» Articles » PMID: 20194865

90Y-edotreotide for Metastatic Carcinoid Refractory to Octreotide

Abstract

Purpose: Metastatic carcinoid is an incurable malignancy whose symptoms, such as diarrhea and flushing, can be debilitating and occasionally life-threatening. Although symptom relief is available with octreotide, the disease eventually becomes refractory to octreotide, leaving no proven treatment options. The goal of this study was to evaluate the clinical effect of using (90)Y-edotreotide to treat symptomatic patients with carcinoid tumors.

Patients And Methods: Patients enrolled had metastatic carcinoid, at least one sign/symptom refractory to octreotide, and at least one measurable lesion. Study treatment consisted of three cycles of 4.4 GBq (120 mCi) (90)Y-edotreotide each, once every 6 weeks.

Results: Ninety patients were enrolled in the study. Using Southwest Oncology Group tumor response criteria, 67 (74.%) of 90 patients (95% CI, 65.4% to 83.4%) were objectively stable or responded. A statistically significant linear trend toward improvement was demonstrated across all 12 symptoms assessed. Median progression-free survival was significantly greater (P = .03) for the 38 patients who had durable diarrhea improvement than the 18 patients who did not (18.2 v 7.9 months, respectively). Adverse events (AEs) were reported in 96.7% (87 of 90) of patients. These AEs consisted primarily of reversible GI events (76 of 90), which could be caused in part by concomitant administration of amino acid solution given to reduce radiation exposure to the kidneys. There was one case each of grade 3 oliguria and grade 4 renal failure, each lasting 6 days.

Conclusion: (90)Y-edotreotide treatment improved symptoms associated with malignant carcinoid among subjects with no treatment alternatives. Treatment was well-tolerated and had an acceptable expected AE profile.

Citing Articles

Treatment Patterns of Pancreatic Neuroendocrine Tumor (pNET) Patients at Two Canadian Cancer Centres.

Nair G, Black M, Baer K, Welch S, Laidley D, Goodwin R Curr Oncol. 2025; 32(2).

PMID: 39996886 PMC: 11853972. DOI: 10.3390/curroncol32020086.


Peptide Receptor Radionuclide Therapy Improves Survival in Patients Who Progress After Resection of Gastroenteropancreatic Neuroendocrine Tumors.

Borbon L, Sherman S, Breheny P, Chandrasekharan C, Menda Y, Bushnell D Ann Surg Oncol. 2024; 32(2):1136-1148.

PMID: 39505730 DOI: 10.1245/s10434-024-16463-7.


Gastroenteropancreatic Neuroendocrine Tumor with Peritoneal Metastasis: A Review of Current Management.

Hounschell C, Higginbotham S, Al-Kasspooles M, Selby L Cancers (Basel). 2024; 16(20).

PMID: 39456565 PMC: 11506451. DOI: 10.3390/cancers16203472.


The University of Iowa Neuroendocrine Tumor Clinic.

Howe J, Menda Y, Chandrasekharan C, Bellizzi A, Quelle D, ODorisio M Endocr Pract. 2024; 31(1):4-18.

PMID: 39349242 PMC: 11700786. DOI: 10.1016/j.eprac.2024.09.018.


Diagnosis, Management and Theragnostic Approach of Gastro-Entero-Pancreatic Neuroendocrine Neoplasms.

Piscopo L, Zampella E, Pellegrino S, Volpe F, Nappi C, Gaudieri V Cancers (Basel). 2023; 15(13).

PMID: 37444593 PMC: 10340335. DOI: 10.3390/cancers15133483.


References
1.
Arnold R, Rinke A, Klose K, Muller H, Wied M, Zamzow K . Octreotide versus octreotide plus interferon-alpha in endocrine gastroenteropancreatic tumors: a randomized trial. Clin Gastroenterol Hepatol. 2005; 3(8):761-71. DOI: 10.1016/s1542-3565(05)00481-7. View

2.
Di Bartolomeo M, Bajetta E, Buzzoni R, Mariani L, Carnaghi C, Somma L . Clinical efficacy of octreotide in the treatment of metastatic neuroendocrine tumors. A study by the Italian Trials in Medical Oncology Group. Cancer. 1996; 77(2):402-8. DOI: 10.1002/(SICI)1097-0142(19960115)77:2<402::AID-CNCR25>3.0.CO;2-4. View

3.
Arnold R, Trautmann M, Creutzfeldt W, Benning R, Benning M, Neuhaus C . Somatostatin analogue octreotide and inhibition of tumour growth in metastatic endocrine gastroenteropancreatic tumours. Gut. 1996; 38(3):430-8. PMC: 1383075. DOI: 10.1136/gut.38.3.430. View

4.
Green S, Weiss G . Southwest Oncology Group standard response criteria, endpoint definitions and toxicity criteria. Invest New Drugs. 1992; 10(4):239-53. DOI: 10.1007/BF00944177. View

5.
Bushnell D, ODorisio T, Menda Y, Carlisle T, Zehr P, Connolly M . Evaluating the clinical effectiveness of 90Y-SMT 487 in patients with neuroendocrine tumors. J Nucl Med. 2003; 44(10):1556-60. View