Department of Oncology, The Affiliated Ganzhou Hospital of Nanchang University, Ganzhou, China.
Department of Oncology, Ganzhou Hospital-Nanfang Hospital, Southern Medical University, Ganzhou, China.
Front Immunol. 2023 Oct 23;14:1274937. doi: 10.3389/fimmu.2023.1274937. eCollection 2023.
Pulmonary sarcomatoid carcinoma (PSC) is a unique subtype of non-small cell lung cancer (NSCLC) with a high degree of malignancy and poor therapeutic effects. With the widespread use of immune checkpoint inhibitors (ICIs) in recent years, few studies have reported that immunotherapy is effective against PSC. As a multi-target anti-vascular targeting agent, anlotinib showed a better anti-tumor effect in various cancer species. The paper reported the therapeutic and side effects of pembrolizumab combined with anlotinib in a patient with advanced PSC.
This is a 73 year old female patient who underwent thoracoscopy right upper lobectomy and was diagnosed as locally advanced PSC. However, the patient experienced tumor recurrence and metastasis 7 weeks after surgery and was unable to tolerate chemoradiotherapy. Moreover, she detected TP53 mutation and found that tumor mutation burden (TMB) and PD-L1 were high expression. Therefore, the patient received pembrolizumab combined with anlotinib treatment. After 15 cycles of treatment, the tumor significantly shrank with no tumor activity. The evaluation of tumor efficacy is partial response (PR). During the treatment period, she experienced one-degree thyroid-stimulating hormone elevation and two-degree hand-foot syndrome. Pembrolizumab and anlotinib was continued for two years as a maintenance treatment. The patient had a good quality of life and no disease progression was observed. Currently, the patient is still alive without tumor progression and has overall survival exceeding 45 months and toxic side effects were tolerable.
Combining ICIs and anti-angiogenic targeted therapy has brought new hope in treating advanced PSC. Additionally, TMB and PD-L1 expression could be potential predictive biomarkers of the efficacy in advanced PSC with immunotherapy.
肺肉瘤样癌(PSC)是一种非小细胞肺癌(NSCLC)的独特亚型,具有高度恶性和较差的治疗效果。近年来,随着免疫检查点抑制剂(ICIs)的广泛应用,很少有研究报道免疫疗法对 PSC 有效。安罗替尼作为一种多靶点抗血管靶向药物,在多种癌症中表现出更好的抗肿瘤作用。本文报道了一例晚期 PSC 患者使用帕博利珠单抗联合安罗替尼的治疗效果和不良反应。
这是一名 73 岁女性患者,行胸腔镜右上肺叶切除术,诊断为局部晚期 PSC。然而,患者在术后 7 周时出现肿瘤复发和转移,无法耐受放化疗。此外,她检测到 TP53 突变,发现肿瘤突变负荷(TMB)和 PD-L1 高表达。因此,患者接受了帕博利珠单抗联合安罗替尼治疗。经过 15 个周期的治疗,肿瘤明显缩小,无肿瘤活性。肿瘤疗效评估为部分缓解(PR)。在治疗期间,她经历了一次甲状腺刺激激素升高和两次一度手足综合征。继续使用帕博利珠单抗和安罗替尼进行两年的维持治疗。患者生活质量良好,未观察到疾病进展。目前,患者仍存活,无肿瘤进展,总生存期超过 45 个月,毒性反应可耐受。
联合使用 ICIs 和抗血管生成靶向治疗为晚期 PSC 的治疗带来了新的希望。此外,TMB 和 PD-L1 表达可能是晚期 PSC 免疫治疗疗效的潜在预测生物标志物。