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A Trial of Cediranib in the Treatment of Patients With Alveolar Soft Part Sarcoma (CASPS) (CASPS)

22 januari 2019 uppdaterad av: Institute of Cancer Research, United Kingdom

A Phase II Trial of Cediranib in the Treatment of Patients With Alveolar Soft Part Sarcoma (CASPS)

The study is a two-arm, randomised, double-blind, international, multi-centre phase II trial of cediranib in Alveolar Soft Part Sarcoma (ASPS).

The study aims to confirm the ability of cediranib to halt disease progression in patients with metastatic ASPS, as measured by the change in tumour size at 24 weeks after randomisation, and to produce objective response according to RECIST criteria.

Studieöversikt

Status

Okänd

Detaljerad beskrivning

Patients aged 16 years and older with a histologically confirmed diagnosis of ASPS will be recruited. Eligible patients will be randomised to receive cediranib (30 mg daily po) or placebo (30 mg daily po) in a 2:1 ratio. At 24 weeks post randomisation, treatment will be unblinded after which time all patients on placebo and those who have not progressed on active treatment will be given cediranib. Treatment will then continue until objective disease progression or death.

Studietyp

Interventionell

Inskrivning (Förväntat)

36

Fas

  • Fas 2

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Brisbane, Australien
        • Princess Alexandra Hospital
      • Sydney, Australien
        • Royal Prince Alfred Hospital
      • Barcelona, Spanien
        • Hospital Santa Cruz i Sant Pau
      • Madrid, Spanien
        • Hospital Puerta de Hierro
      • Zaragoza, Spanien
        • Hospital Miguel Servet
      • Bristol, Storbritannien
        • Bristol Haematology and Oncology Centre
      • London, Storbritannien
        • University College London Hospital
      • London, Storbritannien
        • Royal Marsden Hospital
      • Manchester, Storbritannien
        • Christie Hospital
      • Newcastle-Upon-Tyne, Storbritannien
        • Royal Victoria Infirmary/Freeman Hospital
      • Nottingham, Storbritannien
        • Nottingham University Hospitals

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

16 år och äldre (Barn, Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  1. Histologically confirmed diagnosis of ASPS (central confirmation not required at study entry)
  2. Age 16 years and older
  3. Availability of archived tissue blocks or unstained slides to enable confirmation of t(X;17) translocation
  4. ECOG Performance Status of 0-1
  5. Life expectancy of >12 weeks
  6. Progressive disease as defined by RECIST v1.1 within 6 months prior to randomisation
  7. Measurable metastatic disease using RECISTv1.1, i.e. at least one lesion 10 mm in diameter (15 mm in short axis for nodal lesions) assessable by CT (or MRI for brain metastases).
  8. Patients with brain metastases are permitted provided disease is controlled with a stable dose of corticosteroid and/or non-enzyme inducing anticonvulsant
  9. The capacity to understand the patient information sheet and ability to provide written informed consent
  10. Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures
  11. Able to swallow and retain oral medication

Exclusion Criteria:

  1. Inadequate bone marrow reserve as demonstrated by an absolute neutrophil count ≤1.5 x 109/L or platelet count ≤100 x 109/L
  2. Serum bilirubin ≥ 1.5 x ULN (unless Gilbert's syndrome)
  3. ALT or AST ≥ 2.5 x ULN. If liver metastases are present, ALT or AST > 5 x ULN
  4. Serum creatinine > 1.5 x ULN or a creatinine clearance (calculated or measured) of ≤ 50mL/min
  5. Greater than +1 proteinuria unless urinary protein < 1.5g in a 24 hr period or protein/creatinine ratio < 1.5.
  6. History of significant gastrointestinal impairment, as judged by the Investigator, that would significantly affect the absorption of cediranib.
  7. Patients with a history of poorly controlled hypertension with resting blood pressure >150/100 mmHg in the presence or absence of a stable regimen of anti-hypertensive therapy.
  8. Any evidence of severe or uncontrolled co-morbidities e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease, or active and uncontrolled infection.
  9. Evidence of prolonged QTc >480 msec (using Bazetts correction, for which the formula is: QTc = QT/√RR) or history of familial long QT syndrome.
  10. Significant recent haemorrhage (>30mL bleeding/episode in previous 3 months) or haemoptysis (>5mL fresh blood in previous 4 weeks).
  11. Major thoracic or abdominal surgery in the 14 days prior to entry into the study, or a surgical incision that is not fully healed.
  12. Pregnant or breast-feeding women; women of childbearing potential with a positive pregnancy test prior to receiving study medication; women the intention of pregnancy during study treatment; women of child bearing potential unwilling to have a urine or serum pregnancy test prior to study entry (even if surgically sterilised).
  13. Men and women of childbearing potential unwilling to use adequate birth control measures (e.g. abstinence, oral contraceptives, intrauterine device, barrier method with spermicide, implantable or injectable contraceptives or surgical sterilisation) for the duration of the study and should continue such precautions for 2 weeks after receiving the last study treatment.
  14. History of anticancer (including investigational, non-registered) treatment in the four weeks prior to first dose of cediranib, with the exception of palliative radiotherapy for symptom control.
  15. Previous treatment with cediranib.
  16. Known hypersensitivity to any excipient of cediranib.
  17. History of other malignancies (except for adequately treated basal or squamous cell carcinoma or carcinoma in situ) within 5 years, unless the patient has been disease free for 2 years and there is a tissue diagnosis of the primary cancer of interest from a target lesion.
  18. Other concomitant anti-cancer therapy (including LHRH agonists) except steroids
  19. Recent history of thrombosis
  20. Patients with brain metastases if they are symptomatic requiring increasing steroids in the previous six weeks to study entry or those with evidence of recent and/or active bleeding, or those causing uncontrolled seizures.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Fyrdubbla

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Blinded Cediranib
30mg once daily, oral until disease progression
Placebo-jämförare: Blinded Placebo
30mg, once daily, oral until 24 weeks or disease progression if sooner

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
To evaluate the efficacy of cediranib in the treatment of ASPS by measuring the percentage change in the sum of target marker lesion diameters from randomisation to week 24 (or progression if sooner) compared to treatment with placebo.
Tidsram: 24 Weeks of treatment
24 Weeks of treatment

Sekundära resultatmått

Resultatmått
Tidsram
Response rate at week 24, best response using RECISTv1.1 and best reduction (%) in tumour size
Tidsram: 24 Weeks of treatment
24 Weeks of treatment
Progression-free survival and percentage alive and progression-free at 12 months (APF12)
Tidsram: 12 months of treatment
12 months of treatment
Length of Overall survival
Tidsram: Patients will be followed up every 12 weeks
Patients will be followed up every 12 weeks
The safety and tolerability profile of cediranib in patients with ASPS
Tidsram: Assessments will be made at every study visit (8-12 weekly)
Assessments will be made at every study visit (8-12 weekly)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 juli 2011

Primärt slutförande (Förväntat)

1 juli 2019

Avslutad studie (Förväntat)

1 januari 2020

Studieregistreringsdatum

Först inskickad

11 april 2011

Först inskickad som uppfyllde QC-kriterierna

15 april 2011

Första postat (Uppskatta)

18 april 2011

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

24 januari 2019

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

22 januari 2019

Senast verifierad

1 januari 2019

Mer information

Termer relaterade till denna studie

Nyckelord

Andra studie-ID-nummer

  • ICR-CTSU/2010/10027
  • 2010-021163-33 (EudraCT-nummer)
  • CRUK/10/021 (Annat bidrag/finansieringsnummer: Cancer Research UK)
  • ISRCTN63733470 (Registeridentifierare: Randomised controlled Trials)
  • ISSRECE0036 (Annat bidrag/finansieringsnummer: AstraZeneca)

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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