Spindler Karen-Lise Garm, Christensen Ib Jarle, Nielsen Hans Jørgen, Jakobsen Anders, Brünner Nils
Department of Oncology, Vejle Hospital, Kabbeltoft 25, 7100, Vejle, Denmark,
Tumour Biol. 2015 Jun;36(6):4301-8. doi: 10.1007/s13277-015-3069-z. Epub 2015 Jan 23.
KRAS wild-type (wt) status determines indication for treatment with combination therapy, including epidermal growth factor receptor (EGFR) inhibitors, but still, the overall response rate in KRAS wt patients is less than 40 %. Consequently, the majority of patients will suffer from substantial side effects and no apparent benefit. Tissue inhibitor of metalloproteinases-1 is a glycoprotein, which regulates metalloproteinases and may consequently imply a central role in tumour progression. Furthermore, it is closely related to the EGFR regulation and has shown promising potential as a biomarker in colorectal cancer (CRC). The aim of the present study was to investigate the clinical value of TIMP-1 in patients with metastatic colorectal cancer (mCRC) treated with cetuximab and irinotecan. Patients with chemotherapy-resistant mCRC referred to third-line treatment with cetuximab (initial 400 mg/m(2) followed by weekly 250 mg/m(2))/irinotecan (350 mg/m(2) q3w) were prospectively included in the biomarker study, as previously published. Pre-treatment blood samples were collected, and plasma TIMP-1 was measured by a validated in-house ELISA assay. In addition, carcinoembryonic antigen (CEA) measurement was performed with a standardised method. A total of 107 patients were included in the biomarker study. The median baseline plasma TIMP-1 level was 271.1 ng/ml (range 65.9-1432 ng/ml) with no significant associations with baseline clinical characteristics. Median baseline plasma TIMP-1 levels were significantly higher in patients with early progression compared to patients who achieved disease control, 349 ng/ml (233-398 95 % confidence interval (CI)) and 215 ng/ml (155-289 95 % CI), respectively, p = 0.03, suggesting some association with treatment efficacy. When dividing patients according to TIMP-1 tertiles, the median progression-free survival (PFS) in patients with a high level of TIMP-1 was 2.4 months (95 % CI 2.1-4.1) compared to 3.3 months (95 % CI 2.1-6.2) and 4.7 months (95 % 3.2-7.6) in patients with intermediate or low levels, respectively. Analysis of TIMP-1 as a continuous variable revealed a shorter PFS associated with increasing levels of TIMP-1 (hazard ratio (HR) 1.36). These results translated into a significantly lower overall survival (OS) in patients with a high baseline TIMP-1 level (4.5 months (95 % CI 3.4-5.4)), compared to those with intermediate or low TIMP-1 levels (7.8 months (95 % CI 4.4-13.7) and 12.0 months (95 % CI 10.1-14.3), respectively, p < 0.0001). An 83 % higher hazard for death was revealed (HR = 1.83) with each twofold increase in the TIMP-1 level. Pre-treatment levels of CEA were not associated with any of the baseline characteristics (except primary tumour localisation) or to differences in PFS or OS. The rank correlation between CEA and TIMP-1 was r = 0.50, and a test for interaction between TIMP-1 and CEA (dichotomised at 5 ng/ml) in survival analysis was not significant (p = 0.18). A multivariate analysis for PFS and OS resulted in a model with significant contributions from TIMP-1, KRAS, and the number of metastatic sites. We have confirmed the potential prognostic value of TIMP-1 measurement prior to palliative chemotherapy for mCRC. However, validation in randomised trials will be essential with the perspective of establishing a potential predictive role of plasma TIMP-1 in this setting.
KRAS野生型(wt)状态决定了联合治疗的适应症,包括表皮生长因子受体(EGFR)抑制剂,但KRAS野生型患者的总体缓解率仍低于40%。因此,大多数患者将遭受严重的副作用且无明显益处。金属蛋白酶组织抑制剂-1是一种糖蛋白,它调节金属蛋白酶,因此可能在肿瘤进展中起核心作用。此外,它与EGFR调节密切相关,并已显示出作为结直肠癌(CRC)生物标志物的潜在前景。本研究的目的是探讨金属蛋白酶组织抑制剂-1(TIMP-1)在接受西妥昔单抗和伊立替康治疗的转移性结直肠癌(mCRC)患者中的临床价值。如先前发表的那样,对化疗耐药的mCRC患者进行三线治疗,采用西妥昔单抗(初始剂量400mg/m²,随后每周250mg/m²)/伊立替康(350mg/m²,每3周一次),前瞻性纳入生物标志物研究。收集治疗前血样,采用经过验证的内部ELISA法检测血浆TIMP-1。此外,采用标准化方法进行癌胚抗原(CEA)检测。共有107例患者纳入生物标志物研究。基线血浆TIMP-1水平中位数为271.1ng/ml(范围65.9 - 1432ng/ml),与基线临床特征无显著相关性。与疾病得到控制的患者相比,早期进展患者的基线血浆TIMP-1水平中位数显著更高,分别为349ng/ml(233 - 398,95%置信区间(CI))和215ng/ml(155 - 289,95%CI),p = 0.03,提示与治疗疗效存在一定关联。根据TIMP-1三分位数对患者进行划分时,TIMP-1水平高的患者中位无进展生存期(PFS)为2.4个月(95%CI 2.1 - 4.1),而TIMP-1水平中等或低的患者分别为3.3个月(95%CI 2.1 - 6.2)和4.7个月(95% 3.2 - 7.6)。将TIMP-1作为连续变量分析显示,PFS随TIMP-1水平升高而缩短(风险比(HR)1.36)。这些结果转化为基线TIMP-1水平高的患者总生存期(OS)显著更低(4.5个月(95%CI 3.4 - 5.4)),相比之下,TIMP-1水平中等或低的患者分别为7.8个月(95%CI 4.4 - 13.7)和12.0个月(95%CI 10.1 - 14.3),p < 0.ooo1。TIMP-1水平每增加两倍,死亡风险高83%(HR = 1.83)。治疗前CEA水平与任何基线特征(原发性肿瘤定位除外)或PFS或OS差异均无关联。CEA与TIMP-1的等级相关系数为r = 0.50,在生存分析中TIMP-1与CEA(以5ng/ml为界二分法)之间的相互作用检验无显著性(p = 0.18)。对PFS和OS进行多变量分析得到一个模型,其中TIMP-1、KRAS和转移部位数量有显著贡献。我们已经证实了在mCRC姑息化疗前检测TIMP-1的潜在预后价值。然而,从确定血浆TIMP-1在此情况下的潜在预测作用的角度来看,在随机试验中进行验证至关重要。