Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Safety and Efficacy Study of Famitinib in Patients With Advanced Colorectal Adenocarcinoma（FACT） (FACT)

21 december 2020 bijgewerkt door: Jiangsu HengRui Medicine Co., Ltd.

A Multicenter，Randomized, Double-blind, Placebo-controlled Trial of Famitinib in Patients With Advanced Colorectal Adenocarcinoma

Famitinib is a tyrosin-inhibitor agent targeting at c-Kit, VEGFR2, PDGFR, VEGFR3, Flt1 and Flt3, whose anti-tumor and anti-angiogenesis effects have been validated in preclinical tests. In PhaseⅡb study, a significantly improved Progression Free Survival (PFS) was found in patients with advanced colorectal cancer treated with Famitinib compared to placebo. On the other hand, the toxicity of Famitinib was manageable in both PhaseⅠand Ⅱb studies.

The purpose of this study is to determine whether Famitinib can improve Overall Survival (OS) compared with placebo in total 540 patients with advanced colorectal cancer who have failed in previously received at least two lines of standard chemotherapy.

Studie Overzicht

Toestand

Voltooid

Conditie

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Werkelijk)

543

Fase

  • Fase 3

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

  • China
    • Anhui
      • Hefei, Anhui, China
        • The First Affiliated Hospital of Anhui Medical University
      • Hefei, Anhui, China
        • The Second Affiliated Hospital of Anhui Medical University
    • Beijing
      • Beijing, Beijing, China
        • Beijing Friendship hospital, Capital Medical University
      • Beijing, Beijing, China
        • Chinese Academy of Medical Sciences Cancer Hospital
      • Beijing, Beijing, China
        • Beijing Chao-Yang Hospital, Capital Medical University
      • Beijing, Beijing, China
        • Beijing Cancer Hospital, Peking University
      • Beijing, Beijing, China
        • PLA Hospital 301
    • Chongqing
      • Chongqing, Chongqing, China
        • The Third Affiliated Hospital of the Third Military Medical University
    • Fujian
      • Fuzhou, Fujian, China
        • Fujian Medical University Union Hospital
    • Guangdong
      • Guangzhou, Guangdong, China
        • Cancer center, Sun Yet-sen University
      • Guangzhou, Guangdong, China
        • The First Affiliated Hospital of Guangzhou Medical University of Chinese Medicine
    • Guangxi
      • Nanning, Guangxi, China
        • Cancer Hospital of Guangxi Zhuang Autonomous Region
      • Nanning, Guangxi, China
        • Hospital of Guangxi Zhuang Autonomous Region
    • Hainan
      • Hainan, Hainan, China
        • Hainan General Hospital
    • Heilongjiang
      • Harbin, Heilongjiang, China
        • Harbin Medical University Cancer Hospital
    • Henan
      • Xinxiang, Henan, China
        • The First Affiliated Hospital of Xinxiang Medical University
      • Zhengzhou, Henan, China
        • The First Affiliated Hospital of Zhengzhou University
      • Zhengzhou, Henan, China
        • Cancer Hospital of Henan province
    • Hubei
      • Wuhan, Hubei, China
        • Union Hospital of Tongji Medical College, Huazhong University of Science and Technology
      • Wuhan, Hubei, China
        • Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology
      • Wuhan, Hubei, China
        • Wuhan General Hospital of Guangzhou Military
    • Hunan
      • Changsha, Hunan, China
        • Cancer Hospital of Hunan Province
      • Changsha, Hunan, China
        • The Third Xiangya Hospital of Cental South University
    • Jiangsu
      • Changzhou, Jiangsu, China
        • The First People's Hospital of Changzhou
      • Nanjing, Jiangsu, China
        • The Second Affiliated Hospital of Nanjing Medical University
      • Nanjing, Jiangsu, China
        • Cancer Hospital of Jiangsu Province
      • Xuzhou, Jiangsu, China
        • The Affiliated Hospital of Xuzhou Medical Collage
    • Jiangxi
      • Nanchang, Jiangxi, China
        • The Second Affiliated Hospital of Nanchang University
      • Nanchang, Jiangxi, China
        • Cancer Hospital of Jiangxi Province
    • Jilin
      • Changchun, Jilin, China
        • The first Affiliated Hospital of Jilin University
      • Changchun, Jilin, China
        • Cancer Hospital of Jilin province
    • Liaoning
      • Shenyang, Liaoning, China
        • Cancer Hospital of Liaoning Province
      • Shenyang, Liaoning, China
        • Chinese Medical University First Hospital
    • Shanghai
      • Shanghai, Shanghai, China
        • Shanghai General Hospital
      • Shanghai, Shanghai, China
        • Fudan University Cancer Hospital
      • Shanghai, Shanghai, China
        • Ruijin Hospital, Shanghai Jiaotong University, School of Medicine
      • Shanghai, Shanghai, China
        • Zhongshan Hospital of Fudan University
    • Shanxi
      • Xian, Shanxi, China
        • Cancer Hospital of Shanxi Province
      • Xian, Shanxi, China
        • Tangdu Hospital of The Fouth Military Medical University
    • Tianjin
      • Tianjin, Tianjin, China
        • Cancer Hospital of Tianjin City
      • Tianjin, Tianjin, China
        • People's Hospital of Tianjin City
    • Yunnan
      • Kunming, Yunnan, China
        • Cancer Hospital of Yunnan Province
    • Zhejiang
      • Hangzhou, Zhejiang, China
        • Sir Run Run Shaw Hospital, Zhejiang University, School of Medicine
      • Hangzhou, Zhejiang, China
        • The Second Affiliated Hospital of Zhejiang University School of Medicine

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  1. Male or female patients aged 18 to 75 (including 18 and 75) at the time of Informed Consent
  2. Pathologically confirmed advanced colorectal adenocarcinoma (all the other histological types are excluded)

  3. Treatment failure in previously received standard therapy (at least two lines), which must include 5-Fu, irinotecan and oxaliplatin

    Definition of "treatment failure":

    A.Disease progression during experimental drug treatment or within 3 months after the last treatment, with definite imaging or clinical evidences;

    B.For patients abandoning chemotherapy because of intolerance of advent events, hematologic toxicity is required to reach ≥Grade IV (platelet decrease ≥ Grade III ), and nonhematologic toxicity is required to reach ≥Grade III , according to NCI CTCAE 4.0. Furthermore, the original treatment should be not tolerated any more when it is repeated to the same patient, judged by investigators.

    Note:

    A.When adjuvant therapy including oxaliplatin was previously used, at least 9 courses of FOLFOX (2 weeks regimens), 6 courses of CapeOX (3 week regimen), or 750mg/m^2 cumulative consumption of oxaliplatin, are required. Adjuvant therapy will be regarded as the first-line treatment when disease progressed during or within 6 months after treatments

    B.Monoclonal antibody drugs (bevacizumab, cetuximab, panitumumab, aflibercept, etc.) are allowed to combine with prior chemotherapy.

  4. At least one measurable targeting lesion according to RECIST 1.1 (The diameter of tumor and lymph node lesion should be ≥ 10 mm and 15mm, respectively, with scanning layer ≤ 5 mm and without local treatment)
  5. Eastern Cooperative Oncology Group (ECOG) performance status:0-1.
  6. Life expectancy ≥ 3 months

  7. Adequate function of major organs, meaning the following criteria should be met within 14 days before randomization:

    A.Routine blood test:

    1. Hemoglobin > 90g/L (not received blood transfusion or drugs to incraese RBC, Hb, WBC and PLT in 14 days before screening )
    2. Neutrophils > 1.5×10^9/L

    3. Platelets > 100×10^9/L

      B. Blood biochemistry:

    4. Total bilirubin < 1.25×the upper limit of normal (ULN)
    5. Serum transaminase ≤ 2×ULN (≤ 5×ULN, If existing liver metastases)
    6. Creatinine clearance rate ≥ 60ml/min (Cockcroft-Gault Formula)

    C.Doppler echocardiography assessment: Left ventricular ejection fraction (LVEF) ≥ 50%

  8. Having recovered from impairments of other therapy before taking research drugs (more than 6 weeks from the last treatment of Nitroso or MMC, more than 4 weeks from the last treatment of other cytotoxic drugs, targeted drugs, radiotherapy or operation, with completely healed wound, more than 2 weeks from the last treatment of Chinese traditional and patent medicine)
  9. Signed and dated informed consent
  10. Good compliance of patients and agreement of their family members to cooperate on the follow-up of survival.

Exclusion Criteria:

  1. Second malignancies, except for cured skin basal cell carcinoma and carcinoma in-situ of uterine cervix, before or during screening
  2. Previously received therapy of tyrosine kinase inhibitor agent targeting at VEGFR, e.g. famitinib, sorafenib, sunitinib, regorafenib
  3. Having joined in other clinical trials within 4 weeks
  4. Factors influencing the usage of oral administration (e.g. unable to swallow, chronic diarrhea and intestinal obstruction, etc.)
  5. Having haemorrhage history, ≥ Grade Ⅲ (NCI CTCAE 4.0 ) haemorrhage occurred within 4 weeks before screening
  6. Known central nervous system (CNS) metastasis or having CNS metastasis history before screening. CT or MRI scan should be received 28 days before randomization when CNS metastases is clinically suspected
  7. Uncontrolled hypertension with single medical therapy (systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg), History of unstable angina pectoris or newly diagnosed unstable angina pectoris within 3 months before screening, myocardial infarction events within 6 months before screening, Arrhythmias (QTcF: ≥450ms in male, ≥ 470ms in female) needed long-term treatment of drugs, ≥ class II cardiac insufficiency by New York Heart Association (NYHA) classification
  8. urinary protein ≥ ++ or 24-hour urinary protein ≥ 1.0 g
  9. Chronic untreated wounds or fractures
  10. Tumor invasion around major vessels shown by imaging, high risk of major vascular invasion leading to massive hemorrhage judged by investigators
  11. Abnormal international normalized ratio (INR) of patients with coagulation dysfunction and hemorrhagic tendency at 14 days before randomization. Application of anticoagulants or vitamin K antagonists such as warfarin, heparin or its analogues. However, low doses of warfarin (1mg orally, once daily) or aspirin (between 80mg to 100mg daily) can be used for prevention on the premise of INR ≤ 1.5
  12. Artery/venous thromboembolic events occurred within 1 year before screening, such as cerebral vascular accident (including transient ischemic attack), deep vein thrombosis (except for recovered venous thrombosis judged by investigators, which was caused by venous catheter in previous chemotherapy) and pulmonary embolism, etc.
  13. All female patients who are not surgically sterilized or postmenopausal refusing to take a reliable method of birth control during the study and within 6 months after the last dose of test article. All female patients in breastfeeding period or in child-bearing period with a positive urine or serum pregnancy test result before randomization. All male subjects who are not surgically sterilized refusing to take a reliable method of birth control during the study and within 6 months after the last dose of test article.
  14. Preexisted thyroid dysfunction, thyroid function cannot be controlled within normal range even using medical therapy
  15. History of psychiatric drug abuse and addiction, dysphrenia
  16. Symptomatic pleural effusion, hydropericardium or ascites needed clinical intervention or being stable less than 4 weeks.
  17. History of Immunodeficiency, acquired or congenital immunodeficiency, history of organ transplantation
  18. Known active HBV or HCV infection companion with hepatic dysfunction
  19. Concomitant disease judged by investigators that may bring serious harm to the safety of patients or the completion of this study

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Famitinib arms
Famitinib 25 mg p.o. qd and the medication continued until disease progression or intolerable toxicity or patients withdrawal of consent
Geneesmiddel: Famitinib
25 mg p.o. qd
Placebo-vergelijker: Control arms
Placebo 25 mg p.o. qd and the medication continued until disease progression or intolerable toxicity or patients withdrawal of consent
Geneesmiddel: Placebo
25 mg p.o. qd

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Algehele overleving (OS)
Tijdsspanne: 3 jaar
3 jaar

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Progression Free Survival(PFS)
Tijdsspanne: 1.5 years
1.5 years
Objectief responspercentage (ORR)
Tijdsspanne: 6 maanden
6 maanden
Disease Control Rate(DCR)
Tijdsspanne: 1.5 years
1.5 years
Quality of Life as measured by EORTC QLQ-C30(3.0)
Tijdsspanne: 1.5 years
1.5 years
The incidence of Adverse Events
Tijdsspanne: 3 years
3 years
The severity of Adverse Events
Tijdsspanne: 3 years
3 years

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Jiangsu HengRui Medicine Co., Ltd.

Onderzoekers

  • Hoofdonderzoeker: Ruihua Xu, M.D, Cancer center, Sun Yet-sen University
  • Hoofdonderzoeker: Lin Shen, M.D, Beijing Cancer Hospital, Peking University

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 januari 2015

Primaire voltooiing (Werkelijk)

1 februari 2019

Studie voltooiing (Werkelijk)

1 juli 2019

Studieregistratiedata

Eerst ingediend

26 februari 2015

Eerst ingediend dat voldeed aan de QC-criteria

11 maart 2015

Eerst geplaatst (Schatting)

18 maart 2015

Updates van studierecords

Laatste update geplaatst (Werkelijk)

22 december 2020

Laatste update ingediend die voldeed aan QC-criteria

21 december 2020

Laatst geverifieerd

1 mei 2017

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • HR-FMTN-CRC-FACT

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren