Goldman Jonathan W, Sholl Lynette M, Dacic Sanja, Fishbein Michael C, Murciano-Goroff Yonina R, Rajaram Ravi, Szymczak Sylwia, Szpurka Anna M, Chao Bo H, Drilon Alexander
David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
Front Oncol. 2023 May 18;13:1178313. doi: 10.3389/fonc.2023.1178313. eCollection 2023.
The LIBRETTO-001 trial demonstrated the activity of the selective rearrangement during transfection (RET) inhibitor selpercatinib in advanced fusion-positive non-small cell lung cancer (NSCLC) and resulted in the drug's approval for this indication. A cohort that included neoadjuvant and adjuvant selpercatinib was opened on LIBRETTO-001 for early-stage fusion-positive NSCLC with the primary endpoint of major pathologic response. A patient with a stage IB (cT2aN0M0) fusion-positive NSCLC received 8 weeks of neoadjuvant selpercatinib at 160 mg twice daily followed by surgery. While moderate regression in the primary tumor (stable disease, Response Evaluation Criteria in Solid Tumors (RECIST) guidelines version 1.1) was observed radiologically, assessment via an Independent Pathologic Review Committee revealed a pathologic complete response (0% viable tumor). This consensus assessment by three independent pathologists was aided by fluorescence hybridization testing of a reactive pneumocyte proliferation showing no rearrangement. Neoadjuvant selpercatinib was well-tolerated with only low-grade treatment-emergent adverse events. The activity of prospective preoperative selpercatinib in this case establishes proof of concept of the potential utility of RET inhibitor therapy in early-stage fusion-positive NSCLC.
LIBRETTO-001试验证明了转染期间重排(RET)抑制剂塞尔帕替尼在晚期融合阳性非小细胞肺癌(NSCLC)中的活性,并使该药物获得了这一适应症的批准。在LIBRETTO-001试验中,针对早期融合阳性NSCLC开启了一个包括新辅助和辅助塞尔帕替尼治疗的队列,主要终点为主要病理反应。一名IB期(cT2aN0M0)融合阳性NSCLC患者接受了为期8周的新辅助塞尔帕替尼治疗,每日两次,每次160mg,随后进行手术。虽然影像学上观察到原发肿瘤有中度退缩(疾病稳定,实体瘤疗效评价标准(RECIST)1.1版),但通过独立病理审查委员会评估发现为病理完全缓解(0%存活肿瘤)。三名独立病理学家的这一共识性评估借助了对反应性肺细胞增殖进行的荧光杂交检测,结果显示无重排。新辅助塞尔帕替尼耐受性良好,仅出现低级别治疗中出现的不良事件。该病例中前瞻性术前塞尔帕替尼的活性确立了RET抑制剂治疗在早期融合阳性NSCLC中潜在效用的概念验证。