Selpercatinib is indicated for locally advanced/metastaticRET-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 inRET-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/metastaticRET-activated cancers.
塞尔帕替尼适用于局部晚期/转移性RET激活实体瘤患者,在疾病进展或既往接受过全身治疗后使用。在LIBRETTO-431和LIBRETTO-531研究数据发布前,关于塞尔帕替尼与其它一线治疗方案在RET激活非小细胞肺癌(NSCLC)、甲状腺髓样癌(MTC)及甲状腺癌(TC)中的疗效对比数据较为有限。本研究通过分析LIBRETTO-001的患者数据,比较了一线使用塞尔帕替尼(塞尔帕替尼组)与先接受一线标准治疗、后续再使用塞尔帕替尼(对照组)患者的临床结局,包括治疗终止时间(TTD)、至下次治疗或死亡时间(TTNT-D)、疾病进展时间(TTP)及客观缓解率(ORR)。总体而言,一线塞尔帕替尼组在TTD、TTNT-D和TTP方面均优于一线对照组。TTD的风险比(HR)分别为:NSCLC 0.29、MTC 0.15、TC 0.08;TTNT-D的HR分别为:NSCLC 0.48、MTC 0.11、TC 0.09;TTP的HR分别为:NSCLC 0.54、MTC 0.15、TC 0.12。一线塞尔帕替尼组的ORR显著高于一线对照组(NSCLC:85.3% vs. 39.7%;MTC:82.6% vs. 15.2%;TC:81.8% vs. 31.8%)。对于晚期/转移性RET激活肿瘤患者,一线使用塞尔帕替尼相较于一线对照治疗方案能显著改善临床结局。