Clinical trial · Interventional
Combination Anticancer Therapy of Paclitaxel and Everolimus for Relapsed or Refractory Small Cell Lung Cancer
A Phase I Study of Combination Anticancer Therapy of Paclitaxel and Everolimus for Relapsed or Refractory Small Cell Lung Cancer
NCT01079481CI-TRIAL-00010466completedPhase 1ClinicalTrials.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)
The objective of this phase I study is to determine the maximum tolerated dose (MTD) of combination therapy of paclitaxel and everolimus in small cell lung cancer patient with previous treatment history.
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 |
|---|---|---|---|
| Small Cell Lung Cancer | Lung Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| taxol plus everolimus | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- taxol plus everolimus
- interventionNames
- Drug: taxol plus everolimus
Primary outcomes (1)
- measure
- To determine the maximum tolerated dose (MTD) of everolimus when combined with fixed dose of paclitaxel in small cell lung cancer patients
- timeFrame
- 18 months
Secondary outcomes (2)
- measure
- To evaluate the safety when paclitaxel plus everolimus are given to patients with small cell lung cancer
- timeFrame
- 18 months
- measure
- To evaluate the objective response rate by RECIST 1.1 criteria
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients with histologically or cytologically confirmed small cell lung cancer 2. Regarding a limited disease, the disease in a patient, who had concurrent chemoradiation therapy before, is relapsed or progressing, the patient should have received the first line platinum-based anticancer therapy. The disease should be progressing/relapsed during or after the previous treatment. 3. Regarding an extensive disease, the progression/relapse of the disease during or after the first line platinum-based anticancer therapy should be confirmed. 4. Patient with asymptomatic or treated brain metastasis. 5. Patients without current concomitant chemotherapy 6. Patients without current concomitant radiotherapy 7. Patients who are not receiving chronic treatment with steroids or another immunosuppressive agent. 8. Patients with at least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST). 9. Patients aged 18 years or older 10. ECOG performance status 0-2 11. Adequate organ function as evidenced by the following; Absolute neutrophil count \> 1.5 x 109/L; platelets \> 100 x 109/L; hemoglobin \> 9g/dL; -; total bilirubin ≤1.5 UNL; AST and/or ALT \< 5 UNL; creatinine clearance ≥ 50mL/min. 12. Patients who signed and dated the informed consent form prior to specific study procedures. 13. Patients who can comply with the scheduled follow-up and toxicity management procedure.' Exclusion Criteria: 1. Patients with history of treatment with mTOR inhibitors 2. Pregnant with gastrointestinal problem impairing absorption of drugs 3. Patients who could not use appropriate method of contraception 4. Pregnant or feeding patients 5. Other medically ill patients 6. Severe heart/pulmonary disease 7. DM patients 8. Other malignancy except cured skin cancer or uterine cervix carcinoma in situ 9. High cholesterolemia greater than grade 3 10. Patients with symptomatic brain metastasis 11. Chronic hepatitis or liver cirrhosis (patients with HBsAg positive, IgM anti-HBc positive or HCV Ab positive) 12. Patients receiving immunosuppressant
References
Publications (0)
Data not yet available
No reference posted for this study.