LS301 Uptake in Tumors of Patients Undergoing Liver, Pancreas, or Gastric Surgery

Washington University School of Medicine

Overview

The preclinical data have demonstrated the feasibility of fluorescence-guided tumor resection by the Cancer Vision Googles (CVG) with LS301 in animal models. In this study, the investigators will conduct intraoperative imaging procedures that have minimal interference with ongoing surgery. The underlying hypothesis is that the accurate detection of all cancer cells highlighted by LS301 during surgery will reduce the number of patients with margin positivity to less than 5%, compared to the current surgical paradigm of greater than 15% in pancreatic cancer, for example. The pilot study will obtain critical data required to address the larger question of surgical margin assessment in a full Phase I clinical trial.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

DIAGNOSTIC

Masking

SINGLE

Conditions

Pancreatic Cancer Liver Cancer Gastric Cancer Gastrointestinal Stromal Cancer Metastatic Cancer

Interventions

LS301DRUG

-LS301 is produced at the Optical Radiology Laboratory at Washington University School of Medicine

Cancer Vision GogglesDEVICE

-Non-significant risk device

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Newly diagnosed patients with gastrointestinal cancers, including pancreas, liver, gastric cancer, gastrointestinal stromal tumors, and metastatic cancers undergoing surgical resection as standard of care treatment. * At least 18 years of age. * For the first cohort of patients enrolled, must have an ECG with no prolonged intervals. * Able to understand and willing to sign a written informed consent document. Exclusion Criteria: * Contraindications for surgery. * Receiving any investigational agents. * History of allergic reactions attributed to ICG or other agents used in the study, include known iodide or seafood allergy. We do not expect many of these adverse reactions with LS301 because it is not radioactive and does not possess iodinated counterions. * Presence of underlying lung disease. * Pregnant. Female patients of childbearing potential must have a negative serum or urine pregnancy test no more than 7 days before start of participation. * Breastfeeding. Patients who are breastfeeding are excluded from this study because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with LS301.

Outcomes

Primary Outcomes

Phase I only: Safety of LS301 as measured by incidence of related adverse events per patient

* Safety evaluation includes vital signs, clinical laboratory testing and ECG, measured pre- (within 10-15 minutes or 30 minutes of injection) and post-injection (within 30 minutes or/and at \~60 minutes). * Adverse events will be graded using NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0

Time frame: From time of injection to 1 hour post-injection

Phase I only: Optimal imaging dose of LS301

* The optimal will be the dose at which fewer than 2 dose-limiting toxicities (DLTs) are observed and optimal image quality is observed. It need not be the maximum tolerated dose (MTD) if optimal image quality is observed at a lower dose than the MTD * DLT is defined as any grade 2 or above toxicity that occurs during the hour after injection that is considered possibly, probably, or definitely related to LS301.

Time frame: From time of injection to 1 hour post-injection

Phase II only: Ability of LS301 to predict presence of positive margins

* Margin status called by LS301 and CVG will be compared to the gold standard histopathological results * The histopathological results of margin positivity has the following possible results: margin negative, margin positive at LS301 and CVG identified locations, margin positive at LS301 and CVG unidentified locations. Using LS301 and CVG, the exercised tissue will be considered to be margin positive and have ink marked at the identified locations if any positive margins are observed; otherwise, the margin is considered negative.

Time frame: At the time of pathological analysis (within 2-3 days of surgery)

Data from ClinicalTrials.gov

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