Skip to content

Neoadjuvant chemoradiotherapy combined with surgery in the treatment of potentially operable thoracic squamous cell carcinoma of the esophagus

Neoadjuvant chemoradiotherapy combined with surgery in the treatment of potentially operable thoracic squamous cell carcinoma of the esophagus

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-17011648
Enrollment
Unknown
Registered
2017-06-13
Start date
2016-11-01
Completion date
Unknown
Last updated
2017-06-19

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

Conditions

esophageal cancer

Interventions

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Malignant neoplasm of thoracic esophagus proved by pathology to be squamous cell carcinoma 2. Clinical staging before treatment is locally advanced (T3-4N0-1M0) or locally early with regional lymph node metastasis (T1-2N1M0); 3. expect survival longer than 6 months; 4. Aged 18~65 years old, KPS score >80 (KPS standard, see Appendix 1); 5. Laboratory test indicators must meet the following requirements: Blood: white blood cells than 4.0x10^9/L, neutrophils or 1.5x10^9/L, platelet count, hemoglobin 90g/L or more than 100x10^9/L; Liver and kidney function: serum bilirubin is lower than the maximum normal value of 1.5 times; ALT and AST are lower than the maximum normal value of 1.5 times; BUN and Cr are within the normal range; 6. Patients who have not received formal anti-tumor therapy; 7. Be able to understand the situation of this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. the clinical stage before treatment T4, breaking through the esophageal adventitia invasion and surrounding tissue, esophageal perforation high-risk factors have been anti-tumor treatment (including chemotherapy, radiotherapy, surgery); 2. known or suspected of chemotherapy drugs such as paclitaxel, platinum, platinum and other allergies; 3. having or merging with hemorrhagic disease; 4. other non controllable non operable patients; 5. pregnant and lactating patients; 6. psychological, family, social and other factors lead to the absence of informed consent; 7. because of previous surgery, this operation can not be used for gastric reconstruction of the digestive tract; 8. patients with peripheral neuropathy, CTC grade level is more than 2; 9. patients with a history of other malignancies except those with esophageal cancer, except for non melanoma skin cancer and in situ cervical cancer; 10. the researchers considered unsuitable to participate in this study; 11. there are serious heart, lung, liver and kidney dysfunction, hematopoietic diseases, immune system diseases, cachexia and other intolerance surgery patients.

Design outcomes

Primary

MeasureTime frame
PFS;OS;side effects;

Countries

China

Contacts

Public ContactLiu Fang

General Hospital of PLA medical

liufangfsg@163.com+86 13520469875

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 21, 2026