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Completed

NCT Number: NCT01881620

PET Enhanced CT Scan Performance in Cancer

Hypothesis:

The investigators would like to demonstrate that diagnosis performance of PET/CT scan without and with contrast agent (COMBI TEP), are equivalent or better than those of PET/ non enhanced CT scan (PET scan) associated with an enhanced CT scan. This research project is a pilot study given the few available data concerning this imaging exam reproducibility.

This study is a prospective single center study.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Hypothesis:

We would like to demonstrate that diagnosis performance of PET/CT scan without and with contrast agent (COMBI TEP), are equivalent or better than those of PET/ non enhanced CT scan (PET scan) associated with an enhanced CT scan. This research project is a pilot study given the few available data concerning this imaging exam reproducibility. This study allows us to assess the feasibility of such a large-scale study, but also to evaluate COMBI TEP performance. From these estimates, we can then consider a comparative study to evaluate the performance of COMBI PET.

This study is a prospective single center study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Any patient with a cancerous disease for which PET scan is indicated in the SOR (Standards - Options - Recommendations) FDG PET 2003 updated in 2006 must be included in the trial, in the following locations:

  • Digestive cancers
  • Colorectal cancer
  • Preoperative evaluation in local and metastatic recurrence
  • Location of recurrences, in case of ACE increase in a previously operated patient.
  • Esophageal cancer: initial staging.
  • Pancreatic cancer
  • Initial staging,
  • Differential diagnosis with chronic pancreatitis.
  • Liver cancer: differential diagnosis of liver metastases, cholangiocarcinoma and benign tumors in the case of an isolated hepatic localization.
  • Digestive Endocrine tumors: staging in case of normal pentetreotide scintigraphy.
  • Lung cancer
  • Initial staging,
  • Diagnosis of lung isolated lesion > 1 cm.
  • Head and neck cancer
  • Initial pretreatment staging,
  • Recurrence diagnosis
  • Lymphoma
  • Initial staging of Hodgkin's disease (HD), non-Hodgkin's lymphoma (NHL) and aggressive follicular lymphomas,
  • Diagnosis of minimal residual disease of HD and aggressive NHL,
  • Early assessment of treatment response.
  • Thyroid cancer: suspicion of residual disease or relapse when conventional imaging data are insufficient.
  • Ovarian cancer recurrence
  • Age ≥ 18 years.
  • Chest-abdomen-pelvis enhanced CT scan achieved within 4 weeks before enrollment (with cuts of less than 5 mm).
  • Woman of childbearing age with negative pregnancy test and / or contraception.
  • Patient with informed consent signed.
  • Patient affiliated to social security schemes.

Exclusion criteria

  • Iodine known allergy.
  • Diabetes, excepted if controlled (hemoglucotest ≤ 1.6 g).
  • Known renal failure (creatinine clearance <60ml/min).
  • Indications against Xenetix ®:
  • Hypersensitivity to Xenetix ® or any of the excipients,
  • History of an immediate response or delayed cutaneous reaction to Xenetix ® injection.
  • Thyrotoxicosis.
  • Pregnant or lactating women.
  • Unable to undergo medical follow up for geographical, social or psychological reasons,
  • Private of freedom patient and adult under a legal guardianship or unable to consent.

Treatment and study plan

COMBI TEP : PET / enhanced CT scan

Device

diagnostic imaging exam

Other names: diagnostic imaging exam

Primary outcomes

  1. Inter-observer (B1 and B2) Reproducibility of the PET-CT by Anatomical Regions

    Time frame: 1 year

    The primary endpoint was the inter-observer reproducibility of the interpretation of the combined PET / enhanced CT scan (PET-CT) by anatomical region. Reproducibility was assessed for each of the 5 anatomical regions (thorax, abdomen, pelvis, bone, nervous system). Two independant pairs (B1 and B2), each composed of one nuclear physician and one radiologist interpreted the PET-CT examination and described each of the 5 anatomical régions according to 3 modalities (Presence of suspicious lesion(s); Presence of dubious lesion(s); Absence of suspicious and dubious lesion). The inter-observer reproducibility (inter-pairs of observers) was evaluated for each anatomical region by comparing the interpretations of the two pairs, using the weighted kappa concordance coefficient [ref = Fleiss J, Levin B, Cho Paik M. Statistical methods for rates and proportions. Third ed. 2003.].Interpretation by B1 after PET-CT examination (1 month after). Interpretation by B2 at the end of the study

Secondary outcomes

  1. Inter-observer (B1 and B2) Reproducibility of the PET-CT at a Patient Level

    Time frame: 1 year

    The inter-observer reproducibility of combined PET-CT interpretations has been assessed globally for each patient. Same pairs of observer (B1 and B2) than for the primary endpoint evaluation interpreted the PET-CT examination in a global way and concluded for each patient. A weighted Kappa coefficient has been calculated from an identical methodology to that described for the primary endpoint evaluation. Interpretation by B1 was performed at least 1 month and 1 week after PET-CT examination. Interpretation by B2 was performed at the end of the study

  2. Inter-observer (N1 and B2) Reproducibility of the PET-CT by Anatomical Regions

    Time frame: 1 year

    For each of the 5 anatomical régions (thorax, abdomen, pelvis, bone, nervous system), we evaluated the reproducibility between the interpretations of the PET-CT by the nuclear physician alone (N1) and the independent pair (B2) composed by one nuclear physician and one radiologist . The nuclear physician alone (N1) and the independent pair (B2) interpreted the PET-CT examination independently and described each anatomical region.The inter-observer reproducibility has been evaluated for each anatomical region by comparing the interpretations of the nuclear physician alone and that one of independent pair of nuclear physician and radiologist, using the weighted kappa concordance coefficient [ref = Fleiss J, Levin B, Cho Paik M. Statistical methods for rates and proportions. Third ed. 2003.].Interpretation by nuclear physician alone (N1) was performed within 1 week of PET-CT examination. Interpretation by B2 was performed at the end of the study

  3. Inter-observer (N1 and B2) Reproducibility of the PET-CT at a Patient Level

    Time frame: 1 year

    The inter-observer reproducibility of combined PET-CT interpretations has been assessed globally for each patient. The nuclear physician alone (N1) and the independent pair (B2) interpreted the PET-CT examination independently in a global way and concluded for each patient. The inter-observer reproducibility has been evaluated at patient level by comparing the interpretations of the nuclear physician alone and that one of independent pair of nuclear physician and radiologist, using the weighted kappa concordance coefficient [ref = Fleiss J, Levin B, Cho Paik M. Statistical methods for rates and proportions. Third ed. 2003.]. Interpretation by nuclear physician alone (N1) was performed within 1 week of PET-CT examination. Interpretation by B2 was performed at the end of the study

  4. Intra-observer Reproducibility of Injected CT Scan by Anatomical Regions

    Time frame: 1 year

    For each anatomical region, the reproducibility of the injected CT scan was evaluated. The same radiologist evaluated the two injected CT scans (CT1 and CT2) and interpreted them (Presence of suspicious lesion(s) OR presence of dubious lesion(s) OR absence of suspicious and dubious lesion). Intra-observer reproducibility was analyzed by using the individual analysis by each radiologist. A weighted Kappa concordance coefficient was calculated per anatomical region using a methodology identical to that described for the evaluation of the proncipal endpoint. Interpretation of CT1 was performed befor inclusion. Interpretation of CT2 was performed at the end of the study.

  5. Intra-observer Reproducibility of Injected CT Scanat a Patient Level

    Time frame: 1 year

    The reproducibility of the injected CT scan was evaluated globally for each patient. The same radiologist evaluated the two injected CT scans (CT1 and CT2) and interpreted them (Presence of suspicious lesion(s) OR presence of dubious lesion(s) OR absence of suspicious and dubious lesion). Intra-observer reproducibility was analyzed by using the individual analysis by each radiologist. A weighted Kappa concordance coefficient was calculated using a methodology identical to that described for the evaluation of the proncipal endpoint. Interpretation of CT1 was performed befor inclusion. Interpretation of CT2 was performed at the end of the study.

Sponsors and collaborators

Lead sponsor

Institut Bergonié

Other

Registry information

Official study title

PET / Enhanced CT Scan Performance in Cancer (Positron Emission Tomography Combined With Computed Tomography or Vascular Contrast CT Scan). COMBI TEP Study

Acronym: COMBITEP

Important dates

Study start
2010
Primary completion
2012
Study completion
2015
First posted
Jun 19, 2013
Registry last updated
Nov 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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