Characteristics of Advanced LUNG CANCER at the tIme of Diagnosis in a Large Italian Cohor

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS

About this trial

The distribution of demographic, clinical, radiological, pathological and molecular characteristics of lung cancer at the time of diagnosis, as well as preferential association between elements of those domains, have not been specifically studied in Italy. The aim of the present project is to assess, in a systematic fashion, the demographic, clinical, radiological, pathological and molecular characteristics of advanced lung cancer at the time of diagnosis in a large Italian cohort of consecutive patients referred to two tertiary referral centers.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age >18 years

Suspicion of lung cancer based on imaging (CT and/or PET/CT)

Indication to a biopsy for diagnosis, staging and/or molecular profiling

Disqualifiers

Inability or unwillingness to provide a written informed consent

ECOG performance status (>3) which makes a tissue diagnosis unfeasible

ASA 4 status

TNM Stage I-III

Trial population

Consecutive, treatment-naïve, patients with clinical and radiological suspicion of advanced lung cancer referred for the initial diagnosis/staging/molecular profiling.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Advanced lung cancer patients' group

    Other intervention

    Evaluation of the demographic, clinical, histological and molecular characteristics of advanced lung cancer at the time of Diagnosis

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Distribution of histologic subtypes

The investigators will assess the prevalence of histologic subtypes in patients with advanced lung cancer

Time frame
24 months

Secondary outcomes

1

Distribution of histologic subtypes according to clinical and radiological characteristics

The investigators will assess the prevalence of different histologic subtypes according to clinical and imaging characteristics

Time frame
24 months
2

Molecular profiling

Prevalence of individual molecular markers in patients with advanced non-squamous non-small cell lung cancer histology

Time frame
24 months
3

Time to diagnosis

Time lag between onset of symptoms (if any) and invasive testing

Time frame
24 months

Other outcomes

Sponsors and contacts

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