He Yulong, Tang Xiaorong, Yang Fang, Jiang Qinling, Deng Lin, Lang Wenwang
Department of Oncology, Nanxishan Hospital of the Guangxi Zhuang Autonomous Region, Guilin, Guangxi, China.
Department of Spine Surgery, Guilin People's Hospital, Guilin, Guangxi, China.
Medicine (Baltimore). 2025 Mar 21;104(12):e41953. doi: 10.1097/MD.0000000000041953.
Clinically, approximately 10% to 20% of small cell lung cancer (SCLC) patients do not respond well to initial platinum-based first-line chemotherapy. Knowledge about the clinicopathologic characteristics of these primary drug-resistant populations is limited. This study aimed to explore the clinicopathologic characteristics in SCLC populations insensitive to initial chemotherapy. This study enrolled SCLC patients with insensitivity to initial chemotherapy and analyzed their clinicopathological characteristics. Binary logistic regression analysis was used to determine the independent factors that influence chemosensitivity. The study evaluated 142 cases to determine the clinicopathologic characteristics of SCLC populations with insensitivity to initial chemotherapy. Between the chemotherapy-insensitive group (n = 32) and the chemotherapy-sensitive group (n = 110), no significant differences were observed in sex, age, smoking status, tumor size, lymph-node metastasis, vascular invasion, carcinomatous lymphangitis, mediastinal invasion, superior vena cava syndrome, tumor stage, brain metastases, pleural metastasis, lung metastasis, adrenal metastasis, or the immunohistochemical markers cytokeratin, synaptophysin, chromogranin A, thyroid transcription factor-1, and Ki-67 (all P > .05). However, significant differences in liver metastasis (P = .005), bone metastasis (P < .001), and neural cell adhesion molecule expression (P = .027) were identified. Binary logistic regression analysis revealed that bone metastasis (P = .008) was an independent high-risk factor for insensitivity to initial first-line chemotherapy. Bone metastasis is an independent high-risk factor for insensitivity to initial chemotherapy in SCLC. Enhancing our understanding of SCLC biology and osteoimmuno-oncology could identify new vulnerabilities and better define patient populations that may benefit from tailored clinical treatments to overcome drug resistance.
临床上,约10%至20%的小细胞肺癌(SCLC)患者对初始铂类一线化疗反应不佳。关于这些原发性耐药人群的临床病理特征的了解有限。本研究旨在探讨对初始化疗不敏感的SCLC人群的临床病理特征。本研究纳入了对初始化疗不敏感的SCLC患者,并分析了他们的临床病理特征。采用二元逻辑回归分析来确定影响化疗敏感性的独立因素。该研究评估了142例患者,以确定对初始化疗不敏感的SCLC人群的临床病理特征。在化疗不敏感组(n = 32)和化疗敏感组(n = 110)之间,在性别、年龄、吸烟状况、肿瘤大小、淋巴结转移、血管侵犯、癌性淋巴管炎、纵隔侵犯、上腔静脉综合征、肿瘤分期、脑转移、胸膜转移、肺转移、肾上腺转移或免疫组化标志物细胞角蛋白、突触素、嗜铬粒蛋白A、甲状腺转录因子-1和Ki-67方面均未观察到显著差异(所有P > 0.05)。然而,在肝转移(P = 0.005)、骨转移(P < 0.001)和神经细胞黏附分子表达(P = 0.027)方面发现了显著差异。二元逻辑回归分析显示,骨转移(P = 0.008)是对初始一线化疗不敏感的独立高危因素。骨转移是SCLC对初始化疗不敏感的独立高危因素。加强我们对SCLC生物学和骨免疫肿瘤学的理解可以识别新的脆弱点,并更好地定义可能从定制临床治疗中受益以克服耐药性的患者群体。