Status:

RECRUITING

Tislelizumab Combined With Chemotherapy and Thoracic Radiotherapy in ES-SCLC

Lead Sponsor:

Second Hospital of Shanxi Medical University

Conditions:

Extensive-stage Small-cell Lung Cancer

Eligibility:

All Genders

18-80 years

Phase:

PHASE2

Brief Summary

This study is a single arm, open, multicenter phase II study. The main purpose of this study was to evaluate preliminary efficacy and safety of Tislelizumab combined with thoracic radiotherapy as firs...

Eligibility Criteria

Inclusion

  • Patients aged between 18 to 80 years old (inclusive of 18th and 80th birthdays), male or female, at the time of signing the informed consent form;
  • Confirmed small cell lung cancer of extensive stage by histology or cytology;
  • At least one measurable lesion by imaging studies (according to RECIST 1.1) with a long diameter of ≥10 mm as examined by spiral CT or MRI;
  • Within 3 days prior to treatment, an ECOG score of 0 to 1;
  • No prior antitumor treatment for extensive stage disease (if the patient has previously received chemotherapy and/or radiotherapy in the limited stage of SCLC, the treatment intent must have been curative, and there must be at least a 6-month treatment-free interval between the end of chemotherapy, radiotherapy, or chemoradiotherapy and the diagnosis of extensive stage SCLC);
  • Expected life span of ≥3 months;
  • Good function of vital organs;
  • The subject voluntarily joins this study, signs the informed consent form, has good compliance, and cooperates with follow-up.

Exclusion

  • Concurrent severe respiratory diseases: such as pulmonary fibrosis;
  • Presence of psychiatric disorders, hematologic diseases, autoimmune diseases, and severe primary diseases of the heart, brain, liver, or kidneys;
  • Uncontrolled active infections;
  • Known or suspected allergies to the study medication and its excipients;
  • Female patients who are pregnant or breastfeeding, or women of childbearing potential with a positive baseline pregnancy test;
  • Prior use of antitumor treatment targeting the PD-(L)1 pathway.

Key Trial Info

Start Date :

August 1 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2026

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06536868

Start Date

August 1 2024

End Date

December 31 2026

Last Update

August 5 2024

Active Locations (6)

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Page 1 of 2 (6 locations)

1

Jincheng General Hospital

Jincheng, Shanxi, China, 048000

2

Jinzhong third people's hospital

Jinzhong, Shanxi, China, 032000

3

Second Hospital of Shanxi Medical University

Taiyuan, Shanxi, China, 030000

4

Shanxi Bethune Hospital

Taiyuan, Shanxi, China, 030000