Aoude Lauren G, Bonazzi Vanessa F, Brosda Sandra, Patel Kalpana, Koufariotis Lambros T, Oey Harald, Nones Katia, Wood Scott, Pearson John V, Lonie James M, Arneil Melissa, Atkinson Victoria, Smithers B Mark, Waddell Nicola, Barbour Andrew P
The University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD, 4102, Australia.
QIMR Berghofer Medical Research Institute, Herston, QLD, 4006, Australia.
Sci Rep. 2020 Oct 19;10(1):17687. doi: 10.1038/s41598-020-74956-3.
Patients with late stage resected cutaneous melanoma have poor overall survival (OS) and experience irreversible adverse events from systemic therapy. There is a clinical need to identify biomarkers to predict outcome. Performing germline/tumour whole-exome sequencing of 44 stage III/IV melanoma patients we identified pathogenic germline mutations in CDKN2A, CDK4, ATM, POLH, MRE11A, RECQL4 and XPC, affecting 7/44 patients. These mutations were associated with poor OS (p = 0.0082). We confirmed our findings in The Cancer Genome Atlas (TCGA) human skin cutaneous melanoma cohort where we identified pathogenic variants in 40/455 patients (p = 0.0203). Combining these cohorts (n = 499) further strengthened these findings showing germline carriers had worse OS (p = 0.0009). Additionally, we determined whether tumour mutation burden (TMB) or BRAF status were prognostic markers of survival. Low TMB rate (< 20 Mut/Mb; p = 0.0034) and BRAF p.V600 mutation (p = 0.0355) were associated with worse progression-free survival. Combining these biomarkers indicated that V600 mutant patients had significantly lower TMB (p = 0.0155). This was confirmed in the TCGA (n = 443, p = 0.0007). Integrative analysis showed germline mutation status conferred the highest risk (HR 5.2, 95% CI 1.72-15.7). Stage IV (HR 2.5, 0.74-8.6) and low TMB (HR 2.3, 0.57-9.4) were similar, whereas BRAF V600 status was the weakest prognostic biomarker (HR 1.5, 95% CI 0.44-5.2).
晚期切除的皮肤黑色素瘤患者总体生存率(OS)较低,且会经历全身治疗带来的不可逆不良事件。临床上需要识别生物标志物来预测预后。对44例III/IV期黑色素瘤患者进行种系/肿瘤全外显子测序后,我们在CDKN2A、CDK4、ATM、POLH、MRE11A、RECQL4和XPC中发现了致病种系突变,影响了7/44例患者。这些突变与较差的总生存期相关(p = 0.0082)。我们在癌症基因组图谱(TCGA)人类皮肤黑色素瘤队列中证实了我们的发现,在该队列中我们在40/455例患者中发现了致病变异(p = 0.0203)。合并这些队列(n = 499)进一步强化了这些发现,表明种系携带者的总生存期更差(p = 0.0009)。此外,我们确定肿瘤突变负荷(TMB)或BRAF状态是否为生存的预后标志物。低TMB率(< 20 Mut/Mb;p = 0.0034)和BRAF p.V600突变(p = 0.0355)与较差的无进展生存期相关。综合这些生物标志物表明,V600突变患者的TMB显著更低(p = 0.015)。这在TCGA中得到了证实(n = 443,p = 0.0007)。综合分析表明,种系突变状态带来的风险最高(HR 5.2,95% CI 1.72 - 15.7)。IV期(HR 2.5,0.74 - 8.6)和低TMB(HR 2.3,0.57 - 9.4)相似,而BRAF V600状态是最弱的预后生物标志物(HR 1.5,95% CI 0.44 - 5.2)。