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Rituximab plus multiagent chemotherapy for newly diagnosed CD20-positive acute lymphoblastic leukemia: a prospective phase II study
Background/Aims: We performed a prospective study to determine the efficacy and safety of rituximab including chemotherapy in CD20-positive acute lymphoblastic leukemia (ALL). Methods: Patients with newly diagnosed ALL, aged ≥ 15 years, were eligible for the study if their leukemic blast cells in bo...
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Published in: | The Korean journal of internal medicine 2023-09, Vol.38 (5), p.734 |
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creator | Dong Won Baek Han-seung Park Sang Kyun Sohn Dae Young Kim Inho Kim Jae-sook Ahn Young Rok Do Se Ryeon Lee Hyeon-seok Eom Won-sik Lee Sung-hyun Kim Ho Sup Lee Yoo Jin Lee Joon Ho Moon Je-hwan Lee |
description | Background/Aims: We performed a prospective study to determine the efficacy and safety of rituximab including chemotherapy in CD20-positive acute lymphoblastic leukemia (ALL).
Methods: Patients with newly diagnosed ALL, aged ≥ 15 years, were eligible for the study if their leukemic blast cells in bone marrow expressed CD20 ≥ 20% at the time of diagnosis. Patients received multiagent chemotherapy with rituximab. After achieving complete remission (CR), patients received five cycles of consolidation with concomitant rituximab. Rituximab was administered monthly from day 90 of transplantation for patients who received allogeneic hematopoietic cell transplantation.
Results: In patients with Philadelphia (Ph)-negative ALL, 39 of 41 achieved CR (95.1%), the 2- and 4-year relapse-free survival (RFS) rates were 50.4% and 35.7%, and the 2- and 4-year overall survival (OS) rates were 51.5% and 43.2%, respectively. In the group with Ph-positive ALL, all 32 patients achieved CR, the 2- and 4-year RFS rates were 60.7% and 52.1%, and the 2- and 4-year OS rates were 73.3% and 52.3%, respectively. In the Ph-negative ALL group, patients with higher CD20 positivity experienced more favorable RFS (p < 0.001) and OS (p = 0.06) than those with lower CD20 positivity. Patients who received ≥ 2 cycles of rituximab after transplantation had significantly improved RFS (hazard ratio [HR], 0.31; p = 0.049) and OS (HR, 0.29; p = 0.021) compared with those who received < 2 cycles.
Conclusions: The addition of rituximab to conventional chemotherapy for CD20-positive ALL is effective and tolerable (Clinicaltrials.gov NCT01429610). |
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fullrecord | <record><control><sourceid>kiss</sourceid><recordid>TN_cdi_kiss_primary_4038451</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><kiss_id>4038451</kiss_id><sourcerecordid>4038451</sourcerecordid><originalsourceid>FETCH-kiss_primary_40384513</originalsourceid><addsrcrecordid>eNp9jrFOwzAUAC1EJSLaL-jyfiCSHSdR1bWA6IrYKyd5bZ5qx5afDXjmx6kQM9MNd8PdiaqRsqv7vt3di0o1TV9rLfWD2DDTIKVWqleyq8T3G6X8Rc4MEGxmcNkmMhdcEowzOp9mjCYUOPsIC37aAtNNL55xgsNTI-vgmRJ9IJgxJwRbXJj9YA0nGsFivqIjswcDIXoOOP62YTaMcDwCpzyVtVidjWXc_PFRbF-e3w-v9ZWYTyHe7mI5tVLv2k7p_-0PgoNO6g</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Rituximab plus multiagent chemotherapy for newly diagnosed CD20-positive acute lymphoblastic leukemia: a prospective phase II study</title><source>Open Access: PubMed Central</source><creator>Dong Won Baek ; Han-seung Park ; Sang Kyun Sohn ; Dae Young Kim ; Inho Kim ; Jae-sook Ahn ; Young Rok Do ; Se Ryeon Lee ; Hyeon-seok Eom ; Won-sik Lee ; Sung-hyun Kim ; Ho Sup Lee ; Yoo Jin Lee ; Joon Ho Moon ; Je-hwan Lee</creator><creatorcontrib>Dong Won Baek ; Han-seung Park ; Sang Kyun Sohn ; Dae Young Kim ; Inho Kim ; Jae-sook Ahn ; Young Rok Do ; Se Ryeon Lee ; Hyeon-seok Eom ; Won-sik Lee ; Sung-hyun Kim ; Ho Sup Lee ; Yoo Jin Lee ; Joon Ho Moon ; Je-hwan Lee</creatorcontrib><description>Background/Aims: We performed a prospective study to determine the efficacy and safety of rituximab including chemotherapy in CD20-positive acute lymphoblastic leukemia (ALL).
Methods: Patients with newly diagnosed ALL, aged ≥ 15 years, were eligible for the study if their leukemic blast cells in bone marrow expressed CD20 ≥ 20% at the time of diagnosis. Patients received multiagent chemotherapy with rituximab. After achieving complete remission (CR), patients received five cycles of consolidation with concomitant rituximab. Rituximab was administered monthly from day 90 of transplantation for patients who received allogeneic hematopoietic cell transplantation.
Results: In patients with Philadelphia (Ph)-negative ALL, 39 of 41 achieved CR (95.1%), the 2- and 4-year relapse-free survival (RFS) rates were 50.4% and 35.7%, and the 2- and 4-year overall survival (OS) rates were 51.5% and 43.2%, respectively. In the group with Ph-positive ALL, all 32 patients achieved CR, the 2- and 4-year RFS rates were 60.7% and 52.1%, and the 2- and 4-year OS rates were 73.3% and 52.3%, respectively. In the Ph-negative ALL group, patients with higher CD20 positivity experienced more favorable RFS (p < 0.001) and OS (p = 0.06) than those with lower CD20 positivity. Patients who received ≥ 2 cycles of rituximab after transplantation had significantly improved RFS (hazard ratio [HR], 0.31; p = 0.049) and OS (HR, 0.29; p = 0.021) compared with those who received < 2 cycles.
Conclusions: The addition of rituximab to conventional chemotherapy for CD20-positive ALL is effective and tolerable (Clinicaltrials.gov NCT01429610).</description><identifier>ISSN: 1226-3303</identifier><identifier>EISSN: 2005-6648</identifier><language>kor</language><publisher>대한내과학회</publisher><subject>acute lymphoblastic ; Leukemia ; Rituximab ; Survival</subject><ispartof>The Korean journal of internal medicine, 2023-09, Vol.38 (5), p.734</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Dong Won Baek</creatorcontrib><creatorcontrib>Han-seung Park</creatorcontrib><creatorcontrib>Sang Kyun Sohn</creatorcontrib><creatorcontrib>Dae Young Kim</creatorcontrib><creatorcontrib>Inho Kim</creatorcontrib><creatorcontrib>Jae-sook Ahn</creatorcontrib><creatorcontrib>Young Rok Do</creatorcontrib><creatorcontrib>Se Ryeon Lee</creatorcontrib><creatorcontrib>Hyeon-seok Eom</creatorcontrib><creatorcontrib>Won-sik Lee</creatorcontrib><creatorcontrib>Sung-hyun Kim</creatorcontrib><creatorcontrib>Ho Sup Lee</creatorcontrib><creatorcontrib>Yoo Jin Lee</creatorcontrib><creatorcontrib>Joon Ho Moon</creatorcontrib><creatorcontrib>Je-hwan Lee</creatorcontrib><title>Rituximab plus multiagent chemotherapy for newly diagnosed CD20-positive acute lymphoblastic leukemia: a prospective phase II study</title><title>The Korean journal of internal medicine</title><addtitle>The Korean Journal of Internal Medicine</addtitle><description>Background/Aims: We performed a prospective study to determine the efficacy and safety of rituximab including chemotherapy in CD20-positive acute lymphoblastic leukemia (ALL).
Methods: Patients with newly diagnosed ALL, aged ≥ 15 years, were eligible for the study if their leukemic blast cells in bone marrow expressed CD20 ≥ 20% at the time of diagnosis. Patients received multiagent chemotherapy with rituximab. After achieving complete remission (CR), patients received five cycles of consolidation with concomitant rituximab. Rituximab was administered monthly from day 90 of transplantation for patients who received allogeneic hematopoietic cell transplantation.
Results: In patients with Philadelphia (Ph)-negative ALL, 39 of 41 achieved CR (95.1%), the 2- and 4-year relapse-free survival (RFS) rates were 50.4% and 35.7%, and the 2- and 4-year overall survival (OS) rates were 51.5% and 43.2%, respectively. In the group with Ph-positive ALL, all 32 patients achieved CR, the 2- and 4-year RFS rates were 60.7% and 52.1%, and the 2- and 4-year OS rates were 73.3% and 52.3%, respectively. In the Ph-negative ALL group, patients with higher CD20 positivity experienced more favorable RFS (p < 0.001) and OS (p = 0.06) than those with lower CD20 positivity. Patients who received ≥ 2 cycles of rituximab after transplantation had significantly improved RFS (hazard ratio [HR], 0.31; p = 0.049) and OS (HR, 0.29; p = 0.021) compared with those who received < 2 cycles.
Conclusions: The addition of rituximab to conventional chemotherapy for CD20-positive ALL is effective and tolerable (Clinicaltrials.gov NCT01429610).</description><subject>acute lymphoblastic</subject><subject>Leukemia</subject><subject>Rituximab</subject><subject>Survival</subject><issn>1226-3303</issn><issn>2005-6648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9jrFOwzAUAC1EJSLaL-jyfiCSHSdR1bWA6IrYKyd5bZ5qx5afDXjmx6kQM9MNd8PdiaqRsqv7vt3di0o1TV9rLfWD2DDTIKVWqleyq8T3G6X8Rc4MEGxmcNkmMhdcEowzOp9mjCYUOPsIC37aAtNNL55xgsNTI-vgmRJ9IJgxJwRbXJj9YA0nGsFivqIjswcDIXoOOP62YTaMcDwCpzyVtVidjWXc_PFRbF-e3w-v9ZWYTyHe7mI5tVLv2k7p_-0PgoNO6g</recordid><startdate>20230930</startdate><enddate>20230930</enddate><creator>Dong Won Baek</creator><creator>Han-seung Park</creator><creator>Sang Kyun Sohn</creator><creator>Dae Young Kim</creator><creator>Inho Kim</creator><creator>Jae-sook Ahn</creator><creator>Young Rok Do</creator><creator>Se Ryeon Lee</creator><creator>Hyeon-seok Eom</creator><creator>Won-sik Lee</creator><creator>Sung-hyun Kim</creator><creator>Ho Sup Lee</creator><creator>Yoo Jin Lee</creator><creator>Joon Ho Moon</creator><creator>Je-hwan Lee</creator><general>대한내과학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20230930</creationdate><title>Rituximab plus multiagent chemotherapy for newly diagnosed CD20-positive acute lymphoblastic leukemia: a prospective phase II study</title><author>Dong Won Baek ; Han-seung Park ; Sang Kyun Sohn ; Dae Young Kim ; Inho Kim ; Jae-sook Ahn ; Young Rok Do ; Se Ryeon Lee ; Hyeon-seok Eom ; Won-sik Lee ; Sung-hyun Kim ; Ho Sup Lee ; Yoo Jin Lee ; Joon Ho Moon ; Je-hwan Lee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_40384513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2023</creationdate><topic>acute lymphoblastic</topic><topic>Leukemia</topic><topic>Rituximab</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dong Won Baek</creatorcontrib><creatorcontrib>Han-seung Park</creatorcontrib><creatorcontrib>Sang Kyun Sohn</creatorcontrib><creatorcontrib>Dae Young Kim</creatorcontrib><creatorcontrib>Inho Kim</creatorcontrib><creatorcontrib>Jae-sook Ahn</creatorcontrib><creatorcontrib>Young Rok Do</creatorcontrib><creatorcontrib>Se Ryeon Lee</creatorcontrib><creatorcontrib>Hyeon-seok Eom</creatorcontrib><creatorcontrib>Won-sik Lee</creatorcontrib><creatorcontrib>Sung-hyun Kim</creatorcontrib><creatorcontrib>Ho Sup Lee</creatorcontrib><creatorcontrib>Yoo Jin Lee</creatorcontrib><creatorcontrib>Joon Ho Moon</creatorcontrib><creatorcontrib>Je-hwan Lee</creatorcontrib><collection>KISS</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>The Korean journal of internal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dong Won Baek</au><au>Han-seung Park</au><au>Sang Kyun Sohn</au><au>Dae Young Kim</au><au>Inho Kim</au><au>Jae-sook Ahn</au><au>Young Rok Do</au><au>Se Ryeon Lee</au><au>Hyeon-seok Eom</au><au>Won-sik Lee</au><au>Sung-hyun Kim</au><au>Ho Sup Lee</au><au>Yoo Jin Lee</au><au>Joon Ho Moon</au><au>Je-hwan Lee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rituximab plus multiagent chemotherapy for newly diagnosed CD20-positive acute lymphoblastic leukemia: a prospective phase II study</atitle><jtitle>The Korean journal of internal medicine</jtitle><addtitle>The Korean Journal of Internal Medicine</addtitle><date>2023-09-30</date><risdate>2023</risdate><volume>38</volume><issue>5</issue><spage>734</spage><pages>734-</pages><issn>1226-3303</issn><eissn>2005-6648</eissn><abstract>Background/Aims: We performed a prospective study to determine the efficacy and safety of rituximab including chemotherapy in CD20-positive acute lymphoblastic leukemia (ALL).
Methods: Patients with newly diagnosed ALL, aged ≥ 15 years, were eligible for the study if their leukemic blast cells in bone marrow expressed CD20 ≥ 20% at the time of diagnosis. Patients received multiagent chemotherapy with rituximab. After achieving complete remission (CR), patients received five cycles of consolidation with concomitant rituximab. Rituximab was administered monthly from day 90 of transplantation for patients who received allogeneic hematopoietic cell transplantation.
Results: In patients with Philadelphia (Ph)-negative ALL, 39 of 41 achieved CR (95.1%), the 2- and 4-year relapse-free survival (RFS) rates were 50.4% and 35.7%, and the 2- and 4-year overall survival (OS) rates were 51.5% and 43.2%, respectively. In the group with Ph-positive ALL, all 32 patients achieved CR, the 2- and 4-year RFS rates were 60.7% and 52.1%, and the 2- and 4-year OS rates were 73.3% and 52.3%, respectively. In the Ph-negative ALL group, patients with higher CD20 positivity experienced more favorable RFS (p < 0.001) and OS (p = 0.06) than those with lower CD20 positivity. Patients who received ≥ 2 cycles of rituximab after transplantation had significantly improved RFS (hazard ratio [HR], 0.31; p = 0.049) and OS (HR, 0.29; p = 0.021) compared with those who received < 2 cycles.
Conclusions: The addition of rituximab to conventional chemotherapy for CD20-positive ALL is effective and tolerable (Clinicaltrials.gov NCT01429610).</abstract><pub>대한내과학회</pub><tpages>22</tpages></addata></record> |
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subjects | acute lymphoblastic Leukemia Rituximab Survival |
title | Rituximab plus multiagent chemotherapy for newly diagnosed CD20-positive acute lymphoblastic leukemia: a prospective phase II study |
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