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A Randomized, Double Blind Study Evaluating Paclitaxel With and Without RAD001 in Patients With Gastric Carcinoma After Prior Chemotherapy (AIO-STO-0111)

27. januar 2020 oppdatert av: Prof. Dr. S.E. Al-Batran, Krankenhaus Nordwest

A Randomized, Double-blind, Multi-center Phase III Study Evaluating Paclitaxel With and Without RAD001 in Patients With Gastric Carcinoma Who Have Progressed After Therapy With a Fluoropyrimidine-containing Regimen

Adult patients with gastric carcinoma which has progressed after initial treatment with a fluoropyrimidines-containing regimen will be treated with paclitaxel plus RAD001 or plus placebo. The hypothesis is that patients with RAD001 have significantly prolonged overall survival compared to patients who are treated with paclitaxel alone.

Studieoversikt

Status

Fullført

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

This is a randomized, double-blind, phase III two-arm multi-center study aiming at estimating the relative efficacy of the combination of RAD001 and paclitaxel versus that of paclitaxel alone as second-, third- or fourth-line treatment in terms of hazard ratio of overall survival in patients with gastric cancer who have relapsed after one treatment regimen containing a fluoropyrimidine (e.g., 5-FU, S-1, capecitabine and other 5-FU prodrugs or derivatives). Patients will be randomized in a 1:1 ratio for a total of 240 patients per treatment arm. Randomization will be stratified according to performance status (0-1 versus 2), prior taxan use (yes vs. no) and treatment line (2nd versus 3rd/4th line).

Study treatment will be continued until progression or intolerable toxicity. Patients will be seen at baseline/screening, and weekly for paclitaxel administration and safety assessment until disease progression or discontinuation of trial therapy for other reasons. Radiological tumor assessment will be performed every second cycle (every 8 weeks) or earlier if clinically indicated. Post-study follow-up will be completed every 8 weeks for survival.

Studietype

Intervensjonell

Registrering (Faktiske)

300

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Frankfurt/Main, Tyskland, 60488
        • Krankenhaus Nordwest

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 og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Male or female patients ≥ 18 years old
  • Histologically or cytologically confirmed and documented gastric adenocarcinoma. Adenocarcinomata of the gastro-esophageal junction will be allowed, if they have advanced disease (inoperable, recurrent or metastatic disease).
  • Documented progressive disease during/after one, two or three prior treatments containing 5FU and/or its precursors or derivatives in the palliative setting
  • At least one measurable or evaluable lesion by RECIST as determined by Computed Tomography (CT) Scan or Magnetic Resonance Imaging (MRI)
  • ECOG performance status of 0, 1 or 2
  • The following laboratory parameters:

    • Absolute neutrophil count ≥ 1.5 x 109/L
    • Platelets ≥ 100 x 109/L
    • Hemoglobin (Hgb) ≥ 9 g/dL
    • Serum creatinine ≤ 2 x Upper Limit of Normal (ULN)
    • Adequate liver function:
    • Total serum calcium (corrected for serum albumin) or ionized calcium ≥ LLN
  • Women of childbearing potential must have a negative serum pregnancy test within 7 days of the first administration of study treatments and must be willing to use adequate methods of contraception during the study and for 3 months after last study drug administration.
  • Written informed consent

Exclusion Criteria:

  • Current treatment with any anti cancer therapy or treatment with anti cancer therapy ≤ 2 weeks prior to study treatment start unless rapidly progressing disease is measured
  • Known hypersensitivity to RAD001 (everolimus) or to its excipients, or to other rapamycins (e.g. sirolimus, temsirolimus)
  • Known prior history of hypersensitivity to paclitaxel.
  • Paclitaxel refractory disease, which is defined as a disease progression under or within 12 weeks of last taxan treatment
  • Chronic treatment with steroids (except for oral, topical or local injection) or another immunosuppressive agent
  • Major surgery ≤ 2 weeks prior to starting study treatment or patients who have not recovered from such therapy
  • Lack of resolution of all acute toxic effects (excluding alopecia) of prior chemotherapy, prior radiotherapy, or surgical procedure to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) grade <= 1. Note: Neuropathy due to prior chemotherapy is allowed.
  • Unstable CNS disease

    • Requiring increasing doses of steroids to maintain stable neurological status
    • Deteriorating / changing neurological status
  • Known history of HIV seropositivity (HIV testing is not mandatory) or Hepatitis B or C.
  • Active, bleeding diathesis or on oral anti-vitamin K medication (except low dose warfarin, as long as the INR is <= 2.0)
  • Any other severe and/or uncontrolled medical conditions

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: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: paclitaxel + placebo

Paclitaxel 80 mg/m2 on day 1, day 8 and day 15 of every 28-day cycle.

+ Placebo (2 tablets / day) d1-d28

Paclitaxel 80 mg/m2 on day 1, day 8 and day 15 of every 28-day cycle.
Eksperimentell: paclitaxel + RAD001

Paclitaxel 80 mg/m2 on day 1, day 8 and day 15 of every 28-day cycle.

+ RAD001 10mg (2 x5 mg tablets / day) d1-d28

Paclitaxel 80 mg/m2 on day 1, day 8 and day 15 of every 28-day cycle.
RAD001 10mg (2 x5 mg tablets / day) d1-d28
Andre navn:
  • Certican
  • Everolimus

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
overall survival
Tidsramme: 6 months follow-up
6 months follow-up

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
best overall response
Tidsramme: staging every 8 weeks
staging every 8 weeks
progression-free survival
Tidsramme: staging every 8 weeks
staging every 8 weeks
number of participants with adverse events as a measure of safety and tolerability
Tidsramme: every week until end of treatment
every week until end of treatment
disease control rate
Tidsramme: every 8 weeks
responders + stable disease ≥12 weeks
every 8 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

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)

1. oktober 2011

Primær fullføring (Faktiske)

1. juli 2017

Studiet fullført (Faktiske)

1. oktober 2019

Datoer for studieregistrering

Først innsendt

23. november 2010

Først innsendt som oppfylte QC-kriteriene

24. november 2010

Først lagt ut (Anslag)

25. november 2010

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. januar 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. januar 2020

Sist bekreftet

1. januar 2020

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • CRAD001RDE35T

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

No IPD will be shared.

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .