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A prospective study of survival and prognosis of non small cell lung cancer patients to treatment Oligometastases

A prospective study of survival and prognosis of non small cell lung cancer patients to treatment Oligometastases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15007544
Enrollment
Unknown
Registered
2015-12-08
Start date
2015-12-31
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:treatment Oligometastases and radiotherapy

Sponsors

Henan anti-cancer hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
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 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*1089/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*ULN; 11. renal function: serum creatinine <1.5*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 was serious allergic or idiosyncratic. History, serious pulmonary heart disease; 12. refused or not signed the informed consent to participate in trials; 13. abuse drugs or alcohol addicts; 14. personality or psychiatric disorders, no civil capacity or with limited civil capacity.

Design outcomes

Primary

MeasureTime frame
tumor size;

Countries

China

Contacts

Public ContactJianjun Qin
qinjianjun73@aliyun.com+86 13838008630

Outcome results

None listed

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