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
Hauptverfasser: 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.
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container_end_page 609
container_issue 5
container_start_page 600
container_title Blood
container_volume 137
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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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><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 &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - administration &amp; dosage</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - adverse effects</subject><subject>Clinical Trials and Observations</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Cyclophosphamide - adverse effects</subject><subject>Doxorubicin - administration &amp; 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 &amp; 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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 - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Bridged Bicyclo Compounds, Heterocyclic - administration &amp; dosage</topic><topic>Bridged Bicyclo Compounds, Heterocyclic - adverse effects</topic><topic>Clinical Trials and Observations</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>Cyclophosphamide - adverse effects</topic><topic>Doxorubicin - administration &amp; dosage</topic><topic>Doxorubicin - adverse effects</topic><topic>Fatigue - chemically induced</topic><topic>Female</topic><topic>Gastrointestinal Diseases - chemically induced</topic><topic>Genes, bcl-2</topic><topic>Granulocyte Colony-Stimulating Factor - therapeutic use</topic><topic>Hematologic Diseases - chemically induced</topic><topic>Humans</topic><topic>Infections - etiology</topic><topic>Kaplan-Meier Estimate</topic><topic>Life Sciences</topic><topic>Lymphoma, Large B-Cell, Diffuse - drug therapy</topic><topic>Lymphoma, Large B-Cell, Diffuse - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Proteins - antagonists &amp; inhibitors</topic><topic>Prednisone - administration &amp; dosage</topic><topic>Prednisone - adverse effects</topic><topic>Proto-Oncogene Proteins c-bcl-2 - antagonists &amp; inhibitors</topic><topic>Rituximab - administration &amp; dosage</topic><topic>Rituximab - adverse effects</topic><topic>Sulfonamides - administration &amp; dosage</topic><topic>Sulfonamides - adverse effects</topic><topic>Vincristine - administration &amp; dosage</topic><topic>Vincristine - adverse effects</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - 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>
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identifier ISSN: 0006-4971
ispartof Blood, 2021-02, Vol.137 (5), p.600-609
issn 0006-4971
1528-0020
1528-0020
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7869186
source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
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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