Gadgeel Shirish M, Fajardo Otto, Barlesi Fabrice, Eun Kim Jeong, Kurzrock Razelle, Thomas David M, Jagtiani Ritika, Noe Johannes, Schwemmers Sven, Nikolaidis Christos
Department of Internal Medicine, Division of Hematology/Oncology, Henry Ford Cancer Institute/Henry Ford Health, Detroit, MI 48208, United States.
Real World Data Science, Product Development Data Sciences, F. Hoffmann-La Roche Ltd, Basel 4070, Switzerland.
Oncologist. 2025 May 8;30(5). doi: 10.1093/oncolo/oyaf005.
Anaplastic lymphoma kinase (ALK) fusions can be found in different solid tumors. This study aims to describe the clinical characteristics and investigate survival outcomes of patients with ALK fusion-positive solid tumors (excluding non-small cell lung cancer [NSCLC]) treated with standard-of-care therapies in a real-world setting.
Data for patients with metastatic solid tumors (excluding NSCLC) who had ≥1 Foundation Medicine comprehensive genomic profiling (CGP) test between January 1, 2011 and September 30, 2023, were obtained from a nationwide (US-based) de-identified multi-tumor clinico-genomic database. Patients with ALK wild-type (ALK-WT) tumors were matched with patients with ALK fusion-positive tumors (4:1 ratio) using pre-specified baseline characteristics. Two models were used to analyze survival outcomes: Model 1 used the CGP report date as the index date; Model 2 used the date of metastatic diagnosis as the index date (including adjustment for immortal time bias).
Overall, 22 and 88 patients were included in the ALK fusion-positive and ALK-WT cohorts, respectively. Co-alterations were rare in the ALK fusion-positive cohort. Median overall survival was consistently lower in patients with ALK fusion-positive tumors compared with patients with ALK-WT tumors, across all analyses (hazard ratios between 1.8 and 2.0).
Data from this study suggest that ALK fusions have a negative prognostic effect in metastatic solid tumors and highlight the need for further investigation of ALK inhibitors in the tumor-agnostic setting.
间变性淋巴瘤激酶(ALK)融合可在不同实体瘤中发现。本研究旨在描述ALK融合阳性实体瘤(不包括非小细胞肺癌[NSCLC])患者在真实世界中接受标准治疗的临床特征,并调查其生存结局。
从一个全国性(美国)的去识别化多肿瘤临床基因组数据库中获取2011年1月1日至2023年9月30日期间接受过≥1次Foundation Medicine综合基因组分析(CGP)检测的转移性实体瘤(不包括NSCLC)患者的数据。使用预先指定的基线特征将ALK野生型(ALK-WT)肿瘤患者与ALK融合阳性肿瘤患者按4:1的比例进行匹配。采用两种模型分析生存结局:模型1以CGP报告日期作为索引日期;模型2以转移诊断日期作为索引日期(包括对不朽时间偏倚的调整)。
总体而言,ALK融合阳性队列和ALK-WT队列分别纳入了22例和88例患者。ALK融合阳性队列中的共改变很少见。在所有分析中,ALK融合阳性肿瘤患者的中位总生存期始终低于ALK-WT肿瘤患者(风险比在1.8至2.0之间)。
本研究数据表明,ALK融合在转移性实体瘤中具有负面预后作用,并强调了在肿瘤非特异性环境中进一步研究ALK抑制剂的必要性。