500 Participants Needed

Indocyanine Green Imaging for Solid Tumors

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Overseen ByAzra Din
Age: 18+
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: University of Pennsylvania
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 4 JurisdictionsThis treatment is already approved in other countries

Trial Summary

What is the purpose of this trial?

This is a Phase 1/2 study in patients presenting with any solid tumor and/or diseased tissue even benign nodules presumed to be resectable and at risk for recurrence on pre-operative assessment who are considered to be good surgical candidates to evaluate the safety and efficacy of the image-guided surgery using indocyanine green for intramolecular imaging of solid tumors.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What data supports the effectiveness of the treatment Indocyanine Green (ICG) Imaging for Solid Tumors?

Indocyanine Green (ICG) is a dye that helps doctors see cancer tissues more clearly during surgery by making them glow under special light. Studies show it helps identify tumors and important structures in surgeries for various cancers, like liver and breast cancer, making surgeries more precise.12345

How is the drug Indocyanine Green (ICG) unique for treating solid tumors?

Indocyanine Green (ICG) is unique because it is a dye that, when exposed to near-infrared light, makes tumors glow, helping doctors see and remove them more precisely during surgery. This approach is different from traditional treatments as it uses fluorescence imaging to guide surgical procedures.25678

Eligibility Criteria

This trial is for adults over 18 with any solid tumor or diseased tissue, including benign nodules, that can be surgically removed and may recur. Candidates must be good surgical candidates as determined by their physician or a team of experts and able to give informed consent.

Inclusion Criteria

I have a tumor or diseased tissue that can be surgically removed and might come back.
My doctor agrees I am a good candidate for surgery.
Subject capable of giving informed consent.

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants undergo surgical resection with indocyanine green for intraoperative molecular imaging

1 week
1 visit (in-person)

Follow-up

Participants are monitored for safety and efficacy of indocyanine green post-surgery

Up to 5 days
1 visit (in-person)

Long-term follow-up

Participants are monitored for any long-term effects or recurrence

4 weeks

Treatment Details

Interventions

  • Indocyanine Green
Trial Overview The study tests the safety and effectiveness of using indocyanine green for image-guided surgery in patients with solid tumors. It's designed to see if this method helps surgeons better visualize and remove tumors during operations.
Participant Groups
2Treatment groups
Experimental Treatment
Group I: Cohort 2Experimental Treatment1 Intervention
Patients scheduled to undergo surgical resection for the following cancers (known or suspected) that the safety and dosing/timing of indocyanine green has been fully studied will be enrolled: non-small cell lung cancer, metastatic sarcoma to the lung, brain meningioma.
Group II: Cohort 1Experimental Treatment1 Intervention
Patients scheduled to undergo surgical resection for the following cancers (known or suspected) that the safety and dosing/timing of indocyanine green has not been fully studied will be enrolled: glioma, breast cancer, colon cancer, rectal cancer, head and neck cancer, pulmonary metastasectomy (colorectal mets), thymoma, ovarian cancer, prostate cancer, renal cell carcinoma, thyroid cancer, parathyroid adenoma, mesothelioma, esophageal cancer, pancreas cancer, stomach cancer.

Indocyanine Green is already approved in United States, European Union, China, Japan for the following indications:

🇺🇸
Approved in United States as Indocyanine Green for:
  • Diagnostic imaging agent for various medical procedures including sentinel lymph node mapping
🇪🇺
Approved in European Union as Indocyanine Green for:
  • Diagnostic imaging agent for various medical procedures including sentinel lymph node mapping
🇨🇳
Approved in China as Indocyanine Green for:
  • Diagnostic imaging agent for various medical procedures including sentinel lymph node mapping, liver function testing
🇯🇵
Approved in Japan as Indocyanine Green for:
  • Diagnostic imaging agent for various medical procedures including sentinel lymph node mapping, liver function testing

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Pennsylvania

Lead Sponsor

Trials
2,118
Recruited
45,270,000+

Findings from Research

Indocyanine Green (ICG) is a fluorescent dye that helps surgeons visualize important anatomical structures and blood flow during various surgical procedures, enhancing the identification of tumors and lymphatic mapping.
While the initial evidence for ICG's effectiveness in surgery is promising, more standardized protocols and larger randomized studies are needed to confirm its benefits across general surgical practices.
Indocyanine green (ICG) fluorescence guide for the use and indications in general surgery: recommendations based on the descriptive review of the literature and the analysis of experience.Morales-Conde, S., Licardie, E., Alarcón, I., et al.[2022]
Indocyanine green (ICG) is a fluorescent dye used in various surgical applications, including identifying sentinel lymph nodes and assessing skin perfusion during breast surgeries, highlighting its role in improving surgical outcomes.
ICG's ability to emit fluorescence when illuminated by near-infrared light allows for precise mapping of lymphatic networks and guidance in excising nonpalpable breast cancer, demonstrating its efficacy in oncological and reconstructive procedures.
[Use of indocyanine green angiography in oncological and reconstructive breast surgery].Struk, S., Honart, JF., Qassemyar, Q., et al.[2018]
In a systematic review of 17 studies involving 2274 patients, indocyanine green (ICG) imaging significantly increased the number of retrieved lymph nodes during radical gastrectomy for gastric cancer, suggesting improved surgical efficacy.
The use of ICG also reduced intraoperative blood loss without extending operative time or increasing overall complications, and it was associated with a lower recurrence rate of cancer, although it did not improve the 2-year overall survival rate.
Efficacy of indocyanine green fluorescence imaging-guided lymphadenectomy in radical gastrectomy for gastric cancer: A systematic review and meta-analysis.Dong, B., Zhang, A., Zhang, Y., et al.[2022]

References

Indocyanine green (ICG) fluorescence guide for the use and indications in general surgery: recommendations based on the descriptive review of the literature and the analysis of experience. [2022]
[Use of indocyanine green angiography in oncological and reconstructive breast surgery]. [2018]
Efficacy of indocyanine green fluorescence imaging-guided lymphadenectomy in radical gastrectomy for gastric cancer: A systematic review and meta-analysis. [2022]
Fluorescence-Guided Surgery in the Combined Treatment of Peritoneal Carcinomatosis from Colorectal Cancer: Preliminary Results and Considerations. [2019]
Indocyanine green fluorescence imaging for resection of pulmonary metastasis of hepatocellular carcinoma. [2022]
[Photochemotherapy of cutaneous AIDS-associated Kaposi sarcoma with indocyanine green and laser light]. [2019]
Identification of liver lesions using fluorescence imaging: comparison of methods for administering indocyanine green. [2022]
Indocyanine green and its nanosynthetic particles for the diagnosis and treatment of hepatocellular carcinoma. [2020]
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