Human equilibrative nucleoside transporter 1 gene expression is associated with gemcitabine efficacy in advanced leiomyosarcoma and angiosarcoma

被引:20
作者
Vincenzi, Bruno [1 ]
Stacchiotti, Silvia [2 ]
Collini, Paola [3 ]
Pantano, Francesco [1 ]
Rabitti, Carla [4 ]
Perrone, Giuseppe [4 ]
Iuliani, Michele [5 ]
Baldi, Alfonso [5 ]
Badalamenti, Giuseppe [6 ]
Sanfilippo, Roberta [2 ]
Santini, Daniele [1 ]
Muda, Andrea Onetti [4 ]
Gronchi, Alessandro [7 ]
Casali, Paolo [2 ]
Dei Tos, Angelo Paolo [8 ]
Tonini, Giuseppe [1 ]
机构
[1] Univ Rome, Med Oncol, Campus Biomed,Via Alvaro del Portillo 200, I-00128 Rome, Italy
[2] Fdn IRCCS Ist Nazl Tumori, Med Dept, Sarcoma Unit Canc, Via Venezian 1, I-20133 Milan, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Dept Diagnost Pathol & Lab Med, Via Venezian 1, I-20133 Milan, Italy
[4] Univ Rome, Human Pathol, Campus Biomed,Via Alvaro del Portillo 200,, I-00128 Rome, Italy
[5] Univ Naples 2, Dept Environm Biol & Pharmaceut Sci & Tech, Via A Vivaldi 43, I-81100 Caserta, Italy
[6] Univ Palermo, Dept Surg & Oncol Sci, Via Vespro 131, I-90127 Palermo, Italy
[7] Fdn IRCCS Ist Nazl Tumori, Dept Surg, Via Venezian 1, I-20133 Milan, Italy
[8] Treviso Gen Hosp, Dept Pathol & Mol Genet, Piazza Osped 1, I-31100 Treviso, Italy
关键词
human equilibrative nucleoside transporter 1; gemcitabine; leiomyosarcoma; angiosarcoma; LEVELS PREDICT RESPONSE; PHASE-II TRIAL; PANCREATIC-CANCER; HENT1; SURVIVAL; ADENOCARCINOMA; CHEMOTHERAPY; DOCETAXEL; THERAPY; MULTICENTER;
D O I
10.1038/bjc.2017.187
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The expression of human equilibrative nucleoside transporter 1 (hENT1), the major gemcitabine transporter into cells, has been thoroughly investigated as a predictive marker of response to gemcitabine in pancreatic cancer and biliary tract cancers. Since gemcitabine is widely used in the treatment of leiomyosarcoma and angiosarcoma, we investigated the correlation between hENT1 expression and gemcitabine efficacy in these sarcoma subtypes. Methods: We retrospectively identified 71 patients affected by advanced angiosarcoma (26) or leiomyosarcoma (45) treated within five Italian referral centres for sarcoma; among them, 49 patients (15 angiosarcoma, 34 leiomyosarcoma) were treated with gemcitabine. All tumour samples were analysed for hENT1 expression by real-time PCR. Median 2-(Delta Ct) value was used as the cutoff to dichotomise patients into 'high' expression and 'low' expression groups. Kaplan-Meier analysis was performed to estimate progression-free survival (PFS) and overall survival (OS). Results: We found a significant association between high hENT1 expression levels and favourable outcome in terms of PFS and OS compared to cases with low hENT1 expression in leiomyosarcoma treated with gemcitabine (PFS: 6.8 vs 3.2 months, P = 0.004; OS: 14.9 vs 8.5 months, P = 0.007). In addition, hENT1 overexpression correlated with a significant improvement in PFS (9.3 vs 4.5 months; P = 0.02) and OS (20.6 vs 10.8 months; P = 0.001) in angiosarcoma patients treated with gemcitabine. Conclusions: Our study suggests that higher hENT1 expression are associated to gemcitabine efficacy both in patients with advanced leiomyosarcoma and angiosarcoma.
引用
收藏
页码:340 / 346
页数:7
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