Twice-daily SIB Radiotherapy Versus Standard Radiotherapy for Patients With SCLC

NCT03214003 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 235

Last updated 2023-06-22

No results posted yet for this study

Summary

This trial is a multicenter, perspective, non-blinded, randomized controlled phase 3 trial. In order to establish whether the SIB technique can improve the results of twice-daily chemo-RT for patients with LS-SCLC, the investigators will primarily compare survival of patients treated with standard chemotherapy (cisplatin and etoposide) and either SIB twice-daily RT or standard dose twice-daily RT.

Conditions

  • Small Cell Lung Cancer Limited Stage
  • Radiotherapy

Interventions

RADIATION

SIB

patients will recieve twice-daily radiotherapy by simultaneous integrated boosting technique concurrent with chemotherapy

RADIATION

Standard

patients will recieve standard twice-daily radiotherapy concurrent with chemotherapy

Sponsors & Collaborators

  • Sun Yat-sen University

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Xijing Hospital

    collaborator OTHER
  • Henan Cancer Hospital

    collaborator OTHER_GOV
  • Jilin Provincial Tumor Hospital

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences

    collaborator OTHER
  • Air Force General Hospital of the PLA

    collaborator OTHER_GOV
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Peking University Third Hospital

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Beijing Hospital

    collaborator OTHER_GOV
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Peking University First Hospital

    collaborator OTHER
  • Anhui Shi, MD

    lead OTHER

Principal Investigators

  • Anhui Shi, Doctor · Peking University Cancer Hospital & Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-30
Primary Completion
2021-04-30
Completion
2023-01-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03214003 on ClinicalTrials.gov