Image-guided surgery for tumor agnostic detection of solid tumors using the pH-activated micellar imaging agent ONM-100.

Authors

null

Floris Jan Voskuil

UMCG, Groningen, Netherlands

Floris Jan Voskuil , Pieter Jan Steinkamp , Marjory Koller , Bert van der Vegt , Jan Johannes Doff , Tian Zhao , Jeffrey P. Hartung , Yalia Jayalakshmi , Baran D. Sumer , Jinming Gao , Max J.H. Witjes , Gooitzen Michell Van Dam

Organizations

UMCG, Groningen, Netherlands, University Medical Center Groningen, Groningen, Netherlands, OncoNano Medicine Inc., Southlake, TX, JPH Clinical Development Inc., San Diego, CA, The University of Texas Southwestern Medical Center, Dallas, TX, University of Texas Southwestern Medical Center, Dallas, TX

Research Funding

Pharmaceutical/Biotech Company

Background: ONM-100, a micelle-based polymer imaging agent conjugated to indocyanine green (ICG) and with an exquisitely pH-sensitive binary activation mechanism, may be used for tumor detection. ONM-100 micelles dissociate in acidic environments resulting in activation of the fluorescent ICG tag. As nearly all solid cancer types are acidotic, ONM-100 has the potential to act as a broadly indicated tumor agnostic imaging agent. This first-in-human study investigates the safety and feasibility of ONM-100 as a tumor agnostic imaging agent for intra-operative fluorescent imaging of various solid tumors. Methods: ONM-100 was IV administered 24±8h prior to surgery in a dose escalation scheme (0.1-1.2mg/kg). Patients with histopathologically confirmed breast cancer (BC), head and neck squamous cell carcinoma (HNSCC), colorectal cancer (CRC) and esophageal cancer (EC) were included. Blood was drawn to assess safety and pharmacokinetic data. Intra-operative fluorescence images were collected before and after tumor excision. Post-excision fluorescence images were obtained from serially sliced specimens and correlated with standard histopathological assessment. Results: 30 patients (11 BC, 13 HNSCC, 3 EC, 3 CRC) were enrolled. No ONM-100 related serious adverse events were observed and the agent was well-tolerated. A strong and sharply demarcated fluorescent signal was observed in all patients with vital tumor tissue (median CNR ranging 1.85-14.05) which correlated with tumor on final histopathology. HNSCC and superficially located BC as well as peritoneal metastasis could be clearly visualized in vivo during surgery. In four patients (BC and HNSCC), perioperatively, tumors otherwise unnoticed by the surgeons were detected on the margin or wound bed using fluorescence imaging. Additionally, two BC tumor lesions were detected that were missed by conventional pre-operative imaging and pathological assessment. Conclusions: ONM-100 appears to be safe and enables fluorescent visualization of tumors both in vivo and ex vivo. The first-in-human data demonstrate the feasibility for potential use of ONM-100 for image guided surgery, margin assessment and detection of occult disease. Clinical trial information: NTR 7085.

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Developmental Therapeutics and Tumor Biology (Nonimmuno)

Track

Developmental Therapeutics—Molecularly Targeted Agents and Tumor Biology

Sub Track

Molecular Diagnostics and Imaging

Clinical Trial Registration Number

NTR 7085

Citation

J Clin Oncol 37, 2019 (suppl; abstr 3068)

DOI

10.1200/JCO.2019.37.15_suppl.3068

Abstract #

3068

Poster Bd #

60

Abstract Disclosures