Efficacy of Everolimus Combined with 177Lu-Dotatate in the Treatment of Neuroendocrine Tumors

被引:2
|
作者
Aljubran, Ali [1 ]
Badran, Ahmed [1 ,2 ]
Alrowaily, Mohamed [3 ]
Raef, Hussein [4 ]
Alzahrani, Ahmed M. [1 ]
Almuhaideb, Ahmed [3 ]
Almanea, Hadeel [5 ]
El-Dali, Abdelmoneim [6 ]
Tuli, Mahmoud [3 ,7 ]
Bazarbashi, Shouki [1 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, Dept Med Oncol, Riyadh, Saudi Arabia
[2] Ain Shams Univ, Dept Clin Oncol & Nucl Med, Cairo, Egypt
[3] King Faisal Specialist Hosp & Res Ctr, Dept Radiol, Riyadh, Saudi Arabia
[4] King Faisal Specialist Hosp & Res Ctr, Dept Med, Sect Endocrinol, Riyadh, Saudi Arabia
[5] King Faisal Specialist Hosp & Res Ctr, Dept Pathol, Riyadh, Saudi Arabia
[6] King Faisal Specialist Hosp & Res Ctr, Dept Biostat Epidemiol & Sci Comp, Riyadh, Saudi Arabia
[7] King Fahd Specialist Hosp, Dept Radiol, Damam, Saudi Arabia
关键词
everolimus; neuroendocrine tumors; peptide receptor radionuclide therapy; lutetium Dotatate; SURVIVAL; THERAPY;
D O I
10.1089/cbr.2022.0043
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Both everolimus and peptide receptor radionuclide therapy (PRRT) are approved as monotherapies for advanced neuroendocrine tumors (NETs). Research in animal models showed synergism between the two treatment modalities. This study aimed to evaluate the safety and efficacy of combining everolimus and PRRT in the treatment of unresectable NETs.Methods: Adult patients (>= 18 years) with progressing and unresectable histologically confirmed grade 1-2 NETs of all origins were enrolled. Everolimus was started at a 5 mg daily dose and was increased after the initial three patients to 10 mg daily. Patients were treated concurrently with Lu-177-DOTATATE at an 8-week interval, with planned four cycles. Safety was the primary endpoint, with response rate and progression-free survival (PFS) being secondary.Results: Eleven patients were enrolled. The trial was terminated early for poor accrual. The median age was 51 years (18-64), and 4 were males. The median number of cycles of Lu-177-DOTATATE was 3, and the median cumulative dose was 300 mCi. The most frequent grade 1-2 toxicities were stomatitis (90.9%) and nausea (72.7%). Less frequent were fatigue (63.6%), anorexia, diarrhea, and skin changes (each at a 36.4% rate). Grade 3 toxicities occurred in 36% (fatigue, infection, pneumonitis, neutropenia, and stroke). No patient developed grade 4 toxicity. Treatment was stopped because of progression in three patients, and toxicity in another three patients, in addition, in four patients due to therapy interruption and in one patient who developed stroke. One patient achieved partial response, and nine had stable disease. One patient developed disease progression. At a median follow-up of 18.9 months, three died and one was lost to follow-up. The median PFS was 23.3 months.Conclusions: The combination of everolimus at a dose of 10 mg daily and Lu-177-DOTATATE appears not to be feasible. A larger trial at a lower dose of everolimus is warranted.
引用
收藏
页码:164 / 168
页数:5
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