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Pulmonary Interstitial Lymphography in Early Stage Lung Cancer

Primary Purpose

Lung Cancer, Lung Cancer Non-Small Cell Cancer (NSCLC), Lung Cancer Small Cell Lung Cancer (SCLC)

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Stereotactic Body Radiation Therapy (SBRT)
Computed Tomography (CT)
Cyberknife
Trilogy
True Beam
Iohexol
Iodixanol
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Lung Cancer

Eligibility Criteria

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

INCLUSION CRITERIA

  • Either:

    • Established primary lung cancer/ cancer metastatic to lung, OR
    • Lesion suspicious for malignancy in lung, according to the following criteria:

      • Histopathologically confirmed lung cancer or cancer metastatic to lung, OR
      • Plan for biopsy of suspicious lung mass based on imaging (growth on serial CT scan or nodule/mass with focal hypermetabolism on FDG-PET scan), OR
      • Known metastatic cancer, with metastases to the lung based on imaging
  • Age > 18 years old
  • Eastern Clinical Oncology Group (ECOG) performance status 0, 1 or 2 (Appendix IV)
  • No prior surgery, chemotherapy, or radiation for the current lung tumor

EXCLUSION CRITERIA

  • Prior radiotherapy to thorax
  • Iodine allergy
  • Contraindication to receiving radiotherapy, unless undergoing surgery
  • Pregnant

Sites / Locations

  • Stanford University School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

pulmonary interstitial lymphography

Arm Description

stereotactic body radiation therapy & pulmonary interstitial lymphography

Outcomes

Primary Outcome Measures

- Feasibility and safety of identification of primary nodal drainage for purpose of radiation therapy targeting

Secondary Outcome Measures

- Feasibility of incorporating primary nodal drainage into radiation therapy planning process

Full Information

First Posted
August 23, 2010
Last Updated
April 13, 2018
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT01188486
Brief Title
Pulmonary Interstitial Lymphography in Early Stage Lung Cancer
Official Title
Pulmonary Interstitial Lymphography in Early Stage Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Terminated
Why Stopped
Business decision
Study Start Date
August 2010 (undefined)
Primary Completion Date
April 30, 2017 (Actual)
Study Completion Date
April 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The stereotactic body radiation therapy (SBRT) procedure is an emerging alternative to the standard treatment for early stage non-small cell lung cancer (NSCLC), typically lobectomy with lymphadenectomy. This procedure (lobectomy) does not fulfill the medical need as many patients are poor operative candidates or decline surgery. This study assesses the feasibility of stereotactic body radiation therapy (SBRT) as a tool to produce therapeutically useful computed tomography (CT) scans, using standard water-soluble iodinated compounds as the contrast agents.
Detailed Description
Non-small cell lung cancer (NSCLC) is the most deadly cancer in the world. NSCLC annually causes 150,000 deaths in the US and greater than 1 million worldwide. The standard treatment for early stage NSCLC is lobectomy with lymphadenectomy. However, many patients are poor operative candidates or decline surgery. An emerging alternative is Stereotactic Body Radiation Therapy (SBRT). Mounting evidence from phase 1-2 studies demonstrates that SBRT offers excellent local control. Most SBRT trials focused on small, peripheral tumors in inoperable patients. Increasingly, clinical trials study SBRT in operable patients, often with larger, central tumors. Using clinical staging, a significant proportion of patients harbor occult nodal metastases when undergoing SBRT to the primary tumor alone. Subgroups of patients carry even higher risk of nodal metastases. These nodal metastases frequently would be removed by surgical intervention. However, SBRT, at present, is only directed at the primary tumor, potentially leading to regional failures in otherwise curable patients. To increase the effectiveness of SBRT for lung tumors, the next logical step is to explore whether the highest risk areas of disease spread can be identified and targeted. Regional failure could be reduced and outcome improved in a significant proportion of patients treated with SBRT if the primary nodal drainage (PND) were identified, targeted and treated in addition to the primary tumor. We propose to conduct a study to determine the feasibility of visualizing, by computed tomography (CT) scans, water-soluble iodinated contrast materials after direct injection into the tumor. Integration into radiation therapy treatment planning may also be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Lung Cancer Non-Small Cell Cancer (NSCLC), Lung Cancer Small Cell Lung Cancer (SCLC), Mesothelioma

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
pulmonary interstitial lymphography
Arm Type
Experimental
Arm Description
stereotactic body radiation therapy & pulmonary interstitial lymphography
Intervention Type
Radiation
Intervention Name(s)
Stereotactic Body Radiation Therapy (SBRT)
Intervention Description
Standard of care diagnostic radiotherapy procedure
Intervention Type
Radiation
Intervention Name(s)
Computed Tomography (CT)
Intervention Description
For each participant, 3 chest CT scans will be obtained, 1 before and 2 after interstitial injection of the water-soluble contrast
Intervention Type
Device
Intervention Name(s)
Cyberknife
Intervention Description
Linear accelerator for producing high energy x-rays for radiation therapy.
Intervention Type
Device
Intervention Name(s)
Trilogy
Intervention Description
Linear accelerator for producing high energy x-rays for radiation therapy.
Intervention Type
Device
Intervention Name(s)
True Beam
Intervention Description
Linear accelerator for producing high energy x-rays for radiation therapy.
Intervention Type
Drug
Intervention Name(s)
Iohexol
Other Intervention Name(s)
Omnipaque, Omnipaque in Rediflo prefilled cartridges, Bis(2,3-dihydroxypropyl)-5-[N-(2,3-dihydroxypropyl)-acetamido]-2,4,6-triiodoisophthalamide
Intervention Description
Aqueous solution of a nonionic, water-soluble radiographic contrast medium in prefilled cartridges with a molecular weight of 821.14 (iodine content 46.36%), available at 140, 180, 240, 300, and 350 mgI/mL.
Intervention Type
Drug
Intervention Name(s)
Iodixanol
Other Intervention Name(s)
Visipaque, 5,5´-[(2-hydroxy-1,3-propanediyl)bis (acetylimino)] bis[N,N´-bis(2,3-dihydroxypropyl)-2,4,6- triiodo-1,3- benzenedicarboxamide]
Intervention Description
Aqueous solution of a nonionic, water-soluble, dimeric, isosmolar, radiographic contrast medium with a molecular weight of 1550.20 (iodine content 49.1%), available in 2 concentrations, (270 mgI/mL and 320 mgI/mL.
Primary Outcome Measure Information:
Title
- Feasibility and safety of identification of primary nodal drainage for purpose of radiation therapy targeting
Time Frame
15 months
Secondary Outcome Measure Information:
Title
- Feasibility of incorporating primary nodal drainage into radiation therapy planning process
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA Either: Established primary lung cancer/ cancer metastatic to lung, OR Lesion suspicious for malignancy in lung, according to the following criteria: Histopathologically confirmed lung cancer or cancer metastatic to lung, OR Plan for biopsy of suspicious lung mass based on imaging (growth on serial CT scan or nodule/mass with focal hypermetabolism on FDG-PET scan), OR Known metastatic cancer, with metastases to the lung based on imaging Age > 18 years old Eastern Clinical Oncology Group (ECOG) performance status 0, 1 or 2 (Appendix IV) No prior surgery, chemotherapy, or radiation for the current lung tumor EXCLUSION CRITERIA Prior radiotherapy to thorax Iodine allergy Contraindication to receiving radiotherapy, unless undergoing surgery Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Billy W Loo, Jr, MD, PhD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jonathan Abelson, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Pulmonary Interstitial Lymphography in Early Stage Lung Cancer

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