- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT05191849
Circulating EV Long RNA Profiles in SCLC
Circulating Extracellular Vesicle Long RNA Profiles in the Diagnosis and Prediction of Treatment Response for Small Cell Lung Cancer
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Verwacht)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Jialei Wang, Doctor
- Telefoonnummer: 18017312369
- E-mail: luwangjialei@126.com
Studie Locaties
-
-
Shanghai
-
Shanghai, Shanghai, China, 200032
- Werving
- Cancer hospital Fudan University
-
Contact:
- Jia lei Wang, Master
- Telefoonnummer: 8907 02164175590
- E-mail: luwangjialei@hotmail.com
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Patients volunteered to participate in the study and have signed the informed consent.
- Histological or cytological diagnosis of small cell lung cancer, and no indication of radical surgery or radiotherapy.
- There are measurable lesions defined by RECIST standard v1.1. A lesion can be considered measurable only if the previously irradiated lesion has clear progression after radiotherapy and the previous irradiated lesion is not the sole lesion.
- Initially treated patients who have not received any systematic therapy before. If have received postoperative adjuvant chemotherapy, the time to relapse is at least 6 months from the last adjuvant chemotherapy.
- 18~75 years old; ECOG PS score: 0~1 points; expected survival time is more than 3 months.
- The main organs's function meets the following criteria within 14 days before treatment:
(1)Routine blood test (without blood transfusion within 14 days): a) Hemoglobin (HB) ≥ 90 g / L; b) Absolute neutrophil (ANC) ≥ 1.5 × 109 / L; c) Platelets (PLT) ≥ 80×109/L (2)Biochemical examination: a) Total bilirubin (TBIL) ≤ 1.5 times of the upper limit of the normal (ULN); b) Alanine aminotransferase (ALT) and aspartate aminotransferase AST ≤ 2.5ULN.To patients with liver metastasis, ALT and AST ≤ 5ULN; c) Serum creatinine (Cr) ≤ 1.5ULN or creatinine clearance (CCr) ≥ 60ml / min; (3)Doppler ultrasound assessment: left ventricular ejection fraction (LVEF) ≥ the lower limit of the normal (50%).
7. Patients with previously treated asymptomatic CNS metastases are allowed to participate in this study if all of the following criteria are met: a) No need for continuous corticosteroid therapy for CNS disease; b) No radiotherapy within 14 days prior to enrollment treatment; c) Imaging examination from the end of radiotherapy to screening period shows no CNS progression.
8. Women of childbearing age should agree to conduct contraception (such as intrauterine devices, contraceptives or condoms) during the study and within 6 months after the end of the study; and the serum or urine pregnancy test is negative within 7 days prior to study enrollment and they must be non-lactating patients; Men should agree to conduct contraception during the study and within 6 months after the end of the study.
Exclusion Criteria:
- Histological or cytological diagnosis of small cell and non-small cell mixed lung cancer.
- Patients who have previously received systemic chemotherapy, signal transduction inhibitors, targeted therapies, hormone and endocrine therapy.
- Patients with other malignant tumors occurred within 5 years prior to the enrollment, except those with cured cervical carcinoma in situ and superficial bladder tumors [Ta (non-invasive tumor), Tis (carcinoma in situ) and T1 (tumor infiltrating basement membrane)] , basal or squamous cell skin cancer, and localized prostate cancer and ductal breast carcinoma in situ treated with radical surgery.
- Unresolved toxicity due to any previous treatment above CTC AE (4.0) level 2 or higher, excluding hair loss.
- Patients with symptomatic CNS metastases.
- Patients with uncontrolled pleural, pericardial, or peritoneal effusion requiring repeated drainage.
Patients with any severe and/or uncontrolled disease, including:
- Patients with unsatisfactory blood pressure control (systolic blood pressure >150 mmHg, diastolic blood pressure >90 mmHg).
- Patients with myocardial ischemia or myocardial infarction of Grade I of higher level, arrhythmia (including QTC ≥ 440ms) and congestive heart failure above Grade 2 (New York Heart Association (NYHA) classification).
- Patients with active or uncontrolled severe infection (≥ CTC AE Level 2).
- Patients with a history of immunodeficiency, including HIV-positive or other acquired, congenital immunodeficiency disease, or a history of organ transplantation.
- Patients with poor control of diabetes (fasting blood glucose (FBG)>10mmol/L).
- Patients with urine protein ≥ ++ indicated by routine urine test, and confirmed 24-hour urine protein quantitation > 1.0 g.
- Patients with seizures requiring treatment.
- Patients undergone venous thrombosis events currently or within 6 months, such as cerebrovascular accidents (including transient ischemic attacks), deep vein thrombosis, and pulmonary embolism.
- Patients with a history of psychotropic drug abuse from which they are unable to abstain or with mental disorders.
- Patients who have participated in other clinical trials of anti-tumor drugs within four weeks.
- Patients with severe disease that threaten the safety of themselves or affect the completion of the study according to the investigators' judgment.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Diagnostisch
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
---|---|
Ander: Small Cell Lung Cancer receiving chemotherapy
|
Baseline blood samples are collected before chemotherapy.
Dynamic blood samples are also prospectively collected after 2~4 cycles of chemotherapy, or at the time of disease progression.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Establish a model to predict curative effect
Tijdsspanne: At the end of Cycle 4 (each cycle is 21 days)
|
To detect the difference of exLR profiles of SCLC patients before and after treatment, and the difference of baseline exLR profiles between responders and non-responders.
|
At the end of Cycle 4 (each cycle is 21 days)
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- EXRNA-SCLC-2021
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
Klinische onderzoeken op Blood sample collection
-
Hillel Yaffe Medical CenterOnbekend
-
Teal Health, Inc.Actief, niet wervendHumaan papillomavirus | Infectie met humaan papillomavirus type 16 | Infectie met humaan papillomavirus type 18Verenigde Staten
-
Acorai ABWerving
-
Cliniques universitaires Saint-Luc- Université...Université de LiègeWervingTaaislijmziekte | BiomarkersBelgië
-
Rutgers, The State University of New JerseyNational Cancer Institute (NCI)WervingPeritoneale carcinomatose | Neoplasmata van het spijsverteringsstelsel | Lever en intrahepatisch galwegcarcinoom | Bijlage Carcinoom door AJCC V8 Stage | Colorectaal carcinoom door AJCC V8 Stage | Slokdarmcarcinoom door AJCC V8 Stage | Maagcarcinoom door AJCC V8 StageVerenigde Staten
-
Memorial Sloan Kettering Cancer CenterVoltooidProstaatkankerVerenigde Staten
-
Marmara UniversityVoltooid
-
University of MinnesotaNational Institute on Drug Abuse (NIDA)VoltooidStoornis in het gebruik van middelenVerenigde Staten