Surgical Management in Metastatic Gastrointestinal Stromal Tumor (GIST) Patients After Imatinib Mesylate Treatment

被引:44
|
作者
Yeh, Chun-Nan [1 ]
Chen, Tsung-Wen [1 ]
Tseng, Jeng-Hwei [2 ]
Liu, Yu-Yin [1 ]
Wang, Shang-Yu [1 ]
Tsai, Chun-Yi [1 ]
Chiang, Kun-Chun [1 ]
Hwang, Tsann-Long [1 ]
Jan, Yi-Yin [1 ]
Chen, Miin-Fu [1 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Dept Surg, GIST Team, Tao Yuan, Taiwan
[2] Chang Gung Univ, Chang Gung Mem Hosp, Dept Radiol, GIST Team, Tao Yuan, Taiwan
关键词
surgery; GIST; IMATINIB mesylate; TYROSINE-KINASE INHIBITOR; MUTATIONS; KIT; RESISTANCE; THERAPY; MECHANISMS; RESECTION; SURVIVAL;
D O I
10.1002/jso.21630
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Imatinib mesylate (IM) demonstrates substantial efficacy in most patients with metastatic gastrointestinal stromal tumors (GISTs) However, progression of GIST eventually develops and emerges as a challenge To assess the role of surgery in the multidisciplinary management of GISTs, we studied the surgical outcomes in GIST patients receiving IM. Materials and Methods: Between 2001 and May 2009,. 161 metastatic GIST patients received IM. Among them. 35 patients undergoing 38 surgeries were investigated Patients welt: categorized based on extent of disease before surgery (responsive or stable disease (PR, SI)). local progression (LP), and generalized progression (GP)) Each tumor was investigated for genetic alteration before and after surgery Results: Disease status before surgery was significantly associated with surgical result Gross tumor clearance was achieved in 42.9% of patients with responsive, disease, but only 4 8% of those with focal resistance and 0% of those with disease progression (P = 0.022). GIST patients with PR. SD, and LP had significant better 2-year progression-free survival and overall survival than those with GP. Secondary mutations tended to he found note frequently in GIST patients with LP after surgery than those with response (10/21(47.6%) vs 2/14 (14 3%); P = 007), indicating that surgery may prevent potential development of secondary mutation in GIST patients with response. Secondary kit mutations were also found more frequently with primary exon II mutation than those with exon 9 mutation (38 7% vs 16 7%; P = 0 394) Conclusions: Surgery may benefit selected GIST patients with PR. SI), 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 mutation than those with a primary kit exon 9 mutation. J Surg. Oncol. 2010,102:599-603. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:599 / 603
页数:5
相关论文
共 50 条
  • [1] Imatinib mesylate in the management of gastrointestinal stromal tumours (GIST)
    Kurteva G.P.
    Kurtev P.F.
    memo - Magazine of European Medical Oncology, 2010, 3 (2) : 49 - 52
  • [2] Genetic changes in advanced gastrointestinal stromal tumor (GIST) patients during imatinib mesylate treatment
    Yeh, Chun-Nan
    Chen, Tsung-Wen
    Liu, Feng-Yuan
    Jan, Yi-Yin
    Chen, Miin-Fu
    LANGENBECKS ARCHIVES OF SURGERY, 2006, 391 (06) : 615 - 621
  • [3] Genetic changes in advanced gastrointestinal stromal tumor (GIST) patients during imatinib mesylate treatment
    Chun-Nan Yeh
    Tsung-Wen Chen
    Feng-Yuan Liu
    Yi-Yin Jan
    Miin-Fu Chen
    Langenbeck's Archives of Surgery, 2006, 391 : 615 - 621
  • [4] Surgical treatment of patients with initially inoperable and/or metastatic gastrointestinal stromal tumors (GIST) during therapy with imatinib mesylate
    Rutkowski, P
    Nowecki, Z
    Nyckowski, P
    Dziewirski, W
    Grzesiakowska, U
    Nasierowska-Guttmejer, A
    Krawczyk, M
    Ruka, W
    JOURNAL OF SURGICAL ONCOLOGY, 2006, 93 (04) : 304 - 311
  • [5] Imatinib mesylate for the treatment of gastrointestinal stromal tumor
    Cassier, Philippe A.
    Blay, Jean-Yves
    EXPERT REVIEW OF ANTICANCER THERAPY, 2010, 10 (05) : 623 - 634
  • [6] Clinical Significance of Pathological Complete Response in Patients with Metastatic Gastrointestinal Stromal Tumors after Imatinib Mesylate Treatment - Lessons Learned
    Cheng, Chi-Tung
    Tsai, Chun-Yi
    Yeh, Chun-Nan
    Chiang, Kun-Chun
    Chen, Yen-Yang
    Wang, Shang-Yu
    Chen, Tsung-Wen
    Tseng, Jeng-Hwei
    Jung, Shih-Ming
    Chen, Tse-Ching
    Yeh, Ta-Sen
    ANTICANCER RESEARCH, 2014, 34 (11) : 6617 - 6625
  • [7] Imatinib Escalation or Sunitinib Treatment After First-line Imatinib in Metastatic Gastrointestinal Stromal Tumor Patients
    Hsu, Chih-Chieh
    Wu, Chiao-En
    Chen, Jen-Shi
    Tseng, Jeng-Hwei
    Chiang, Kun-Chun
    Liu, Yu-Yin
    Tsai, Chun-Yi
    Cheng, Chi-Tung
    Chen, Tsung-Wen
    Jan, Yi-Yin
    Yeh, Ta-Sen
    Chen, Yen-Yang
    Yeh, Chun-Nan
    ANTICANCER RESEARCH, 2014, 34 (09) : 5029 - 5036
  • [8] A metastatic case of gastrointestinal stromal tumor (GIST) treated with imatinib mesylate (Glivec®) in Mali
    Diallo, D. A.
    Ly, M.
    Diallo, G.
    Dembele, A. K.
    Toure, M.
    Toure, B. A.
    Kone, A.
    Sidibe, S.
    Dembele, M.
    Traore, C.
    CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 2011, 35 (10) : 675 - 677
  • [9] Preoperative imatinib mesylate for unresectable or locally advanced primary gastrointestinal stromal tumors (GIST)
    Fiore, M.
    Palassini, E.
    Fumagalli, E.
    Pilotti, S.
    Tamborini, E.
    Stacchiotti, S.
    Pennacchioli, E.
    Casali, P. G.
    Gronchi, A.
    EJSO, 2009, 35 (07): : 739 - 745
  • [10] Efficacy of surgery and imatinib mesylate in the treatment of advanced gastrointestinal stromal tumor: a systematic review
    Cirocchi, Roberto
    Farinella, Eriberto
    La Mura, Francesco
    Cavaliere, Davide
    Avenia, Nicola
    Verdecchia, Giorgio Maria
    Giustozzi, Gianmario
    Noya, Giuseppe
    Sciannameo, Francesco
    TUMORI JOURNAL, 2010, 96 (03): : 392 - 399