Castellanos Luz E, Yedururi Sireesha, Waguespack Steven G
Department of Endocrine Neoplasia and Hormonal Disorders and Department of Pediatrics-Patient Care, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Department of Abdominal Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
J Endocr Soc. 2025 Jun 5;9(8):bvaf098. doi: 10.1210/jendso/bvaf098. eCollection 2025 Aug.
Few data exist regarding larotrectinib therapy in pediatric fusion-positive papillary thyroid cancer (PTC), especially its effects on redifferentiation in radioactive iodine-refractory (RAIR) disease.
To describe redifferentiation effects and disease outcomes in patients with stage 2 pediatric PTC following treatment with larotrectinib ± RAI.
A retrospective case series at a tertiary cancer center of patients with fusion-positive pediatric PTC and RAIR pulmonary metastases treated with larotrectinib and considered for I therapy. Tumor response was assessed utilizing RECIST 1.1.
Four patients (aged 6-16 years at PTC diagnosis; 50% female) were treated with larotrectinib 100 mg twice a day for a median of 14 months (range 6-30 months). Treatment was well tolerated, except for grade 3 hypocalcemia in 1 patient with pre-existing hypoparathyroidism. All patients had tumor shrinkage (-25% to -100%) in target and nontarget pulmonary metastases. On diagnostic I thyroid scans, any RAI uptake was identified in only 2 patients, and therapeutic I did not cause further incremental tumor shrinkage in the patients treated, despite robust pulmonary uptake on the post-therapy scans. After stopping larotrectinib and with a mean follow-up of 38 months (range 26-48 months), 2 patients had stable disease and 2 had clinically insignificant tumor progression.
Although larotrectinib can have a redifferentiation effect in pediatric fusion-positive PTC, therapy with I may not lead to an incremental benefit in established RAIR disease. Significant structural disease progression did not occur after cessation of larotrectinib, suggesting that a drug holiday can safely be considered in this population.
关于拉罗替尼治疗儿童融合阳性乳头状甲状腺癌(PTC)的数据很少,尤其是其对放射性碘难治性(RAIR)疾病再分化的影响。
描述2期儿童PTC患者接受拉罗替尼±放射性碘(RAI)治疗后的再分化效果和疾病转归。
在一家三级癌症中心对接受拉罗替尼治疗并考虑进行碘治疗的融合阳性儿童PTC和RAIR肺转移患者进行回顾性病例系列研究。使用RECIST 1.1评估肿瘤反应。
4例患者(PTC诊断时年龄6 - 16岁;50%为女性)接受拉罗替尼100mg每日两次治疗,中位治疗时间为14个月(范围6 - 30个月)。除1例既往有甲状旁腺功能减退的患者出现3级低钙血症外,治疗耐受性良好。所有患者的靶病灶和非靶病灶肺转移瘤均有缩小(-25%至-100%)。在诊断性碘甲状腺扫描中,仅2例患者发现有任何放射性碘摄取,并且治疗性碘并未导致接受治疗的患者肿瘤进一步缩小,尽管治疗后扫描显示肺部有明显摄取。停用拉罗替尼后,平均随访38个月(范围26 - 48个月),2例患者病情稳定,2例患者有临床意义不显著的肿瘤进展。
虽然拉罗替尼在儿童融合阳性PTC中可产生再分化作用,但在已确诊的RAIR疾病中,碘治疗可能不会带来额外益处。停用拉罗替尼后未发生明显的结构性疾病进展,提示在该人群中可以安全地考虑药物假期。