Moniz Camila Motta Venchiarutti, Riechelmann Rachel Pimenta, Oliveira Suilane Coelho Ribeiro, Bariani Giovanni Mendonça, Rivelli Thomas Giollo, Ortega Cintia, Pereira Allan Andresson Lima, Meireles Sibele Inácio, Franco Rejane, Chen Andre, Bonadio Renata Colombo, Nahas Caio, Sabbaga Jorge, Coudry Renata Almeida, Braghiroli Maria Ignez, Hoff Paulo Marcelo
Instituto do Cancer do Estado de Sao Paulo (ICESP), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.
Instituto D'Or de Pesquisa e Ensino - IDOR, Sao Paulo, SP, BR.
J Cancer. 2021 Oct 16;12(23):7018-7025. doi: 10.7150/jca.57678. eCollection 2021.
Although Chemoradiation (CRT) is the curative treatment for SCCAC, many patients present primary resistance. Since it is a rare tumor, response predictors remain unknown. We performed a prospective cohort study to evaluate biomarkers associated with CRT response, progression-free survival (PFS), and overall survival (OS). The primary endpoint was response at 6 months (m). Tumor DNA and HPV were analyzed by next-generation sequencing, while KI-67 and PD-L1 by immunohistochemistry in tumor tissue. Seventy-eight patients were recruited between October/2011 and December/2015, and 75 were response evaluable. The median age was 57 years, 65% (n=49) were stage III and 12% (n=9) were HIV positive (HIV+). At 6m, 62.7% (n=47) presented CR. On multivariate analyses, stage II patients were 4.7 more likely to achieve response than stage III (OR, 4.70; 95%CI, 1.36-16.30; p=0.015). HIV+ was associated with a worse response (OR, 5.72; 95%CI, 2.5-13.0; p<0.001). 5-year PFS and OS rates were 63.3% and 76.4%, respectively, with a median follow up of 66m. On multivariate analyses, older age (HR 1.06, p=0.022, 95%IC 1.01-1.11) and absence of CR at 6m (HR 3.36, p=0.007, 95%IC 1.39-8.09) were associated with inferior OS. The 5-year OS rate was 62.5% in HIV+ group compared to 78% among HIV- pts, although this difference was not statistically significant (p=0.4). and mutations, HPV, Ki-67 expression, and PD-L1 expression, were not associated with PFS and OS. Clinical stage III and HIV+ were associated with worse response to CRT at 6m. The absence of CR was the main factor associated with poor 5-year OS.
尽管放化疗(CRT)是鳞状细胞癌(SCCAC)的根治性治疗方法,但许多患者存在原发性耐药。由于这是一种罕见肿瘤,反应预测指标仍然未知。我们进行了一项前瞻性队列研究,以评估与CRT反应、无进展生存期(PFS)和总生存期(OS)相关的生物标志物。主要终点是6个月(m)时的反应。肿瘤DNA和人乳头瘤病毒(HPV)通过二代测序进行分析,而Ki-67和程序性死亡受体配体1(PD-L1)在肿瘤组织中通过免疫组织化学进行分析。2011年10月至2015年12月期间招募了78例患者,75例可进行反应评估。中位年龄为57岁,65%(n = 49)为III期,12%(n = 9)为HIV阳性(HIV+)。在6个月时,62.7%(n = 47)出现完全缓解(CR)。多因素分析显示,II期患者达到反应的可能性比III期高4.7倍(比值比[OR],4.70;95%置信区间[CI],1.36 - 16.30;p = 0.015)。HIV+与较差的反应相关(OR,5.72;95%CI,2.5 - 13.0;p <0.001)。5年PFS率和OS率分别为63.3%和76.4%,中位随访时间为66个月。多因素分析显示,年龄较大(风险比[HR] 1.06,p = 0.022,95%置信区间1.01 - 1.11)和6个月时未达到CR(HR 3.36,p = 0.007,95%置信区间1.39 - 8.09)与较差的OS相关。HIV+组的5年OS率为62.5%,而HIV阴性患者为78%,尽管这种差异无统计学意义(p = 0.4)。 以及 突变、HPV、Ki-67表达和PD-L1表达与PFS和OS无关。临床III期和HIV+与6个月时CRT反应较差相关。未达到CR是与5年OS较差相关的主要因素。