Y90 selective internal radiation therapy and peptide receptor radionuclide therapy for the treatment of metastatic neuroendocrine tumors: combination or not?

被引:8
|
作者
Yilmaz, Ebru [1 ]
Engin, Muege Nur [1 ]
Ozkan, Zeynep Gozde [1 ]
Kovan, Bilal [1 ]
Buyukkaya, Fikret [1 ]
Poyanli, Arzu [2 ]
Saglam, Sezer [4 ]
Basaran, Mert [3 ]
Turkmen, Cuneyt [1 ]
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Nucl Med, Istanbul, Turkey
[2] Istanbul Univ, Istanbul Fac Med, Dept Radiol, Istanbul, Turkey
[3] Istanbul Univ, Istanbul Fac Med, Dept Med Oncol, Istanbul, Turkey
[4] Demiroglu Bilim Univ, Dept Med Oncol, Istanbul, Turkey
关键词
Lu-177-octreotate; Y-90; microspheres; neuroendocrine tumors; peptide receptor radionuclide therapy; selective internal radiation therapy; RADIOEMBOLIZATION; LU-177-DOTATATE; MICROSPHERES; EFFICACY; NETS;
D O I
10.1097/MNM.0000000000001284
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background Peptide receptor radionuclide therapy and selective internal radiation therapy are effective radionuclide therapy modalities for unresectable metastatic neuroendocrine tumor patients that cannot be controlled with somatostatin analogs. The present study is intended to evaluate the therapeutic efficacy and toxicity of the combined therapy of selective internal radiation therapy and peptide receptor radionuclide therapy and stand-alone selective internal radiation therapy in patients with neuroendocrine tumor, a liver-dominant disease. Methods This cohort consists of 27 patients with metastatic neuroendocrine tumor and liver-dominant disease. They were grouped as the patients who were treated with selective internal radiation therapy for unresectable liver metastasis (n = 15) and the patients who received a combination of selective internal radiation therapy and peptide receptor radionuclide therapy (n = 12) for hepatic and extrahepatic metastasis. Treatment efficacy and treatment-associated toxicity were retrospectively assessed in both groups. Results The objective treatment response and stable disease were found in 13 patients (86.6%) in the selective internal radiation therapy group and eight patients (66.6%) in the selective internal radiation therapy + peptide receptor radionuclide therapy group. The median overall survival rate was found to be 34.9 months, in the selective internal radiation therapy group and 67.5 months in the selective internal radiation therapy + peptide receptor radionuclide therapy group (P = 0.217). The median progression-free survival data was not reached, and the mean values of progression-free survival were 53.1 +/- 9.9 months in the selective internal radiation therapy group, and 27.2 +/- 5.9 months in the selective internal radiation therapy + peptide receptor radionuclide therapy group (P = 0.561). Temporary lymphopenia was the most common side effect. Grade 1-2 hepatotoxicity was observed to be 6.6% in the selective internal radiation therapy group, while it was not observed in selective internal radiation therapy + peptide receptor radionuclide therapy group. Conclusions In the neuroendocrine tumors with liver-dominant metastatic disease, personalized selective internal radiation therapy and peptide receptor radionuclide therapy and their combinations result in increased survival rates. Selective internal radiation therapy alone could be an effective treatment in patients with liver-limited and -dominant disease.
引用
收藏
页码:1242 / 1249
页数:8
相关论文
共 50 条
  • [21] Tumor Cystic Necrosis Following Peptide Receptor Radionuclide Therapy in Neuroendocrine Tumors
    Ladwa, Rahul
    Wen Hong, Hooi
    Wyld, David
    Pattison, David A.
    Burge, Matthew
    CLINICAL NUCLEAR MEDICINE, 2018, 43 (03) : 186 - 187
  • [22] Selective internal radiation therapy: an effective treatment for hormonal syndromes in pancreatic neuroendocrine tumors
    Zubiri, Leyre
    Bilbao, Jose I.
    Rodriguez, Javier
    Sangro, Bruno
    HEPATIC ONCOLOGY, 2018, 5 (02)
  • [23] The Impact of Radiological Response to Peptide Receptor Radionuclide Therapy on Overall Survival in Patients With Metastatic Midgut Neuroendocrine Tumors
    Yalchin, Mehmet
    Oliveira, Amelia
    Theocharidou, Eleni
    Pencharz, Deborah
    Navalkissoor, Shaunak
    Quigley, Ann-Marie
    Walker, Martin
    Caplin, Martyn
    Toumpanakis, Christos
    CLINICAL NUCLEAR MEDICINE, 2017, 42 (03) : E135 - E141
  • [24] Indications of Peptide Receptor Radionuclide Therapy (PRRT) in Gastroenteropancreatic and Pulmonary Neuroendocrine Tumors: An Updated Review
    Camus, Baptiste
    Cottereau, Anne-Segolene
    Palmieri, Lola-Jade
    Dermine, Solene
    Tenenbaum, Florence
    Brezault, Catherine
    Coriat, Romain
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (06) : 1 - 18
  • [25] Alpha-emitter Peptide Receptor Radionuclide Therapy in Neuroendocrine Tumors
    Bhimaniya, Sudhir
    Shah, Hina
    Jacene, Heather A.
    PET CLINICS, 2024, 19 (03) : 341 - 349
  • [26] Combination treatments to enhance peptide receptor radionuclide therapy of neuroendocrine tumours
    Adant, Samuel
    Shah, Girish M.
    Beauregard, Jean-Mathieu
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2020, 47 (04) : 907 - 921
  • [27] Combination treatments to enhance peptide receptor radionuclide therapy of neuroendocrine tumours
    Samuel Adant
    Girish M. Shah
    Jean-Mathieu Beauregard
    European Journal of Nuclear Medicine and Molecular Imaging, 2020, 47 : 907 - 921
  • [28] Neuroendocrine Tumors and Peptide Receptor Radionuclide Therapy: When Is the Right Time?
    Hope, Thomas A.
    Pavel, Marianne
    Bergsland, Emily K.
    JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (24) : 2818 - +
  • [29] Peptide receptor radionuclide therapy for metastatic paragangliomas
    Pinato, David J.
    Black, James R. M.
    Ramaswami, Ramya
    Tan, Tricia M.
    Adjogatse, Delali
    Sharma, Rohini
    MEDICAL ONCOLOGY, 2016, 33 (05)
  • [30] Peptide receptor radionuclide therapy (PRRT) in metastatic neuroendocrine tumors of unknown primary (CUP-NETs)
    Baum, Richard P.
    Wang, Peipei
    Jakobsson, Vivianne
    Zhao, Tianzhi
    Schuchardt, Christiane
    Khong, Pek-Lan
    Zhang, Jingjing
    THERANOSTICS, 2024, 14 (01): : 133 - 142