Clinical trial · Interventional
Extensive Stage Sclc Patients Who Were Benefit From First-line Treatment Accept Temozolomide Maintain Therapeutic
Lobaplatin Combined With Etoposide for First-line Treatment in Extensive Stage Sclc Then Benefit Patients Follow up Temozolomide Maintain Therapeutic
NCT02972320CI-TRIAL-00024893unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study evaluates temozolomide maintain therapeutic efficacy and safety in extensive stage SCLC who has clinical benefit from etoposide combined Los platinum (EL) scheme in the first line treatment.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Extensive Stage Small Cell Lung Cancer | Lung Small Cell Carcinoma | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| temozolomide | Drug | Temozolomide | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- temozolomide maintain therapeutic
- description
- Lobaplatin combined with etoposide for first-line treatment of extensive stage small cell lung cancer,then clinical benefit patients for temozolomide maintain therapeutic.This study have only one arm which temozolomide maintain at dose of 150mg/m2 D1-5 Q4W.
- interventionNames
- Drug: temozolomide
Primary outcomes (1)
- measure
- Progression-Free Survival in the first line of chemotherapy
- timeFrame
- 6 months
- description
- The first day of treatment to the date that disease progression is reported
Secondary outcomes (3)
- measure
- Overall Survival (OS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. aged 18 to 70 years old, men and women are not limited; 2. confirmed by histopathological examination SCLC; 3. clinical stage for patients with extensive stage (except for the case of pleural effusion) 4. patients has no drug treatment history 5. the implementation of palliative radiotherapy for metastatic lesions, surgical treatment, after the end of treatment over 14 days. 6. there can be measured lesions (non radiation exposure site) of patients (RECIST) evaluation; 7. physical condition score ECOG PS:0-1 8. more than expected survival time over 3 months Exclusion Criteria: 1. the previous platinum compounds have a history of allergies; 2. active ulcer patients; 3. Patients with primary lung lesions were treated with radiotherapy; 4. chest X-ray showed clear interstitial pneumonia or patients with pulmonary fibrosis; 5. the need for treatment of brain metastases in the active phase 6. there are more serious tumor invasion, superior vena cava syndrome, or in the middle volume of malignant pleural effusion, abdominal effusion or pericardial effusion, not yet control; 7. there is a serious infection, ADH abnormal secretion syndrome, poor control of diabetes,the need for the treatment of patients with severe complications such as vena cava syndrome
References
Publications (0)
Data not yet available
No reference posted for this study.