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Real-world study of patients with recurrent or metastatic esophageal cancer in city/county-level hospitals in high-incidence areas of esophageal cancer

Real-world study of patients with recurrent or metastatic esophageal cancer in city/county-level hospitals in high-incidence areas of esophageal cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089404
Enrollment
Unknown
Registered
2024-09-09
Start date
2024-09-30
Completion date
Unknown
Last updated
2024-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Cancer

Interventions

Sponsors

Gaozhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Retrospective Part: 1. Patients who visited the study department between January 1, 2022, and August 29, 2024; 2. Patients with recurrent or distant metastatic esophageal cancer confirmed by pathology or clinically (AJCC 8th Edition); 3. Inoperable locally advanced patients who cannot or are unwilling to accept definitive treatment (including definitive chemoradiotherapy or definitive radiotherapy, etc.) may also be considered for enrollment; 4. Patients who have progressed or recurred after neoadjuvant or adjuvant therapy may also be considered for enrollment; 5. Age = 18 years old; 6. Complete medical records. Prospective Part: 1. Patients with recurrent or distant metastatic squamous cell carcinoma of the esophagus confirmed by pathology or clinically (AJCC 8th Edition); 2. Age = 18 years old; 3. First-line patients who have not received systemic treatment or are in the process of first-line systemic treatment containing tislelizumab, with no less than four courses of first-line treatment, and continue to receive tislelizumab in the second-line after progression; 4. Second-line patients must have received at least four courses of PD-1/PD-L1 other than tislelizumab during first-line treatment, and patients with PD within 6 months of first-line treatment are excluded; 5. Intend to receive tislelizumab treatment; 6. Good compliance and willingness to accept long-term follow-up.

Exclusion criteria

Exclusion criteria: 1. Participating simultaneously in another clinical study that is blinded; 2. Having other active malignant tumors or multiple primary cancers; 3. Pregnant or lactating women, or men and women planning to conceive during the study period; 4. Other situations deemed unsuitable for inclusion in the study by the investigator.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
OS;=3 TRAE;irAE;

Countries

China

Contacts

Public ContactWen Zunbei

Gaozhou People's Hospital

13828607806@139.com+86 138 2860 7806

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026