In vitro method for the diagnosis of lung cancer
AssigneesFundacióN Para La InvestigacióN MéDica Aplicada, Advanced Marker Discovery, S.L.
InventorsJackeline Agorreta Arrazubi, Daniel Ajona Martínez-Polo, Luis Montuenga Badía, María Josefa Pajares Villandiego, Rubén Pío Osés
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Abstract
In vitro method for the diagnosis of lung cancer. The present invention is generally related to diagnostic assays. In particular, the present invention refers to the use of at least C4c fragment as diagnostic and prognostic lung cancer marker. C4c fragment can also be useful to estimate lung cancer risk and to decide whether a medical regimen has to be initiated and to determine whether the medical regimen initiated is efficient.
Claims16
In vitro method for the diagnosis or screening of lung cancer in a subject which comprises:
- a. Determining the level of at least C4c fragment in a plasma sample isolated from the subject;
- and
- b. Comparing the C4c fragment level determined in step (a) with a reference control level of said C4c fragment, and
- c. Wherein if the C4c fragment level determined in step (a) is higher than the reference control level, it is indicative that the subject suffers from lung cancer.
In vitro method for deciding whether to administer a medical treatment to a subject suspected of suffering from lung cancer which comprises:
- a. Determining the level of at least C4c fragment in a plasma sample isolated from the subject;
- and
- b. Comparing the C4c fragment level determined in step (a) with a reference control level of said C4c fragment, and
- c. Wherein if the C4c fragment level determined in step (a) is higher than the reference control level, a medical treatment suitable for the treatment of lung cancer is selected to be administered to the patient.
In vitro method for determining the efficacy of a medical regimen in a patient already diagnosed with lung cancer which comprises:
- a. Measuring the level of at least C4c fragment in a plasma sample isolated from the patient prior to the administration of the medical regimen;
- and
- b. Measuring the level of said C4c fragment in a sample from the patient once started the administration of the medical regimen;
- and
- c. Comparing the C4c fragment levels measured in steps (a) and (b), in such a way that if the C4c fragment level measured in step (b) is lower than the C4c fragment level measured in step (a), it is indicative that the medical regimen is effective in the treatment of lung cancer.
In vitro method for determining the efficacy of a medical regimen in a patient already diagnosed with lung cancer comprising:
- a. Measuring the level of at least C4c fragment in a plasma from the patient once started the administration of the medical regimen;
- and
- b. Comparing the C4c fragment level measured in step (i) with a reference control level of the C4c fragment, and
- c. Wherein, if the C4c fragment level measured in step a) is not higher than the reference control level, it is indicative that the medical regimen is effective in the treatment of lung cancer.
In vitro method, according to any of the previous claims, wherein the step a) comprises measuring the level of C4c fragment and prolactin, C4c fragment and CYFRA 21-1, C4c fragment and C-reactive protein (CRP), C4c fragment and prolactin and CYFRA 21-1, C4c fragment and prolactin and CRP, C4c fragment and CYFRA 21-1 and CRP, or C4c fragment and CYFRA 21-1 and CRP and prolactin.
In vitro method, according to any of the previous claims, wherein the lung cancer is selected from the group consisting of non-small cell lung cancer and small-cell lung carcinoma.
In vitro method, according to any of the previous claims, wherein the subject to be diagnosed or screened is an individual at high-risk for lung cancer.
In vitro method, according to any of the previous claims, characterized in that it is an immunoassay.
Use of at least C4c fragment in the in vitro diagnosis of lung cancer.
Dependencies are inferred from the claim text.