Sun Yat-sen University Cancer Center
Guanzhou, Guangdong, 510060, China
NCT Number: NCT04005170
Definitive chemoradiotherapy (CRT) is the standard treatment option for unresectable esophageal cancer (EC). However, as high as more than 40% of EC patients experienced locoregional recurrence after concurrent CRT. Immunotherapy targeting the PD-1/PD-L1 checkpoints has demonstrated promising activity in advanced EC. The aim of this study was to evaluate the efficacy and safety of the combination of toripalimab (an anti-PD-1 antibody) combined with definitive CRT in locally advanced esophageal squamous cell carcinoma (ESCC).
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Notify Me18 year–70 year
All sexes
Interventional
Phase 2
Guanzhou, Guangdong, 510060, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients received toripalimab 240 mg on days 1 and 22 during radiotherapy followed by a maintenance phase of toripalimab IV 240 mg every 3 weeks for up to 1 year.
Other names: JS-001
Patients received 5 cycles of paclitaxel/cisplatin (paclitaxel 50mg/m2 and cisplatin 25 mg/m2) on days 1, 8, 15, 22, 29 during radiotherapy.
Other names: TP
All patients received external-beam radiation using intensity-modulated radiotherapy. The prescribed dose is 50.4 Gy in 28 fractions over 5-6 weeks.
Other names: IMRT
Time frame: 3 months after chemoradiotherapy (plus or minus 14 days)
Tumor response was evaluated 3 months after the completion of chemoradiotherapy based on CT or PET-CT scans, endoscopy with biopsies.
Time frame: From date of randomization until the date of death from any cause or the date of last follow-up, whichever came first, assessed up to 24 months
The 2-year overall survival of the whole group
Time frame: From date of randomization until the date of death from any cause or the date of first documented disease progression whichever came first, assessed up to 24 months
The 2-year progression-free survival of the whole group
Time frame: From date of first CR/PR to the date of first PD according to RECIST criteria, assessed up to 24 months
Tumor response was evaluated every two months after chemoradiotherapy according to RECIST criteria
Time frame: From the start of treatment to 2 year after the completion of treatment
Toxicity of treatment was evaluated according to CTCAE 4.0
Time frame: Baseline biopsies of primary tumor in esophagus
To investigate the impact of programmed cell death-ligand 1 (PD-L1) expression on clinical response
Time frame: Baseline biopsies of primary tumor in esophagus
To investigate the impact of indoleamine 2,3-dioxygenase 1 (IDO1) expression on clinical response
Mian XI
Other
A Phase II Trial of Combination of Toripalimab and Definitive Chemoradiotherapy in Esophageal Squamous Cell Carcinoma
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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