Selpercatinib in RET-fusion positive metastatic non-small cell lung cancer: achievements and gray areas

被引:2
作者
Belluomini, Lorenzo [1 ,2 ]
Avancini, Alice [1 ,2 ,3 ]
Pasqualin, Luca [1 ,2 ]
Insolda, Jessica [1 ,2 ]
Sposito, Marco [1 ,2 ]
Menis, Jessica [1 ,2 ]
Tregnago, Daniela [1 ,2 ]
Trestini, Ilaria [1 ,2 ]
Ferrara, Miriam Grazia [4 ,5 ]
Bria, Emilio [4 ,5 ]
Milella, Michele [1 ,2 ]
Pilotto, Sara [1 ,2 ]
机构
[1] Univ Verona, Dept Med, Sect Oncol, Sch Med, Verona, Italy
[2] Verona Univ Hosp Trust, Verona, Italy
[3] Univ Verona, Dept Neurosci Biomed & Movement Sci, Verona, Italy
[4] Fdn Policlin Univ Agostino Gemelli IRCCS, Comprehens Canc Ctr, Rome, Italy
[5] Univ Cattolica Sacro Cuore, Med Oncol, Rome, Italy
关键词
Non-small-cell-lung cancer; selpercatinib; RET fusion; efficacy; safety; OPEN-LABEL; ACQUIRED-RESISTANCE; CLINICAL-OUTCOMES; TARGETING RET; SOLID TUMORS; NSCLC; PRALSETINIB; INHIBITION; EFFICACY; PHASE-2;
D O I
10.1080/14737140.2022.2093190
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Selpercatinib is a RET selective tyrosine kinase inhibitor with nanomolar potency against diverse RET alterations, including fusions, activating point mutations, and acquired resistance mutations. Rearranged during transfection (RET) gene is a validated target in non-small-cell lung cancer (NSCLC). Selpercatinib is currently approved for adult patients with metastatic RET fusion-positive NSCLC. Areas covered This review summarizes the efficacy and safety data of selpercatinib in the treatment landscape of RET fusion-positive NSCLC. Expert opinion Globally considered, selpercatinib is an optimal treatment choice, in terms of both (systemic and intracranial) efficacy and safety, in patients affected by advanced NSCLC harboring RET fusions as a driver mechanism. Future challenges include the identification of the most appropriate placement for selpercatinib in the treatment algorithm of RET fusion-positive NSCLC (including early stages), the clarification of resistance mechanisms, as well as of its role in EGFR-mutant NSCLC undergoing progression during osimertinib driven by RET alterations.
引用
收藏
页码:785 / 794
页数:10
相关论文
共 67 条
[1]   Direct interactions among Ret, GDNF and GFRα1 molecules reveal new insights into the assembly of a functional three-protein complex [J].
Amoresano, A ;
Incoronato, M ;
Monti, G ;
Pucci, P ;
de Franciscis, V ;
Cerchia, L .
CELLULAR SIGNALLING, 2005, 17 (06) :717-727
[2]  
Baby Sheon, 2021, Cancer Treat Res Commun, V28, P100423, DOI 10.1016/j.ctarc.2021.100423
[3]   RET Rearrangement as a Predictor of Unresponsiveness to Immunotherapy in Non-Small Cell Lung Cancer: Report of Two Cases with Review of the Literature [J].
Baglivo, Sara ;
Ludovini, Vienna ;
Moretti, Riccardo ;
Bellezza, Guido ;
Sidoni, Angelo ;
Roila, Fausto ;
Metro, Giulio .
ONCOLOGY AND THERAPY, 2020, 8 (02) :333-339
[4]  
Bauer TM, 2021, CANCER RES, V81
[5]  
Besse B., 2021, J CLIN ONCOL, V39
[6]  
Brandhuber B., 2016, AACR NCI EORTC INT C
[7]  
CURIGLIANO G, 2021, J CLIN ONCOL, V39
[8]   Rethinking treatment for RET-altered lung and thyroid cancers: selpercatinib approval by the EMA [J].
Della Corte, C. M. ;
Morgillo, F. .
ESMO OPEN, 2021, 6 (01)
[9]   Durability of efficacy and safety with selpercatinib in patients (pts) with RET fusion plus non-small cell lung cancer (NSCLC) [J].
Drilon, A. ;
Subbiah, V. ;
Gautschi, O. ;
Tomasini, P. ;
De Braud, F. G. M. ;
Solomon, B. ;
Tan, D. Shao-Weng ;
Alonso, G. ;
Wolf, J. ;
Park, K. ;
Goto, K. ;
Soldatenkova, V. ;
Szymczak, S. ;
Barker, S. ;
Puri, T. ;
Lin, A. B. ;
Loong, H. H. F. ;
Besse, B. .
ANNALS OF ONCOLOGY, 2022, 33 :S43-S43
[10]   Efficacy of Selpercatinib in RET Fusion-Positive Non-Small-Cell Lung Cancer [J].
Drilon, A. ;
Oxnard, G. R. ;
Tan, D. S. W. ;
Loong, H. H. F. ;
Johnson, M. ;
Gainor, J. ;
McCoach, C. E. ;
Gautschi, O. ;
Besse, B. ;
Cho, B. C. ;
Peled, N. ;
Weiss, J. ;
Kim, Y. -J. ;
Ohe, Y. ;
Nishio, M. ;
Park, K. ;
Patel, J. ;
Seto, T. ;
Sakamoto, T. ;
Rosen, E. ;
Shah, M. H. ;
Barlesi, F. ;
Cassier, P. A. ;
Bazhenova, L. ;
De Braud, F. ;
Garralda, E. ;
Velcheti, V. ;
Satouchi, M. ;
Ohashi, K. ;
Pennell, N. A. ;
Reckamp, K. L. ;
Dy, G. K. ;
Wolf, J. ;
Solomon, B. ;
Falchook, G. ;
Ebata, K. ;
Nguyen, M. ;
Nair, B. ;
Zhu, E. Y. ;
Yang, L. ;
Huang, X. ;
Olek, E. ;
Rothenberg, S. M. ;
Goto, K. ;
Subbiah, V. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (09) :813-824