De Braud Filippo, Deschler-Baier Barbara, Morris John C, Worden Francis, Han Yimei, Kiiskinen Urpo, Jen Min-Hua, Barker Scott S, Szymczak Sylwia, Gilligan Adrienne M
Department of Oncology and Hematology-Oncology, University of Milan, 20133 Milan, Italy.
Department of Internal Medicine, University Hospital Würzburg, 97080 Würzburg, Germany.
Cancers (Basel). 2023 Dec 27;16(1):140. doi: 10.3390/cancers16010140.
Selpercatinib is indicated for locally advanced/metastatic -activated solid tumors after progression or following prior systemic therapies. Until the recently published data from LIBRETTO-431 and LIBRETTO-531, there were limited effectiveness data comparing selpercatinib with other first-line treatments in -activated non-small cell lung cancer (NSCLC), medullary thyroid cancer (MTC), and thyroid cancer (TC). This study analyzed patient data from LIBRETTO-001 and compared the outcomes (time to treatment discontinuation {TTD}, time to next treatment or death {TTNT-D}, time to progression {TTP}, and the objective response rate {ORR}) of first-line selpercatinib (selpercatinib arm) use with the outcomes of first-line standard therapies in patients who then received selpercatinib in later lines of treatment (comparator arm). Overall, the first-line selpercatinib arm had a longer TTD, TTNT-D, and TTP versus the first-line comparator arm. The hazard ratios (HRs) for TTD were 0.29 (NSCLC), 0.15 (MTC), 0.08 (TC); for TTNT-D, the HRs were 0.48 (NSCLC), 0.11 (MTC), 0.09 (TC); and for TTP, the HRs were 0.54 (NSCLC), 0.15 (MTC), and 0.12 (TC). The ORR was higher for first-line selpercatinib versus the first-line comparator (NSCLC: 85.3% vs. 39.7%; MTC: 82.6% vs. 15.2%; and TC: 81.8% vs. 31.8%). First-line selpercatinib use is associated with improved outcomes compared to first-line comparator therapies for patients with advanced/metastatic -activated cancers.
塞尔帕替尼适用于疾病进展后或先前接受全身治疗后的局部晚期/转移性活性实体瘤。在LIBRETTO - 431和LIBRETTO - 531最近公布数据之前,在活性非小细胞肺癌(NSCLC)、甲状腺髓样癌(MTC)和甲状腺癌(TC)中,将塞尔帕替尼与其他一线治疗进行疗效比较的数据有限。本研究分析了LIBRETTO - 001的患者数据,并比较了一线使用塞尔帕替尼(塞尔帕替尼组)与一线标准治疗(比较组)的患者后续接受塞尔帕替尼治疗后的结局(治疗中断时间{TTD}、下次治疗或死亡时间{TTNT - D}、疾病进展时间{TTP}和客观缓解率{ORR})。总体而言,与一线比较组相比,一线塞尔帕替尼组的TTD、TTNT - D和TTP更长。TTD的风险比(HR)分别为0.29(NSCLC)、0.15(MTC)、0.08(TC);TTNT - D的HR分别为0.48(NSCLC)、0.11(MTC)、0.09(TC);TTP的HR分别为0.54(NSCLC)、0.15(MTC)和0.12(TC)。一线塞尔帕替尼的ORR高于一线比较组(NSCLC:85.3%对vs . 39.7%;MTC:82.6%对vs . 15.2%;TC:81.8%对vs . 31.8%)。对于晚期/转移性活性癌症患者,与一线比较疗法相比,一线使用塞尔帕替尼与更好的结局相关。