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5FU and Octreotide Long-acting Release (LAR) for Neuroendocrine Tumors

Continuous 5-fluorouracil Infusion Plus Long Acting Octreotide in Advanced Well Differentiated Neuroendocrine Carcinomas. A Phase II Trial of the Piemonte Oncology Network.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00953394
Enrollment
29
Registered
2009-08-06
Start date
2002-02-28
Completion date
2006-12-31
Last updated
2009-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuroendocrine Tumors

Keywords

octreotide LAR, neuroendocrine carcinoma, metronomic 5fluorouracil

Brief summary

Well differentiated neuroendocrine carcinomas have low proliferative activity and conventional chemotherapy is not recommended. Metronomic chemotherapy, i.e. the frequent administration of cytotoxic drugs at low doses, has demonstrated antiangiogenetic properties. Since well differentiated NE carcinomas are highly vascular, there is a rationale for testing metronomic chemotherapy in this clinical setting. A phase II study was designed to test the activity of protracted 5-fluorouracil (5FU) infusion plus long-acting release (LAR) octreotide for patients with neuroendocrine carcinoma.

Detailed description

Metastatic or locally advanced well differentiated neuroendocrine carcinoma were treated with 5Fluorouracil protracted intravenous infusion (200 mg/m2 daily) plus Octreotide LAR (20 mg monthly). Primary Endpoint: the response to treatment, evaluated according to the RECIST criteria. Secondary Endpoints: * toxicity, graded according to the NCI-CTG criteria; * symptomatic response: evaluated according to the changes in both the frequency and intensity of symptoms; * biochemical response: evaluated considering the changes in the tumor marker levels (circulating Chromogranin A); * time to progression and survival: were measured from the date of treatment start to the date of progression and the date of last follow-up or death, respectively.

Interventions

DRUGcontinuous 5 fluouracil infusion plus long-acting octreotide

long-acting octreotide acetate at a dose of 20 mg was administered intramuscularly every 4 weeks. 5fluorouracil was given as a protracted continuous infusion without interruption at a daily dose of 200 mg/m2 of body-surface area through an elastomeric pump connected to a central venous access.

Sponsors

University of Turin, Italy
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* histological diagnosis of well-differentiated neuroendocrine carcinoma according to the World Health Organization (WHO) classification; * locally advanced or metastatic disease not amenable to surgery with radical intent; * at least one measurable target lesion; * radiological documentation of progressive disease; * ECOG performance status grade \<=2; * life expectancy \>12 weeks; * adequate bone marrow reserve; * adequate hepatic and renal function; * ability to comply with the protocol procedures (including geographic accessibility); * written informed consent.

Exclusion criteria

* non-malignant systemic disease or conditions that precluded patients from receiving the study therapy; * second primary malignancies and previous systemic antineoplastic treatment including somatostatin analogues; * history of prior malignancy, excepted for cured non-melanoma skin cancer, and cured in situ cervical carcinoma.

Design outcomes

Primary

MeasureTime frame
disease free survival50 months

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026