Neoadjuvant Imatinib in Locally Advanced Gastrointestinal Stromal Tumors (GIST): The EORTC STBSG Experience

P Rutkowski, A Gronchi, P Hohenberger, S Bonvalot, P Schoffski, S Bauer, E Fumagalli, P Nyckowski, BP Nguyen, JM Kerst, M Fiore, E Bylina, M Hoiczyk, A Cats, PG Casali, A le Cesne, J Treckmann, E Stoeckle, JHW (Johannes) de Wilt, Stefan SleijferR Tielen, W de Graaf, Kees Verhoef, F van Coevorden

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Preoperative imatinib therapy of locally advanced GIST may facilitate resection and decrease morbidity of the procedure. We have pooled databases from 10 EORTC STBSG sarcoma centers and analyzed disease-free survival (DFS) and disease-specific survival (DSS) in 161 patients with locally advanced, nonmetastatic GISTs who received neoadjuvant imatinib. OS was calculated from start of imatinib therapy for locally advanced disease until death or last follow-up (FU) after resection of the GIST. DFS was calculated from date of resection to date of disease recurrence or last FU. Median FU time was 46 months. The primary tumor was located in the stomach (55 %), followed by rectum (20 %), duodenum (10 %), ileum/jejunum/other (11 %), and esophagus (3 %). The tumor resection after preoperative imatinib (median time on therapy, 40 weeks) was R0 in 83 %. Only two patients have demonstrated disease progression during neoadjuvant therapy. Five-year DSS/DFS rates were 95/65 %, respectively, median OS was 104 months, and median DFS was not reached. There were 56 % of patients who continued imatinib after rese Our analysis comprising the largest group of GIST patients treated with neoadjuvant imatinib in routine practice indicates excellent long-term results of combined therapy in locally advanced GISTs.
Original languageUndefined/Unknown
Pages (from-to)2937-2943
Number of pages7
JournalAnnals of Surgical Oncology
Issue number9
Publication statusPublished - 2013

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