Ciardiello Davide, Famiglietti Vincenzo, Napolitano Stefania, Esposito Lucia, Pietrantonio Filippo, Avallone Antonio, Maiello Evaristo, Cremolini Chiara, Troiani Teresa, Martinelli Erika, Ciardiello Fortunato, Martini Giulia
Oncologia Medica, Dipartimento di Medicina di Precisione, Università degli Studi della Campania "L. Vanvitelli", Naples, Italy; Oncologia Medica, Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Oncologia Medica, Dipartimento di Medicina di Precisione, Università degli Studi della Campania "L. Vanvitelli", Naples, Italy.
Clin Colorectal Cancer. 2022 Jun;21(2):141-148. doi: 10.1016/j.clcc.2022.01.005. Epub 2022 Jan 16.
High neutrophil-to-lymphocyte ratio (NLR) is a poor prognostic factor in metastatic colorectal cancer (mCRC). Here we provide final results of CAVE mCRC trial, of cetuximab plus avelumab rechallenge in chemo-refractory mCRC patients and investigated the predictive role of NLR.
All the 77 patients enrolled were included in the analysis. A cut-off of 3 was used to correlate baseline NLR with with overall survival (OS) and with progression free survival (PFS), in intention to treat (ITT) and in circulating tumor DNA (ctDNA) RAS/BRAF Wild Type (WT) patients.
In ITT population, NLR <3 (49%) group had median overall survival (mOS) of 17.8 months, vs. 8.9 months in NLR ≥ 3 group (51%) [HR 0.50, (CI 95% 0.3-0.8), P = .006]. Median progression free survival (mPFS) was 3.9 months in NLR <3 group and 3.5 months in NLR≥3 [HR 0.79, (CI 95% 0.5-1.24), P = .3]. In ctDNA RAS/BRAF WT population, mOS was 22 months in NLR <3 group (48%), vs. 8.9 months in NLR ≥3 group (52%), [HR 0.38, (CI 95% 0.19-0.75), P = .005]. A trend towards increased mPFS was observed in patients with NLR <3 versus NLR ≥3: 5.3 vs. 3.6 months [HR: 0.79, (CI 95% 0.44-1.4), P = .43]. In contrast, NLR did not correlate either with PFS or OS in ctDNA RAS/BRAF mutated patients.
In the exploratory analysis of the CAVE mCRC trial, baseline NLR <3 significantly correlated with improved survival and may represent a potential predictive biomarker of cetuximab plus avelumab rechallenge activity in ctDNA RAS/BRAF WT patients, that must be confirmed in randomized studies.
高中性粒细胞与淋巴细胞比值(NLR)是转移性结直肠癌(mCRC)的不良预后因素。在此,我们提供了CAVE mCRC试验的最终结果,该试验针对化疗难治性mCRC患者使用西妥昔单抗联合阿维鲁单抗再次治疗,并研究了NLR的预测作用。
纳入分析的所有77例患者。采用截断值3将基线NLR与总生存期(OS)和无进展生存期(PFS)进行关联,分析意向性治疗(ITT)人群以及循环肿瘤DNA(ctDNA)RAS/BRAF野生型(WT)患者。
在ITT人群中,NLR<3(49%)组的中位总生存期(mOS)为17.8个月,而NLR≥3组(51%)为8.9个月[HR 0.50,(95%CI 0.3 - 0.8),P = 0.006]。NLR<3组的中位无进展生存期(mPFS)为3.9个月,NLR≥3组为3.5个月[HR 0.79,(95%CI 0.5 - 1.24),P = 0.3]。在ctDNA RAS/BRAF WT人群中,NLR<3组(48%)的mOS为22个月,而NLR≥3组(52%)为8.9个月,[HR 0.38,(95%CI 0.19 - 0.75),P = 0.005]。观察到NLR<3的患者与NLR≥3的患者相比,mPFS有增加趋势:5.3个月对3.6个月[HR:0.79,(95%CI 0.44 - 1.4),P = 0.43]。相比之下,在ctDNA RAS/BRAF突变患者中,NLR与PFS或OS均无相关性。
在CAVE mCRC试验的探索性分析中,基线NLR<3与生存期改善显著相关,可能代表ctDNA RAS/BRAF WT患者中西妥昔单抗联合阿维鲁单抗再次治疗活性的潜在预测生物标志物,这必须在随机研究中得到证实。