- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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)
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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
Registrering (Forventet)
Fase
- Fase 3
Kontakter og plasseringer
Studiesteder
-
-
Shanghai
-
Shanghai, Shanghai, Kina, 200433
- Rekruttering
- Medical Department, Shanghai Pulmonary Hospital
-
Underetterforsker:
- Jie Zhang, MD
-
Underetterforsker:
- Huiwei Qi, MD
-
Underetterforsker:
- Fengying Wu, MD
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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 .
|
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.
|
|
Aktiv komparator: 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.
|
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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
CTCAE grade 4 of the blood marrow
Tidsramme: 24 months
|
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
|
24 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective response rate
Tidsramme: Tumor assessment 6-8 weeks after the initiation of chemotherapy
|
The objective tumour response rate will be calculated as the percentage of evaluable patients with complete response (CR) and partial response (PR).
|
Tumor assessment 6-8 weeks after the initiation of chemotherapy
|
|
Progression free survival
Tidsramme: 12 months
|
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.
|
12 months
|
|
Overall survival
Tidsramme: 24 months
|
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.
|
24 months
|
|
Quality of life
Tidsramme: 24 months
|
Data on QoL will be assessed using the Functional Assessment of Cancer Therapy - Lung (FACT-L) for every patients.
|
24 months
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Caicun Zhou, Ph.D, Tongji University Affiliated Shanghai Pulmonary Hospital
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i luftveiene
- Neoplasmer
- Lungesykdommer
- Neoplasmer etter nettsted
- Neoplasmer i luftveiene
- Thoracale neoplasmer
- Karsinom, bronkogent
- Bronkiale neoplasmer
- Lungeneoplasmer
- Karsinom, ikke-småcellet lunge
- Molekylære mekanismer for farmakologisk virkning
- Antineoplastiske midler
- Tubulin modulatorer
- Antimitotiske midler
- Mitosemodulatorer
- Antineoplastiske midler, fytogene
- Paklitaksel
- Albuminbundet paklitaksel
Andre studie-ID-numre
- SPAP
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