Zhou Jie, Cao Kexin, Wei Jin-Xia, Wang Biao, Li Meng-Jie, Zhu Jian, Ai Guo-Ping, Liu Qiu-Lian
Department of Respiratory Oncology, Renmin Hospital of Qingxian, Cangzhou, China.
Department of Thoracic Surgery, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Front Immunol. 2025 Apr 17;16:1552547. doi: 10.3389/fimmu.2025.1552547. eCollection 2025.
Recent studies have shown that immunotherapy improves survival outcomes for patients with a late staged cancer. However, in a small number of cases do not benefit from this treatment and instead experience rapid tumor progression, known as hyperprogressive disease (HPD). Currently, HPD is provisionally defined as occurring within two months of receiving immunotherapy. Is HPD that occurs after two months associated with immunotherapy? The existing literature does not provide an answer.
A 59-year-old woman was diagnosed with unresectable squamous cell carcinoma of the lung. She received four months (6 cycles) of chemotherapy with albumin-bound paclitaxel and cisplatin, along with immunotherapy using Camrelizumab. After treatment, the lesion in the patient's lung were significantly reduced. However, because the tumor did not disappear and due to the limitations dose of the chemotherapy drugs using for body, the patient turned to receive stereotactic radiation therapy (2 Gy per fraction). After 10 fractions of radiotherapy, the lesion in the patient's lung significantly increased. The enlarged lesion was pathologically analyzed through a percutaneous lung biopsy and was confirmed to be squamous cell carcinoma. Following the cessation of radiotherapy, four cycles of targeted segment arterial chemoembolization resulted in another significant reduction in the lung lesion.
This report is the first to present HPD after 5 months of immunotherapy, marking the longest recorded occurrence of this phenomenon. This particular case of post-immunotherapy HPD achieved satisfactory results through targeted segment arterial chemoembolization, offering a potential approach for managing this side effect.
近期研究表明,免疫疗法可改善晚期癌症患者的生存结局。然而,少数患者无法从这种治疗中获益,反而经历肿瘤快速进展,即超进展性疾病(HPD)。目前,HPD被暂行定义为在接受免疫疗法后两个月内出现。那么,在两个月后出现的HPD是否与免疫疗法有关?现有文献并未给出答案。
一名59岁女性被诊断为不可切除的肺鳞状细胞癌。她接受了四个月(6个周期)的白蛋白结合型紫杉醇和顺铂化疗,以及使用卡瑞利珠单抗的免疫疗法。治疗后,患者肺部病灶明显缩小。然而,由于肿瘤并未消失,且考虑到化疗药物对身体的剂量限制,患者转而接受立体定向放射治疗(每次分割剂量2Gy)。放疗10次后,患者肺部病灶显著增大。通过经皮肺穿刺活检对增大的病灶进行病理分析,确诊为鳞状细胞癌。放疗结束后,四个周期的靶向节段性动脉化疗栓塞术使肺部病灶再次显著缩小。
本报告首次呈现了免疫疗法5个月后出现的HPD,这是该现象记录中出现时间最长的。这例免疫治疗后HPD的特殊病例通过靶向节段性动脉化疗栓塞术取得了满意效果,为处理这种副作用提供了一种可能的方法。