A Real-world Study of Adebrelimab Combined With Chemotherapy±Chest Radiotherapy in Patients With Extensive Stage Small Cell Lung Cancer

NCT ID: NCT06323265

Last Updated: 2024-03-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-03-26

Study Completion Date

2026-04-01

Brief Summary

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The purpose of this study is to assess efficacy and safety of patients who receive Adebrelimab combined with chemotherapy±chest radiotherapy as first-line treatment of extensive stage small cell lung cancer in the real world.

Detailed Description

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Conditions

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Extensive Stage Small Cell Lung Cancer

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Experimental

Adebrelimab + chemotherapy

Intervention Type DRUG

Adebrelimab: 1200mg, d1, iv (30-60min), Q3W ,up to progressive disease or toxicity intolerable Chemotherapy: etoposide 100mg/m2,d1-3,iv;carboplatin AUC=5-6,d1,iv;or cisplatin 75mg/m2,d1,iv,Q3W,4 cycles;

±chest radiotherapy

Intervention Type RADIATION

Chest radiotherapy: 3Gy/15f-18f or 2Gy/20f-25f

Interventions

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Adebrelimab + chemotherapy

Adebrelimab: 1200mg, d1, iv (30-60min), Q3W ,up to progressive disease or toxicity intolerable Chemotherapy: etoposide 100mg/m2,d1-3,iv;carboplatin AUC=5-6,d1,iv;or cisplatin 75mg/m2,d1,iv,Q3W,4 cycles;

Intervention Type DRUG

±chest radiotherapy

Chest radiotherapy: 3Gy/15f-18f or 2Gy/20f-25f

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

1. Age:≥18 years old;
2. Patients with extensive stage small cell lung cancer confirmed by histopathology;
3. Normal function of major organs;
4. Participants were willing to join in this study, and written informed consent, good adherence, cooperate with the follow-up.

Exclusion Criteria

1. Patients with drug allergy sufferers;
2. Serious and uncontrolled organic lesions or infections, such as decompensated heart, lung, kidney failure, etc;
3. History of psychiatric drugs abuse and can't quit or patients with mental disorders;
4. The researchers think inappropriate.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hebei Medical University Fourth Hospital

OTHER

Sponsor Role lead

Responsible Party

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Jun wang

Study Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Jun Wang

Shijiazhuang, Hebei, China

Site Status RECRUITING

Countries

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China

Facility Contacts

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Jun Wang

Role: primary

13931182128

Other Identifiers

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ARL-SCLC-001

Identifier Type: -

Identifier Source: org_study_id

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