Safety and efficacy of ibrutinib in combination with rituximab and lenalidomide in previously untreated follicular and marginal zone lymphoma: An open label, phase 2 study
Background Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent non‐Hodgkin lymphomas (iNHL). Median survival for iNHL is approximately 20 years. Because standard treatments are not curative, patients often receive multiple lines of therapy with associated toxicity—rationally desig...
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Veröffentlicht in: | Cancer 2024-03, Vol.130 (6), p.876-885 |
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creator | Gordon, Max J. Feng, Lei Strati, Paolo Lee, Hun Ju Hagemeister, Fredrick B. Westin, Jason R. Samaniego, Felipe Marques‐Piubelli, Mario L. Vega Vazquez, Francisco Parra Cuentas, Edwin R. Solis‐Soto, Luisa M. Ma, Wencai Wang, Jing Claret, Linda Averill, Barbara Ibanez, Karina Fayad, Luis E. Flowers, Christopher R. Green, Michael R. Davis, R. Eric Neelapu, Sattva S. Fowler, Nathan H. Nastoupil, Loretta J. |
description | Background
Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent non‐Hodgkin lymphomas (iNHL). Median survival for iNHL is approximately 20 years. Because standard treatments are not curative, patients often receive multiple lines of therapy with associated toxicity—rationally designed, combination therapies with curative potential are needed. The immunomodulatory drug lenalidomide was evaluated in combination with rituximab for the frontline treatment of FL in the phase 3 RELEVANCE study. Ibrutinib, an oral Bruton tyrosine kinase inhibitor, is active in NHL and was evaluated in combination with lenalidomide, rituximab, and ibrutinib (IRR) in a phase 1 study.
Methods
The authors conducted an open‐label, phase 2 clinical trial of IRR for previously untreated FL and MZL. The primary end point was progression‐free survival (PFS) at 24 months.
Results
This study included 48 participants with previously untreated FL grade 1–3a (N = 38), or MZL (N = 10). Participants received 12, 28‐day cycles of lenalidomide (15 mg, days 1–21 cycle 1; 20 mg, cycles 2–12), rituximab (375 mg/m2 weekly in cycle 1; day 1 cycles 2‐12), and ibrutinib 560 mg daily. With a median follow‐up of 65.3 months, the estimated PFS at 24 months was 78.8% (95% confidence interval [CI], 68.0%–91.4%) and 60‐month PFS was 59.7% (95% CI, 46.6%–76.4%). One death occurred unrelated to disease progression. Grade 3–4 adverse events were observed in 64.6%, including 50% with grade 3–4 rash.
Conclusions
IRR is highly active as frontline therapy for FL and MZL. Compared to historical results with lenalidomide and rituximab, PFS is similar with higher grade 3–4 toxicity, particularly rash. The study was registered with ClinicalTrials.gov (NCT02532257).
After 5 years of follow‐up from a phase 2 clinical trial of ibrutinib, lenalidomide, and rituximab in previously untreated patients with follicular and marginal zone lymphoma, the 5‐year progression‐free survival rate was 59.7% and the overall survival rate was 97.9%. |
doi_str_mv | 10.1002/cncr.35114 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2892272580</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2892272580</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3164-de5caa41ff459dc2fb62eec816a4d3cda9ff0a599995ac0655eec8e3d2049bf83</originalsourceid><addsrcrecordid>eNp9kU2LFDEQhoMo7uzqxR8gAS8i9pqPTk_H2zK4KiwKfoC3Jp1UnCzppE26Xdu_5J80PbN68GBdQpGnHqh6EXpEyTklhL3QQadzLiit76ANJXJbEVqzu2hDCGkrUfMvJ-g05-vSbpng99EJ38pWcCE36NdHZWFasAoGg7VOK73gaLHr0zy54HrsAtZx6F1Qk4sB37hpj5Ob5h9uUP1hzkNQ3pk4OAMrPib47uKc_YLnMCVQExhso_dOz16lw8yg0tei9PhnDID9Moz7OKiX-CLgOELAXvXgn-NxrzJghvM0m-UBumeVz_Dw9j1Dny9ffdq9qa7ev367u7iqNKdNXRkQWqmaWlsLaTSzfcMAdEsbVRuujZLWEiVkKaE0aYRYf4EbRmrZ25afoadH75jitxny1A0ua_BeBShrdayVjJVLtqSgT_5Br-Ocyl6FkpzIljT1Sj07UjrFnBPYbkzlemnpKOnWCLs1wu4QYYEf3yrnfgDzF_2TWQHoEbhxHpb_qLrdu92Ho_Q3-sGqjQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2930980640</pqid></control><display><type>article</type><title>Safety and efficacy of ibrutinib in combination with rituximab and lenalidomide in previously untreated follicular and marginal zone lymphoma: An open label, phase 2 study</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Gordon, Max J. ; Feng, Lei ; Strati, Paolo ; Lee, Hun Ju ; Hagemeister, Fredrick B. ; Westin, Jason R. ; Samaniego, Felipe ; Marques‐Piubelli, Mario L. ; Vega Vazquez, Francisco ; Parra Cuentas, Edwin R. ; Solis‐Soto, Luisa M. ; Ma, Wencai ; Wang, Jing ; Claret, Linda ; Averill, Barbara ; Ibanez, Karina ; Fayad, Luis E. ; Flowers, Christopher R. ; Green, Michael R. ; Davis, R. Eric ; Neelapu, Sattva S. ; Fowler, Nathan H. ; Nastoupil, Loretta J.</creator><creatorcontrib>Gordon, Max J. ; Feng, Lei ; Strati, Paolo ; Lee, Hun Ju ; Hagemeister, Fredrick B. ; Westin, Jason R. ; Samaniego, Felipe ; Marques‐Piubelli, Mario L. ; Vega Vazquez, Francisco ; Parra Cuentas, Edwin R. ; Solis‐Soto, Luisa M. ; Ma, Wencai ; Wang, Jing ; Claret, Linda ; Averill, Barbara ; Ibanez, Karina ; Fayad, Luis E. ; Flowers, Christopher R. ; Green, Michael R. ; Davis, R. Eric ; Neelapu, Sattva S. ; Fowler, Nathan H. ; Nastoupil, Loretta J.</creatorcontrib><description>Background
Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent non‐Hodgkin lymphomas (iNHL). Median survival for iNHL is approximately 20 years. Because standard treatments are not curative, patients often receive multiple lines of therapy with associated toxicity—rationally designed, combination therapies with curative potential are needed. The immunomodulatory drug lenalidomide was evaluated in combination with rituximab for the frontline treatment of FL in the phase 3 RELEVANCE study. Ibrutinib, an oral Bruton tyrosine kinase inhibitor, is active in NHL and was evaluated in combination with lenalidomide, rituximab, and ibrutinib (IRR) in a phase 1 study.
Methods
The authors conducted an open‐label, phase 2 clinical trial of IRR for previously untreated FL and MZL. The primary end point was progression‐free survival (PFS) at 24 months.
Results
This study included 48 participants with previously untreated FL grade 1–3a (N = 38), or MZL (N = 10). Participants received 12, 28‐day cycles of lenalidomide (15 mg, days 1–21 cycle 1; 20 mg, cycles 2–12), rituximab (375 mg/m2 weekly in cycle 1; day 1 cycles 2‐12), and ibrutinib 560 mg daily. With a median follow‐up of 65.3 months, the estimated PFS at 24 months was 78.8% (95% confidence interval [CI], 68.0%–91.4%) and 60‐month PFS was 59.7% (95% CI, 46.6%–76.4%). One death occurred unrelated to disease progression. Grade 3–4 adverse events were observed in 64.6%, including 50% with grade 3–4 rash.
Conclusions
IRR is highly active as frontline therapy for FL and MZL. Compared to historical results with lenalidomide and rituximab, PFS is similar with higher grade 3–4 toxicity, particularly rash. The study was registered with ClinicalTrials.gov (NCT02532257).
After 5 years of follow‐up from a phase 2 clinical trial of ibrutinib, lenalidomide, and rituximab in previously untreated patients with follicular and marginal zone lymphoma, the 5‐year progression‐free survival rate was 59.7% and the overall survival rate was 97.9%.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.35114</identifier><identifier>PMID: 37985359</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adenine - analogs & derivatives ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Exanthema ; Exanthema - chemically induced ; Exanthema - drug therapy ; Humans ; Immunomodulation ; Immunotherapy ; indolent lymphoma ; Kinases ; Labels ; Lenalidomide - therapeutic use ; Lymphoma ; Lymphoma, B-Cell, Marginal Zone - drug therapy ; Lymphoma, Follicular - drug therapy ; Lymphoma, Follicular - pathology ; non‐Hodgkin lymphoma (NHL) ; Piperidines ; Rituximab ; Survival ; Targeted cancer therapy ; targeted therapy ; Toxicity ; Tyrosine</subject><ispartof>Cancer, 2024-03, Vol.130 (6), p.876-885</ispartof><rights>2023 American Cancer Society.</rights><rights>2024 American Cancer Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3164-de5caa41ff459dc2fb62eec816a4d3cda9ff0a599995ac0655eec8e3d2049bf83</cites><orcidid>0000-0003-3940-4451 ; 0000-0002-9524-3990 ; 0000-0002-6324-2096</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.35114$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.35114$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37985359$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gordon, Max J.</creatorcontrib><creatorcontrib>Feng, Lei</creatorcontrib><creatorcontrib>Strati, Paolo</creatorcontrib><creatorcontrib>Lee, Hun Ju</creatorcontrib><creatorcontrib>Hagemeister, Fredrick B.</creatorcontrib><creatorcontrib>Westin, Jason R.</creatorcontrib><creatorcontrib>Samaniego, Felipe</creatorcontrib><creatorcontrib>Marques‐Piubelli, Mario L.</creatorcontrib><creatorcontrib>Vega Vazquez, Francisco</creatorcontrib><creatorcontrib>Parra Cuentas, Edwin R.</creatorcontrib><creatorcontrib>Solis‐Soto, Luisa M.</creatorcontrib><creatorcontrib>Ma, Wencai</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Claret, Linda</creatorcontrib><creatorcontrib>Averill, Barbara</creatorcontrib><creatorcontrib>Ibanez, Karina</creatorcontrib><creatorcontrib>Fayad, Luis E.</creatorcontrib><creatorcontrib>Flowers, Christopher R.</creatorcontrib><creatorcontrib>Green, Michael R.</creatorcontrib><creatorcontrib>Davis, R. Eric</creatorcontrib><creatorcontrib>Neelapu, Sattva S.</creatorcontrib><creatorcontrib>Fowler, Nathan H.</creatorcontrib><creatorcontrib>Nastoupil, Loretta J.</creatorcontrib><title>Safety and efficacy of ibrutinib in combination with rituximab and lenalidomide in previously untreated follicular and marginal zone lymphoma: An open label, phase 2 study</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Background
Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent non‐Hodgkin lymphomas (iNHL). Median survival for iNHL is approximately 20 years. Because standard treatments are not curative, patients often receive multiple lines of therapy with associated toxicity—rationally designed, combination therapies with curative potential are needed. The immunomodulatory drug lenalidomide was evaluated in combination with rituximab for the frontline treatment of FL in the phase 3 RELEVANCE study. Ibrutinib, an oral Bruton tyrosine kinase inhibitor, is active in NHL and was evaluated in combination with lenalidomide, rituximab, and ibrutinib (IRR) in a phase 1 study.
Methods
The authors conducted an open‐label, phase 2 clinical trial of IRR for previously untreated FL and MZL. The primary end point was progression‐free survival (PFS) at 24 months.
Results
This study included 48 participants with previously untreated FL grade 1–3a (N = 38), or MZL (N = 10). Participants received 12, 28‐day cycles of lenalidomide (15 mg, days 1–21 cycle 1; 20 mg, cycles 2–12), rituximab (375 mg/m2 weekly in cycle 1; day 1 cycles 2‐12), and ibrutinib 560 mg daily. With a median follow‐up of 65.3 months, the estimated PFS at 24 months was 78.8% (95% confidence interval [CI], 68.0%–91.4%) and 60‐month PFS was 59.7% (95% CI, 46.6%–76.4%). One death occurred unrelated to disease progression. Grade 3–4 adverse events were observed in 64.6%, including 50% with grade 3–4 rash.
Conclusions
IRR is highly active as frontline therapy for FL and MZL. Compared to historical results with lenalidomide and rituximab, PFS is similar with higher grade 3–4 toxicity, particularly rash. The study was registered with ClinicalTrials.gov (NCT02532257).
After 5 years of follow‐up from a phase 2 clinical trial of ibrutinib, lenalidomide, and rituximab in previously untreated patients with follicular and marginal zone lymphoma, the 5‐year progression‐free survival rate was 59.7% and the overall survival rate was 97.9%.</description><subject>Adenine - analogs & derivatives</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Exanthema</subject><subject>Exanthema - chemically induced</subject><subject>Exanthema - drug therapy</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>Immunotherapy</subject><subject>indolent lymphoma</subject><subject>Kinases</subject><subject>Labels</subject><subject>Lenalidomide - therapeutic use</subject><subject>Lymphoma</subject><subject>Lymphoma, B-Cell, Marginal Zone - drug therapy</subject><subject>Lymphoma, Follicular - drug therapy</subject><subject>Lymphoma, Follicular - pathology</subject><subject>non‐Hodgkin lymphoma (NHL)</subject><subject>Piperidines</subject><subject>Rituximab</subject><subject>Survival</subject><subject>Targeted cancer therapy</subject><subject>targeted therapy</subject><subject>Toxicity</subject><subject>Tyrosine</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhoMo7uzqxR8gAS8i9pqPTk_H2zK4KiwKfoC3Jp1UnCzppE26Xdu_5J80PbN68GBdQpGnHqh6EXpEyTklhL3QQadzLiit76ANJXJbEVqzu2hDCGkrUfMvJ-g05-vSbpng99EJ38pWcCE36NdHZWFasAoGg7VOK73gaLHr0zy54HrsAtZx6F1Qk4sB37hpj5Ob5h9uUP1hzkNQ3pk4OAMrPib47uKc_YLnMCVQExhso_dOz16lw8yg0tei9PhnDID9Moz7OKiX-CLgOELAXvXgn-NxrzJghvM0m-UBumeVz_Dw9j1Dny9ffdq9qa7ev367u7iqNKdNXRkQWqmaWlsLaTSzfcMAdEsbVRuujZLWEiVkKaE0aYRYf4EbRmrZ25afoadH75jitxny1A0ua_BeBShrdayVjJVLtqSgT_5Br-Ocyl6FkpzIljT1Sj07UjrFnBPYbkzlemnpKOnWCLs1wu4QYYEf3yrnfgDzF_2TWQHoEbhxHpb_qLrdu92Ho_Q3-sGqjQ</recordid><startdate>20240315</startdate><enddate>20240315</enddate><creator>Gordon, Max J.</creator><creator>Feng, Lei</creator><creator>Strati, Paolo</creator><creator>Lee, Hun Ju</creator><creator>Hagemeister, Fredrick B.</creator><creator>Westin, Jason R.</creator><creator>Samaniego, Felipe</creator><creator>Marques‐Piubelli, Mario L.</creator><creator>Vega Vazquez, Francisco</creator><creator>Parra Cuentas, Edwin R.</creator><creator>Solis‐Soto, Luisa M.</creator><creator>Ma, Wencai</creator><creator>Wang, Jing</creator><creator>Claret, Linda</creator><creator>Averill, Barbara</creator><creator>Ibanez, Karina</creator><creator>Fayad, Luis E.</creator><creator>Flowers, Christopher R.</creator><creator>Green, Michael R.</creator><creator>Davis, R. Eric</creator><creator>Neelapu, Sattva S.</creator><creator>Fowler, Nathan H.</creator><creator>Nastoupil, Loretta J.</creator><general>Wiley Subscription Services, Inc</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>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3940-4451</orcidid><orcidid>https://orcid.org/0000-0002-9524-3990</orcidid><orcidid>https://orcid.org/0000-0002-6324-2096</orcidid></search><sort><creationdate>20240315</creationdate><title>Safety and efficacy of ibrutinib in combination with rituximab and lenalidomide in previously untreated follicular and marginal zone lymphoma: An open label, phase 2 study</title><author>Gordon, Max J. ; Feng, Lei ; Strati, Paolo ; Lee, Hun Ju ; Hagemeister, Fredrick B. ; Westin, Jason R. ; Samaniego, Felipe ; Marques‐Piubelli, Mario L. ; Vega Vazquez, Francisco ; Parra Cuentas, Edwin R. ; Solis‐Soto, Luisa M. ; Ma, Wencai ; Wang, Jing ; Claret, Linda ; Averill, Barbara ; Ibanez, Karina ; Fayad, Luis E. ; Flowers, Christopher R. ; Green, Michael R. ; Davis, R. Eric ; Neelapu, Sattva S. ; Fowler, Nathan H. ; Nastoupil, Loretta J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3164-de5caa41ff459dc2fb62eec816a4d3cda9ff0a599995ac0655eec8e3d2049bf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adenine - analogs & derivatives</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Exanthema</topic><topic>Exanthema - chemically induced</topic><topic>Exanthema - drug therapy</topic><topic>Humans</topic><topic>Immunomodulation</topic><topic>Immunotherapy</topic><topic>indolent lymphoma</topic><topic>Kinases</topic><topic>Labels</topic><topic>Lenalidomide - therapeutic use</topic><topic>Lymphoma</topic><topic>Lymphoma, B-Cell, Marginal Zone - drug therapy</topic><topic>Lymphoma, Follicular - drug therapy</topic><topic>Lymphoma, Follicular - pathology</topic><topic>non‐Hodgkin lymphoma (NHL)</topic><topic>Piperidines</topic><topic>Rituximab</topic><topic>Survival</topic><topic>Targeted cancer therapy</topic><topic>targeted therapy</topic><topic>Toxicity</topic><topic>Tyrosine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gordon, Max J.</creatorcontrib><creatorcontrib>Feng, Lei</creatorcontrib><creatorcontrib>Strati, Paolo</creatorcontrib><creatorcontrib>Lee, Hun Ju</creatorcontrib><creatorcontrib>Hagemeister, Fredrick B.</creatorcontrib><creatorcontrib>Westin, Jason R.</creatorcontrib><creatorcontrib>Samaniego, Felipe</creatorcontrib><creatorcontrib>Marques‐Piubelli, Mario L.</creatorcontrib><creatorcontrib>Vega Vazquez, Francisco</creatorcontrib><creatorcontrib>Parra Cuentas, Edwin R.</creatorcontrib><creatorcontrib>Solis‐Soto, Luisa M.</creatorcontrib><creatorcontrib>Ma, Wencai</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Claret, Linda</creatorcontrib><creatorcontrib>Averill, Barbara</creatorcontrib><creatorcontrib>Ibanez, Karina</creatorcontrib><creatorcontrib>Fayad, Luis E.</creatorcontrib><creatorcontrib>Flowers, Christopher R.</creatorcontrib><creatorcontrib>Green, Michael R.</creatorcontrib><creatorcontrib>Davis, R. Eric</creatorcontrib><creatorcontrib>Neelapu, Sattva S.</creatorcontrib><creatorcontrib>Fowler, Nathan H.</creatorcontrib><creatorcontrib>Nastoupil, Loretta J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gordon, Max J.</au><au>Feng, Lei</au><au>Strati, Paolo</au><au>Lee, Hun Ju</au><au>Hagemeister, Fredrick B.</au><au>Westin, Jason R.</au><au>Samaniego, Felipe</au><au>Marques‐Piubelli, Mario L.</au><au>Vega Vazquez, Francisco</au><au>Parra Cuentas, Edwin R.</au><au>Solis‐Soto, Luisa M.</au><au>Ma, Wencai</au><au>Wang, Jing</au><au>Claret, Linda</au><au>Averill, Barbara</au><au>Ibanez, Karina</au><au>Fayad, Luis E.</au><au>Flowers, Christopher R.</au><au>Green, Michael R.</au><au>Davis, R. Eric</au><au>Neelapu, Sattva S.</au><au>Fowler, Nathan H.</au><au>Nastoupil, Loretta J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety and efficacy of ibrutinib in combination with rituximab and lenalidomide in previously untreated follicular and marginal zone lymphoma: An open label, phase 2 study</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2024-03-15</date><risdate>2024</risdate><volume>130</volume><issue>6</issue><spage>876</spage><epage>885</epage><pages>876-885</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>Background
Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent non‐Hodgkin lymphomas (iNHL). Median survival for iNHL is approximately 20 years. Because standard treatments are not curative, patients often receive multiple lines of therapy with associated toxicity—rationally designed, combination therapies with curative potential are needed. The immunomodulatory drug lenalidomide was evaluated in combination with rituximab for the frontline treatment of FL in the phase 3 RELEVANCE study. Ibrutinib, an oral Bruton tyrosine kinase inhibitor, is active in NHL and was evaluated in combination with lenalidomide, rituximab, and ibrutinib (IRR) in a phase 1 study.
Methods
The authors conducted an open‐label, phase 2 clinical trial of IRR for previously untreated FL and MZL. The primary end point was progression‐free survival (PFS) at 24 months.
Results
This study included 48 participants with previously untreated FL grade 1–3a (N = 38), or MZL (N = 10). Participants received 12, 28‐day cycles of lenalidomide (15 mg, days 1–21 cycle 1; 20 mg, cycles 2–12), rituximab (375 mg/m2 weekly in cycle 1; day 1 cycles 2‐12), and ibrutinib 560 mg daily. With a median follow‐up of 65.3 months, the estimated PFS at 24 months was 78.8% (95% confidence interval [CI], 68.0%–91.4%) and 60‐month PFS was 59.7% (95% CI, 46.6%–76.4%). One death occurred unrelated to disease progression. Grade 3–4 adverse events were observed in 64.6%, including 50% with grade 3–4 rash.
Conclusions
IRR is highly active as frontline therapy for FL and MZL. Compared to historical results with lenalidomide and rituximab, PFS is similar with higher grade 3–4 toxicity, particularly rash. The study was registered with ClinicalTrials.gov (NCT02532257).
After 5 years of follow‐up from a phase 2 clinical trial of ibrutinib, lenalidomide, and rituximab in previously untreated patients with follicular and marginal zone lymphoma, the 5‐year progression‐free survival rate was 59.7% and the overall survival rate was 97.9%.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37985359</pmid><doi>10.1002/cncr.35114</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3940-4451</orcidid><orcidid>https://orcid.org/0000-0002-9524-3990</orcidid><orcidid>https://orcid.org/0000-0002-6324-2096</orcidid></addata></record> |
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source | MEDLINE; Access via Wiley Online Library |
subjects | Adenine - analogs & derivatives Antineoplastic Combined Chemotherapy Protocols - adverse effects Exanthema Exanthema - chemically induced Exanthema - drug therapy Humans Immunomodulation Immunotherapy indolent lymphoma Kinases Labels Lenalidomide - therapeutic use Lymphoma Lymphoma, B-Cell, Marginal Zone - drug therapy Lymphoma, Follicular - drug therapy Lymphoma, Follicular - pathology non‐Hodgkin lymphoma (NHL) Piperidines Rituximab Survival Targeted cancer therapy targeted therapy Toxicity Tyrosine |
title | Safety and efficacy of ibrutinib in combination with rituximab and lenalidomide in previously untreated follicular and marginal zone lymphoma: An open label, phase 2 study |
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