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

Not Applicable

Completed

• Conditions: Small Cell Lung Cancer Limited Stage; Radiotherapy
• Interventions: Radiation: Standard; Radiation: SIB

• Registration Number: NCT03214003
• Lead Sponsor: Anhui Shi, MD

Brief 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.

Detailed Description

Three hundred and twenty-six patients with a histological or cytological proven diagnosis of SCLC will be recruited from 35 centers in 14 areas including provinces, municipalities and autonomous region, from May 2017 to May 2020.

Study Timeline

• Study Start: 2017-06-30
• Study First Submitted: 2017-07-05
• Study First Submitted QC: 2017-07-10
• Study First Posted: 2017-07-11
• Primary Completion: 2021-04-30
• Study Completion: 2023-01-30
• Status Verified: 2023-06
• Last Update Submitted: 2023-06-19
• Last Update Posted: 2023-06-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 235

Inclusion Criteria

• Read the patient information and Sign the informed consent before enrollment
• Either sex, age ≥18 and ≤70
• Histologically or cytologically confirmed SLCL
• Limited stage disease(AJCC, 2009 version 7), stage I-III(T any, N any, M0) that can be safely treated with definitive radiation doses, excludes T3-4 due to multiple lung nodules that are too extensive or have tumor/nodal volume that is too large to be encompassed in a tolerable radiation plan, clinical nonmalignant diagnosis by investigator when the pleural is too few to obtain cytological evidence.
• measurable lesion according RECIST 1.1
• PS ECOG 0-1
• having zero to two cycles of systemic chemotherapy with etoposide and cisplatin (cisplatin 60-80 mg/m2 at day1 or divided into two to three days, etoposide 100-120 mg/m2 at day 1 to 3, Q21d, and the treatment delay between two cycles shouldn't be more than 14days).
• patients especially female patients must satisfy the investigator that they are not pregnant, or are not of childbearing potential, or are using adequate contraception. Man must also use adequate contraception
• adequate haematological function: white blood cell ≥3.0×109/L , neutrophils ≥1.5×109/L, platelet ≥100×109/L, hemoglobin ≥90g/L.
• adequate liver and renal function: total bilirubin ≤1.5 ×upper limit normal , alanine transaminase and aspartate aminotransferase ≤1.5 ×upper limit normal, normal serum creatinine and/or calculated creatinine clearance ≥60ml/min.

Exclusion Criteria

• prior surgical resection of the primary tumor or prior RT for lung cancer
• mixed small-cell and non-small-cell histological features
• contemporaneous immunotherapy or target therapy
• pregnancy or lactation
• physical or mental disease that could impact treatment plan
• unable to understand the trial, or could not follow the process
• to refuse the sign the informed consent.
• no history of previous malignancy in the past 5 years (except non-melanomatous skin or in situ servix carcinoma)
• be allergic to any known protocol in this trail
• be enrolled in other clinical trial in past 30days

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
BID group	Standard	Patients in this group will receive concurrent twice-daily standard radiotherapy (95%PTV 45Gy in 30 twice-daily fractions over 3 weeks, 5 days per week, without SIB) and chemotherapy (etoposide and cisplatin).
SIB group	SIB	Patients in this group will receive concurrent twice-daily radiotherapy by SIB technique (95%PGTV 54Gy, 95%PTV 45Gy,both in 30 twice-daily fractions over 3 weeks, 5 days per week) and chemotherapy (etoposide and cisplatin).

Primary Outcome Measures

Name	Time	Method
Overall survival	5 years	from the starting date of treatment until the date of death from any cause

Secondary Outcome Measures

Name	Time	Method
Local Progression Free Survival	5 years	from the starting date of treatment until the date of local disease progression
health related quality of life	from baseline, immediately after radiotherapy and an average of 3 months up to 24 months. Then through study completion, an average of 6 months.From date of randomization until the date of death from any cause, assessed up to 120 months.	assessed from completed questionnaires. Assessments using Physicians Global Assessment to measure quality of life.
Metastasis Free Survival	5 years	from the staring date of treatment until the date of distant metastasis
acute and late toxicity	from baseline, immediately after radiotherapy and an average of 1 week up to 12 weeks, an average of 3 months up to 24 months. Up to 120 weeks.	acute toxicity (defined as toxicity occurring between the start of treatment and up to 3 months after completion of treatment, and assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events \[version 5.0\]), late toxicity (more than 3 months after completion of treatment, and assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events \[version 5.0\])

Trial Locations

Locations (1)

Beijing Cancer Hospital; 🇨🇳 Beijing, China