Patterns of Care, Prognosis, and Survival in Patients with Metastatic Gastrointestinal Stromal Tumors (GIST) Refractory to First-Line Imatinib and Second-Line Sunitinib

被引:42
作者
Italiano, Antoine [1 ,14 ]
Cioffi, Angela [1 ,2 ]
Coco, Paola [3 ]
Maki, Robert G. [1 ,4 ]
Schoffski, Patrick [5 ,6 ]
Rutkowski, Piotr [7 ]
Le Cesne, Axel [2 ]
Duffaud, Florence [8 ]
Adenis, Antoine [9 ]
Isambert, Nicolas [10 ]
Bompas, Emmanuelle [11 ]
Blay, Jean-Yves [12 ]
Casali, Paolo [2 ]
Keohan, Mary Louise [1 ]
Toulmonde, Maud [14 ]
Antonescu, Cristina R. [1 ]
Debiec-Rychter, Maria [13 ]
Coindre, Jean-Michel [14 ]
Bui, Binh [14 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[2] Inst Gustave Roussy, Villejuif, France
[3] Ist Tumori, Milan, Italy
[4] Mt Sinai Sch Med, Dept Med Pediat, New York, NY USA
[5] Catholic Univ Louvain, Univ Hosp Leuven, Leuven Canc Inst, Expt Oncol Lab, B-3000 Louvain, Belgium
[6] Catholic Univ Louvain, Dept Gen Med Oncol, B-3000 Louvain, Belgium
[7] Sklodowska Curie Mem Canc Ctr & Inst Oncol, Warsaw, Poland
[8] Hop Enfants La Timone, Marseille, France
[9] Ctr Oscar Lambret, F-59020 Lille, France
[10] Ctr Georges Francois Leclerc, Dijon, France
[11] Ctr Rene Gauducheau, F-44035 Nantes, France
[12] Ctr Leon Berard, F-69373 Lyon, France
[13] Katholieke Univ Leuven Hosp, Dept Human Genet, Louvain, Belgium
[14] Inst Bergonie, Bordeaux, France
关键词
MUTATIONS; NILOTINIB; RESISTANT; SORAFENIB; KIT;
D O I
10.1245/s10434-011-2120-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Data regarding the management and outcome of patients with metastatic gastrointestinal stromal tumors (GIST) refractory to 1st-line imatinib and 2nd-line sunitinib are limited. Medical records of 223 imatinib-resistant and sunitinib-resistant GIST who were treated in 11 major referral centers were reviewed. The three most frequent drugs used in the 3rd-line setting were: nilotinib n = 67 (29.5%), sorafenib n = 55 (24.5%), and imatinib n = 40 (17.5%). There were 18 patients (8%) who received best supportive care (BSC) only. The median progression-free survival (PFS) and overall survival (OS) on 3rd-line treatment were 3.6 months [95% confidence interval (95% CI), 3.1-4.1] and 9.2 months (95% CI, 7.5-10.9), respectively. Multivariate analysis showed that, in the 3rd-line setting, albumin level and KIT/PDGFRA mutational status were significantly associated with PFS, whereas performance status and albumin level were associated with OS. After adjustment for prognostic factors, nilotinib and sorafenib provided the best PFS and OS. Rechallenge with imatinib was also associated with improved OS in comparison with BSC. In the 3rd-line setting, rechallenge with imatinib provided limited clinical benefit but was superior to BSC. Sorafenib and nilotinib have significant clinical activity in imatinib-resistant and sunitinib-resistant GIST and may represent an alternative for rechallenge with imatinib.
引用
收藏
页码:1551 / 1559
页数:9
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