Chemoradiotherapy for Patients With Oligometastatic Colorectal Cancer (OLGA)
Capecitabine and Bevacizumab With Radiotherapy After 3-6 Months Chemotherapy for Patients With Oligometastatic Colorectal Cancer (OLGA Trial)
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Studientyp
Einschreibung (Tatsächlich)
Einschreibung
Phase
Phase
- Phase 2
Kontakte und Standorte
Studienorte
-
-
-
Hamburg, Deutschland
- University Hospital Hamburg-Eppendorf
-
-
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Patients with histologically confirmed diagnosis of stage IV (UICC) colorectal cancer
- Oligometastatic disease, defined as at least one measureable lesion with size > 1cm (RECIST v1.1) to a maximum of 3 sites and 5 lesions suitable for radiotherapy according to the dose constraints for normal tissue
- Patients being neither progressive nor resectable after 3-6 months of first line chemotherapy (combination chemotherapy, at least chemo-doublet) with bevacizumab
- maximum treatment interruption after induction therapy of 6 weeks
- ECOG performance status ≤ 1
- Life expectancy > 3 months
- Age ≥ 18 years
- Haematologic function: ANC ≥ 1.5 x 109/L, platelets ≥ 75 x109/L
- INR < 1.5 within 7 days prior to starting study treatment. aPTT < 1.5 ULN within 7 days prior to starting study treatment
- adequate liver function as measured by serum transaminases (AST & ALT) ≤ 5 x ULN and a total bilirubin ≤1.5 x ULN
- adequate renal function: serum creatinine ≤ 1.5 x ULN
- signed, written informed consent
- ability to swallow tablets
Exclusion Criteria:
- treatment with any other investigational agent, or participation in another clinical trial within 30 days prior to entering this study
- prior radiotherapy for metastatic lesions (prior radiotherapy for primary tumor allowed if followed by complete resection and no sign for local recurrence at the time of enrolment)
- Pre history or evidence upon physical/neurological examination of CNS disease (unrelated to cancer) (unless adequately treated with standard medical therapy) e.g. uncontrolled seizures
- fertile women (< 2 years after last menstruation) and women of childbearing potential unwilling or unable to use effective means of contraception (oral contraceptives, intrauterine contraceptive device, barrier method of contraception in conjunction with spermicidal gel or surgically sterile)
- pregnancy or lactation
- Positive serum pregnancy test within 7 days of starting study treatment in pre-menopausal women and women < 2 years after the onset of menopause. Note: a negative test has to be reconfirmed by a urine test, should the 7-day window be exceeded.
- Past or current history (within the last 2 years prior to treatment start) of other malignancies except metastatic colorectal cancer (patients with curatively treated basal and squamous cell carcinoma of the skin or in situ carcinoma of the cervix are eligible).
- Known DPD-insufficiency
- Active inflammatory bowel disease or other bowel disease causing chronic diarrhea (defined as > 4 loose stools per day)
- Serious, non-healing wound, ulcer or bone fracture.
- Evidence of bleeding diathesis or coagulopathy.
- Urine dipstick for proteinuria >2+. If urine dipstick is 2+, 24-hour urine must demonstrate 1 g of protein in 24 hours for patient to be eligible.
- Major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to first treatment with study medication.
- Clinically significant cardiovascular disease, for example CVA, myocardial infarction (£ 12 months before treatment start), unstable angina pectoris, NYHA Class II CHF, arrhythmia requiring medication, or uncontrolled hypertension.
- Evidence of any other disease, metabolic dysfunction, physical examination finding or laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or puts the patient at high risk for treatment-related complications.
- Concomitant therapy with sorivudin or chemical analogues like brivudin
- Known hypersensitivity or contraindication to the drugs used in the trial (eg: capecitabine, bevacizumab)
- Inability or unwillingness to comply with the protocol.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: Chemoradiation
Chemoradiation with different radiotherapy regimes (depending on location and size of irradiated lesions; e.g.
conventional radiotherapy with a total dose of 35 Gy, delivered in 2.5Gy fractions for 14 days or intensity-modulated and image-guided radiotherapy with a total dose of 40 Gy, delivered in 4.0 Gy fractions for 10 days or 3-8 fractions with 8-15 Gy) combined with bevacizumab (7.5mg/kg day 1) and capecitabine (825mg/m2 bid on day 1-5, 8-12 and 15-19)
|
825mg/m2 per os bid
7.5 mg/kg
(conventional or intensity-modulated and image-guided radiotherapy)
|
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Progression free survival rate
Zeitfenster: 12 months
|
Progression free survival rate at 12 months after start of induction treatment (PFSR@12)
|
12 months
|
Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Gesamtüberleben (OS)
Zeitfenster: 36 Monate
|
36 Monate
|
|
|
Time to progression (TTP) in 2 cohorts
Zeitfenster: 24 months
|
Time to progression (TTP) in 2 cohorts:
|
24 months
|
|
Overall Response Rate
Zeitfenster: 12 months
|
Efficacy of the investigational therapy shown by the Overall Response Rate (CR and PR) according to RECIST v1.1
|
12 months
|
|
Quality of life (QoL)
Zeitfenster: 12 months
|
Quality of life using the EORTC QLQ-C30 and the module CR29
|
12 months
|
|
Prognostic and predictive value of PET scan
Zeitfenster: at baseline and 2 months after chemoradiation
|
Prognostic and predictive value of PET scan at baseline and at 2 months after chemoradiation
|
at baseline and 2 months after chemoradiation
|
|
Toxicity
Zeitfenster: 12 months
|
Number of adverse events, according to NCI CTCAE v4.0)
|
12 months
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Ermittler
Ermittler
- Hauptermittler: Cordula Petersen, Prof., Universitätsklinikum Hamburg-Eppendorf
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Studienbeginn
Primärer Abschluss (Tatsächlich)
Primärer Abschluss
Studienabschluss (Tatsächlich)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Erkrankungen des Verdauungssystems
- Pathologische Prozesse
- Neubildungen
- Neubildungen nach Standort
- Gastrointestinale Neubildungen
- Neoplasmen des Verdauungssystems
- Magen-Darm-Erkrankungen
- Darmerkrankungen
- Darmerkrankungen
- Darmtumoren
- Rektale Erkrankungen
- Neoplastische Prozesse
- Kolorektale Neubildungen
- Neoplasma Metastasierung
- Physiologische Wirkungen von Arzneimitteln
- Molekulare Mechanismen der pharmakologischen Wirkung
- Antimetaboliten, antineoplastisch
- Antimetaboliten
- Antineoplastische Mittel
- Antineoplastische Mittel, immunologische
- Angiogenese-Inhibitoren
- Angiogenese-modulierende Mittel
- Wuchsstoffe
- Wachstumshemmer
- Capecitabin
- Bevacizumab
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- OLGA
- 2011-005296-16 (EudraCT-Nummer)
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