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Hyperpolarized Pyruvate Injection in Subjects With Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Hyperpolarized Pyruvate (13C) injection
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Cancer focused on measuring Prostate Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

INCLUSION CRITERIA:

  1. The subject has biopsy-proven prostate cancer and is either undergoing active surveillance ("watchful waiting") or pre primary local treatment for prostate cancer (i.e., prior to either radiation therapy or radical prostatectomy).
  2. The subject is able and willing to comply with study procedures and provide signed and dated informed consent.
  3. The subject has concordant MRI/1H MRSI findings from a prior MR staging exam performed within 8 weeks of the 13C MRSI exam performed in this study with IMP, or is willing to undergo MRI/1H MRSI in connection with the study exam.
  4. Negative test for hepatitis B and hepatitis C.
  5. Eastern Cooperative Oncology Group Performance Status of 0 or 1.

  6. Laboratory criteria for protocol entry:

    • Absolute neutrophil count (ANC) >/= 1500 cells/microLiters
    • Hemoglobin >/= 9.0 gm/dL
    • Platelets >/= 100,000 cells/microLiters
    • Estimated creatinine clearance >/= 60 mL/min (by the Cockcroft Gault equation)
    • Bilirubin within normal range
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) within normal range
  7. Willing to use contraception during and for 1 month after completion of the study.

EXCLUSION CRITERIA:

  1. The subject has received, or is scheduled to receive, another IMP from 1 month before to 1 month after inclusion in this study.
  2. Current or prior androgen deprivation therapy; previous use of a 5-alpha reductase inhibitor is allowed, provided it was discontinued at least 1 month prior to study entry.
  3. Poorly controlled hypertension, with blood pressure at study entry >150/90.
  4. Contraindication for or inability to tolerate MRI examination.
  5. Prostate biopsy within 12 weeks prior to study entry.
  6. BMI of less than 18.5 or greater than 32. At the 0.43 ml/kg dose, subject body weight should be less than or equal to 100 kg owing to limitations in the amount of IMP available.
  7. Congestive heart failure or New York Heart Association (NYHA) status >2.
  8. A past or present medical history of clinically significant electrocardiogram (EKG) abnormalities, including QT prolongation, a family history of prolonged QT interval syndrome, or myocardial infarction (MI) less than 1 year ago with ensuing unstable EKG.
  9. Ongoing acute or chronic pulmonary bronchospastic disease, including a history of chronic obstructive pulmonary disease or asthma, with an exacerbation within the past year.

Sites / Locations

  • University of California San Francisco

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

1

2

3

Arm Description

0.14 ml/kg bw - hyperpolarized pyruvate

0.28 ml/kg bw - hyperpolarized pyruvate

0.43 ml/kg bw - hyperpolarized pyruvate

Outcomes

Primary Outcome Measures

Number of Participants with Adverse Events as a Measure of Safety and Tolerability.
Assessment of the occurrence of clinically significant changes in safety variables from baseline. Safety endpoints include monitoring for the occurrence of treatment-emergent AEs. Monitoring will occur to evaluate for dose-limiting toxicity. Dose-Limiting Toxicity (DLT) is defined as any toxicity greater than or equal to grade 2, 3 or 4, attributable to the imaging agent and occurring within 7 days after administration. The maximum tolerated dose will be the dose level at which <33% DLT occurs.

Secondary Outcome Measures

to determine the time course and imaging window that provides the best signal-to-noise ratio (SNR) of the presence of hyperpolarized pyruvate (13C).
The optimum 13C imaging window for maximizing lactate SNR will be determined as the period of time after injection in which hyperpolarized lactate reaches a maximal plateau in the prostate. This plateau results from opposing processes of lactate production from pyruvate and T1 decay (for pre-clinical studies this plateau occurred approximately between 35 and 55 seconds).
To determine the kinetics and prostate metabolism of hyperpolarized pyruvate (13C)
For the subjects receiving 3-D 13C spectroscopic imaging (the second 3 subjects per dose cohort as well as the expansion cohorts), a fast 13C MRSI sequence will be used to acquire data from the prostate at a time defined by the kinetic studies (approximately 40 seconds after intravenous administration of hyperpolarized pyruvate).

Full Information

First Posted
October 13, 2010
Last Updated
October 1, 2015
Sponsor
University of California, San Francisco
Collaborators
GE Healthcare
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1. Study Identification

Unique Protocol Identification Number
NCT01229618
Brief Title
Hyperpolarized Pyruvate Injection in Subjects With Prostate Cancer
Official Title
A Phase 1 Ascending-dose Study to Assess the Safety and Tolerability and Imaging Potential of Hyperpolarized Pyruvate (13C) Injection in Subjects With Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Francisco
Collaborators
GE Healthcare

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Current imaging options do not assess prostate cancer well. This study will combine two magnetic resonance imaging modalities, MRI and MRSI, in order to determine the utility to physicians and patients with prostate cancer in making treatment decisions and seeing how well various types of treatment work. Hyperpolarized pyruvate (13C) is an investigational product that may enhance the imaging capability of MRI and MRSI. Hyperpolarized pyruvate will be injected into the body to determine how it is metabolized and how it's metabolism can be assessed using MR imaging. The purpose of this study is to determine the safety and metabolism of hyperpolarized pyruvate in humans, and how this can be used to increase the effectiveness of MR imaging with regards to patient care.
Detailed Description
This is a phase 1 clinical study of an investigational medicinal product (IMP), hyperpolarized Pyruvate (13C) Injection. The study includes the acquisition of magnetic resonance (MR) data and will be performed in men with prostate cancer and intact prostates. A standard dose-escalation design will be used; initially, 6 subjects will receive IMP at each dose level. As data on both the dynamics of arrival of the IMP and potential imaging efficacy are needed at each dose level, requiring the use of separate MR acquisition sequences, a modified 3+3 design will be applied in each dose cohort. The first 3 subjects will undergo dynamic 13C imaging to define the kinetics of delivery and metabolism of IMP, and the second 3 subjects will undergo 13C MR spectroscopic imaging (MRSI) to obtain 3-dimensional (3-D) spatial information about metabolism of IMP in regions of the prostate with and without cancer involvement. After the apparent maximum tolerated dose (MTD) has been established, there will be an expansion of the 3-D imaging cohort to 6 subjects (9 subjects in total at this dose level) to obtain additional information regarding safety at the MTD. If >2 subjects from this cohort of 9 subjects experience a dose-limiting toxicity (DLT), the next lower dose will be defined as the MTD. At the dose level with the highest contrast to noise ratio (dose level less than or equal to the MTD) there will be an expansion of the imaging cohort to include another 15 subjects for a total of 18 subjects who undergo 13C 3-D scanning at this dose, to obtain exploratory information concerning the time course and SNR (signal to noise ratio) of the presence of hyperpolarized [1 13C] pyruvate and its metabolites in regions of cancer and benign prostate tissues. The information provided by these data will be used to develop the MR imaging protocol for future clinical trials that will seek to address the sensitivity and specificity of the technology.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
0.14 ml/kg bw - hyperpolarized pyruvate
Arm Title
2
Arm Type
Experimental
Arm Description
0.28 ml/kg bw - hyperpolarized pyruvate
Arm Title
3
Arm Type
Experimental
Arm Description
0.43 ml/kg bw - hyperpolarized pyruvate
Intervention Type
Drug
Intervention Name(s)
Hyperpolarized Pyruvate (13C) injection
Other Intervention Name(s)
[1-13C]pyruvic acid, AH111710
Intervention Description
single hyperpolarized pyruvate IV (intravenous) injection followed by MR imaging scans (MRI and MRSI)
Primary Outcome Measure Information:
Title
Number of Participants with Adverse Events as a Measure of Safety and Tolerability.
Description
Assessment of the occurrence of clinically significant changes in safety variables from baseline. Safety endpoints include monitoring for the occurrence of treatment-emergent AEs. Monitoring will occur to evaluate for dose-limiting toxicity. Dose-Limiting Toxicity (DLT) is defined as any toxicity greater than or equal to grade 2, 3 or 4, attributable to the imaging agent and occurring within 7 days after administration. The maximum tolerated dose will be the dose level at which <33% DLT occurs.
Time Frame
7 days
Secondary Outcome Measure Information:
Title
to determine the time course and imaging window that provides the best signal-to-noise ratio (SNR) of the presence of hyperpolarized pyruvate (13C).
Description
The optimum 13C imaging window for maximizing lactate SNR will be determined as the period of time after injection in which hyperpolarized lactate reaches a maximal plateau in the prostate. This plateau results from opposing processes of lactate production from pyruvate and T1 decay (for pre-clinical studies this plateau occurred approximately between 35 and 55 seconds).
Title
To determine the kinetics and prostate metabolism of hyperpolarized pyruvate (13C)
Description
For the subjects receiving 3-D 13C spectroscopic imaging (the second 3 subjects per dose cohort as well as the expansion cohorts), a fast 13C MRSI sequence will be used to acquire data from the prostate at a time defined by the kinetic studies (approximately 40 seconds after intravenous administration of hyperpolarized pyruvate).

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: The subject has biopsy-proven prostate cancer and is either undergoing active surveillance ("watchful waiting") or pre primary local treatment for prostate cancer (i.e., prior to either radiation therapy or radical prostatectomy). The subject is able and willing to comply with study procedures and provide signed and dated informed consent. The subject has concordant MRI/1H MRSI findings from a prior MR staging exam performed within 8 weeks of the 13C MRSI exam performed in this study with IMP, or is willing to undergo MRI/1H MRSI in connection with the study exam. Negative test for hepatitis B and hepatitis C. Eastern Cooperative Oncology Group Performance Status of 0 or 1. Laboratory criteria for protocol entry: Absolute neutrophil count (ANC) >/= 1500 cells/microLiters Hemoglobin >/= 9.0 gm/dL Platelets >/= 100,000 cells/microLiters Estimated creatinine clearance >/= 60 mL/min (by the Cockcroft Gault equation) Bilirubin within normal range Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) within normal range Willing to use contraception during and for 1 month after completion of the study. EXCLUSION CRITERIA: The subject has received, or is scheduled to receive, another IMP from 1 month before to 1 month after inclusion in this study. Current or prior androgen deprivation therapy; previous use of a 5-alpha reductase inhibitor is allowed, provided it was discontinued at least 1 month prior to study entry. Poorly controlled hypertension, with blood pressure at study entry >150/90. Contraindication for or inability to tolerate MRI examination. Prostate biopsy within 12 weeks prior to study entry. BMI of less than 18.5 or greater than 32. At the 0.43 ml/kg dose, subject body weight should be less than or equal to 100 kg owing to limitations in the amount of IMP available. Congestive heart failure or New York Heart Association (NYHA) status >2. A past or present medical history of clinically significant electrocardiogram (EKG) abnormalities, including QT prolongation, a family history of prolonged QT interval syndrome, or myocardial infarction (MI) less than 1 year ago with ensuing unstable EKG. Ongoing acute or chronic pulmonary bronchospastic disease, including a history of chronic obstructive pulmonary disease or asthma, with an exacerbation within the past year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles Ryan, M.D.
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18922937
Citation
Albers MJ, Bok R, Chen AP, Cunningham CH, Zierhut ML, Zhang VY, Kohler SJ, Tropp J, Hurd RE, Yen YF, Nelson SJ, Vigneron DB, Kurhanewicz J. Hyperpolarized 13C lactate, pyruvate, and alanine: noninvasive biomarkers for prostate cancer detection and grading. Cancer Res. 2008 Oct 15;68(20):8607-15. doi: 10.1158/0008-5472.CAN-08-0749.
Results Reference
background
PubMed Identifier
12930897
Citation
Ardenkjaer-Larsen JH, Fridlund B, Gram A, Hansson G, Hansson L, Lerche MH, Servin R, Thaning M, Golman K. Increase in signal-to-noise ratio of > 10,000 times in liquid-state NMR. Proc Natl Acad Sci U S A. 2003 Sep 2;100(18):10158-63. doi: 10.1073/pnas.1733835100. Epub 2003 Aug 20.
Results Reference
background
PubMed Identifier
17392247
Citation
Hricak H, Choyke PL, Eberhardt SC, Leibel SA, Scardino PT. Imaging prostate cancer: a multidisciplinary perspective. Radiology. 2007 Apr;243(1):28-53. doi: 10.1148/radiol.2431030580. Erratum In: Radiology. 2007 Oct;245(1):302.
Results Reference
background
PubMed Identifier
16685733
Citation
Swanson MG, Zektzer AS, Tabatabai ZL, Simko J, Jarso S, Keshari KR, Schmitt L, Carroll PR, Shinohara K, Vigneron DB, Kurhanewicz J. Quantitative analysis of prostate metabolites using 1H HR-MAS spectroscopy. Magn Reson Med. 2006 Jun;55(6):1257-64. doi: 10.1002/mrm.20909.
Results Reference
background
PubMed Identifier
18727052
Citation
Tessem MB, Swanson MG, Keshari KR, Albers MJ, Joun D, Tabatabai ZL, Simko JP, Shinohara K, Nelson SJ, Vigneron DB, Gribbestad IS, Kurhanewicz J. Evaluation of lactate and alanine as metabolic biomarkers of prostate cancer using 1H HR-MAS spectroscopy of biopsy tissues. Magn Reson Med. 2008 Sep;60(3):510-6. doi: 10.1002/mrm.21694.
Results Reference
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Hyperpolarized Pyruvate Injection in Subjects With Prostate Cancer

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