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Clinical study of irinotecan and platinum sequential chemotherapy with EP in the treatment of extensive stage small cell lung cancer

Clinical study of irinotecan and platinum sequential chemotherapy with EP in the treatment of extensive stage small cell lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-16009325
Enrollment
Unknown
Registered
2016-10-08
Start date
2017-01-01
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

small cell lung cancer

Interventions

EP Group:Etoposide (VP-16), 100/m2, intravenous drip, D1 ~ D3
cisplatin (DDP), 25 mg/m2, intravenous drip, D1 ~ D3 days. 21 d for 1 cycles, 4 cycles.

Sponsors

Huangshi Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. In line with the Chinese Association for cancer, lung cancer, Specialized Committee issued the diagnostic criteria "China lung cancer clinical guidelines (2010 Edition)". By the histopathological or cytology, diagnosis is clear for the patients with a wide range of SCLC. And the chest abdominal enhanced CT, the whole body bone scan, MRI scan, are confirmed as the wide range of SCLC,according to the staging method developed by the United States veterans of lung cancer research group (VALG); 2. Man and woman aged 18-72 years old; 3. The general situation is good, the KPS score is more than 70 points, and the survival time is 3 months or more; 4. ECOG score of 0 to 1 points; 5. Cases can be first diagnosed patients, also be the patients of recurrence and metastasis after surgery or radiotherapy after not by the treatment; If received adjuvant chemotherapy, from the end of adjuvant chemotherapy at least interval of more than half a year; at least a measurement of tumor lesions. Spiral CT. The maximum diameter must be larger than or equal to 10mm, ordinary or physical examination. The maximum diameter must be equal to or greater than 10mm; 6. Patients with asymptomatic brain metastases, or patients with brain metastases after treatment for more than a week; 7. Blood, heart, lung and liver showed no obvious abnormal. 8. To support the understanding of this experiment, and willing to sign the consent form of chemotherapy and informed consent, voluntary testing, good compliance.

Exclusion criteria

Exclusion criteria: (1) Patients who did not meet the inclusion criteria; (2) Patients with severe heart disease, brain blood vessels, liver and kidney, and blood coagulation system; (3) Women during pregnancy or lactation; (4) Participating in other drug trials.

Design outcomes

Primary

MeasureTime frame
short-term therapeutic effectiveness;KPS score;progression-free survival (PFS);Overall survival (OS);toxicity;

Countries

China

Contacts

Public ContactJiang Lan

Huangshi Central Hospital

304188944@qq.com+86 15335888931

Outcome results

None listed

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