Circulating EV Long RNA Profiles in SCLC

Small Cell Lung Cancer Clinical Trial

Official title:

Circulating Extracellular Vesicle Long RNA Profiles in the Diagnosis and Prediction of Treatment Response for Small Cell Lung Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05191849
• Other study ID #: EXRNA-SCLC-2021
• Status: Recruiting
• Phase: N/A
• Start date: October 25, 2021
• Est. completion date: October 25, 2024

Study information

• Verified date: December 2021
• Source: Fudan University
• Contact: Jialei Wang, Doctor
• Phone: 18017312369
• Email: luwangjialei[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To identify the circulating extracellular vesicle long RNA (exLR) profiles in small cell lung cancer (SCLC) and explore the potential of exLR as biomarkers to predict the therapeutic effect of SCLC.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: October 25, 2024
• Est. primary completion date: April 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Patients volunteered to participate in the study and have signed the informed consent.

2. Histological or cytological diagnosis of small cell lung cancer, and no indication of radical surgery or radiotherapy.

3. 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.

4. 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.

5. 18~75 years old; ECOG PS score: 0~1 points; expected survival time is more than 3 months.

6. 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:

1. Histological or cytological diagnosis of small cell and non-small cell mixed lung cancer.

2. Patients who have previously received systemic chemotherapy, signal transduction inhibitors, targeted therapies, hormone and endocrine therapy.

3. 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.

4. Unresolved toxicity due to any previous treatment above CTC AE (4.0) level 2 or higher, excluding hair loss.

5. Patients with symptomatic CNS metastases.

6. Patients with uncontrolled pleural, pericardial, or peritoneal effusion requiring repeated drainage.

7. Patients with any severe and/or uncontrolled disease, including:

1. Patients with unsatisfactory blood pressure control (systolic blood pressure >150 mmHg, diastolic blood pressure >90 mmHg).

2. 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).

3. Patients with active or uncontrolled severe infection (= CTC AE Level 2).

4. Patients with a history of immunodeficiency, including HIV-positive or other acquired, congenital immunodeficiency disease, or a history of organ transplantation.

5. Patients with poor control of diabetes (fasting blood glucose (FBG)>10mmol/L).

6. Patients with urine protein = ++ indicated by routine urine test, and confirmed 24-hour urine protein quantitation > 1.0 g.

7. Patients with seizures requiring treatment.

8. Patients undergone venous thrombosis events currently or within 6 months, such as cerebrovascular accidents (including transient ischemic attacks), deep vein thrombosis, and pulmonary embolism.

9. Patients with a history of psychotropic drug abuse from which they are unable to abstain or with mental disorders.

10. Patients who have participated in other clinical trials of anti-tumor drugs within four weeks.

11. Patients with severe disease that threaten the safety of themselves or affect the completion of the study according to the investigators' judgment.

Related Conditions & MeSH terms

• Lung Neoplasms
• Small Cell Lung Cancer
• Small Cell Lung Carcinoma

Intervention

Diagnostic Test:
• Blood sample collection
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.

Locations

Country	Name	City	State
China	Cancer hospital Fudan University	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Fudan University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Establish a model to predict curative effect	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)