2010
DOI: 10.1002/jso.21630
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Surgical management in metastatic gastrointestinal stromal tumor (GIST) patients after imatinib mesylate treatment

Abstract: Surgery may benefit selected GIST patients with PR, SD, and LP, especially for patients with LP because patients with LP had comparable survival to that of patients with responsive lesion. Surgery may prevent potential development of secondary mutations in selected patients with response after IM treatment. Secondary kit mutation was found more frequently in GIST patients with a primary kit exon 11 mutation than those with a primary kit exon 9 mutation.

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Cited by 50 publications
(32 citation statements)
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“…If those lesions are not removable, escalation of the dose of imatinib or a switch to sunitinib should be considered. Although there was no prospective study to evaluate the efficacy of local treatment for focal progression in GIST, retrospective analyses have suggested that some cases with focal progression may benefit from local treatment [38,60]. On the other hand, there was a study showing the potential risk of rapid disease progression within a short period of time after local treatment [39].…”
Section: Medical Treatment Of Gistsmentioning
confidence: 99%
“…If those lesions are not removable, escalation of the dose of imatinib or a switch to sunitinib should be considered. Although there was no prospective study to evaluate the efficacy of local treatment for focal progression in GIST, retrospective analyses have suggested that some cases with focal progression may benefit from local treatment [38,60]. On the other hand, there was a study showing the potential risk of rapid disease progression within a short period of time after local treatment [39].…”
Section: Medical Treatment Of Gistsmentioning
confidence: 99%
“…It is also indicated in those who have a widespread metastatic disease or a recurrence after resection. There is a survival benefit of cytoreductive surgery following preoperative imatinib in patients responding to preoperative imatinib [51,[55][56][57][58][59][60][61][62] . The lesion is assessed within 3 mo of initiating therapy to determine if it has become resectable.…”
Section: Unresectable Metastatic or Recurrent Diseasementioning
confidence: 99%
“…In cases where the tumor remains unresectable, imatinib is continued indefinitely until there is evi- dence of tumor progression. Continuation of TKI therapy life-long for palliation of symptoms forms an essential component of best supportive care [9,18,27,29,51,[56][57][58][59][60][61][62] . Options for patients with progressive disease or with widespread systemic disease and good performance status (0-2) include continuation of imatinib at the same dose, dose escalation up to 800 mg in the absence of severe adverse drug reactions or switching to sunitinib [29,[44][45][46]51,53,55] .…”
Section: Unresectable Metastatic or Recurrent Diseasementioning
confidence: 99%
“…It is believed to occur through development of a secondary acquired KIT mutation [19]. Sunitinib another molecule inhibitor of receptor tyrosine kinases has been shown to be an effective second-line therapy for patients with GISTs [20,21].…”
Section: Fine-needle Biopsymentioning
confidence: 99%