Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience

Abstract The long‐term effects of tyrosine kinase inhibitors (TKIs), including imatinib, and surgical intervention on advanced gastrointestinal stromal tumor (GIST) were evaluated. All 379 patients had metastatic or recurrent GIST and started 400 mg/d imatinib at the Asan Medical Center in periods 1...

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Main Authors: Jwa Hoon Kim, Min‐Hee Ryu, Changhoon Yoo, Heejung Chae, Hana Na, Moyoul Beck, Beom Su Kim, Moon‐Won Yoo, Jeong Hwan Yook, Byung Sik Kim, Ki‐Hun Kim, Chan Wook Kim, Yoon‐Koo Kang
Format: Article
Language:English
Published: Wiley 2019-03-01
Series:Cancer Medicine
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Online Access:https://doi.org/10.1002/cam4.1994
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author Jwa Hoon Kim
Min‐Hee Ryu
Changhoon Yoo
Heejung Chae
Hana Na
Moyoul Beck
Beom Su Kim
Moon‐Won Yoo
Jeong Hwan Yook
Byung Sik Kim
Ki‐Hun Kim
Chan Wook Kim
Yoon‐Koo Kang
author_facet Jwa Hoon Kim
Min‐Hee Ryu
Changhoon Yoo
Heejung Chae
Hana Na
Moyoul Beck
Beom Su Kim
Moon‐Won Yoo
Jeong Hwan Yook
Byung Sik Kim
Ki‐Hun Kim
Chan Wook Kim
Yoon‐Koo Kang
author_sort Jwa Hoon Kim
collection DOAJ
description Abstract The long‐term effects of tyrosine kinase inhibitors (TKIs), including imatinib, and surgical intervention on advanced gastrointestinal stromal tumor (GIST) were evaluated. All 379 patients had metastatic or recurrent GIST and started 400 mg/d imatinib at the Asan Medical Center in periods 1 and 2 [2001‐2007 (33.2%) and 2008‐2014 (66.8%), respectively]. Men constituted 60.4%; median patient age and tumor size at the initiation of imatinib were 58.6 (14.6‐85.5) years and 51 (0‐324) mm, respectively, without differences between periods except for older age and less preimatinib surgery in period 2. Response and disease control rates with imatinib in measurable GIST were 63.1% and 94.3%, respectively, without differences between periods. More patients in period 2 underwent surgical resection for TKI‐responsive diseases within the first 2 years (24.9%, P = 0.006). With a median follow‐up of 6.1 years (2.5‐16.0) in survivors, median progression‐free survival (PFS) was 5.4 years [95% confidence interval (CI), 4.0‐6.9]. Subsequent sunitinib (P = 0.066) and regorafenib (P = 0.003) were more commonly administered in period 2. Median overall survival (OS) was 8.8 years (95% CI, 7.8‐9.7). PFS with imatinib (P = 0.002) and OS (P = 0.019) were significantly longer in period 2. Young age, smaller tumor size at the initiation of imatinib, KIT exon 11 mutation, surgical intervention, and period 2 were favorable factors for PFS and OS. Patients with advanced GIST showed better prognosis with the optimal use of imatinib, along with active surgical intervention and more common use of subsequent TKIs in period 2.
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spelling doaj-art-aede1e5457f34f26aa500166828ca9c92025-01-31T08:47:42ZengWileyCancer Medicine2045-76342019-03-01831034104310.1002/cam4.1994Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experienceJwa Hoon Kim0Min‐Hee Ryu1Changhoon Yoo2Heejung Chae3Hana Na4Moyoul Beck5Beom Su Kim6Moon‐Won Yoo7Jeong Hwan Yook8Byung Sik Kim9Ki‐Hun Kim10Chan Wook Kim11Yoon‐Koo Kang12Department of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaDepartment of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaDepartment of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaDepartment of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaDepartment of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaDepartment of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaDepartment of Surgery, Asan Medical Center University of Ulsan College of Medicine Seoul KoreaDepartment of Surgery, Asan Medical Center University of Ulsan College of Medicine Seoul KoreaDepartment of Surgery, Asan Medical Center University of Ulsan College of Medicine Seoul KoreaDepartment of Surgery, Asan Medical Center University of Ulsan College of Medicine Seoul KoreaDepartment of Surgery, Asan Medical Center University of Ulsan College of Medicine Seoul KoreaDepartment of Surgery, Asan Medical Center University of Ulsan College of Medicine Seoul KoreaDepartment of Oncology Asan Medical Center, University of Ulsan College of Medicine Seoul KoreaAbstract The long‐term effects of tyrosine kinase inhibitors (TKIs), including imatinib, and surgical intervention on advanced gastrointestinal stromal tumor (GIST) were evaluated. All 379 patients had metastatic or recurrent GIST and started 400 mg/d imatinib at the Asan Medical Center in periods 1 and 2 [2001‐2007 (33.2%) and 2008‐2014 (66.8%), respectively]. Men constituted 60.4%; median patient age and tumor size at the initiation of imatinib were 58.6 (14.6‐85.5) years and 51 (0‐324) mm, respectively, without differences between periods except for older age and less preimatinib surgery in period 2. Response and disease control rates with imatinib in measurable GIST were 63.1% and 94.3%, respectively, without differences between periods. More patients in period 2 underwent surgical resection for TKI‐responsive diseases within the first 2 years (24.9%, P = 0.006). With a median follow‐up of 6.1 years (2.5‐16.0) in survivors, median progression‐free survival (PFS) was 5.4 years [95% confidence interval (CI), 4.0‐6.9]. Subsequent sunitinib (P = 0.066) and regorafenib (P = 0.003) were more commonly administered in period 2. Median overall survival (OS) was 8.8 years (95% CI, 7.8‐9.7). PFS with imatinib (P = 0.002) and OS (P = 0.019) were significantly longer in period 2. Young age, smaller tumor size at the initiation of imatinib, KIT exon 11 mutation, surgical intervention, and period 2 were favorable factors for PFS and OS. Patients with advanced GIST showed better prognosis with the optimal use of imatinib, along with active surgical intervention and more common use of subsequent TKIs in period 2.https://doi.org/10.1002/cam4.1994gastrointestinal stromal tumorimatinib mesylatesurvival
spellingShingle Jwa Hoon Kim
Min‐Hee Ryu
Changhoon Yoo
Heejung Chae
Hana Na
Moyoul Beck
Beom Su Kim
Moon‐Won Yoo
Jeong Hwan Yook
Byung Sik Kim
Ki‐Hun Kim
Chan Wook Kim
Yoon‐Koo Kang
Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience
Cancer Medicine
gastrointestinal stromal tumor
imatinib mesylate
survival
title Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience
title_full Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience
title_fullStr Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience
title_full_unstemmed Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience
title_short Long‐term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors: A 14‐year, single‐center experience
title_sort long term survival outcome with tyrosine kinase inhibitors and surgical intervention in patients with metastatic or recurrent gastrointestinal stromal tumors a 14 year single center experience
topic gastrointestinal stromal tumor
imatinib mesylate
survival
url https://doi.org/10.1002/cam4.1994
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