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Randomized study of first-line pemetrexed (Pe) plus platinum (P) followed by second-line docetaxel (D) versus first-line DP followed by second-line Pe in advanced non-small cell lung cancer

Randomized study of first-line pemetrexed (Pe) plus platinum (P) followed by second-line docetaxel (D) versus first-line DP followed by second-line Pe in advanced non-small cell lung cancer

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004696
Enrollment
Unknown
Registered
2014-01-17
Start date
2014-01-01
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

Lung cancer

Interventions

A:first-line pemetrexed (Pe) plus platinum (P) follo
B:first-line DP followed by second-line Pe

Sponsors

The Affiliated Hospital of Guiyang Medical University/Guizhou Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) histologically or cytology confirmed inoperable non-squamous NSCLC; 2)newly diagnosed stage IV disease according to the staging system of the 2009 American Joint Committee on Cancer (AJCC); 3) an age of 18–75 years; 4) a Karnofsky Performance Status score =70%; 5) adequate bone marrow, liver and renal function; neutrophils = 1.5×109/L, platelets 80×109/L, hemoglobin =80g/L, AST and ALT =2× the upper limit of the institutional normal range, total bilirubin =1.25× the upper limit of the institutional normal range, and creatinine concentration =120 µmol/L;

Exclusion criteria

Exclusion criteria: 1) a history involving thoracic surgery, radiotherapy or chemotherapy; 2) pregnancy or lactation; 3) previous malignancy or other concomitant malignant disease; 4)allergy to any chemotherapeutics.

Design outcomes

Primary

MeasureTime frame
Overall surviva;

Secondary

MeasureTime frame
progression-free surviva;

Countries

China

Contacts

Public ContactSu Shengfa
sushengfa2005@163.com+86 851 6513076

Outcome results

None listed

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