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- Klinische proef NCT02058433
Safety Study of Individual Paclitaxel Dose Adjustment Based on Pharmacokinetics in Non-Small Cell Lung Cancer (NSCLC)
Phase 3, Randomized, Open-label Study of the Safety of Individual Paclitaxel Dose Adjustment Based on Pharmacokinetic Follow up Versus Conventional Dosage in First-line Treatment in Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Primary end point: Common Terminology Criteria for Adverse Events(CTCAE) grade 4.
Secondary end point:Objective Response Rate(ORR),Progression Free Survival(PFS),Overall Survival(OS),Quality Of Life(QOL) etc.
Studietype
Inschrijving (Verwacht)
Fase
- Fase 3
Contacten en locaties
Studie Locaties
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Shanghai
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Shanghai, Shanghai, China, 200433
- Werving
- Medical Department, Shanghai Pulmonary Hospital
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Onderonderzoeker:
- Jie Zhang, MD
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Onderonderzoeker:
- Huiwei Qi, MD
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Onderonderzoeker:
- Fengying Wu, MD
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
For inclusion in the study treatment period patients must fulfil all of the following criteria:
- Provision of informed consent.
- Male or female aged 18 years and over.
- Histologically or cytologically confirmed non-small cell lung carcinoma.
- Locally advanced Stage not amenable to local therapy (e.g. pleural effusion) or metastatic disease.
- No prior chemotherapy, biological (including targeted therapies such as Epidermal Growth Factor Receptor(EGFR) and Vascular Epidermal Growth Factor (VEGF) inhibitors) or immunological therapy. Patients who are willing to accept with paclitaxel and carboplatin as adjuvant chemotherapy will be eligible.
- World Health Organization (WHO) performance status (PS) of 0 to 2.
- Females of child-bearing potential must have negative serum pregnancy test. Sexually active males and females (of childbearing potential) willing to practice contraception during the study.
Laboratory values within the range, as defined below, within two weeks of randomization:
- Absolute neutrophils count(ANC)≥2.0×109/L
- Platelets≥100×109/L
- Serum bilirubin≤2×ULN; Aspartate transaminase(AST) and alanine tansaminase (ALT) ≤2.5×ULN(≤5×ULN if liver metastases)
- Creatinine clearance≥60ml/min
- Measurable disease according to Response Evaluation Criteria in Solid Tumors(RECIST) criteria with at least one measurable lesion not previously irradiated.
- Life expectancy ≥12 weeks.
Exclusion Criteria:
Any of the following is regarded as a criterion for exclusion from the study:
- As judged by the investigator, any evidence of severe or uncontrolled systemic disease (e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease).
- Newly diagnosed Central Nervous System (CNS) metastases that have not yet been definitively treated with surgery and/or radiation.
- Known severe hypersensitivity to carboplatin, paclitaxel or any of the excipients of these products.Known severe hypersensitivity to pre-medications required for treatment with carboplatin / paclitaxel doublet chemotherapy.
- Prior treatment with paclitaxel.
- Current treatment with target drug and biological therapy.
- Pregnant or lactating woman.
- Prior chemotherapy, biological (including targeted therapies such as Epidermal Growth Factor Receptor(EGFR) and Vascular Epidermal Growth Factor (VEGF) inhibitors) or immunological therapy were received even if treatment was not paclitaxel and was completed in 4 weeks before day1 of study treatment.
- Other co-existing malignancies or malignancies diagnosed within the last 5 years with the exception of basal cell carcinoma or cervical cancer in situ.
- Life expectancy of less than 12 weeks.
- Unable to tolerate carboplatin / paclitaxel doublet chemotherapy, as judged by the investigator.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: pharmacokinetics group
Based on pharmacokinetics.
Observe safety and efficacy.
In first cycle a fixed Paclitaxel dose depends on BSA.
In subsequent cycles the dosage of Paclitaxel will be adjusted depending on pharmacokinetics follow up .
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Based on pharmacokinetics.
Observe the toxicity in an individual patient after a fixed Paclitaxel dose depending on BSA and then the dosage of Paclitaxel is adjusted depending on pharmacokinetics follow up to avoid excess toxicity in subsequent cycles.
Based on body surface area.
The dosage of Paclitaxel is based on the BSA of the patient.
Paclitaxel/carboplatin up to 4 cycles or disease progression or intolerable toxicity.
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Actieve vergelijker: Body surface area(BSA) group
Based on body surface area.
The dosage of Paclitaxel is based on the BSA of the patient.
Paclitaxel/carboplatin up to 4 cycles or disease progression or intolerable toxicity.
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Based on pharmacokinetics.
Observe the toxicity in an individual patient after a fixed Paclitaxel dose depending on BSA and then the dosage of Paclitaxel is adjusted depending on pharmacokinetics follow up to avoid excess toxicity in subsequent cycles.
Based on body surface area.
The dosage of Paclitaxel is based on the BSA of the patient.
Paclitaxel/carboplatin up to 4 cycles or disease progression or intolerable toxicity.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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CTCAE grade 4 of the blood marrow
Tijdsspanne: 24 months
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Record the number of CTCAE grade 4 of the blood marrow such as Leukocytes, Neutrophils,Platelets and Hemoglobin in two treatment groups since the initiation of chemotherapy
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24 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Objective response rate
Tijdsspanne: Tumor assessment 6-8 weeks after the initiation of chemotherapy
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The objective tumour response rate will be calculated as the percentage of evaluable patients with complete response (CR) and partial response (PR).
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Tumor assessment 6-8 weeks after the initiation of chemotherapy
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Progression free survival
Tijdsspanne: 12 months
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Progression Free Survival (PFS) is defined as the time from randomization to the first documentation of objective disease progression (PD) or death from any cause.
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12 months
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Overall survival
Tijdsspanne: 24 months
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Overall survival(OS) is defined as the interval between the date of randomization and the date of patient death due to any cause, or the last date the patient was known to be alive.
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24 months
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Quality of life
Tijdsspanne: 24 months
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Data on QoL will be assessed using the Functional Assessment of Cancer Therapy - Lung (FACT-L) for every patients.
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24 months
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Caicun Zhou, Ph.D, Tongji University Affiliated Shanghai Pulmonary Hospital
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Ziekten van de luchtwegen
- Neoplasmata
- Longziekten
- Neoplasmata per site
- Neoplasmata van de luchtwegen
- Thoracale neoplasmata
- Carcinoom, bronchogeen
- Bronchiale neoplasmata
- Longneoplasmata
- Carcinoom, niet-kleincellige long
- Moleculaire mechanismen van farmacologische werking
- Antineoplastische middelen
- Tubuline-modulatoren
- Antimitotische middelen
- Mitose modulatoren
- Antineoplastische middelen, fytogeen
- Paclitaxel
- Albumine-gebonden paclitaxel
Andere studie-ID-nummers
- SPAP
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