Hypofraction Radiotherapy for Locally Advanced Non-small Cell Lung Cancer

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-70
SponsorAnhui Provincial Hospital

About this trial

Definitive concurrent chemoradiotherapy followed by durvalumab (Pacific protocol) has been the standard modality for stage III locally advanced non-small cell lung cancer. In spite of the median overall survival of 47.5 months, there still existed 38.5% and 6.9% patients who finally developed intra-thorax and extra-thorax recurrence respectively in long-term follow-up. The relatively low local control rate has been the bottleneck for further improvement of overall survival. Hypofraction radiotherapy has been validated to be able to increase the local control rate in two prospective trials. Therefore, this trial is designed to explore the safety and primary efficacy of hypofraction radiotherapy followed by immune checkpoint inhibitors for stage III locally advanced non-small cell lung cancer.

Eligibility criteria

Qualifiers

18-70 years old;

Eastern Cooperative Oncology Group (ECOG) 0-1;

Non-small cell lung cancer including squamous cell carcinoma, adenocarcinoma, adenosquamous carcinoma, large-cell carcinoma;

Wild-type of driven genes;

Disqualifiers

Younger than 18 years old or older than 70 years old;

ECOG>1;

Small-cell lung cancer and other neuroendocrine carcinoma including typical or atypical carcinoid, large-cell neuroendocrine carcinoma;

Mutant type of driven genes;

Trial design

Treatments tested in this trial

  • High-dose fractionated radiotherapy
  • Low-dose fractionated radiotherapy

Treatment groups

36 Participants
are divided into 2 treatment groups

Sponsors and collaborators