An Efficacy and Safety Study to Assess [18F]-ML-10 in Detecting Response of Tumors to Chemotherapy and Radiation

NCT ID: NCT01260480

Last Updated: 2010-12-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-12-31

Brief Summary

The purpose of this study is to determine whether [18F]-ML-10 used in conjunction with PET imaging is effective as an imaging tool for the early detection of response of oncological tumors in the lungs,head and neck to chemoradiation therapy.

The study will evaluate the potential of [18F]-ML-10 used in conjunction with PET imaging to distinguish early during the course of chemoradiation therapy between a tumor that responds to the therapy, and a tumor that does not respond to the therapy. Currently, this distinction is available to the physician several weeks or months after completion of therapy, using anatomical imaging (for example Computed Tomography [CT] or Magnetic Resonance Imaging [MRI]).

Conditions

Carcinoma, Non-Small-Cell Lung; Head and Neck Neoplasms

Keywords

Carcinoma, non-small-cell lung; Head and neck neoplasms; Diagnostic imaging

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

[18F]-ML-10

Group Type: EXPERIMENTAL

[18F]-ML-10 in conjunction with PET imaging

Intervention Type: OTHER

Subjects will receive two to three intravenous (IV) doses of \[18F\]-ML-10. The dose for each \[18F\]-ML-10 dose will be 5.50 MBq/Kg or 0.15 mCi/Kg but will not exceed 500.00 MBq (13.50 mCi) per administration.

Interventions

[18F]-ML-10 in conjunction with PET imaging

Subjects will receive two to three intravenous (IV) doses of \[18F\]-ML-10. The dose for each \[18F\]-ML-10 dose will be 5.50 MBq/Kg or 0.15 mCi/Kg but will not exceed 500.00 MBq (13.50 mCi) per administration.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

Male or female patients with either:

Newly diagnosed non small cell lung cancer (NSCLC) (Group A) who meet the following criteria:

• Previously untreated, histologically or cytologically confirmed stage IIB, IIIA or IIIB disease, without evidence of distant metastases
• A measurable primary tumor with at least one diameter > 2 cm or primary tumor extending to one or more lymph nodes which cannot be distinctively delineated as confirmed by a diagnostic quality chest CT performed within 4 weeks prior to initiation of the concurrent CRT.
• Planned to receive concurrent chemoradiotherapy as definitive treatment. The radiation dose should not exceed 70 Gy.
• Undergone the following minimum workup to confirm disease staging within 4 weeks prior to initiation of the concurrent CRT:

• GBCA-enhanced Brain MRI or contrast enhanced CT if there are signs or symptoms suggesting brain metastases within the past 2 months.
• If necessary to confirm stage of disease, an upper abdomen CT scan will be performed.
• whole-body FDG PET/CT; OR
• Newly diagnosed squamous cell carcinoma of the head and neck (SCCHN) (Group B) who meet the following criteria:

• Previously untreated, histologically or cytologically confirmed (from the primary tumor and/or lymph nodes) stage III-IV disease without evidence of distant metastases.
• A measurable (i) primary tumor with at least one diameter ≥2 cm and (ii) lymph node with at least one diameter ≥ 2 cm as confirmed by a diagnostic quality neck CT performed within 4 weeks prior to initiation of the concurrent CRT.
• Planned to receive concurrent chemoradiotherapy as definitive treatment. The radiation dose should not exceed 70 Gy.
• Have undergone the following minimum workup to confirm disease staging within 4 weeks prior to initiation of the concurrent CRT:
• Whole-body FDG PET/CT.
• Patients ≥ 18 years of age.
• Able to comply with lying still during the PET/CT imaging session which may last for up to 3 hrs with intermediate breaks.
• ECOG performance status of 0, 1 or 2.
• Adequate renal function and adequate hepatic function, as assessed by standard laboratory criteria and defined as:
• Serum creatinine ≤ 1.2 times the Upper Limit of Normal (ULN).
• Total bilirubin ≤ 1.5 times the ULN.
• Asparagine aminotransferase (AST) and/or alanineaminotransferase (ALT) ≤ 2.5 times the ULN (grade 1 according to the NCI-CTCAE v.3).
• Women of child-bearing potential must have a negative blood pregnancy test at screening and use an adequate and medically acceptable contraceptive method.
• Willing and able to comply with the protocol requirements.
• Able to provide written informed consent.

Exclusion Criteria

• Predominant small cell carcinoma histology.
• Pure bronchioalveolar cell carcinoma histology.
• Treatment planned with chemotherapy other than a platinum-based doublet regimen.
• Malignant pleural or pericardial effusions.
• Any contraindication to perform CT with IV contrast agent.

• Histology other than squamous cell carcinoma.
• Treatment planned with chemotherapy other than a platinum-based regimen.
• Treatment planned with cetuximab.
• Treatment with induction chemotherapy.
• Any contraindication to CT with IV contrast agent.
• Evidence of distant metastases.
• Patients who, based on the investigator's judgment, have other unstable medical conditions that may preclude safe and complete study participation.
• Treatment with any investigational drug, device or biologic agent within 30 days prior to administration of [18F]-ML-10.
• Pregnancy or lactation.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Aposense Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Aposense

Principal Investigators

Heron Dwight, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh Medical Center

David Sher, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

BWH, Harvard

Aaron Allen, MD

Role: STUDY_DIRECTOR

Rabin Medical Center

Locations

BWH

Boston, Massachusetts, United States

Site Status: RECRUITING

Holy Name Medical Center

Teaneck, New Jersey, United States

Site Status: RECRUITING

Mount Sinai

New York, New York, United States

Site Status: RECRUITING

University of Pittsburgh

Pittsburgh, Pennsylvania, United States

Site Status: RECRUITING

Countries

United States

Facility Contacts

David Sher, MD

Role: primary

Benjamin Rosenbluth, MD

Role: primary

Lale Kostakoglu, MD, MPH

Role: primary

Heron Dwight, MD

Role: primary

Other Identifiers

NST-CA007

Identifier Type: -

Identifier Source: org_study_id