Case Report: Complete pathologic response to neoadjuvant selpercatinib in a patient with resectable early-stage RET fusion-positive non-small cell lung cancer

被引:3
|
作者
Goldman, Jonathan W. [1 ]
Sholl, Lynette M. [2 ,3 ]
Dacic, Sanja [4 ]
Fishbein, Michael C. [1 ]
Murciano-Goroff, Yonina R. [5 ]
Rajaram, Ravi [6 ]
Szymczak, Sylwia [7 ]
Szpurka, Anna M. [8 ]
Chao, Bo H. [9 ]
Drilon, Alexander [5 ,10 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Brigham & Womens Hosp, Dept Pathol, Boston, MA USA
[3] Harvard Med Sch, Boston, MA USA
[4] Yale Sch Med, Dept Pathol, New Haven, CT USA
[5] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Cardiovasc Surg, Houston, TX USA
[7] Eli Lilly & Co, LoxoLilly, Warsaw, Poland
[8] Eli Lilly & Co, LoxoLilly, Indianapolis, IN USA
[9] Eli Lilly & Co, LoxoLilly, New York, NY USA
[10] Weill Cornell Med Coll, Dept Med, New York, NY USA
来源
FRONTIERS IN ONCOLOGY | 2023年 / 13卷
关键词
RET fusion; selective RET inhibitor; NSCLC; neoadjuvant; major pathologic response; pathologic complete response; case report;
D O I
10.3389/fonc.2023.1178313
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The LIBRETTO-001 trial demonstrated the activity of the selective rearrangement during transfection (RET) inhibitor selpercatinib in advanced RET 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 RET fusion-positive NSCLC with the primary endpoint of major pathologic response. A patient with a stage IB (cT2aN0M0) KIF5B-RET 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 RET fluorescence in situ 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 RET fusion-positive NSCLC.
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页数:5
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