Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor
Background: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. The clinical management of patients with metastatic GISTs is exceptionally challenging due to their poor prognosis. Apatinib is a multiple tyrosine kinase inhibitor. Here, we pre...
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doaj-3a62ac81ea80462e99706897669ae2332020-11-25T02:18:32ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2019-06-01910.3389/fonc.2019.00470455081Apatinib Treatment in Metastatic Gastrointestinal Stromal TumorZhaolun Cai0Xin Chen1Bo Zhang2Dan Cao3Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, ChinaDepartment of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, ChinaDepartment of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, ChinaDepartment of Abdominal Oncology, Cancer Center of West China Hospital, Sichuan University, Chengdu, ChinaBackground: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. The clinical management of patients with metastatic GISTs is exceptionally challenging due to their poor prognosis. Apatinib is a multiple tyrosine kinase inhibitor. Here, we present the unique case with metastatic GISTs who derived clinical benefit from apatinib following the failure of imatinib and sunitinib.Case presentation: A 57-year-old man was admitted to our hospital diagnosed with metastatic and recurrent GISTs following surgical resection. Fifty-four months after the first-line imatinib treatment, he developed progressive disease and then was treated with cytoreductive surgery combined with imatinib. Disease progression occurred after 7 months. He then received second-line sunitinib and achieved a progression-free survival of 11 months. Apatinib mesylate was then administered. Follow-up imaging revealed a stable disease. Progression-free survival following apatinib therapy was at least 8 months. The only toxicities were hypertension and proteinuria, which were both controllable and well-tolerated.Conclusions: Treatment with apatinib provides an additional option for the treatment of patients with GISTs refractory to imatinib and sunitinib.https://www.frontiersin.org/article/10.3389/fonc.2019.00470/fullapatinibgastrointestinal stromal tumorsGISTsmetastaticvascular endothelial growth factor receptor |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhaolun Cai Xin Chen Bo Zhang Dan Cao |
spellingShingle |
Zhaolun Cai Xin Chen Bo Zhang Dan Cao Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor Frontiers in Oncology apatinib gastrointestinal stromal tumors GISTs metastatic vascular endothelial growth factor receptor |
author_facet |
Zhaolun Cai Xin Chen Bo Zhang Dan Cao |
author_sort |
Zhaolun Cai |
title |
Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor |
title_short |
Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor |
title_full |
Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor |
title_fullStr |
Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor |
title_full_unstemmed |
Apatinib Treatment in Metastatic Gastrointestinal Stromal Tumor |
title_sort |
apatinib treatment in metastatic gastrointestinal stromal tumor |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2019-06-01 |
description |
Background: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. The clinical management of patients with metastatic GISTs is exceptionally challenging due to their poor prognosis. Apatinib is a multiple tyrosine kinase inhibitor. Here, we present the unique case with metastatic GISTs who derived clinical benefit from apatinib following the failure of imatinib and sunitinib.Case presentation: A 57-year-old man was admitted to our hospital diagnosed with metastatic and recurrent GISTs following surgical resection. Fifty-four months after the first-line imatinib treatment, he developed progressive disease and then was treated with cytoreductive surgery combined with imatinib. Disease progression occurred after 7 months. He then received second-line sunitinib and achieved a progression-free survival of 11 months. Apatinib mesylate was then administered. Follow-up imaging revealed a stable disease. Progression-free survival following apatinib therapy was at least 8 months. The only toxicities were hypertension and proteinuria, which were both controllable and well-tolerated.Conclusions: Treatment with apatinib provides an additional option for the treatment of patients with GISTs refractory to imatinib and sunitinib. |
topic |
apatinib gastrointestinal stromal tumors GISTs metastatic vascular endothelial growth factor receptor |
url |
https://www.frontiersin.org/article/10.3389/fonc.2019.00470/full |
work_keys_str_mv |
AT zhaoluncai apatinibtreatmentinmetastaticgastrointestinalstromaltumor AT xinchen apatinibtreatmentinmetastaticgastrointestinalstromaltumor AT bozhang apatinibtreatmentinmetastaticgastrointestinalstromaltumor AT dancao apatinibtreatmentinmetastaticgastrointestinalstromaltumor |
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