorcontrib><creatorcontrib>Meulemans, Bart</creatorcontrib><creatorcontrib>Tonino, Sanne</creatorcontrib><creatorcontrib>Raemaekers, John</creatorcontrib><creatorcontrib>André, Marc</creatorcontrib><title>Long-Term Follow-Up of the Response-Adapted Intergroup EORTC/LYSA/FIL H10 Trial for Localized Hodgkin Lymphoma</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>JCO
The primary analysis of the Early positron emission tomography (ePET) Response-Adapted Treatment in localized Hodgkin Lymphoma H10 Trial demonstrated that in ePET-negative patients, the risk of relapse increased when involved-node radiotherapy (INRT) was omitted and that in ePET-positive patients, switching from doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) to bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPesc) significantly improved 5-year progression-free survival (PFS). Here, we report the final results of a preplanned analysis at a 10-year follow-up. In the favorable (F) ePET-negative group, the 10-year PFS rates were 98.8% versus 85.4% (hazard ratio [HR], 13.2; 95% CI, 3.1 to 55.8;
value for noninferiority = .9735; difference test
< .0001) in favor of ABVD + INRT; in the unfavorable (U) ePET-negative group, the 10-year PFS rates were 91.4% and 86.5% (HR, 1.52; 95% CI, 0.84 to 2.75;
value for noninferiority = .8577; difference test
= .1628). In ePET-positive patients, the difference in terms of PFS between standard ABVD and intensified BEACOPPesc was no longer statistically significant (HR, 0.67; 95% CI, 0.37 to 1.20;
= .1777). In conclusion, the present long-term analysis confirms that in ePET-negative patients, the omission of INRT is associated with lower 10-year PFS. Instead, in ePET-positive patients, no significant difference between standard and experimental arms emerged although intensification with BEACOPPesc was safe, with no increase in late adverse events, namely, second malignancies.</description><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Bleomycin</subject><subject>CLINICAL TRIAL UPDATES</subject><subject>Dacarbazine</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin</subject><subject>Follow-Up Studies</subject><subject>Hodgkin Disease - diagnostic imaging</subject><subject>Hodgkin Disease - drug therapy</subject><subject>Hodgkin Disease - pathology</subject><subject>Humans</subject><subject>Neoplasm Recurrence, Local - drug therapy</subject><subject>Prednisone</subject><subject>Procarbazine - adverse effects</subject><subject>Vinblastine</subject><subject>Vincristine</subject><issn>0732-183X</issn><issn>1527-7755</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1v2zAMhoVhxZp1u-086LhDnYiSHVmnIQiaJoWBAF0KtCdBsajEm225ktOi-_Xz-oX2xAMfviT4EPIN2Bg4Y5OL-XrMxZiBTLMPZAQZl4mUWfaRjJgUPIFcXB-TzzH-ZgzSXGSfyLGQaioFwIi0hW93yQZDQxe-rv19ctVR72i_R3qJsfNtxGRmTdejpau2x7AL_tDRs_XlZj4pbn7NJotVQZfA6CZUpqbOB1r40tTV32Fi6e3uT9XS4qHp9r4xX8iRM3XEr8_1hFwtzjbzZVKsz1fzWZGUIs_6RCmRKnDb1KJ1gktAI5BxNp3K1OQISknGrFE5WJA8tc6gTeXWbUE4J1gqTsjPp9zusG3Qltj2wdS6C1VjwoP2ptLvO2211zt_p2H4GWNcDQk_nhOCvz1g7HVTxRLr2rToD1HzXDGZ5ZmEAT19QsvgYwzoXvcA0_8d6cGR5kI_Ohrw729ve4VfpIh_90-MAQ</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Federico, Massimo</creator><creator>Fortpied, Catherine</creator><creator>Stepanishyna, Yana</creator><creator>Gotti, Manuel</creator><creator>van der Maazen, Richard</creator><creator>Cristinelli, Caterina</creator><creator>Re, Alessandro</creator><creator>Plattel, Wouter</creator><creator>Lazarovici, Julien</creator><creator>Merli, Francesco</creator><creator>Specht, Lena</creator><creator>Schiano de Colella, Jean-Marc</creator><creator>Hutchings, Martin</creator><creator>Versari, Annibale</creator><creator>Edeline, Véronique</creator><creator>Stamatoulas, Aspasia</creator><creator>Girinsky, Theodore</creator><creator>Ricardi, Umberto</creator><creator>Aleman, Berthe</creator><creator>Meulemans, Bart</creator><creator>Tonino, Sanne</creator><creator>Raemaekers, John</creator><creator>André, Marc</creator><general>Wolters Kluwer Health</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9889-3796</orcidid><orcidid>https://orcid.org/0000-0003-0360-9172</orcidid><orcidid>https://orcid.org/0000-0003-2306-6590</orcidid><orcidid>https://orcid.org/0000-0003-4406-7621</orcidid><orcidid>https://orcid.org/0000-0003-3873-1741</orcidid><orcidid>https://orcid.org/0000-0002-0979-7883</orcidid><orcidid>https://orcid.org/0000-0002-8675-2435</orcidid><orcidid>https://orcid.org/0000-0002-7884-193X</orcidid><orcidid>https://orcid.org/0000-0002-6902-2190</orcidid><orcidid>https://orcid.org/0000-0001-9923-4808</orcidid><orcidid>https://orcid.org/0000-0003-1156-6395</orcidid><orcidid>https://orcid.org/0000-0001-7101-810X</orcidid><orcidid>https://orcid.org/0000-0001-7321-5254</orcidid><orcidid>https://orcid.org/0000-0002-5757-3569</orcidid><orcidid>https://orcid.org/0000-0001-9828-9460</orcidid><orcidid>https://orcid.org/0009-0000-3496-7445</orcidid></search><sort><creationdate>20240101</creationdate><title>Long-Term Follow-Up of the Response-Adapted Intergroup EORTC/LYSA/FIL H10 Trial for Localized Hodgkin Lymphoma</title><author>Federico, Massimo ; 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The primary analysis of the Early positron emission tomography (ePET) Response-Adapted Treatment in localized Hodgkin Lymphoma H10 Trial demonstrated that in ePET-negative patients, the risk of relapse increased when involved-node radiotherapy (INRT) was omitted and that in ePET-positive patients, switching from doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) to bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPPesc) significantly improved 5-year progression-free survival (PFS). Here, we report the final results of a preplanned analysis at a 10-year follow-up. In the favorable (F) ePET-negative group, the 10-year PFS rates were 98.8% versus 85.4% (hazard ratio [HR], 13.2; 95% CI, 3.1 to 55.8;
value for noninferiority = .9735; difference test
< .0001) in favor of ABVD + INRT; in the unfavorable (U) ePET-negative group, the 10-year PFS rates were 91.4% and 86.5% (HR, 1.52; 95% CI, 0.84 to 2.75;
value for noninferiority = .8577; difference test
= .1628). In ePET-positive patients, the difference in terms of PFS between standard ABVD and intensified BEACOPPesc was no longer statistically significant (HR, 0.67; 95% CI, 0.37 to 1.20;
= .1777). In conclusion, the present long-term analysis confirms that in ePET-negative patients, the omission of INRT is associated with lower 10-year PFS. Instead, in ePET-positive patients, no significant difference between standard and experimental arms emerged although intensification with BEACOPPesc was safe, with no increase in late adverse events, namely, second malignancies.</abstract><cop>United States</cop><pub>Wolters Kluwer Health</pub><pmid>37967311</pmid><doi>10.1200/JCO.23.01745</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9889-3796</orcidid><orcidid>https://orcid.org/0000-0003-0360-9172</orcidid><orcidid>https://orcid.org/0000-0003-2306-6590</orcidid><orcidid>https://orcid.org/0000-0003-4406-7621</orcidid><orcidid>https://orcid.org/0000-0003-3873-1741</orcidid><orcidid>https://orcid.org/0000-0002-0979-7883</orcidid><orcidid>https://orcid.org/0000-0002-8675-2435</orcidid><orcidid>https://orcid.org/0000-0002-7884-193X</orcidid><orcidid>https://orcid.org/0000-0002-6902-2190</orcidid><orcidid>https://orcid.org/0000-0001-9923-4808</orcidid><orcidid>https://orcid.org/0000-0003-1156-6395</orcidid><orcidid>https://orcid.org/0000-0001-7101-810X</orcidid><orcidid>https://orcid.org/0000-0001-7321-5254</orcidid><orcidid>https://orcid.org/0000-0002-5757-3569</orcidid><orcidid>https://orcid.org/0000-0001-9828-9460</orcidid><orcidid>https://orcid.org/0009-0000-3496-7445</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Antineoplastic Combined Chemotherapy Protocols - adverse effects Bleomycin CLINICAL TRIAL UPDATES Dacarbazine Disease-Free Survival Doxorubicin Follow-Up Studies Hodgkin Disease - diagnostic imaging Hodgkin Disease - drug therapy Hodgkin Disease - pathology Humans Neoplasm Recurrence, Local - drug therapy Prednisone Procarbazine - adverse effects Vinblastine Vincristine |
title | Long-Term Follow-Up of the Response-Adapted Intergroup EORTC/LYSA/FIL H10 Trial for Localized Hodgkin Lymphoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T03%3A36%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long-Term%20Follow-Up%20of%20the%20Response-Adapted%20Intergroup%20EORTC/LYSA/FIL%20H10%20Trial%20for%20Localized%20Hodgkin%20Lymphoma&rft.jtitle=Journal%20of%20clinical%20oncology&rft.au=Federico,%20Massimo&rft.date=2024-01-01&rft.volume=42&rft.issue=1&rft.spage=19&rft.epage=25&rft.pages=19-25&rft.issn=0732-183X&rft.eissn=1527-7755&rft_id=info:doi/10.1200/JCO.23.01745&rft_dat=%3Cproquest_pubme%3E2890758571%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2890758571&rft_id=info:pmid/37967311&rfr_iscdi=true |