Actively Recruiting
Hypofractionated Radiotherapy Combined with Immunotherapy for Limited-stage Small-cell Lung Cancer
Led by Anhui Provincial Hospital · Updated on 2024-09-19
45
Participants Needed
1
Research Sites
160 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Concurrent chemoradiotherapy has long been the standard modality for locally advanced small-cell lung cancer, which could achieve median overall survival of 25 mos. Conventional fractionation of 66Gy/33f and hyperfractionation of 45Gy/30f twice daily have been acknowledged as the two standard radiotherapy modalities according to CONVERT study. With the introduction of immune checkpoint inhibitors, ADRIATIC study concluded that consolidative Durvalumab after concurrent chemoradiotherapy could achieve a far longer median overall survival of 55.9 months compared with 33.4 months for concurrent chemoradiotherapy. Recently, several studies have demonstrated the safety and efficacy of hypofractionated radiotherapy (3 to 4 Gy) for limited-stage small-cell lung cancer. Hypofractionated radiotherapy processes the advantage of short treatment duration compared with conventional fractionated radiotherapy, which may allow the early participation of immunotherapy. Therefore, we suppose that whether hypofractionated radiotherapy combined with immunotherapy could improve the survival of limited-stage of small-cell lung cancer.
CONDITIONS
Official Title
Hypofractionated Radiotherapy Combined with Immunotherapy for Limited-stage Small-cell Lung Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between 18 and 70 years old
- Performance status (ECOG) of 0 or 1
- Adequate organ function to tolerate chemotherapy, immunotherapy, and radiotherapy
- Diagnosed with small-cell lung cancer
- Limited stage confirmed by cranial MRI, chest CT, abdominal ultrasound, bone scan, or PET-CT
- Signed informed consent
You will not qualify if you...
- Younger than 18 or older than 70 years old
- Performance status (ECOG) greater than 1
- Inadequate organ function to tolerate chemotherapy, immunotherapy, and radiotherapy
- Diagnosed with non-small cell lung cancer or other neuroendocrine carcinomas including typical or atypical carcinoid, large-cell neuroendocrine carcinoma
- Extensive stage confirmed by cranial MRI, chest CT, abdominal ultrasound, bone scan, or PET-CT
- No signed informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Anhui Provicial Hospital
Hefei, Anhui, China, 230011
Actively Recruiting
Research Team
D
Dong Qian, M.D.
CONTACT
X
Xiao-Yang Li
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
0
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