Liu Zhenzhen, Li Na, Liu Jiaqiu, Li Jielin, Sun Jingfei, Zehentmayr Franz, Gomez-Randulfe Igor, Liang Yuan
Department of Thoracic Cancer 1, Cancer Hospital of Dalian University of Technology, Liaoning Cancer Hospital & Institute, Shenyang, China.
Department of Medical Oncology, Ward 2, Xincheng Hospital, Tieling Central Hospital, Tieling, China.
J Thorac Dis. 2025 Apr 30;17(4):2730-2740. doi: 10.21037/jtd-2025-541. Epub 2025 Apr 27.
-deficient undifferentiated thoracic tumor (-UT) are very aggressive high-grade malignant tumors associated with poor prognosis. It is typically diagnosed at an advanced stage. Response to conventional therapeutic approaches is particularly poor and there is no specific targeted drug for this mutation site. Currently, there are no guidelines regarding the standard treatment for this disease.
In November 2021, a 71-year-old Chinese male was diagnosed with metastatic -UT in liver and brain. Molecular analysis showed a mutation in exon 10 and a programmed death-ligand 1 (PD-L1) tumor proportion score (TPS) of <1%. From January 2022, the patient received a combination of camrelizumab, bevacizumab, pemetrexed, and carboplatin for four cycles, followed by camrelizumab, bevacizumab, and pemetrexed maintenance therapy for 31 cycles. The last treatment was on June 25, 2024. Imaging follow-up revealed a tumor reduction of approximately 50% as the best response. To date, the progression-free survival (PFS) has surpassed 32 months.
To our knowledge, this is the first patient with -UT treated with this regimen. The first-line combined regimen containing immunotherapy plus antiangiogenic therapy and chemotherapy demonstrated durable treatment response in this case. This may represent a novel treatment option for this group of patients. Prospective studies will be required to validate the efficacy and safety of this therapy.
δ-缺乏未分化胸段肿瘤(δ-UT)是极具侵袭性的高级别恶性肿瘤,预后较差。其通常在晚期被诊断出来。对传统治疗方法的反应特别差,且针对该突变位点没有特异性靶向药物。目前,对于这种疾病尚无标准治疗指南。
2021年11月,一名71岁中国男性被诊断为肝脏和脑转移δ-UT。分子分析显示第10外显子突变,程序性死亡配体1(PD-L1)肿瘤比例评分(TPS)<1%。自2022年1月起,患者接受卡瑞利珠单抗、贝伐单抗、培美曲塞和卡铂联合治疗4个周期,随后接受卡瑞利珠单抗、贝伐单抗和培美曲塞维持治疗31个周期。最后一次治疗是在2024年6月25日。影像学随访显示最佳反应为肿瘤缩小约50%。迄今为止,无进展生存期(PFS)已超过32个月。
据我们所知,这是首例接受该方案治疗的δ-UT患者。包含免疫治疗加抗血管生成治疗和化疗的一线联合方案在该病例中显示出持久的治疗反应。这可能代表了这组患者的一种新的治疗选择。需要进行前瞻性研究以验证该治疗的疗效和安全性。