Prophylactic Cranial Irradiation in Extensive-stage Small Cell Lung Cancer

Sponsor
Chinese Academy of Medical Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT04947774
Collaborator
(none)
100
1
23
4.4

Study Details

Study Description

Brief Summary

The prognosis of extensive-stage small cell lung cancer is still very poor, even for those who received chemotherapy and immunotherapy. This experimental study is a real-world research design to evaluate the effectiveness and safety of prophylactic cranial irradiation in patients with extensive-stage small cell lung cancer who with first-line chemotherapy combined with immunotherapy.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Prophylactic Cranial Irradiation

Detailed Description

This study is a prospective trial. This study included ES-SCLC patients who response after standard first-line treatment, and aimed to explore the safety and effectiveness of prophylactic cranial irradiation in this treatment modality.

The primary endpoint is progression-free survival in the brain.The secondary endpoints includes OS, PFS. The indicators for evaluating safety are the incidence and severity of adverse events.The exploratory endpoint is the molecular biomarkers for efficacy and toxicity predicting from tumor tissue and peripheral blood TMB.

The trial was designed by the National Cancer Center/Cancer Hospital of the Chinese Academy of Medical Sciences and Peking Union Medical College. The hypothesis is that preventive brain irradiation is safe and effective in the treatment of extensive SCLC combined with chemotherapy and immunotherapy.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Real-world Study of Prophylactic Cranial Irradiation After Immunotherapy Combined With Chemotherapy for Extensive-stage Small Cell Lung Cancer
Actual Study Start Date :
Nov 1, 2020
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
prophylactic cranial irradiation group

The extensive-stage SCLC patients will receive prophylactic cranial irradiation after standard first-line chemotherapy combined with immunotherapy, until disease progression or death.

Radiation: Prophylactic Cranial Irradiation
The extensive-stage SCLC patients will receive prophylactic cranial irradiation ±immunotherapy after standard first-line chemotherapy combined with immunotherapy, until disease progression or death
Other Names:
  • Immunotherapy
  • Observation group

    Patients with extensive-stage SCLC do not receive preventive craniocerebral irradiation after standard first-line chemotherapy combined with immunotherapy until the disease progresses or death.

    Outcome Measures

    Primary Outcome Measures

    1. Progression-free survival in the brain [1 year]

      The length of time during and after treatment for a disease in which the patient lives with the disease but the intracranial lesions do not worsen

    Secondary Outcome Measures

    1. Progression-free survival (PFS) [1 year]

      The length of time during and after the treatment of a disease that a patient lives with the disease but it does not get worse

    2. Overall survival (OS) [1 year]

      The time from treatment to death from any cause

    3. Adverse events [1 year]

      The incidence and severity of adverse events related to treatments

    4. The cognitive function of the patient [1 year]

      Use the Montreal Cognitive Screening Scale (MoCA) to score, the total score is 30 points, ≥26 points are normal

    Other Outcome Measures

    1. Exploratory end point including biomarkers [1 year]

      To explore the correlation of PD-L1 expression in tumor tissue , TCR, ctDNA in peripheral blood and efficacy

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Sign written informed consent;

    • With extensive small cell lung cancer;

    • Previously received first-line standard chemotherapy, with treatment response of CR or PR;

    • Can tolerate the radiotherapy process;

    • Be over 18 years old

    • Life expectancy ≥ 12 weeks;

    • With the Eastern Cancer Cooperative Group (ECOG) score 0-1

    • After the systemic treatment was received, there was no brain metastasis on MR before brain preventive irradiation.

    Exclusion Criteria:
    • Exclude subjects with central nervous system (CNS) metastasis at the first diagnosis;

    • Pregnancy or breastfeeding;

    • Any other conclusive medical, psychiatric and/or social reasons determined by the researcher;

    • Subjects who have previously suffered from other malignant tumors (excluding non-melanoma skin cancer and the following carcinoma in situ: bladder, stomach, colon, endometrial, cervical/dysplasia, melanoma or breast cancer) are not allowed to participate in the study. Unless he/she has been in complete remission at least 2 years before enrolling in the study, and does not need to receive other treatments or does not need to receive other treatments during the study;

    • Researchers believe that the treatment methods used in the study can cause harm or cause basic diseases whose toxicity is difficult to judge when judging adverse events.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cancer Insititute and Hosiptal of Chinese Academy of Medical Sciences Beijing Beijing China 100021

    Sponsors and Collaborators

    • Chinese Academy of Medical Sciences

    Investigators

    • Study Director: Bi Nan, MD, Cancer Hospital, CAMS and PUMC

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Luhua Wang, Professor, Chinese Academy of Medical Sciences
    ClinicalTrials.gov Identifier:
    NCT04947774
    Other Study ID Numbers:
    • NCC2622
    First Posted:
    Jul 1, 2021
    Last Update Posted:
    Sep 22, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Luhua Wang, Professor, Chinese Academy of Medical Sciences
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 22, 2021