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Prospective multicenter randomized clinical study phase IV oligo transfer timing of radiotherapy for non small cell lung cancer

Prospective multicenter randomized clinical study phase IV oligo transfer timing of radiotherapy for non small cell lung cancer

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004170
Enrollment
Unknown
Registered
2014-01-02
Start date
2014-01-20
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

NSCLC in stage IV with oligo metastases

Interventions

A:adjuvant chemotherapy and radiotherapy
B:neoadjuvant chemotherapy + adjuvant chemotherapy and radiotherapy

Sponsors

Cancer Hospital of Sichuan province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. voluntary and signed written informed consent; 2. aged 18 to 75 years, sex not limited; 3. pathology or cytology in the diagnosis of NSCLC (squamous cell carcinoma, adenocarcinoma and large cell carcinoma); 4. primary tumors can measure; 5. distant organ metastases number = 5, and metastasis can be measured; 6. Karnofsky score >70; 7. survival is expected to exceed 3 months; 8. reproductive age women should ensure that before entering the study period contraception; 9. HB =100 g/L, WBC =4 × 10^9/L, platelet = 100 × 10^9/L; 10. liver function: the upper limit of normal value of ALT, AST< (ULN) 1.5 times, total bilirubin <1.5 x ULN; 11. renal function: serum creatinine <1.5 x ULN; 12. patients have good compliance to treatment and follow-up of acceptance.

Exclusion criteria

Exclusion criteria: 1. Do not meet the inclusion criteria for patients with pathologic type and primary site. 2. to pemetrexed, cisplatin, docetaxel and contrast medium allergy. 3. distant organ metastases number > 5. 4. the primary tumor, lymph node and metastases has underwent surgical operation (biopsy except). 5. the primary tumor, lymph node and metastases had radiotherapy. 6. had molecular targeted therapy. 7. had received chemotherapy or immunotherapy. 8. suffered from other malignant tumors. 9. in January received other drug test subjects. 10. pregnant or lactating women and treatment observation period rejected contraception in female. 11. There is serious allergic or idiosyncratic. 12. History, serious pulmonary heart disease. 13. refused or not signed the informed consent to participate in trials. 14. abuse drugs or alcohol addicts. 15. personality or psychiatric disorders, no civil capacity or with limited civil capacity.

Design outcomes

Primary

MeasureTime frame
tumor size;

Countries

China

Contacts

Public ContactLi Tao

Cancer Hospital of Sichuan province

litaoxmf@126.com+86 18908178818

Outcome results

None listed

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