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Study to Evaluate the Safety of Combining Two Radionuclide Therapies to Treat Mid-gut Neuroendocrine Tumors

Primary Purpose

Neuroendocrine Tumor, Malignant, Neuroendocrine Tumor Gastrointestinal, Hormone-Secreting

Status

Active

Phase

Early Phase 1

Locations

United States

Study Type

Interventional

Intervention

90Y-DOTA-3-Tyr-Octreotide

131I-MIBG

About this trial

This is an interventional treatment trial for Neuroendocrine Tumor, Malignant focused on measuring 3-Iodobenzylguanidine, dose-response relationship, radiation, theranostic, radionuclide, MIBG, DOTA

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

A 2-step eligibility is utilized for this study.

STEP 1:

Inclusion Criteria:

Ability to understand and the willingness to provide informed consent.
A pathologically confirmed (histology or cytology) malignant neoplasm that is determined to be well-differentiated neuroendocrine tumor (i.e. grade 1 or grade 2). The primary tumor location should be known or believed to be midgut, or pheochromocytoma, or paraganglioma.
Disease not amenable to curative intent treatment (primarily surgery) and in addition has shown either clinical or radiographic progression on all available (non-radionuclidic) therapies known to confer clinical benefit.
SSTR positive sites as demonstrated by either SSTR2 positivity (2+ or 3+ intensity and greater than 10% tumor cell occupying the receptors) or a nuclear medicine scan utilizing 111In-DTPA-Phe3-Octreotide (Octreoscan™) or 68Ga-DOTA-tyr3-Octreotide within 12 months prior to anticipated C1D1 demonstrating SSTR positive tumor sites
≥1 tumor site must have demonstrated uptake equal to or greater than normal liver as documented by nuclear scan imaging
≥1 evaluable site of disease measuring ≥ 1.5 cm in diameter on CT or MRI as measured per RECIST
≥ 18 to 70 years at the time of study drug administration.
Karnofsky Performance Status at least 70%
Agrees to contraception.

Exclusion criteria:

Patients who are considered a fall risk.
Women who are pregnant or breast feeding.
Surgery, radiation or chemotherapy within 4 weeks of proposed step 1 start date.
Prior peptide-receptor radiotherapy (PRRT).
Investigational drug within 4 weeks of proposed step 1 start date.
More than one concurrent, malignant disease.
History of congestive heart failure and cardiac ejection fraction ≤ 40%.
Patients for whom, in the opinion of their physician, a 24-hour discontinuation of somatostatin analogue therapy represents a health risk.
Patients who are unable to discontinue medications known to affect MIBG uptake
Proteinuria, grade 2 (i.e., ≥ 2+proteinuria).
Long-acting somatostatin analogue treatment within 14 days of proposed step 1 start date.
Prior external beam radiation involving kidneys (scatter doses of < 500 cGy to a single kidney or radiation to < 50% of a single kidney is acceptable).
Prior external beam radiation (including brachytherapy) involving 25% of bone marrow (excluding scatter doses of ≤ 5 Gy).
History of allergic reactions attributed to compounds of similar chemical or biologic composition to 90Y-DOTA-tyr3-Octreotide, Octreoscan®, 68Ga-Octreotide, or 131I-MIBG.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

If a subject meets STEP 1 criteria, a serial SPECT scan is performed for dosimetry. Step 2 criteria must be met and verified prior to therapy initiation.

STEP 2:

Inclusion Criteria:

Subjects must demonstrate at least one of the following:
- One or more MIBG+ and DOTATOC- tumors in addition to one or more DOTATOC+ tumors, and/or,
- One or more tumor sites where the calculated "safe" radiation tumor dose is higher by at least 25% with a combination of 131I-MIBG and 90Y-DOTATOC than it is with 90Y DOTATOC alone, or,
Within 2 weeks of study drug administration for therapeutic intent, patients must have normal organ and marrow function as defined below:
- absolute neutrophil count ≥ 2000 cells/mm3
- platelets ≥100,000 cells/mm3
- total bilirubin <1.5 x institutional ULN for age and weight
- AST(SGOT) ≤ 2.5 x institutional ULN
- ALT (SGPT) ≤ 2.5 x institutional ULN
- eGFR ≥ 50 mL/min/1.73 m2 (Cockroft Gault formula)

Sites / Locations

Holden Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

Experimental

Arm Label

Cohort 1

Cohort 2

Cohort 3

Cohort -1 (alternative cohort)

Cohort 2.1 (renal alternative)

Cohort 2.2 (bone marrow alternative)

Cohort 3.1 (renal alternative)

Cohort 3.2 (bone marrow alternative)

Arm Description

This is the initial treatment arm. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 150 centiGray (cGy) Radiation exposure to the kidneys is limited to 1900 centiGray (cGy)

This treatment arm is opened if Cohort 1 is successful. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 200 centiGray (cGy) Radiation exposure to the kidneys is limited to 2300 centiGray (cGy)

This treatment arm is opened if Cohort 2 is successful. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 250 centiGray (cGy) Radiation exposure to the kidneys is limited to 2300 centiGray (cGy)

This treatment arm is opened if Cohort 1 is not tolerated. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 100 centiGray (cGy) Radiation exposure to the kidneys is limited to 1500 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

This treatment arm is opened if the kidney radiation exposure was not tolerated in cohort 2. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 200 centiGray (cGy) Radiation exposure to the kidneys is limited to 1500 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

This treatment arm is opened if the kidney radiation exposure was not tolerated in cohort 2. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 100 centiGray (cGy) Radiation exposure to the kidneys is limited to 2300 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

This treatment arm is opened if the kidney radiation exposure was not tolerated in cohort 3. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 250 centiGray (cGy) Radiation exposure to the kidneys is limited to 1900 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

This treatment arm is opened if the kidney radiation exposure was not tolerated in cohort 2. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 150 centiGray (cGy) Radiation exposure to the kidneys is limited to 2300 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

Outcomes

Primary Outcome Measures

glomular filtration rate (eGFR)

Evaluate renal toxicity using eGFR measurement

urine protein

Evaluate renal toxicity using urine protein measurement

platelet count decreased

Evaluate bone marrow toxicity using platelet counts

absolute neutrophil count decreased

Evaluate bone marrow toxicity using absolute neutrophil count

Secondary Outcome Measures

Progression free survival (PFS)

From day 1 of therapy to documented disease progression in CT or MRI as per RECIST criteria

Overall survival (OS)

From start of treatment (cycle 1, day 1) until the date of death from any cause.

Full Information

NCT ID

NCT03044977

First Posted

February 2, 2017

Last Updated

August 15, 2023

Sponsor

David Bushnell

Collaborators

National Institutes of Health (NIH), National Cancer Institute (NCI), Holden Comprehensive Cancer Center

1. Study Identification

Unique Protocol Identification Number

NCT03044977

Brief Title

Study to Evaluate the Safety of Combining Two Radionuclide Therapies to Treat Mid-gut Neuroendocrine Tumors

Official Title

Phase 1 Trial Using 131I MIBG and 90Y DOTATOC in a Dosimetrically Determined Optimal Combination for Therapy of Selected Patients With Midgut Neuroendocrine Tumors.

Study Type

Interventional

2. Study Status

Record Verification Date

August 2023

Overall Recruitment Status

Active, not recruiting

Study Start Date

May 7, 2017 (Actual)

Primary Completion Date

December 2025 (Anticipated)

Study Completion Date

December 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor-Investigator

Name of the Sponsor

David Bushnell

Collaborators

National Institutes of Health (NIH), National Cancer Institute (NCI), Holden Comprehensive Cancer Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Yes

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

This study is designed to identify the best tolerated doses of [131]Iodine-MIBG and [90]Yttrium-DOTATOC when co-administered to treat midgut neuroendocrine tumors. These drugs (131I-MIBG, 90Y-DOTATOC) are radioactive drugs, known as radionuclide therapy. Currently, the safest and best tolerated doses of these drugs (when combined together) is unknown.

Detailed Description

[131]Iodine-MIBG and [90]Yttrium-DOTATOC are radioactive drugs designed to treat specific tumor cells. These drugs are a combination of the radiation (131-Iodine, 90-Yttrium) and a protein that targets the tumor cell (MIBG or DOTATOC). Because these proteins are attracted to, and stick to, the tumor, the radiation is centered in the tumors. This kills more tumor cells and minimizes radiation-damage to healthy tissues, like the heart and lungs. Two organs still absorb some of the radiation, though: bone marrow and the kidney. These organs limit how much radiation can be given to tumors, but we don't know how much radiation is too much. Too much radiation to bone marrow can result in anemia. Too much radiation to the kidneys can result in kidney failure. From prior radiation therapies, we have a general idea of how much radiation we can give safely. 131I-MIBG and 90Y-DOTATOC have never been given together. We want to give them together because many times, tumors are actually groups of different types of cells. This means, not all the cells respond to therapy the same way. If some tumor cells survive therapy, the tumor will continue to grow and eventually come back. We know some mid-gut neuroendocrine tumors (NETs) have targets for DOTATOC and some other mid-gut NETs have targets for MIBG. We also have now identified that some people with mid-gut NETs have different tumors: some with targets for MIBG and some with targets for DOTATOC. For these people, this means treating only with 131I-MIBG or 90Y-DOTATOC will not be enough to treat their cancer. They need both radioactive drugs. Because we are combining these radioactive drugs, this study is known as a first-in-man study. We are also using a special imaging to help us estimate the radiation dose to the bone marrow and to the kidneys. This is what decides the final dose of 131I-MIBG and 90Y-DOTATOC. Before receiving therapy, participants will be asked to undergo imaging to verify they have both MIBG and DOTATOC tumor types: participants are given very small doses of radioactive drugs a special camera (SPECT/CT) collects images (scans) imaging (scans) are done over 3 calendar days blood samples are taken at that time, too, to measure the circulating amount of tracer doses If the scans show a participant has both MIBG and DOTATOC tumors, therapy is given: a customized dose of 90Y-DOTATOC is given on day 1 of a treatment cycle. This is given outpatient. a customized dose of 131I-MIBG is given on day 2 of a treatment cycle. This is given inpatient (admitted to the hospital). participants are monitored through blood tests to identify the side effects of therapy. Each participant can have up to 2 cycles of therapy. The cycles are 12 weeks apart. The doses for 90Y-DOTATOC and 131I-MIBG are decided based on radiation to the bone marrow and radiation to the kidney. Doses are decided by how well other participants have done on this study. Participants have life long follow-up for this study. This is very important, because a study like this has not been done.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Neuroendocrine Tumor, Malignant, Neuroendocrine Tumor Gastrointestinal, Hormone-Secreting

Keywords

3-Iodobenzylguanidine, dose-response relationship, radiation, theranostic, radionuclide, MIBG, DOTA

7. Study Design

Primary Purpose

Treatment

Study Phase

Early Phase 1

Interventional Study Model

Single Group Assignment

Model Description

dose-escalation design

Masking

None (Open Label)

Allocation

Non-Randomized

Enrollment

20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title

Cohort 1

Arm Type

Experimental

Arm Description

Arm Title

Cohort 2

Arm Type

Experimental

Arm Description

Arm Title

Cohort 3

Arm Type

Experimental

Arm Description

Arm Title

Cohort -1 (alternative cohort)

Arm Type

Experimental

Arm Description

Arm Title

Cohort 2.1 (renal alternative)

Arm Type

Experimental

Arm Description

Arm Title

Cohort 2.2 (bone marrow alternative)

Arm Type

Experimental

Arm Description

This treatment arm is opened if the kidney radiation exposure was not tolerated in cohort 2. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 100 centiGray (cGy) Radiation exposure to the kidneys is limited to 2300 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

Arm Title

Cohort 3.1 (renal alternative)

Arm Type

Experimental

Arm Description

Arm Title

Cohort 3.2 (bone marrow alternative)

Arm Type

Experimental

Arm Description

This treatment arm is opened if the kidney radiation exposure was not tolerated in cohort 2. 131I-MIBG and 90Y-DOTATOC are administered once per cycle, for up to 2 cycles 12 weeks apart. Radiation exposure to the bone marrow is limited to 150 centiGray (cGy) Radiation exposure to the kidneys is limited to 2300 centiGray (cGy) No further dose evaluations are done after this cohort is completed.

Intervention Type

Drug

Intervention Name(s)

90Y-DOTA-3-Tyr-Octreotide

Other Intervention Name(s)

90Y DOTATOC

Intervention Description

Peptide receptor radiotherapy (PRRT) using Yttrium-90 as the active radionuclide. For intravenous administration only.

Intervention Type

Drug

Intervention Name(s)

131I-MIBG

Intervention Description

Peptide receptor radiotherapy (PRRT) using Iodine-131 as the active radionuclide. For intravenous administration only.

Primary Outcome Measure Information:

Title

glomular filtration rate (eGFR)

Description

Evaluate renal toxicity using eGFR measurement

Time Frame

4 and 8 weeks after each treatment, then at 3, 6, & 9 months after the last treatment

Title

urine protein

Description

Evaluate renal toxicity using urine protein measurement

Time Frame

Monthly beginning 4 weeks after the first treatment through 6 months after the last treatment

Title

platelet count decreased

Description

Evaluate bone marrow toxicity using platelet counts

Time Frame

Weeks 4, 5, 6, 7, 8 after each therapy and then 3, 6, & 12 months after the last treatment

Title

absolute neutrophil count decreased

Description

Evaluate bone marrow toxicity using absolute neutrophil count

Time Frame

Weeks 4, 5, 6, 7, 8 after each therapy and then 3, 6, & 12 months after the last treatment

Secondary Outcome Measure Information:

Title

Progression free survival (PFS)

Description

From day 1 of therapy to documented disease progression in CT or MRI as per RECIST criteria

Time Frame

Every 6 months for up to 5 years

Title

Overall survival (OS)

Description

From start of treatment (cycle 1, day 1) until the date of death from any cause.

Time Frame

Up to 5 years

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Maximum Age & Unit of Time

80 Years

Accepts Healthy Volunteers

Eligibility Criteria

A 2-step eligibility is utilized for this study. STEP 1: Inclusion Criteria: Ability to understand and the willingness to provide informed consent. A pathologically confirmed (histology or cytology) malignant neoplasm that is determined to be well-differentiated neuroendocrine tumor (i.e. grade 1 or grade 2). The primary tumor location should be known or believed to be midgut, or pheochromocytoma, or paraganglioma. Disease not amenable to curative intent treatment (primarily surgery) and in addition has shown either clinical or radiographic progression on all available (non-radionuclidic) therapies known to confer clinical benefit. SSTR positive sites as demonstrated by either SSTR2 positivity (2+ or 3+ intensity and greater than 10% tumor cell occupying the receptors) or a nuclear medicine scan utilizing 111In-DTPA-Phe3-Octreotide (Octreoscan™) or 68Ga-DOTA-tyr3-Octreotide within 12 months prior to anticipated C1D1 demonstrating SSTR positive tumor sites ≥1 tumor site must have demonstrated uptake equal to or greater than normal liver as documented by nuclear scan imaging ≥1 evaluable site of disease measuring ≥ 1.5 cm in diameter on CT or MRI as measured per RECIST ≥ 18 to 70 years at the time of study drug administration. Karnofsky Performance Status at least 70% Agrees to contraception. Exclusion criteria: Patients who are considered a fall risk. Women who are pregnant or breast feeding. Surgery, radiation or chemotherapy within 4 weeks of proposed step 1 start date. Prior peptide-receptor radiotherapy (PRRT). Investigational drug within 4 weeks of proposed step 1 start date. More than one concurrent, malignant disease. History of congestive heart failure and cardiac ejection fraction ≤ 40%. Patients for whom, in the opinion of their physician, a 24-hour discontinuation of somatostatin analogue therapy represents a health risk. Patients who are unable to discontinue medications known to affect MIBG uptake Proteinuria, grade 2 (i.e., ≥ 2+proteinuria). Long-acting somatostatin analogue treatment within 14 days of proposed step 1 start date. Prior external beam radiation involving kidneys (scatter doses of < 500 cGy to a single kidney or radiation to < 50% of a single kidney is acceptable). Prior external beam radiation (including brachytherapy) involving 25% of bone marrow (excluding scatter doses of ≤ 5 Gy). History of allergic reactions attributed to compounds of similar chemical or biologic composition to 90Y-DOTA-tyr3-Octreotide, Octreoscan®, 68Ga-Octreotide, or 131I-MIBG. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. If a subject meets STEP 1 criteria, a serial SPECT scan is performed for dosimetry. Step 2 criteria must be met and verified prior to therapy initiation. STEP 2: Inclusion Criteria: Subjects must demonstrate at least one of the following: One or more MIBG+ and DOTATOC- tumors in addition to one or more DOTATOC+ tumors, and/or, One or more tumor sites where the calculated "safe" radiation tumor dose is higher by at least 25% with a combination of 131I-MIBG and 90Y-DOTATOC than it is with 90Y DOTATOC alone, or, Within 2 weeks of study drug administration for therapeutic intent, patients must have normal organ and marrow function as defined below: absolute neutrophil count ≥ 2000 cells/mm3 platelets ≥100,000 cells/mm3 total bilirubin <1.5 x institutional ULN for age and weight AST(SGOT) ≤ 2.5 x institutional ULN ALT (SGPT) ≤ 2.5 x institutional ULN eGFR ≥ 50 mL/min/1.73 m2 (Cockroft Gault formula)

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

David Bushnell, MD

Organizational Affiliation

University of Iowa

Official's Role

Study Chair

Facility Information:

Facility Name

Holden Comprehensive Cancer Center

City

Iowa City

State/Province

Iowa

ZIP/Postal Code

52242

Country

United States

12. IPD Sharing Statement

Plan to Share IPD

Yes

IPD Sharing Plan Description

Information will be distributed via clinicaltrials.gov and shared as per the filed NIH data sharing plan

IPD Sharing Time Frame

Typically, after completion of study

IPD Sharing Access Criteria

A data sharing agreement will need to be filed for sharing the individual participant data. A contract may be required.

Citations:

PubMed Identifier

26116109

Citation

Bushnell DL, Madsen MT, O'cdorisio T, Menda Y, Muzahir S, Ryan R, O'dorisio MS. Feasibility and advantage of adding (131)I-MIBG to (90)Y-DOTATOC for treatment of patients with advanced stage neuroendocrine tumors. EJNMMI Res. 2014 Dec;4(1):38. doi: 10.1186/s13550-014-0038-2. Epub 2014 Sep 10.

Results Reference

background

PubMed Identifier

16595501

Citation

Madsen MT, Bushnell DL, Juweid ME, Menda Y, O'Dorisio MS, O'Dorisio T, Besse IM. Potential increased tumor-dose delivery with combined 131I-MIBG and 90Y-DOTATOC treatment in neuroendocrine tumors: a theoretic model. J Nucl Med. 2006 Apr;47(4):660-7.

Results Reference

background

Links:

URL

https://uihc.org/neuroendocrine-spore-overview

Description

The website describing the Specialized Programs of Research Excellence in Neuroendocrine Cancers that supports this clinical trial.

Learn more about this trial

Study to Evaluate the Safety of Combining Two Radionuclide Therapies to Treat Mid-gut Neuroendocrine Tumors

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