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病例报告:一名同时诊断为可切除非小细胞肺癌和伴有血小板衍生生长因子受体A(PDGFRA)重排的髓系肿瘤患者,接受新辅助化疗免疫疗法和伊马替尼联合治疗后获得病理完全缓解:将临床试验数据转化为实际临床应用

Case Report: Pathologic complete response in a patient with simultaneous diagnoses of resectable NSCLC and myeloid neoplasm with PDGFRA rearrangement treated with concurrent neoadjuvant chemoimmunotherapy and imatinib: translating clinical trial data to real-world practice.

作者信息

Sussman Chad B, Shah Minal, Amin Kausha, Fanaroff Rachel, Krause Eric, Duong Vu H, Rosner Samuel

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, United States.

Medical Oncology and Hematology, Medstar Health, California, MD, United States.

出版信息

Front Oncol. 2025 Jul 28;15:1589126. doi: 10.3389/fonc.2025.1589126. eCollection 2025.

Abstract

Neoadjuvant chemoimmunotherapy has become an established treatment approach in resectable non-small cell lung cancer (NSCLC). The utilization of neoadjuvant immune checkpoint blockade (ICB) and coordination of care in the real-world setting present important challenges, with limited data available for patients with multiple synchronous primary malignancies. This case describes a 57-year-old man with simultaneous diagnoses of resectable stage IIIA NSCLC and -rearranged myeloid neoplasm who received neoadjuvant chemotherapy and nivolumab in combination with imatinib prior to definitive resection. The treatment course was uncomplicated, resulting in a complete pathologic response and resolution of the eosinophilia. Our report highlights the decision-making involved in pursuing combined systemic therapy of the patient's multiple malignancies and in navigating barriers related to tissue availability for biomarker testing. Approaches to neoadjuvant immunotherapy in early-stage NSCLC can be successful but must remain adaptable to reliably manage complex patient presentations in real-world, non-clinical trial settings.

摘要

新辅助化疗免疫疗法已成为可切除非小细胞肺癌(NSCLC)的既定治疗方法。在现实环境中,新辅助免疫检查点阻断(ICB)的应用和护理协调面临重大挑战,对于患有多个同步原发性恶性肿瘤的患者,可用数据有限。本病例描述了一名57岁男性,同时被诊断为可切除的IIIA期NSCLC和重排髓系肿瘤,在进行根治性切除之前接受了新辅助化疗以及纳武单抗联合伊马替尼治疗。治疗过程顺利,实现了完全病理缓解并解决了嗜酸性粒细胞增多问题。我们的报告强调了在对患者的多种恶性肿瘤进行联合全身治疗以及应对与生物标志物检测的组织可用性相关障碍时所涉及的决策过程。早期NSCLC的新辅助免疫疗法可以取得成功,但必须保持适应性,以便在现实世界的非临床试验环境中可靠地管理复杂的患者情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/12336442/b0ab6b23a4d6/fonc-15-1589126-g001.jpg

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