Long-term results of adjuvant imatinib mesylate in localized, high-risk, primary gastrointestinal stromal tumor: ACOSOG Z9000 (Alliance) intergroup phase 2 trial

To conduct the first adjuvant trial of imatinib mesylate for treatment of gastrointestinal stromal tumor (GIST). GIST is the most common sarcoma. Although surgical resection has been the mainstay of therapy for localized, primary GIST, postoperative tumor recurrence is common. The KIT protooncogene...

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Veröffentlicht in:Annals of surgery 2013-09, Vol.258 (3), p.422-429
Hauptverfasser: DeMatteo, Ronald P, Ballman, Karla V, Antonescu, Cristina R, Corless, Christopher, Kolesnikova, Violetta, von Mehren, Margaret, McCarter, Martin D, Norton, Jeffrey, Maki, Robert G, Pisters, Peter W T, Demetri, George D, Brennan, Murray F, Owzar, Kouros
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container_end_page 429
container_issue 3
container_start_page 422
container_title Annals of surgery
container_volume 258
creator DeMatteo, Ronald P
Ballman, Karla V
Antonescu, Cristina R
Corless, Christopher
Kolesnikova, Violetta
von Mehren, Margaret
McCarter, Martin D
Norton, Jeffrey
Maki, Robert G
Pisters, Peter W T
Demetri, George D
Brennan, Murray F
Owzar, Kouros
description To conduct the first adjuvant trial of imatinib mesylate for treatment of gastrointestinal stromal tumor (GIST). GIST is the most common sarcoma. Although surgical resection has been the mainstay of therapy for localized, primary GIST, postoperative tumor recurrence is common. The KIT protooncogene or, less frequently, platelet-derived growth factor receptor alpha is mutated in GIST; the gene products of both are inhibited by imatinib mesylate. This was a phase II, intergroup trial led by the American College of Surgeons Oncology Group, registered at ClinicalTrials.gov as NCT00025246. From September 2001 to September 2003, we accrued 106 patients who had undergone complete gross tumor removal but were deemed at high risk for recurrence. Patients were prescribed imatinib 400 mg per day for 1 year and followed with serial radiologic evaluation. The primary endpoint was overall survival (OS). After a median follow-up of 7.7 years, the 1-, 3-, and 5-year OS rates were 99%, 97%, and 83%, which compared favorably with a historical 5-year OS rate of 35%. The 1-, 3-, and 5-year recurrence-free survival (RFS) rates were 96%, 60%, and 40%. On univariable analysis, age and mitotic rate were associated with OS. On multivariable analysis, the RFS rate was lower with increasing tumor size, small bowel site, KIT exon 9 mutation, high mitotic rate, and older age. Adjuvant imatinib in patients with primary GIST who are at high risk of recurrence prolongs OS compared with that of historical controls. Optimal duration of adjuvant therapy remains undefined. (NCT00025246).
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GIST is the most common sarcoma. Although surgical resection has been the mainstay of therapy for localized, primary GIST, postoperative tumor recurrence is common. The KIT protooncogene or, less frequently, platelet-derived growth factor receptor alpha is mutated in GIST; the gene products of both are inhibited by imatinib mesylate. This was a phase II, intergroup trial led by the American College of Surgeons Oncology Group, registered at ClinicalTrials.gov as NCT00025246. From September 2001 to September 2003, we accrued 106 patients who had undergone complete gross tumor removal but were deemed at high risk for recurrence. Patients were prescribed imatinib 400 mg per day for 1 year and followed with serial radiologic evaluation. The primary endpoint was overall survival (OS). After a median follow-up of 7.7 years, the 1-, 3-, and 5-year OS rates were 99%, 97%, and 83%, which compared favorably with a historical 5-year OS rate of 35%. The 1-, 3-, and 5-year recurrence-free survival (RFS) rates were 96%, 60%, and 40%. On univariable analysis, age and mitotic rate were associated with OS. On multivariable analysis, the RFS rate was lower with increasing tumor size, small bowel site, KIT exon 9 mutation, high mitotic rate, and older age. Adjuvant imatinib in patients with primary GIST who are at high risk of recurrence prolongs OS compared with that of historical controls. Optimal duration of adjuvant therapy remains undefined. 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The 1-, 3-, and 5-year recurrence-free survival (RFS) rates were 96%, 60%, and 40%. On univariable analysis, age and mitotic rate were associated with OS. On multivariable analysis, the RFS rate was lower with increasing tumor size, small bowel site, KIT exon 9 mutation, high mitotic rate, and older age. Adjuvant imatinib in patients with primary GIST who are at high risk of recurrence prolongs OS compared with that of historical controls. Optimal duration of adjuvant therapy remains undefined. (NCT00025246).</abstract><cop>United States</cop><pmid>23860199</pmid><doi>10.1097/SLA.0b013e3182a15eb7</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Journals@Ovid Complete; PubMed Central
subjects Adolescent
Adult
Aged
Antineoplastic Agents - therapeutic use
Benzamides - therapeutic use
Chemotherapy, Adjuvant
Drug Administration Schedule
Female
Follow-Up Studies
Gastrointestinal Neoplasms - drug therapy
Gastrointestinal Neoplasms - mortality
Gastrointestinal Neoplasms - surgery
Gastrointestinal Stromal Tumors - drug therapy
Gastrointestinal Stromal Tumors - mortality
Gastrointestinal Stromal Tumors - surgery
Humans
Imatinib Mesylate
Male
Middle Aged
Neoplasm Recurrence, Local - prevention & control
Piperazines - therapeutic use
Pyrimidines - therapeutic use
Risk
Survival Analysis
Treatment Outcome
Young Adult
title Long-term results of adjuvant imatinib mesylate in localized, high-risk, primary gastrointestinal stromal tumor: ACOSOG Z9000 (Alliance) intergroup phase 2 trial
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