Phase 2
Completed N=179
Cabazitaxel Compared to Topotecan for the Treatment of Small Cell Lung Cancer
Source: ClinicalTrials.gov NCT01500720 ↗Enrolled (actual)
179
Serious AEs
43.5%
Results posted
Apr 2015
Primary outcomePrimary: Progression Free Survival (PFS) — 1.4; 3.0 months — p=<0.0001
Summary
Primary Objective:
To demonstrate progression free survival (PFS) improvement for cabazitaxel compared to topotecan in participants with sensitive or resistant/refractory small cell lung cancer following a first line platinum based chemotherapy.
Secondary Objectives:
* To assess disease progression free rate at 12 weeks
* To assess Response Rate (Response Evaluation Criteria in Solid Tumor [RECIST] 1.1) and duration of response
* To assess Overall Survival (OS)
* To assess the Safety (National Cancer Institute - Common Toxicity Criteria [NCI-CTC] version 4.03)
* To assess the Health-Related Quality of Life (HRQoL)
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Progression Free Survival (PFS) |
1.4; 3.0 | <0.0001 sig |
| SECONDARY Overall Survival |
5.2; 6.8 | — |
| SECONDARY Progression Free Rate at Week 12 |
18.9; 52.8 | — |
| SECONDARY Overall Objective Tumor Response Rate |
0; 10.1 | — |
Eligibility Criteria
Inclusion criteria
- Histological/cytological proven locally advanced or metastatic small cell lung cancer with progressive disease during or after first line platinum based chemotherapy
- Male or female greater than or equal to (>=) 18 years (or country's legal age of majority if greater than [>]18 years)
- Participants with measurable disease, Response Evaluation Criteria in Solid Tumors (RECIST) (version 1.1)
- Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to ( 1 (National Cancer Institute Common Terminology Criteria [NCI CTCAE] v4.03) at the time of randomization
- Uncontrolled Central Nervous System (CNS) metastases: participants with CNS metastases may have previous irradiation, only participants with stable disease or response to irradiation who are without CNS symptoms and on a maximum steroid dose of dexamethasone 8 mg daily or equivalent could be included
- Participants with known leptomeningeal metastases
- History of other, invasive neoplasm requiring ongoing therapy
- Participation in another clinical trial and any concurrent treatment with any investigational drug within 30 days prior to randomization
- Any of the following within 6 months prior to study enrollment: myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft, New York Heart Association class III or IV congestive heart failure, stroke or transient ischemic attack
- Any severe acute or chronic medical condition, which could impair the ability of the participant to participate in the study or interfere with interpretation of study results
- Known Human Immunodeficiency Virus (HIV) disease, or active hepatitis B or C (systematic testing was not required)
- Pregnant or breast-feeding woman. Positive serum or urine pregnancy test prior to randomization
- Participant with reproductive potential (M/F) who did not agree to use an accepted and effective method of contraception during the study treatment period and for at least 6 months after the completion of the study treatment. The definition of "effective method of contraception" was based on the investigator's judgment. Effective method of contraception should also be adapted to local regulation
- History of hypersensitivity to polysorbate 80
- Inadequate organ and bone marrow function as evidenced by:
- Hemoglobin less than [ 2.5 x Upper Limit of Normal (ULN)
- Alkaline Phosphatase (AP) >2.5 x ULN. In case of liver metastases AP >5 x ULN
- Total bilirubin >1.0 x ULN
- Serum Creatinine >1.5 x ULN. If creatinine 1.0 - 1.5 x ULN, creatinine clearance will be calculated according to Chronic Kidney Disease Epidemiology Collaboration formula, and creatinine clearance <60 milliliter per minute (mL/min) was exclude the participant.
The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
Data sourced from ClinicalTrials.gov (NCT01500720). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.