BRCA1 haplotype and clinical benefit of trabectedin in soft-tissue sarcoma patients

被引:18
|
作者
Laroche-Clary, A. [1 ,2 ]
Chaire, V. [1 ,2 ]
Le Morvan, V. [1 ,2 ]
Neuville, A. [2 ]
Bertucci, F. [3 ]
Salas, S. [4 ]
Sanfilippo, R. [5 ]
Pourquier, P. [1 ,2 ]
Italiano, A. [1 ,2 ]
机构
[1] INSERM, U916, Bordeaux, France
[2] Inst Bergonie, Bordeaux, France
[3] Inst Paoli Calmettes, Marseille, France
[4] Hop La Timone, Assistance Publ Hop Marseille, Marseille, France
[5] Inst Nazl Tumori, Dept Canc Med, Adult Sarcoma Med Oncol Unit, Milan, Italy
关键词
sarcoma; polymorphism; BRCA1; trabectedin; predictive biomarkers; DNA-REPAIR PATHWAYS; PHASE-II; NUCLEOTIDE-EXCISION; BREAST-CANCER; ECTEINASCIDIN-743; CHEMOTHERAPY; SURVIVAL; ET-743; MAINTENANCE; SIGNATURE;
D O I
10.1038/bjc.2014.624
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study aimed to determine whether the BRCA1 haplotype was associated with trabectedin efficacy in soft-tissue sarcoma (STS) patients. Methods: We analysed BRCA1 single-nucleotide polymorphisms (SNPs) in tumour specimens from 135 advanced STS patients enrolled in published phase 2 trials or in a compassionate-use programme of trabectedin. Forty-four advanced STS patients treated with doxorubicin and 85 patients with localised STS served as controls. The 6-month nonprogression rate and overall survival (OS) were analysed according to BRCA1 haplotype using log-rank tests. Results: A favourable BRCA1 haplotype (presence of at least one AAAG allele) was significantly associated with an improved 6-month nonprogression rate. It was the only variable significantly associated with OS. No correlations were found between outcomes for patients with localised or advanced STS treated with doxorubicin. Conclusions: The BRCA1 haplotype represents a potential DNA repair biomarker that can be used for the prediction of response to trabectedin in STS patients.
引用
收藏
页码:688 / 692
页数:5
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