Pilskog Martin, Beisland Christian, Akslen Lars A, Bostad Leif, Haug Åse, Heinrich Daniel, Hjelle Karin M, Straume Oddbjørn
Centre for Cancer Biomarkers CCBIO, University of Bergen, Bergen, Norway.
Department of Oncology, Haukeland University Hospital, 5021, Bergen, Norway.
BMC Urol. 2017 Aug 31;17(1):74. doi: 10.1186/s12894-017-0267-6.
Sunitinib has become mainstay first line treatment for patients with metastatic renal clear cell carcinoma (mRCC). Still, useful predictive markers of response are lacking and urgently needed for clinical decision making.
In the present study we investigated the predictive value of standard serum markers as well as clinical markers, including C-reactive protein (CRP), Neutrophil to Lymphocyte ratio (NLR) and early hypertension (eHTN) in an unselected prospective patient population treated with sunitinib for mRCC. Forty-six patients were enrolled in a prospective single-arm study of predictive markers for sunitinib response. Response rates according to RECIST 1.1 were used as primary end-point. Secondary objectives were to evaluate prognostic value of the candidate markers with regard to progression free survival (PFS) and overall survival (OS). In addition, toxicity rates and quality of life was recorded.
Median PFS and OS was 9.1 months and 15.0 months, respectively. Of 38 patients evaluable for response, 1 patient had complete response (CR), 7 had partial response (PR), 18 had stable disease (SD) and 12 had progressive disease (PD). Normal CRP at baseline was significantly associated with objective response (CR + PR) (p = 0.01). Normal CRP was also significantly associated with improved PFS and OS (Log rank, p = 0.05 and <0.01, respectively). Early hypertension, NLR and IMDC risk score were not significantly associated with response rates or survival.
Baseline CRP was a significant predictive factor of sunitinib response and a prognostic factor of survival. Baseline CRP might be a useful biomarker in the treatment planning of mRCC. Due to the relatively small sample size, our results need to be confirmed in larger studies.
舒尼替尼已成为转移性肾透明细胞癌(mRCC)患者的一线主要治疗药物。然而,目前仍缺乏有效的反应预测标志物,临床决策急需此类标志物。
在本研究中,我们调查了标准血清标志物以及临床标志物,包括C反应蛋白(CRP)、中性粒细胞与淋巴细胞比值(NLR)和早期高血压(eHTN)在接受舒尼替尼治疗的未经选择的mRCC前瞻性患者群体中的预测价值。46例患者纳入了舒尼替尼反应预测标志物的前瞻性单臂研究。根据实体瘤疗效评价标准(RECIST)1.1版的反应率作为主要终点。次要目标是评估候选标志物对无进展生存期(PFS)和总生存期(OS)的预后价值。此外,记录了毒性发生率和生活质量。
PFS和OS的中位数分别为9.1个月和15.0个月。在38例可评估反应的患者中,1例完全缓解(CR),7例部分缓解(PR),18例病情稳定(SD),12例病情进展(PD)。基线时CRP正常与客观反应(CR + PR)显著相关(p = 0.01)。CRP正常也与改善的PFS和OS显著相关(对数秩检验,p分别为0.05和<0.01)。早期高血压、NLR和国际转移性肾细胞癌数据库(IMDC)风险评分与反应率或生存率无显著相关性。
基线CRP是舒尼替尼反应的重要预测因素和生存的预后因素。基线CRP可能是mRCC治疗计划中的有用生物标志物。由于样本量相对较小,我们的结果需要在更大规模的研究中得到证实。