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C11-Erlotinib PET/CT as a Tool for Identification and Characterization of Tumor With High Expression of Epidermal Growth Factor Receptor(EGFR).

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01717807
Acronym
EGFR; PET/CT
Enrollment
30
Registered
2012-10-30
Start date
2013-04-30
Completion date
Unknown
Last updated
2012-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer, Pancreatic Cancer

Keywords

epithelial growth factor receptors, lung cancer, advanced tumor of pancrease, erlotinib, C11-Erlotinib PET/CT

Brief summary

The EGFR is one of the most frequently overexpressed proteins in various cancers including lung cancer, and is related to tumor progression and resistance to most treatments. New treatment strategies targeting EGFR have been developed: although much work remains to be done, erlotinib has already established itself as part of the therapeutic armamentarium against cancer(A review of erlotinib and its clinical use. Tang PA, Tsao MS, Moore MJ. Expert Opin Pharmacotherapy. 2006 Feb;7(2):177-93.) Noninvasive PET/CT imaging of EGFR expression activity and mutation status in NSCLC could aid in the selection of patients for individualized therapy with EGFR kinase inhibitors. Whole-body noninvasive PET/CT imaging could estimate treatment-responsive vs. -resistant tumor burden before the initiation of therapy with EGFR inhibitors. The purposes of the study are: 1. To adjust an optimal treatment for patients with tumors that have high expression of EGFR by identification of this type of cancer using C11-Erlotinib PET/CT during pretreatment work-up; as well as to follow up after treatment response. 2. To recognize patients with advanced pancreatic cancer responding to treatment with erlotinib and to distinguish them from non-responders.

Interventions

OTHERC11-Erlotinib PET/CT

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients with NSC type of lung cancer with high expression of EGFR who are candidates for erlotinib as second / third line of treatment; * patients with advanced pancreatic tumor who are candidates for complex gemcitabine and erlotinib treatment.

Exclusion criteria

* lack of histological diagnosis; * not a candidate for erlotinib; * pregnancy.

Design outcomes

Primary

MeasureTime frame
Measure of extent and intensity ( by standardized uptake value - SUV) of C11-Erlotinib accumulation by tumors and metastasis before and after treatment

Secondary

MeasureTime frame
size of tumor and metastasis (mm)

Countries

Israel

Contacts

Primary ContactMarina Orevi, MD
marinaor@hadassah.org.il
Backup ContactEyal Mishani, Phd
eyalmi@ekmd.huji.ac.il

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026