- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03917069
Nab-PCE vs PC for MM After Failure of Anti-PD-1
15. april 2019 oppdatert av: Jun GUO, Peking University Cancer Hospital & Institute
Nab-paclitaxel Plus Carboplatin Combined Endostatin Versus Solvent-based Paclitaxel Plus Carboplatin in the Treatment of Advanced Melanoma After the Failure of PD-1 Treatment #A Randomized Controlled, Open, Multicenter Trial
This is a randomized controlled clinical trial of nab-paclitaxel + carboplatin
- Endostatin for advanced melanoma after failure of PD-1 therapy. The aim was to evaluate the efficacy and safety of nab-paclitaxel+carboplatin
- endostatin versus combination of paclitaxel and carboplatin in patients with advanced melanoma after failure of PD-1 therapy.
Studieoversikt
Status
Ukjent
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
The enrollment time is expected to be 1.5 year and the observation time is 2 years.
The regimen were performed on a 28-day/21-day cycle respectively.
Subjects who met the entry criteria were treated in a 2:1 group according to a randomized list: the treatment group was treated with nab-paclitaxel + carboplatin + endostatin regimen, and the control group was treated with paclitaxel + carboplatin.
In this trial, the efficacy is evaluated every 8 weeks until disease progression or unacceptable toxicity,or until the investigator deemed that the patient's condition was unacceptable for further treatment.
The follow-up period was 24 months after the end of treatment (follow-up patient survival information and new anti-tumor treatment).
The planning enrolled sample size for nab-paclitaxel + carboplatin + endostatin group and paclitaxel-carboplatin group were 90 patients and 45 patients, respectively.
Studietype
Intervensjonell
Registrering (Forventet)
145
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Beijing
-
Beijing, Beijing, Kina, 100142
- Rekruttering
- Beijing Cancer Hospital
-
Ta kontakt med:
- Lili Mao, Dr
- Telefonnummer: 861013261859885
- E-post: yunzhongmanbu7848@163.com
-
Ta kontakt med:
- Lu Si
- Telefonnummer: 861088196956
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 70 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Age ≥ 18 years old, ≤ 70 years old, male or female;
- Histological or pathological diagnosis of advanced melanoma, and progressed after anti-PD-1 treatment (disease progression or unacceptable toxicity);
- The patient has at least one (RECIST 1.1 standard) measurable lesion, which needs to be detected by spiral CT or MRI, and the tumor lesion has at least one single diameter ≥ 1 cm;
- ECOG PS is 0 or 1 (see Annex 1 for standards);
- The estimated survival period is ≥12 weeks;
- no chemotherapy contraindications, including normal peripheral blood, liver and kidney function and electrocardiogram are basically normal; Peripheral blood: neutrophils ≥1.5×109/L, platelets≥90×109/ L, hemoglobin≥90 g/L; Renal function: normal serum creatinine; For patients with non-metastatic liver function impairment: alanine, aspartate aminotransferase ≤ 2.5 ULN, For patients with metastatic liver dysfunction: alanine, aspartate aminotransferase ≤ 5 ULN;
- Patients who have undergone topical treatment for asymptomatic brain metastases can be enrolled and have a clinical stable status of at least 4 weeks.
- Patients voluntarily participate in and sign an informed consent form.
- contraindications for the use of no carboplatin, paclitaxel, entropic and albumin paclitaxel
Exclusion Criteria:
- Known HIV, hepatitis B/C virus positive status or history of active tuberculosis (testing prior to randomisation is not required)
- Received any investigational drug within 28 days or 5 half-lives of the planned first dose of this study treatment.
- Active infection requiring systemic therapy.
- A known history of another malignancy or concurrent malignancy unless the patient is disease-free for a minimum of 1 year, is completely treated and is at low-risk of recurrence.
- Patients with a history or evidence of cardiovascular risk,
- History or evidence of interstitial lung disease or active non-infectious pneumonitis.
- Serious or unstable pre-existing medical conditions or other conditions that could interfere with the patient's safety, consent, or compliance.
- Pregnant or breastfeeding females, or expecting to conceive or father children within the projected period of study treatment (52 weeks followed by 4 months following end of study treatment).
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: nab-paclitaxel + endostatin+ carboplatin
nab-paclitaxel + endostatin+ carboplatin nab-paclitaxel 260mg/m2, d1 +Carboplatin AUC=5, d1 +endostatin 15mg, d1-14 q28d
|
nab-paclitaxel 260mg/m2 d1+Carboplatin AUC=5 d1+ endostatin 15mg d1-14,q28d
|
|
Aktiv komparator: paclitaxel+carboplatin
paclitaxel+carboplatin paclitaxel 175 mg/m2, d1+ Carboplatin AUC=5, d1 q21d
|
paclitaxel 175 mg/m2 d1+Carboplatin AUC=5 d1, q21d
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression free survival (PFS)
Tidsramme: 3 years
|
The time from treatment to tumor progression or death
|
3 years
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective response rate (ORR)
Tidsramme: At the end of Cycle 2 (each cycle is 28 days)
|
response evaluation disease progression defined by Response Evaluation Criteria in Solid Tumors (RECIST, version 1.1) criteria. response (PR), refers to the number of cases with complete and partial response after treatment as a percentage of the total number of evaluable cases |
At the end of Cycle 2 (each cycle is 28 days)
|
|
Disease Control Rate (DCR)
Tidsramme: At the end of Cycle 2 (each cycle is 28 days)
|
The disease control rate was the proportion of patients with complete remission, partial remission and stability (SD) in all patients.
|
At the end of Cycle 2 (each cycle is 28 days)
|
|
overall survival (OS)
Tidsramme: 3 years
|
OS was defined as the time from the date of the first administration of trial regimen to the date of death from any cause (event) or last follow-up (censored data).
|
3 years
|
|
Adverse events (AE)
Tidsramme: 3 years
|
Adverse events (AE) were monitored on an ongoing basis and classified according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), version 4.0.
Patients were assessed for toxicities before each administration, and toxicity was graded accordingly
|
3 years
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Etterforskere
- Hovedetterforsker: Jun Guo, Dr., Peking University Cancer Hospital & Institute
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
23. mars 2019
Primær fullføring (Forventet)
30. september 2021
Studiet fullført (Forventet)
30. september 2022
Datoer for studieregistrering
Først innsendt
12. april 2019
Først innsendt som oppfylte QC-kriteriene
15. april 2019
Først lagt ut (Faktiske)
16. april 2019
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
17. april 2019
Siste oppdatering sendt inn som oppfylte QC-kriteriene
15. april 2019
Sist bekreftet
1. april 2019
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2019NPCE
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
JA
IPD-planbeskrivelse
De-identified individual participant data for all primary and secondary outcome measures will be made available.
IPD-delingstidsramme
Data will be available within 6 months of study completion.
Tilgangskriterier for IPD-deling
data access requests will be reviewed by an external Independent Review Panel.Requestors will be required to sign a Data Access Agreement.
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
- SEVJE
- ICF
- ANALYTIC_CODE
- CSR
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
produkt produsert i og eksportert fra USA
Nei
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