基于免疫治疗的复合egfr突变的少转移性肺肉瘤样癌的特殊反应:1例报告。

IF 3.2 Q3 Medicine
Journal of Immunotherapy and Precision Oncology Pub Date : 2025-08-22 eCollection Date: 2025-08-01 DOI:10.36401/JIPO-25-7
Ayushi Gianchandani, Darshana Desai, Janani Sambath, Darshana Patil, Prashant Kumar, Shambhavi Singh, Chetan Madre, Ruturaj Deshpande, Anjali Parab, Niyati Shah, Darshit Shah, Pritam Kataria, Shrikanth Atluri, Marzi Mehta, Aditya Shreenivas, Rajan Datar, Razelle Kurzrock, Sewanti Limaye
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引用次数: 0

摘要

肺肉瘤样癌(PSC)是一种罕见的侵袭性非小细胞肺癌(NSCLC)亚型,治疗方案有限,预后差。EGFR突变通常对基于酪氨酸激酶抑制剂(TKIs)的靶向治疗有反应,但通常与免疫治疗耐药有关。我们报告一例少转移性PSC携带复合EGFR突变(p.G719C和S768I)。尽管患者连续接受EGFR TKIs治疗,包括奥西替尼、阿法替尼和莫博替尼,并联合化疗,但患者仍表现出疾病进展。治疗策略随后转变为pembrolizumab联合卡铂和紫杉醇的免疫治疗,导致显着的反应。鉴于该疾病的低转移性和持续的反应,进行了双侧肾上腺切除术,显示出完全的病理反应。患者治疗后无疾病,随访影像学无复发迹象。该病例挑战了egfr突变的非小细胞肺癌不能从免疫治疗中获益的传统范式,突出了罕见亚型(如PSC)替代治疗方法的潜力。我们的研究结果强调了综合分子分析和个性化治疗策略对优化侵袭性和难治性肺癌预后的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exceptional Response to Immunotherapy-based Treatment in Compound <i>EGFR</i>-Mutated Oligometastatic Pulmonary Sarcomatoid Carcinoma: A Case Report.

Exceptional Response to Immunotherapy-based Treatment in Compound <i>EGFR</i>-Mutated Oligometastatic Pulmonary Sarcomatoid Carcinoma: A Case Report.

Exceptional Response to Immunotherapy-based Treatment in Compound <i>EGFR</i>-Mutated Oligometastatic Pulmonary Sarcomatoid Carcinoma: A Case Report.

Exceptional Response to Immunotherapy-based Treatment in Compound EGFR-Mutated Oligometastatic Pulmonary Sarcomatoid Carcinoma: A Case Report.

Pulmonary sarcomatoid carcinoma (PSC) is a rare and aggressive subtype of non-small cell lung cancer (NSCLC) with limited treatment options and poor prognosis. EGFR mutations generally respond to tyrosine kinase inhibitors (TKIs)-based targeted therapy but are typically associated with resistance to immunotherapy. We report a case of oligometastatic PSC harboring compound EGFR mutations (p.G719C and S768I). The patient exhibited disease progression despite sequential treatment with EGFR TKIs, including osimertinib, afatinib, and mobocertinib, in combination with chemotherapy. The treatment strategy was then shifted to immunotherapy with pembrolizumab alongside carboplatin and paclitaxel, leading to a remarkable response. Given the oligometastatic nature of the disease and the sustained response, bilateral adrenalectomy was performed, revealing a complete pathological response. The patient remains disease-free posttreatment, with no evidence of recurrence on follow-up imaging. This case challenges the conventional paradigm that EGFR-mutated NSCLC does not benefit from immunotherapy, highlighting the potential for an alternative treatment approach in rare subtypes such as PSC. Our findings emphasize the importance of comprehensive molecular profiling and a personalized treatment strategy to optimize outcomes in aggressive and refractory lung cancers.

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