Dasatinib in Pediatric Patients With Chronic Myeloid Leukemia in Chronic Phase: Results From a Phase II Trial

Purpose Safe, effective treatments are needed for pediatric patients with chronic myeloid leukemia in chronic phase (CML-CP). Dasatinib is approved for treatment of adults and children with CML-CP. A phase I study determined suitable dosing for children with Philadelphia chromosome-positive (Ph+) le...

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Veröffentlicht in:Journal of clinical oncology 2018-05, Vol.36 (13), p.1330-1338
Hauptverfasser: Gore, Lia, Kearns, Pamela R, de Martino, Maria Lucia, Lee, De Souza, Carmino Antonio, Bertrand, Yves, Hijiya, Nobuko, Stork, Linda C, Chung, Nack-Gyun, Cardos, Rocio Cardenas, Saikia, Tapan, Fagioli, Franca, Seo, Jong Jin, Landman-Parker, Judith, Lancaster, Donna, Place, Andrew E, Rabin, Karen R, Sacchi, Mariana, Swanink, Rene, Zwaan, C Michel
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container_end_page 1338
container_issue 13
container_start_page 1330
container_title Journal of clinical oncology
container_volume 36
creator Gore, Lia
Kearns, Pamela R
de Martino, Maria Lucia
Lee
De Souza, Carmino Antonio
Bertrand, Yves
Hijiya, Nobuko
Stork, Linda C
Chung, Nack-Gyun
Cardos, Rocio Cardenas
Saikia, Tapan
Fagioli, Franca
Seo, Jong Jin
Landman-Parker, Judith
Lancaster, Donna
Place, Andrew E
Rabin, Karen R
Sacchi, Mariana
Swanink, Rene
Zwaan, C Michel
description Purpose Safe, effective treatments are needed for pediatric patients with chronic myeloid leukemia in chronic phase (CML-CP). Dasatinib is approved for treatment of adults and children with CML-CP. A phase I study determined suitable dosing for children with Philadelphia chromosome-positive (Ph+) leukemias. Methods CA180-226/NCT00777036 is a phase II, open-label, nonrandomized prospective trial of patients < 18 years of age receiving dasatinib. There are three cohorts: (1) imatinib-resistant/intolerant CML-CP, (2) imatinib-resistant/intolerant CML in accelerated/blast phase or Ph+ acute lymphoblastic leukemia (n = 17), and (3) newly diagnosed CML-CP treated with tablets or powder for oral suspension. Major cytogenetic response > 30% for imatinib-resistant/intolerant patients and complete cytogenetic response (CCyR) > 55% for newly diagnosed patients were of clinical interest. Results Of 113 patients with CML-CP, 14 (48%) who were imatinib-resistant/intolerant and 61 (73%) who were newly diagnosed remained on treatment at time of analysis. Major cytogenetic response > 30% was reached by 3 months in the imatinib-resistant/intolerant group and CCyR > 55% was reached by 6 months in the newly diagnosed CML-CP group. CCyR and major molecular response by 12 months, respectively, were 76% and 41% in the imatinib-resistant/intolerant group and 92% and 52% in newly diagnosed CML-CP group. Progression-free survival by 48 months was 78% and 93% in the imatinib-resistant/intolerant and newly diagnosed CML-CP groups, respectively. No dasatinib-related pleural or pericardial effusion, pulmonary edema, or pulmonary arterial hypertension were reported. Bone growth and development events were reported in 4% of patients. Conclusion In the largest prospective trial to date in children with CML-CP, we demonstrate that dasatinib is a safe, effective treatment of pediatric CML-CP. Target responses to first- or second-line dasatinib were met early, and deep molecular responses were observed. Safety of dasatinib in pediatric patients was similar to that observed in adults; however, no cases of pleural or pericardial effusion or pulmonary arterial hypertension were reported.
doi_str_mv 10.1200/JCO.2017.75.9597
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Dasatinib is approved for treatment of adults and children with CML-CP. A phase I study determined suitable dosing for children with Philadelphia chromosome-positive (Ph+) leukemias. Methods CA180-226/NCT00777036 is a phase II, open-label, nonrandomized prospective trial of patients &lt; 18 years of age receiving dasatinib. There are three cohorts: (1) imatinib-resistant/intolerant CML-CP, (2) imatinib-resistant/intolerant CML in accelerated/blast phase or Ph+ acute lymphoblastic leukemia (n = 17), and (3) newly diagnosed CML-CP treated with tablets or powder for oral suspension. Major cytogenetic response &gt; 30% for imatinib-resistant/intolerant patients and complete cytogenetic response (CCyR) &gt; 55% for newly diagnosed patients were of clinical interest. Results Of 113 patients with CML-CP, 14 (48%) who were imatinib-resistant/intolerant and 61 (73%) who were newly diagnosed remained on treatment at time of analysis. Major cytogenetic response &gt; 30% was reached by 3 months in the imatinib-resistant/intolerant group and CCyR &gt; 55% was reached by 6 months in the newly diagnosed CML-CP group. CCyR and major molecular response by 12 months, respectively, were 76% and 41% in the imatinib-resistant/intolerant group and 92% and 52% in newly diagnosed CML-CP group. Progression-free survival by 48 months was 78% and 93% in the imatinib-resistant/intolerant and newly diagnosed CML-CP groups, respectively. No dasatinib-related pleural or pericardial effusion, pulmonary edema, or pulmonary arterial hypertension were reported. Bone growth and development events were reported in 4% of patients. Conclusion In the largest prospective trial to date in children with CML-CP, we demonstrate that dasatinib is a safe, effective treatment of pediatric CML-CP. Target responses to first- or second-line dasatinib were met early, and deep molecular responses were observed. Safety of dasatinib in pediatric patients was similar to that observed in adults; however, no cases of pleural or pericardial effusion or pulmonary arterial hypertension were reported.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2017.75.9597</identifier><identifier>PMID: 29498925</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>ORIGINAL REPORTS</subject><ispartof>Journal of clinical oncology, 2018-05, Vol.36 (13), p.1330-1338</ispartof><rights>2018 by American Society of Clinical Oncology 2018 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-9c3dab88fc0d0c14f73b6e50bb5c8792d803f2a6e1085fdff60a0e036d0c43053</citedby><cites>FETCH-LOGICAL-c396t-9c3dab88fc0d0c14f73b6e50bb5c8792d803f2a6e1085fdff60a0e036d0c43053</cites></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/29498925$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gore, Lia</creatorcontrib><creatorcontrib>Kearns, Pamela R</creatorcontrib><creatorcontrib>de Martino, Maria Lucia</creatorcontrib><creatorcontrib>Lee</creatorcontrib><creatorcontrib>De Souza, Carmino Antonio</creatorcontrib><creatorcontrib>Bertrand, Yves</creatorcontrib><creatorcontrib>Hijiya, Nobuko</creatorcontrib><creatorcontrib>Stork, Linda C</creatorcontrib><creatorcontrib>Chung, Nack-Gyun</creatorcontrib><creatorcontrib>Cardos, Rocio Cardenas</creatorcontrib><creatorcontrib>Saikia, Tapan</creatorcontrib><creatorcontrib>Fagioli, Franca</creatorcontrib><creatorcontrib>Seo, Jong Jin</creatorcontrib><creatorcontrib>Landman-Parker, Judith</creatorcontrib><creatorcontrib>Lancaster, Donna</creatorcontrib><creatorcontrib>Place, Andrew E</creatorcontrib><creatorcontrib>Rabin, Karen R</creatorcontrib><creatorcontrib>Sacchi, Mariana</creatorcontrib><creatorcontrib>Swanink, Rene</creatorcontrib><creatorcontrib>Zwaan, C Michel</creatorcontrib><title>Dasatinib in Pediatric Patients With Chronic Myeloid Leukemia in Chronic Phase: Results From a Phase II Trial</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Purpose Safe, effective treatments are needed for pediatric patients with chronic myeloid leukemia in chronic phase (CML-CP). Dasatinib is approved for treatment of adults and children with CML-CP. A phase I study determined suitable dosing for children with Philadelphia chromosome-positive (Ph+) leukemias. Methods CA180-226/NCT00777036 is a phase II, open-label, nonrandomized prospective trial of patients &lt; 18 years of age receiving dasatinib. There are three cohorts: (1) imatinib-resistant/intolerant CML-CP, (2) imatinib-resistant/intolerant CML in accelerated/blast phase or Ph+ acute lymphoblastic leukemia (n = 17), and (3) newly diagnosed CML-CP treated with tablets or powder for oral suspension. Major cytogenetic response &gt; 30% for imatinib-resistant/intolerant patients and complete cytogenetic response (CCyR) &gt; 55% for newly diagnosed patients were of clinical interest. Results Of 113 patients with CML-CP, 14 (48%) who were imatinib-resistant/intolerant and 61 (73%) who were newly diagnosed remained on treatment at time of analysis. Major cytogenetic response &gt; 30% was reached by 3 months in the imatinib-resistant/intolerant group and CCyR &gt; 55% was reached by 6 months in the newly diagnosed CML-CP group. CCyR and major molecular response by 12 months, respectively, were 76% and 41% in the imatinib-resistant/intolerant group and 92% and 52% in newly diagnosed CML-CP group. Progression-free survival by 48 months was 78% and 93% in the imatinib-resistant/intolerant and newly diagnosed CML-CP groups, respectively. No dasatinib-related pleural or pericardial effusion, pulmonary edema, or pulmonary arterial hypertension were reported. Bone growth and development events were reported in 4% of patients. Conclusion In the largest prospective trial to date in children with CML-CP, we demonstrate that dasatinib is a safe, effective treatment of pediatric CML-CP. Target responses to first- or second-line dasatinib were met early, and deep molecular responses were observed. Safety of dasatinib in pediatric patients was similar to that observed in adults; however, no cases of pleural or pericardial effusion or pulmonary arterial hypertension were reported.</description><subject>ORIGINAL REPORTS</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpVkc1LAzEQxYMoWqt3T5Kjl62TpNlsPAhSvyoViyh6C9ls1kb3oya7gv-9KVXR08Cb95tJ5iF0QGBEKMDxzeRuRIGIkeAjyaXYQAPCqUiE4HwTDUAwmpCMPe-g3RBeAcg4Y3wb7VA5lpmkfIDqcx105xqXY9fguS2c7rwzeB5F23QBP7lugScL3zZRvf20VesKPLP9m62dXjE_vflCB3uC723oq8hd-rbGeq3i6RQ_eKerPbRV6irY_e86RI-XFw-T62R2dzWdnM0Sw2TaJdKwQudZVhoowJBxKVieWg55zk0mJC0yYCXVqSWQ8bIoyxQ0WGBpdI8ZcDZEp-u5yz6vbWHiT7yu1NK7WvtP1Wqn_ncat1Av7YfikkoaLzZER98DfPve29Cp2gVjq0o3tu2DikcHJlImRbTC2mp8G4K35e8aAmqVkooprQChBFerlCJy-Pd5v8BPLOwLq9aOyw</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Gore, Lia</creator><creator>Kearns, Pamela R</creator><creator>de Martino, Maria Lucia</creator><creator>Lee</creator><creator>De Souza, Carmino Antonio</creator><creator>Bertrand, Yves</creator><creator>Hijiya, Nobuko</creator><creator>Stork, Linda C</creator><creator>Chung, Nack-Gyun</creator><creator>Cardos, Rocio Cardenas</creator><creator>Saikia, Tapan</creator><creator>Fagioli, Franca</creator><creator>Seo, Jong Jin</creator><creator>Landman-Parker, Judith</creator><creator>Lancaster, Donna</creator><creator>Place, Andrew E</creator><creator>Rabin, Karen R</creator><creator>Sacchi, Mariana</creator><creator>Swanink, Rene</creator><creator>Zwaan, C Michel</creator><general>American Society of Clinical Oncology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180501</creationdate><title>Dasatinib in Pediatric Patients With Chronic Myeloid Leukemia in Chronic Phase: Results From a Phase II Trial</title><author>Gore, Lia ; 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Dasatinib is approved for treatment of adults and children with CML-CP. A phase I study determined suitable dosing for children with Philadelphia chromosome-positive (Ph+) leukemias. Methods CA180-226/NCT00777036 is a phase II, open-label, nonrandomized prospective trial of patients &lt; 18 years of age receiving dasatinib. There are three cohorts: (1) imatinib-resistant/intolerant CML-CP, (2) imatinib-resistant/intolerant CML in accelerated/blast phase or Ph+ acute lymphoblastic leukemia (n = 17), and (3) newly diagnosed CML-CP treated with tablets or powder for oral suspension. Major cytogenetic response &gt; 30% for imatinib-resistant/intolerant patients and complete cytogenetic response (CCyR) &gt; 55% for newly diagnosed patients were of clinical interest. Results Of 113 patients with CML-CP, 14 (48%) who were imatinib-resistant/intolerant and 61 (73%) who were newly diagnosed remained on treatment at time of analysis. Major cytogenetic response &gt; 30% was reached by 3 months in the imatinib-resistant/intolerant group and CCyR &gt; 55% was reached by 6 months in the newly diagnosed CML-CP group. CCyR and major molecular response by 12 months, respectively, were 76% and 41% in the imatinib-resistant/intolerant group and 92% and 52% in newly diagnosed CML-CP group. Progression-free survival by 48 months was 78% and 93% in the imatinib-resistant/intolerant and newly diagnosed CML-CP groups, respectively. No dasatinib-related pleural or pericardial effusion, pulmonary edema, or pulmonary arterial hypertension were reported. Bone growth and development events were reported in 4% of patients. Conclusion In the largest prospective trial to date in children with CML-CP, we demonstrate that dasatinib is a safe, effective treatment of pediatric CML-CP. Target responses to first- or second-line dasatinib were met early, and deep molecular responses were observed. Safety of dasatinib in pediatric patients was similar to that observed in adults; however, no cases of pleural or pericardial effusion or pulmonary arterial hypertension were reported.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>29498925</pmid><doi>10.1200/JCO.2017.75.9597</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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title Dasatinib in Pediatric Patients With Chronic Myeloid Leukemia in Chronic Phase: Results From a Phase II Trial
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