Surgical interventions for focal progression of advanced gastrointestinal stromal tumors during imatinib therapy

被引:49
作者
Hasegawa, Junichi [1 ]
Kanda, Tatsuo [2 ]
Hirota, Seiichi
Fukuda, Masafumi [3 ]
Nishitani, Akiko [1 ]
Takahashi, Tsuyoshi [1 ]
Kurosaki, Isao [2 ]
Tsutsui, Shusaku [4 ]
Hatakeyama, Katsuyoshi [2 ]
Nishida, Toshirou [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Niigata Univ, Grad Sch Med & Dent Surg, Div Digest & Gen Surg, Niigata, Japan
[3] Niigata Univ, Brain Res Inst, Dept Neurosurg, Niigata 95021, Japan
[4] Osaka Univ, Grad Sch Med, Dept Internal Med, Osaka, Japan
关键词
gastrointestinal stromal tumor; imatinib mesylate; molecular target therapy; resistance; surgical interventions;
D O I
10.1007/s10147-007-0657-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Although imatinib has shown high activity in the majority of patients with advanced gastrointestinal stromal tumors (GIST), it has become clear that secondary resistance appears during chronic therapy. The aim of this study was to retrospectively analyze the safety and prognostic effects of surgical interventions for focal progression during imatinib treatment. Methods. Between January 2002 and May 2005, 16 patients who had focal lesions of secondary-resistant GIST to imatinib treatment (male/female, 12:4; median age, 62 years) underwent surgical interventions such as resection, radio-frequency ablation, and their combination. Results. Postoperative complications, including liver abscess, bile leak, wound infection, and ileus were mostly mild, and the patients recovered with conservative therapy. There was no hospital death. The median time to progression (TTP) of all patients was 5.5 months, and only one patient died of the disease; the others are alive after a median follow up of 12.4 months. Patients with complete resections of resistant lesions (n = 7) showed significantly better median TTP than those with incomplete resections (n = 9; P = 0.014). The impact of curability on focal lesions with secondary resistance was mainly significant in patients with tumors of stomach origin (P = 0.013), and a smaller number (P = 0.014) and smaller size (P = 0.018) of resistant lesions. Overall survival was 100% at 1 year and 75% at 2 years. Conclusion. Our study indicates that surgical interventions in patients with GIST resistant to imatinib therapy are efficacious when complete resections are performed, when the lesions are of gastric origin, when the number of lesions is lower, and when the lesions are a smaller size.
引用
收藏
页码:212 / 217
页数:6
相关论文
共 20 条
[1]   Resection of residual disease in patients with metastatic gastrointestinal stromal tumors responding to treatment with imatinib [J].
Bauer, S ;
Hartmann, JT ;
de Wit, M ;
Lang, H ;
Grabellus, F ;
Antoch, G ;
Niebel, W ;
Erhard, J ;
Ebeling, P ;
Zeth, M ;
Taeger, G ;
Seeber, S ;
Flasshove, M ;
Schütte, J .
INTERNATIONAL JOURNAL OF CANCER, 2005, 117 (02) :316-325
[2]   Consensus meeting for the management of gastrointestinal stromal tumors - Report of the GIST Consensus Conference of 20-21 March 2004, under the auspices of ESMO [J].
Blay, JY ;
Bonvalot, S ;
Casali, P ;
Choi, H ;
Debiec-Richter, M ;
Dei Tos, AP ;
Emile, JF ;
Gronchi, A ;
Hogendoorn, PCW ;
Joensuu, H ;
Le Cesne, A ;
Mac Clure, J ;
Maurel, J ;
Nupponen, N ;
Ray-Coquard, I ;
Reichardt, P ;
Sciot, R ;
Stroobants, S ;
van Glabbeke, M ;
van Oosterom, A ;
Demetri, GD .
ANNALS OF ONCOLOGY, 2005, 16 (04) :566-578
[3]   Imatinib resistance in gastrointestinal stromal tumors [J].
Chen L.L. ;
Sabripour M. ;
Andtbacka R.H.I. ;
Patel S.R. ;
Feig B.W. ;
Macapinlac H.A. ;
Choi H. ;
Wu E.F. ;
Frazier M.L. ;
Benjamin R.S. .
Current Oncology Reports, 2005, 7 (4) :293-299
[4]   Two hundred gastrointestinal stromal tumors - Recurrence patterns and prognostic factors for survival [J].
DeMatteo, RP ;
Lewis, JJ ;
Leung, D ;
Mudan, SS ;
Woodruff, JM ;
Brennan, MF .
ANNALS OF SURGERY, 2000, 231 (01) :51-58
[5]   Clinical management of gastrointestinal stromal tumors: Before and after STI-571 [J].
DeMatteo, RP ;
Heinrich, MC ;
El-Rifai, WM ;
Demetri, G .
HUMAN PATHOLOGY, 2002, 33 (05) :466-477
[6]  
Demetri G.D., 2004, J NATL COMPR CANC NE, V2, pS1
[7]   Phase 3, multicenter, randomized, double-blind, placebo-controlled trial of SU11248 in patients (pts) following failure of imatinib for metastatic GIST [J].
Demetri, GD ;
van Oosterom, AT ;
Blackstein, M ;
Garrett, C ;
Shah, M ;
Heinrich, M ;
McArthur, G ;
Judson, I ;
Baum, CM ;
Casali, PG .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (16) :308S-308S
[8]   Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors [J].
Demetri, GD ;
von Mehren, M ;
Blanke, CD ;
Van den Abbeele, AD ;
Eisenberg, B ;
Roberts, PJ ;
Heinrich, MC ;
Tuveson, DA ;
Singer, S ;
Janicek, M ;
Fletcher, JA ;
Silverman, SG ;
Silberman, SL ;
Capdeville, R ;
Kiese, B ;
Peng, B ;
Dimitrijevic, S ;
Druker, BJ ;
Corless, C ;
Fletcher, CDM ;
Joensuu, H .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (07) :472-480
[9]  
Gronchi A, 2005, J CLIN ONCOL, V23, p825S
[10]  
Hohenberger P, 2006, J CLIN ONCOL, V24, p520S