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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04790708
Other study ID # 160990
Secondary ID 2016-005129-35
Status Recruiting
Phase N/A
First received
Last updated
Start date July 2, 2018
Est. completion date June 30, 2023

Study information

Verified date March 2021
Source University Hospital of Ferrara
Contact Mirco Bartolomei, MD
Phone 0532236082
Email m.bartolomei@ospfe.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The rationale behind the purpose of this study lays on: - the evidence that PRRT could represent a valuable treatment for the majority of patients with neuroendocrine tumor (NET) in disease progression, operated or inoperable, presenting lesions expressing somatostatin receptors and for which standard treatments are not already available; - the current impossibility of acquiring on the market radiolabelled analogues of somatostatin used for PRRT with marketing authorisation; - the need to collect a larger case history than in previous studies; - the need to stratify the various histotypes based on the response obtained; - the need to define new treatment schemes that guarantee the maximum efficacy and the lowest possible toxicity - with low cumulative (and per cycle) activities radiopharmaceutical and according to the concept of dose hyperfractionation - with a view to an optimal balance between risk and benefit.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date June 30, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 1. Age =18 years, of both sexes, of any ethnicity; - 2. Cyto-histological and immunohistochemical diagnosis of NET; - 3. Evaluation of the cell proliferation index by studying Ki-67 and / or E3 ubiquitin-protein ligase (MIB-1). - 4. Illness measurable according to RECIST 1.1 criteria by imaging conventional (CT with contrast medium or MRI with contrast medium) not earlier than two months with respect to enrollment; - 5. Elevated expression of somatostatin receptors documented by PET-CT with 68Ga-DOTATOC in the target lesion (s). It is defined as "high expression of somatostatin receptors "a ratio of Maximum standardized uptake value (SUVmax) lesion / Mean standardized uptake value (SUVmean) muscle = 4: 1 calculated with semi-quantitative analysis on examination PET-CT with 68Ga-DOTATOC; - 6. Dosage of Chromogranin A (and any other specific markers) not prior to two months of enrollment; - 7. Evaluation of glucose metabolism in the target lesion (s) by PET-CT with 18F-FDG; - 8. Preserved haematological, hepatic and renal parameters, in particular: white blood cells =2500 / µL; platelets = 90000 / µL; hemoglobin = 9 gr / dL; creatinine = 2 mg / dL; bilirubin = 2.5 mg / dL - 9. Eastern Cooperative Oncology Group (ECOG) performance status =2; - 10. Life expectancy = 6 months; - 11. Stable or progressive disease, at any stage, both in operated patients that inoperable; - 12. Absence of standard treatments already documented and of equal effectiveness; - 13. Absence of surgical, chemotherapy and / or radiotherapy treatments for at least 30 days. On the other hand, patients in therapy with somatostatin analogues or biologics, such as mechanistic target of rapamycin (m-TOR) inhibitors; - 14. Voluntary participation in the study by signing the consent form informed, after reading and complete understanding of the information notes. Exclusion Criteria: - 1. Lack of the requirements listed above; - 2. State of pregnancy; - 3. Breastfeeding and relative refusal to suspend breastfeeding; - 4. Participation in another therapeutic experimental clinical protocol in the four weeks prior to the PRRT; - 5. Bone marrow invasion of disease> 25% confirmed; - 6. Previous extensive radiotherapy treatments.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Lutetium-177 (177Lu)-DOTATOC
5 cycles of 3,7 e 5,55 gigabequerel (GBq) of 177Lu-DOTATOC every 8-10 weeks. Cumulative activity: 18,5 e 27,75 GBq
Yttrium-90 (90Y)-DOTATOC
5 cycles of 1,85 e 2,775 GBq of 90Y-DOTATOC every 8-10 weeks. Cumulative activity: 9,25 e 13,875 GBq
177Lu-DOTATOC + 90Y-DOTATOC
3 cycles of 3,7 e 5,55 GBq of 177Lu-DOTATOC alternated with 2 cycles of 1,85 e 2,775 GBq of 90Y-DOTATOC every 8-10 weeks. Cumulative activity: 18,5 e 27,75 GBq of 177Lu-DOTATOC and 9,25 e 13,875 GBq of 90Y-DOTATOC
Re-treatment 177Lu-DOTATOC
3 cycles of 3,7 e 5,55 GBq of 177Lu-DOTATOC every 8-10weeks. Cumulative activity: 11,1 e 16,65 GBq of 177Lu-DOTATOC
Re-treatment 90Y-DOTATOC
3 cycles of 1,85 e 2,775 GBq of 90Y-DOTATOC every 8-10 weeks Cumulative activity: 5,55 e 8,325 GBq of 90Y-DOTATOC

Locations

Country Name City State
Italy University Hospital of Ferrara Ferrara

Sponsors (1)

Lead Sponsor Collaborator
University Hospital of Ferrara

Country where clinical trial is conducted

Italy, 

References & Publications (91)

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* Note: There are 91 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Disease Control Rate Post-treatment evaluation will be performed with:
a clinical examination;
a comparative morphological re-evaluation, using version 1.1 of Response evaluation criteria in solid tumors (RECIST criteria) on Computed Tomography (CT);
a comparative functional re-evaluation, performed both on 18F-2-fluoro-2-deoxy-D-glucose (18F-FDG) positron emission computed tomography (PET/CT) and Gallium-68 (68Ga)-DOTATOC PET/CT using visual and semi-quantitative parameters (such as SUVmax).
Based on all these parameters, Disease Control Rate will be labelled as: Complete Response (CR), Partial Response (PR), Stable Disease (SD), or Progression Disease (PD).
12 months
Secondary Progression Free Survival Progression free survival is defined as the time intercurrent from treatment start to the date of first observation of documented disease progression or death due to any cause. 6 months
Secondary Overall Survival Overall survival is defined as the time intercurrent from treatment start to the date of death due to any cause, or the date of last contact. 6 months
Secondary Evaluation of PRRT Safety The evaluation of Treatment-Emergent Adverse Events, defined as any G3/G4 toxicity. The evaluation will be performed during every treatment cycle and after 12, 18, 24, 30, 36 and 42 months after the last treatment cycle and will be based on version 4.0 of Common Terminology Criteria for Adverse Events (CTC-AE) toxicity criteria. 6 months
Secondary Evaluation of Quality of Life Quality of Life (QoL) will be evaluated with quality of life questionnaire, version 3 (QLQ-C30) by European Organisation for Research and Treatment of Cancer (EORTC). The questionnaire includes five functional scales, three symptom scales, a global health status / QoL scale, and six single items.
All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level.
6 months
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