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:4
|
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.
引用
收藏
页数:5
相关论文
共 50 条
  • [41] Neoadjuvant chemoimmunotherapy achieved a pathologic complete response in stage IIIA lung adenocarcinoma harboring RET fusion: a case report
    Dai, Minqian
    Wang, Na
    Xia, Qin
    Liao, Yongde
    Cao, Wei
    Fan, Jun
    Zhou, Diwei
    Wang, Sihua
    Nie, Xiu
    FRONTIERS IN IMMUNOLOGY, 2024, 14
  • [42] Cytomegalovirus viremia and hepatitis B reactivation in patient with RET fusion-positive non-small cell lung cancer treated with pralsetinib
    Lehman, Alanna
    Perissinotti, Anthony
    Aitken, Sam
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2024,
  • [43] Response to the Selective RET Inhibitor Selpercatinib (LOXO-292) in a Patient With RET Fusion-positive Atypical Lung Carcinoid
    Kander, Elizabeth M.
    Shah, Manisha H.
    Zhou, Ye
    Goyal, Ashima
    Palmer, Joshua D.
    Owen, Dwight H.
    Shilo, Konstantin
    Patel, Gopal
    Raval, Raju R.
    Gonzalez, Javier
    Nguyen, Michele
    Olek, Elizabeth
    Kherani, Jennifer
    Rothenberg, S. Michael
    Konda, Bhavana
    CLINICAL LUNG CANCER, 2021, 22 (03) : E442 - E445
  • [44] Patient-Reported Outcomes with Selpercatinib Among Patients with RET Fusion-Positive Non-Small Cell Lung Cancer in the Phase I/II LIBRETTO-001 Trial
    Minchom, Anna
    Tan, Aaron C.
    Massarelli, Erminia
    Subbiah, Vivek
    Boni, Valentina
    Robinson, Bruce
    Wirth, Lori J.
    Hess, Lisa M.
    Jen, Min-Hua
    Kherani, Jennifer
    Olek, Elizabeth
    McCoach, Caroline E.
    ONCOLOGIST, 2022, 27 (01): : 22 - 29
  • [45] Sustained Clinical Response to 4th-Line Therapy with Selpercatinib in RET Fusion-Positive Combined Small Cell Lung Cancer
    Huang, Yan
    Dai, Shuang
    Yin, Wenlian
    Luo, Feng
    Li, Yan
    ONCOTARGETS AND THERAPY, 2023, 16 : 1015 - 1020
  • [46] The efficacy and safety of selective RET inhibitors in RET fusion-positive non-small cell lung cancer: a meta-analysis
    Ke, Jun-yi
    Huang, Shu
    Jing, Zhi-tao
    Duan, Min-chao
    INVESTIGATIONAL NEW DRUGS, 2023, 41 (05) : 768 - 776
  • [47] The efficacy and safety of selective RET inhibitors in RET fusion-positive non-small cell lung cancer: a meta-analysis
    Jun-yi Ke
    Shu Huang
    Zhi-tao Jing
    Min-chao Duan
    Investigational New Drugs, 2023, 41 : 768 - 776
  • [48] COEXISTENT SARCOIDOSIS MIMICS METASTASIS IN A PATIENT WITH EARLY-STAGE NON-SMALL CELL LUNG CANCER: A CASE REPORT
    Zhao, Xiang
    Cheng, Yuan
    Wang, Wei
    SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES, 2024, 41 (01)
  • [49] Remarkable response to low dose of selpercatinib in a patient with RET-rearranged non-small cell lung cancer
    Sakakibara-Konishi, Jun
    Takahashi, Hirofumi
    Ito, Kenichiro
    Ikari, Tomoo
    Ikezawa, Yasuyuki
    Kitai, Hidenori
    Furuta, Megumi
    Takashima, Yuta
    Shoji, Tetsuaki
    Fukudo, Masahide
    Konno, Satoshi
    RESPIRATORY MEDICINE CASE REPORTS, 2025, 53
  • [50] Novel qPCR screen for efficient and reliable identification of RET fusion-positive non-small cell lung cancer
    Schweitzer, Brock Lloyd
    Smith, Rebecca B.
    Skelton, Rachel
    Vincent, Ryan
    McMahon, Frank
    Handshoe, John
    Morris, Stephan Wade
    Hout, David Richard
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)