Division of Medical Oncology, National Jewish Health, Denver, Colorado, USA.
Clin Cancer Res. 2010 Nov 1;16(21):5260-8. doi: 10.1158/1078-0432.CCR-10-0994. Epub 2010 Sep 16.
We conducted a phase II study to assess the efficacy of continuous dosing of sunitinib in patients with flurodeoxyglucose positron emission tomography (FDG-PET)-avid, iodine-refractory well-differentiated thyroid carcinoma (WDTC) and medullary thyroid cancer (MTC) and to assess for early response per FDG-PET.
Patients had metastatic, iodine-refractory WDTC or MTC with FDG-PET-avid disease. Sunitinib was administered at 37.5 mg daily on a continuous basis. The primary end point was response rate per Response Evaluation Criteria in Solid Tumors (RECIST). Secondary end points included toxicity, overall survival, and time to progression. We conducted an exploratory analysis of FDG-PET response after 7 days of treatment.
Thirty-five patients were enrolled (7 MTC, 28 WDTC), and 33 patients were evaluable for disease response. The primary end point, objective response rate per RECIST, was 11 patients (31%; 95% confidence interval, 16-47%). There were 1 complete response (3%), 10 partial responses (28%), and 16 patients (46%) with stable disease. Progressive disease was seen in 6 patients (17%). The median time to progression was 12.8 months (95% confidence interval, 8.9 months-not reached). Repeat FDG-PET was done on 22 patients. The median percent change in average standardized uptake values was -11.7%, -13.9%, and 8.6% for patients with RECIST response, stable disease, and progressive disease, respectively. Differences between response categories were statistically significant (P = 0.03). The most common toxicities seen included fatigue (11%), neutropenia (34%), hand/foot syndrome (17%), diarrhea (17%), and leukopenia (31%). One patient on anticoagulation died of gastrointestinal bleeding.
Continuous administration of sunitinib was effective in patients with iodine-refractory WDTC and MTC. Further study is warranted.
我们进行了一项 II 期研究,以评估连续剂量的舒尼替尼在氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)阳性、碘难治性分化型甲状腺癌(WDTC)和髓样甲状腺癌(MTC)患者中的疗效,并评估 FDG-PET 的早期反应。
患者患有转移性、碘难治性 WDTC 或 MTC,且 FDG-PET 阳性。舒尼替尼以 37.5mg 每天连续给药。主要终点是根据实体瘤反应评估标准(RECIST)评估的反应率。次要终点包括毒性、总生存期和无进展生存期。我们对治疗 7 天后的 FDG-PET 反应进行了探索性分析。
共入组 35 例患者(7 例 MTC,28 例 WDTC),33 例患者可评估疾病反应。主要终点,RECIST 评估的客观缓解率为 11 例(31%;95%置信区间,16-47%)。1 例完全缓解(3%),10 例部分缓解(28%),16 例患者(46%)疾病稳定。6 例患者(17%)疾病进展。中位无进展生存期为 12.8 个月(95%置信区间,8.9 个月-未达到)。对 22 例患者进行了重复 FDG-PET。RECIST 反应、疾病稳定和疾病进展患者的平均标准化摄取值的平均百分比变化分别为-11.7%、-13.9%和 8.6%。反应类别之间的差异具有统计学意义(P = 0.03)。最常见的毒性包括疲劳(11%)、中性粒细胞减少(34%)、手足综合征(17%)、腹泻(17%)和白细胞减少(31%)。1 例正在抗凝的患者死于胃肠道出血。
连续给予舒尼替尼对碘难治性 WDTC 和 MTC 患者有效。需要进一步研究。