Highly favourable outcomes with peptide receptor radionuclide therapy (PRRT) for metastatic rectal neuroendocrine neoplasia (NEN)

被引:19
作者
Kong, Grace [1 ,2 ]
Grozinsky-Glasberg, Simona [3 ]
Hofman, Michael S. [1 ,2 ]
Akhurst, Tim [1 ,2 ]
Meirovitz, Amichay [4 ,5 ]
Maimon, Ofra [4 ,5 ]
Krausz, Yodphat [6 ]
Godefroy, Jeremy [6 ]
Michael, Michael [2 ,7 ]
Gross, David J. [3 ]
Hicks, Rodney J. [1 ,2 ,8 ]
机构
[1] Peter MacCallum Canc Ctr, Ctr Canc Imaging, 305 Grattan St, Melbourne, Vic 3000, Australia
[2] Peter MacCallum Canc Ctr, Neuroendocrine Serv, Melbourne, Vic, Australia
[3] Hadassah Hebrew Univ, Med Ctr, Neuroendocrine Tumour Unit, Dept Endocrinol & Metab, Jerusalem, Israel
[4] Hadassah Hebrew Univ, Med Ctr, Dept Oncol, Jerusalem, Israel
[5] Hadassah Hebrew Univ, Med Ctr, Radiat Therapy Unit, Jerusalem, Israel
[6] Hadassah Hebrew Univ, Med Ctr, Dept Nucl Med, Jerusalem, Israel
[7] Peter MacCallum Canc Ctr, Div Canc Med, Melbourne, Vic, Australia
[8] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic, Australia
关键词
PRRT; Rectal; Neuroendocrine; Lutetium; Radionuclide therapy; ENETS CONSENSUS GUIDELINES; TUMORS; GRADE; LU-177-OCTREOTATE; EPIDEMIOLOGY; CHEMOTHERAPY; MANAGEMENT; UPDATE;
D O I
10.1007/s00259-018-4196-8
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
PurposeRectal neuroendocrine neoplasia (NEN) is more common than other NEN origins, but is less commonly metastatic. However, when present, distant disease carries a particularly poor prognosis. Evidence guiding optimal treatment of such patients is lacking. We assessed PRRT outcomes in patients with somatostatin receptor (SSTR) positive metastatic rectal NEN from two referral centres.MethodsPatients treated with PRRT were retrospectively reviewed. Morphologic (RECIST 1.1), SSTR imaging responses and toxicity were assessed 3months post-PRRT. Kaplan-Meier estimate was used to determine progression-free survival (PFS) and overall survival (OS) from start of PRRT.ResultsTwenty-seven consecutive patients (M=20, age 31-81 years) were reviewed. The majority (70%) had ENETs grade 2 disease (19 patients), three had Grade 3, one Grade 1, and four not documented. Overall, 63% (10/16 patients with available FDG PET/CT) had FDG avid disease. Twenty-six patients were treated for disease progression. Most had Lu-177-DOTA-octreotate with median cumulative activity of 30GBq, median fourcycles. 14 patients had radiosensitising chemotherapy (5FU or capecitabine). At 3months post-PRRT, CT disease control rate (DCR) was 96%: partial response was observed in 70% (19/27) and stable disease in 26%. All but one had partial SSTR imaging response. The median PFS was 29months. Ten patients died, with median overall survival 81months with a median follow-up of 67months. Seventeen patients had further treatments after initial PRRT (10 had further cycles of PRRT). Three patients had grade 3 lymphopenia, without significant renal toxicity, MDS or leukaemia.ConclusionOur results indicate high efficacy and morphologic responses with minimal toxicity and very encouraging survival from PRRT in patients with metastatic rectal NEN despite the adverse prognostic features of this cohort. Further prospective PRRT trials are warranted in this subgroup.
引用
收藏
页码:718 / 727
页数:10
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