Rogers Jane E, Jácome Alexandre A A, Ohinata Aki, Wolff Robert, Morris Van K, Johnson Benny, Mehdizadeh Amir, Rothschild Nicole D, Ahmed Shahab U, Guerra Jennifer L, Eng Cathy
M.D. Anderson Cancer Center Pharmacy Clinical Programs and Cancer Center, Department of Gastrointestinal Medical Oncology, University of Texas , Houston, TX, USA.
Cancer Center, OncoBio Comprehensive Cancer Center , Nova Lima, Brazil.
Expert Rev Anticancer Ther. 2020 Oct;20(10):901-908. doi: 10.1080/14737140.2020.1810573. Epub 2020 Sep 2.
Metastatic squamous cell carcinoma anal cancer (SCCA) is rare. Prospective data recommends front-line platinum doublet combinations and second-line anti-programmed death-1 therapy. Standard therapy beyond these treatments are currently unknown. We evaluated anti-EGFR monoclonal antibody (mAb) outcomes in metastatic SCCA.
Metastatic SCCA patients given anti-EGFR mAb from Oct 2011-May 2018 were included. Primary endpoints included best response, progression-free survival, and overall survival.
56 patients were evaluated with a median of one prior therapy. Most patients (~90%) received anti-EGFR mAbs with chemotherapy. Response rate (any response) was 41%. Median PFS was 4.3 months with a median OS of 16 M. Seven patients with disease control proceeded onto maintenance therapy (anti-EGFR mAb ± a fluoropyrimidine) with a median PFS of 13.8 M. Next generation sequencing of 16 pts (28%) showed 4 pts had a PIK3CA mutation with 3 of these 4 patients demonstrating progression on initial restaging.
Our analysis suggests anti-EGFR mAb therapy with chemotherapy provides clinical benefit in previously treated metastatic SCCA. Our maintenance therapy and the role of PIK3CA MT outcomes were thought-provoking.
Metastatic SCCA patients have limited options; therefore, anti-EGFR mAbs may provide benefit in the treatment armamentarium and should be further explored.
转移性鳞状细胞癌肛门癌(SCCA)较为罕见。前瞻性数据推荐一线铂类双联化疗方案以及二线抗程序性死亡-1治疗。目前尚不清楚这些治疗之外的标准疗法。我们评估了抗表皮生长因子受体(EGFR)单克隆抗体(mAb)在转移性SCCA中的疗效。
纳入2011年10月至2018年5月接受抗EGFR mAb治疗的转移性SCCA患者。主要终点包括最佳缓解、无进展生存期和总生存期。
对56例患者进行了评估,这些患者之前接受的治疗中位数为一种。大多数患者(约90%)接受了抗EGFR mAb联合化疗。缓解率(任何缓解)为41%。中位无进展生存期为4.3个月,中位总生存期为十六个月。7例病情得到控制的患者继续接受维持治疗(抗EGFR mAb±氟嘧啶),中位无进展生存期为13.8个月。对16例患者(28%)进行的二代测序显示,4例患者存在PIK3CA突变,这4例患者中有3例在初始重新分期时病情进展。
我们的分析表明,抗EGFR mAb联合化疗在既往接受过治疗的转移性SCCA中具有临床益处。我们的维持治疗以及PIK3CA突变结果的作用发人深省。
转移性SCCA患者的治疗选择有限;因此,抗EGFR mAb可能在治疗手段中发挥作用,应进一步探索。