A phase 2 study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma
The phase 2 CAVALLI (NCT02055820) study assessed efficacy and safety of venetoclax, a selective B-cell lymphoma-2 (Bcl-2) inhibitor, with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in first-line (1L) diffuse large B-cell lymphoma (DLBCL), including patients de...
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Veröffentlicht in: | Blood 2021-02, Vol.137 (5), p.600-609 |
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creator | Morschhauser, Franck Feugier, Pierre Flinn, Ian W. Gasiorowski, Robin Greil, Richard Illés, Árpád Johnson, Nathalie A. Larouche, Jean-François Lugtenburg, Pieternella J. Patti, Caterina Salles, Gilles A. Trněný, Marek de Vos, Sven Mir, Farheen Samineni, Divya Kim, Su Y. Jiang, Yanwen Punnoose, Elizabeth Sinha, Arijit Clark, Emma Spielewoy, Nathalie Humphrey, Kathryn Bazeos, Alexandra Zelenetz, Andrew D. |
description | The phase 2 CAVALLI (NCT02055820) study assessed efficacy and safety of venetoclax, a selective B-cell lymphoma-2 (Bcl-2) inhibitor, with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in first-line (1L) diffuse large B-cell lymphoma (DLBCL), including patients demonstrating Bcl-2 protein overexpression by immunohistochemistry (Bcl-2 IHC+). Eligible patients were ≥18 years of age and had previously untreated DLBCL, Eastern Cooperative Oncology Group performance status ≤2, and International Prognostic Index 2 to 5. Venetoclax 800 mg (days 4-10, cycle 1; days 1-10, cycles 2-8) was administered with rituximab (8 cycles) and cyclophosphamide, doxorubicin, vincristine, and prednisone (6-8 cycles) in 21-day cycles. Primary end points were safety, tolerability, and complete response (CR) at end of treatment (EOT). Secondary end points were progression-free survival (PFS) and overall survival. Comparative analyses used covariate-adjusted R-CHOP controls from the GOYA/BO21005 study, an appropriate contemporary benchmark for safety and efficacy. Safety and efficacy analyses included 206 patients. CR rate at EOT was 69% in the overall population and was maintained across Bcl-2 IHC+ subgroups. With a median follow-up of 32.2 months, trends were observed for improved investigator-assessed PFS for venetoclax plus R-CHOP in the overall population (hazard ratio [HR], 0.61; 95% confidence interval [CI], 0.43-0.87) and Bcl-2 IHC+ subgroups (HR, 0.55; 95% CI, 0.34-0.89) vs R-CHOP. Despite a higher incidence of grade 3/4 hematologic adverse events (86%), related mortality was not increased (2%). Chemotherapy dose intensity was similar in CAVALLI vs GOYA. The addition of venetoclax to R-CHOP in 1L DLBCL demonstrates increased, but manageable, myelosuppression and the potential of improved efficacy, particularly in high-risk Bcl-2 IHC+ patient subgroups.
•The phase 2 CAVALLI study assessed efficacy and safety of venetoclax + R-CHOP in patients with DLBCL, including Bcl-2+ subpopulations.•Venetoclax + R-CHOP showed potential for improved efficacy vs R-CHOP alone, supporting further investigation of venetoclax in Bcl-2+ DLBCL.
[Display omitted] |
doi_str_mv | 10.1182/blood.2020006578 |
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•The phase 2 CAVALLI study assessed efficacy and safety of venetoclax + R-CHOP in patients with DLBCL, including Bcl-2+ subpopulations.•Venetoclax + R-CHOP showed potential for improved efficacy vs R-CHOP alone, supporting further investigation of venetoclax in Bcl-2+ DLBCL.
[Display omitted]</description><identifier>ISSN: 0006-4971</identifier><identifier>ISSN: 1528-0020</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.2020006578</identifier><identifier>PMID: 33538797</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject><![CDATA[Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bridged Bicyclo Compounds, Heterocyclic - administration & dosage ; Bridged Bicyclo Compounds, Heterocyclic - adverse effects ; Clinical Trials and Observations ; Cyclophosphamide - administration & dosage ; Cyclophosphamide - adverse effects ; Doxorubicin - administration & dosage ; Doxorubicin - adverse effects ; Fatigue - chemically induced ; Female ; Gastrointestinal Diseases - chemically induced ; Genes, bcl-2 ; Granulocyte Colony-Stimulating Factor - therapeutic use ; Hematologic Diseases - chemically induced ; Humans ; Infections - etiology ; Kaplan-Meier Estimate ; Life Sciences ; Lymphoma, Large B-Cell, Diffuse - drug therapy ; Lymphoma, Large B-Cell, Diffuse - genetics ; Male ; Middle Aged ; Neoplasm Proteins - antagonists & inhibitors ; Prednisone - administration & dosage ; Prednisone - adverse effects ; Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors ; Rituximab - administration & dosage ; Rituximab - adverse effects ; Sulfonamides - administration & dosage ; Sulfonamides - adverse effects ; Vincristine - administration & dosage ; Vincristine - adverse effects ; Young Adult]]></subject><ispartof>Blood, 2021-02, Vol.137 (5), p.600-609</ispartof><rights>2021 American Society of Hematology</rights><rights>2021 by The American Society of Hematology.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2021 by The American Society of Hematology 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-667bc6a4a586d2c06f273adc8fa7621bc31d9e7e6f1acbefb41ca18f2c41b34a3</citedby><cites>FETCH-LOGICAL-c481t-667bc6a4a586d2c06f273adc8fa7621bc31d9e7e6f1acbefb41ca18f2c41b34a3</cites><orcidid>0000-0003-1403-6883 ; 0000-0002-6735-8651 ; 0000-0002-3714-9824 ; 0000-0002-6952-6073 ; 0000-0003-1225-8757 ; 0000-0002-9541-8666</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33538797$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.univ-lille.fr/hal-04200631$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Morschhauser, Franck</creatorcontrib><creatorcontrib>Feugier, Pierre</creatorcontrib><creatorcontrib>Flinn, Ian W.</creatorcontrib><creatorcontrib>Gasiorowski, Robin</creatorcontrib><creatorcontrib>Greil, Richard</creatorcontrib><creatorcontrib>Illés, Árpád</creatorcontrib><creatorcontrib>Johnson, Nathalie A.</creatorcontrib><creatorcontrib>Larouche, Jean-François</creatorcontrib><creatorcontrib>Lugtenburg, Pieternella J.</creatorcontrib><creatorcontrib>Patti, Caterina</creatorcontrib><creatorcontrib>Salles, Gilles A.</creatorcontrib><creatorcontrib>Trněný, Marek</creatorcontrib><creatorcontrib>de Vos, Sven</creatorcontrib><creatorcontrib>Mir, Farheen</creatorcontrib><creatorcontrib>Samineni, Divya</creatorcontrib><creatorcontrib>Kim, Su Y.</creatorcontrib><creatorcontrib>Jiang, Yanwen</creatorcontrib><creatorcontrib>Punnoose, Elizabeth</creatorcontrib><creatorcontrib>Sinha, Arijit</creatorcontrib><creatorcontrib>Clark, Emma</creatorcontrib><creatorcontrib>Spielewoy, Nathalie</creatorcontrib><creatorcontrib>Humphrey, Kathryn</creatorcontrib><creatorcontrib>Bazeos, Alexandra</creatorcontrib><creatorcontrib>Zelenetz, Andrew D.</creatorcontrib><title>A phase 2 study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma</title><title>Blood</title><addtitle>Blood</addtitle><description>The phase 2 CAVALLI (NCT02055820) study assessed efficacy and safety of venetoclax, a selective B-cell lymphoma-2 (Bcl-2) inhibitor, with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in first-line (1L) diffuse large B-cell lymphoma (DLBCL), including patients demonstrating Bcl-2 protein overexpression by immunohistochemistry (Bcl-2 IHC+). Eligible patients were ≥18 years of age and had previously untreated DLBCL, Eastern Cooperative Oncology Group performance status ≤2, and International Prognostic Index 2 to 5. Venetoclax 800 mg (days 4-10, cycle 1; days 1-10, cycles 2-8) was administered with rituximab (8 cycles) and cyclophosphamide, doxorubicin, vincristine, and prednisone (6-8 cycles) in 21-day cycles. Primary end points were safety, tolerability, and complete response (CR) at end of treatment (EOT). Secondary end points were progression-free survival (PFS) and overall survival. Comparative analyses used covariate-adjusted R-CHOP controls from the GOYA/BO21005 study, an appropriate contemporary benchmark for safety and efficacy. Safety and efficacy analyses included 206 patients. CR rate at EOT was 69% in the overall population and was maintained across Bcl-2 IHC+ subgroups. With a median follow-up of 32.2 months, trends were observed for improved investigator-assessed PFS for venetoclax plus R-CHOP in the overall population (hazard ratio [HR], 0.61; 95% confidence interval [CI], 0.43-0.87) and Bcl-2 IHC+ subgroups (HR, 0.55; 95% CI, 0.34-0.89) vs R-CHOP. Despite a higher incidence of grade 3/4 hematologic adverse events (86%), related mortality was not increased (2%). Chemotherapy dose intensity was similar in CAVALLI vs GOYA. The addition of venetoclax to R-CHOP in 1L DLBCL demonstrates increased, but manageable, myelosuppression and the potential of improved efficacy, particularly in high-risk Bcl-2 IHC+ patient subgroups.
•The phase 2 CAVALLI study assessed efficacy and safety of venetoclax + R-CHOP in patients with DLBCL, including Bcl-2+ subpopulations.•Venetoclax + R-CHOP showed potential for improved efficacy vs R-CHOP alone, supporting further investigation of venetoclax in Bcl-2+ DLBCL.
[Display omitted]</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - administration & dosage</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - adverse effects</subject><subject>Clinical Trials and Observations</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Cyclophosphamide - adverse effects</subject><subject>Doxorubicin - administration & dosage</subject><subject>Doxorubicin - adverse effects</subject><subject>Fatigue - chemically induced</subject><subject>Female</subject><subject>Gastrointestinal Diseases - chemically induced</subject><subject>Genes, bcl-2</subject><subject>Granulocyte Colony-Stimulating Factor - therapeutic use</subject><subject>Hematologic Diseases - chemically induced</subject><subject>Humans</subject><subject>Infections - etiology</subject><subject>Kaplan-Meier Estimate</subject><subject>Life Sciences</subject><subject>Lymphoma, Large B-Cell, Diffuse - drug therapy</subject><subject>Lymphoma, Large B-Cell, Diffuse - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Proteins - antagonists & inhibitors</subject><subject>Prednisone - administration & dosage</subject><subject>Prednisone - adverse effects</subject><subject>Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors</subject><subject>Rituximab - administration & dosage</subject><subject>Rituximab - adverse effects</subject><subject>Sulfonamides - administration & dosage</subject><subject>Sulfonamides - adverse effects</subject><subject>Vincristine - administration & dosage</subject><subject>Vincristine - adverse effects</subject><subject>Young Adult</subject><issn>0006-4971</issn><issn>1528-0020</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc-P1CAUxxujccfVuyfDUQ9dgVJKPZiMk9UxmWSN0TOh9LHF0NIFOjr__TLOuv5IPEEe3-_n8d63KJ4TfEGIoK87531_QTHFGPO6EQ-KFampKHGuPCxWx2rJ2oacFU9i_IYxYRWtHxdnVVVXommbVXGzRvOgIiCKYlr6A_IG7WGC5LVTP9Dslog-l5vt1SekIjI2xFQ6OwFKAVQaYUrI-IBmlWy-R_TdpgH11pglM50K14DelRqcQ-4wzoMf1dPikVEuwrO787z4-v7yy2Zb7q4-fNysd6VmgqSS86bTXDFVC95TjbmhTaV6LYxqOCWdrkjfQgPcEKU7MB0jWhFhqGakq5iqzou3J-68dCP0On8vKCfnYEcVDtIrK_9-mewgr_1eNoK3RPAMeHUCDP_YtuudPNYwy3vnFdmTrH151yz4mwVikqONx7HVBH6JkjLBGa_bFmcpPkl18DEGMPdsguUxVfkzVfk71Wx58eco94ZfMWbBm5MA8kL3FoKMOuehobcBdJK9t_-n3wJIrLOM</recordid><startdate>20210204</startdate><enddate>20210204</enddate><creator>Morschhauser, Franck</creator><creator>Feugier, Pierre</creator><creator>Flinn, Ian W.</creator><creator>Gasiorowski, Robin</creator><creator>Greil, Richard</creator><creator>Illés, Árpád</creator><creator>Johnson, Nathalie A.</creator><creator>Larouche, Jean-François</creator><creator>Lugtenburg, Pieternella J.</creator><creator>Patti, Caterina</creator><creator>Salles, Gilles A.</creator><creator>Trněný, Marek</creator><creator>de Vos, Sven</creator><creator>Mir, Farheen</creator><creator>Samineni, Divya</creator><creator>Kim, Su Y.</creator><creator>Jiang, Yanwen</creator><creator>Punnoose, Elizabeth</creator><creator>Sinha, Arijit</creator><creator>Clark, Emma</creator><creator>Spielewoy, Nathalie</creator><creator>Humphrey, Kathryn</creator><creator>Bazeos, Alexandra</creator><creator>Zelenetz, Andrew D.</creator><general>Elsevier Inc</general><general>American Society of Hematology</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>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1403-6883</orcidid><orcidid>https://orcid.org/0000-0002-6735-8651</orcidid><orcidid>https://orcid.org/0000-0002-3714-9824</orcidid><orcidid>https://orcid.org/0000-0002-6952-6073</orcidid><orcidid>https://orcid.org/0000-0003-1225-8757</orcidid><orcidid>https://orcid.org/0000-0002-9541-8666</orcidid></search><sort><creationdate>20210204</creationdate><title>A phase 2 study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma</title><author>Morschhauser, Franck ; Feugier, Pierre ; Flinn, Ian W. ; Gasiorowski, Robin ; Greil, Richard ; Illés, Árpád ; Johnson, Nathalie A. ; Larouche, Jean-François ; Lugtenburg, Pieternella J. ; Patti, Caterina ; Salles, Gilles A. ; Trněný, Marek ; de Vos, Sven ; Mir, Farheen ; Samineni, Divya ; Kim, Su Y. ; Jiang, Yanwen ; Punnoose, Elizabeth ; Sinha, Arijit ; Clark, Emma ; Spielewoy, Nathalie ; Humphrey, Kathryn ; Bazeos, Alexandra ; Zelenetz, Andrew D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-667bc6a4a586d2c06f273adc8fa7621bc31d9e7e6f1acbefb41ca18f2c41b34a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Combined Chemotherapy Protocols - 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Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morschhauser, Franck</au><au>Feugier, Pierre</au><au>Flinn, Ian W.</au><au>Gasiorowski, Robin</au><au>Greil, Richard</au><au>Illés, Árpád</au><au>Johnson, Nathalie A.</au><au>Larouche, Jean-François</au><au>Lugtenburg, Pieternella J.</au><au>Patti, Caterina</au><au>Salles, Gilles A.</au><au>Trněný, Marek</au><au>de Vos, Sven</au><au>Mir, Farheen</au><au>Samineni, Divya</au><au>Kim, Su Y.</au><au>Jiang, Yanwen</au><au>Punnoose, Elizabeth</au><au>Sinha, Arijit</au><au>Clark, Emma</au><au>Spielewoy, Nathalie</au><au>Humphrey, Kathryn</au><au>Bazeos, Alexandra</au><au>Zelenetz, Andrew D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A phase 2 study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2021-02-04</date><risdate>2021</risdate><volume>137</volume><issue>5</issue><spage>600</spage><epage>609</epage><pages>600-609</pages><issn>0006-4971</issn><issn>1528-0020</issn><eissn>1528-0020</eissn><abstract>The phase 2 CAVALLI (NCT02055820) study assessed efficacy and safety of venetoclax, a selective B-cell lymphoma-2 (Bcl-2) inhibitor, with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in first-line (1L) diffuse large B-cell lymphoma (DLBCL), including patients demonstrating Bcl-2 protein overexpression by immunohistochemistry (Bcl-2 IHC+). Eligible patients were ≥18 years of age and had previously untreated DLBCL, Eastern Cooperative Oncology Group performance status ≤2, and International Prognostic Index 2 to 5. Venetoclax 800 mg (days 4-10, cycle 1; days 1-10, cycles 2-8) was administered with rituximab (8 cycles) and cyclophosphamide, doxorubicin, vincristine, and prednisone (6-8 cycles) in 21-day cycles. Primary end points were safety, tolerability, and complete response (CR) at end of treatment (EOT). Secondary end points were progression-free survival (PFS) and overall survival. Comparative analyses used covariate-adjusted R-CHOP controls from the GOYA/BO21005 study, an appropriate contemporary benchmark for safety and efficacy. Safety and efficacy analyses included 206 patients. CR rate at EOT was 69% in the overall population and was maintained across Bcl-2 IHC+ subgroups. With a median follow-up of 32.2 months, trends were observed for improved investigator-assessed PFS for venetoclax plus R-CHOP in the overall population (hazard ratio [HR], 0.61; 95% confidence interval [CI], 0.43-0.87) and Bcl-2 IHC+ subgroups (HR, 0.55; 95% CI, 0.34-0.89) vs R-CHOP. Despite a higher incidence of grade 3/4 hematologic adverse events (86%), related mortality was not increased (2%). Chemotherapy dose intensity was similar in CAVALLI vs GOYA. The addition of venetoclax to R-CHOP in 1L DLBCL demonstrates increased, but manageable, myelosuppression and the potential of improved efficacy, particularly in high-risk Bcl-2 IHC+ patient subgroups.
•The phase 2 CAVALLI study assessed efficacy and safety of venetoclax + R-CHOP in patients with DLBCL, including Bcl-2+ subpopulations.•Venetoclax + R-CHOP showed potential for improved efficacy vs R-CHOP alone, supporting further investigation of venetoclax in Bcl-2+ DLBCL.
[Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33538797</pmid><doi>10.1182/blood.2020006578</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-1403-6883</orcidid><orcidid>https://orcid.org/0000-0002-6735-8651</orcidid><orcidid>https://orcid.org/0000-0002-3714-9824</orcidid><orcidid>https://orcid.org/0000-0002-6952-6073</orcidid><orcidid>https://orcid.org/0000-0003-1225-8757</orcidid><orcidid>https://orcid.org/0000-0002-9541-8666</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-4971 |
ispartof | Blood, 2021-02, Vol.137 (5), p.600-609 |
issn | 0006-4971 1528-0020 1528-0020 |
language | eng |
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subjects | Adolescent Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Bridged Bicyclo Compounds, Heterocyclic - administration & dosage Bridged Bicyclo Compounds, Heterocyclic - adverse effects Clinical Trials and Observations Cyclophosphamide - administration & dosage Cyclophosphamide - adverse effects Doxorubicin - administration & dosage Doxorubicin - adverse effects Fatigue - chemically induced Female Gastrointestinal Diseases - chemically induced Genes, bcl-2 Granulocyte Colony-Stimulating Factor - therapeutic use Hematologic Diseases - chemically induced Humans Infections - etiology Kaplan-Meier Estimate Life Sciences Lymphoma, Large B-Cell, Diffuse - drug therapy Lymphoma, Large B-Cell, Diffuse - genetics Male Middle Aged Neoplasm Proteins - antagonists & inhibitors Prednisone - administration & dosage Prednisone - adverse effects Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors Rituximab - administration & dosage Rituximab - adverse effects Sulfonamides - administration & dosage Sulfonamides - adverse effects Vincristine - administration & dosage Vincristine - adverse effects Young Adult |
title | A phase 2 study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma |
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