- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01759238
Chemoradiotherapy for Patients With Oligometastatic Colorectal Cancer (OLGA)
29. juni 2022 oppdatert av: Universitätsklinikum Hamburg-Eppendorf
Capecitabine and Bevacizumab With Radiotherapy After 3-6 Months Chemotherapy for Patients With Oligometastatic Colorectal Cancer (OLGA Trial)
This study tries to evaluate the role of chemoradiation with capecitabine and bevacizumab in oligometastatic patients neither being progressive nor resectable after chemotherapy.
Studieoversikt
Status
Avsluttet
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Combining chemoradiation with an antiangiogenic agent has a strong biological rationale, and preclinical studies consistently show an increase in radiosensitization with combined treatment.
It is well described that hypoxia or HIF-1 expression is associated with a lower radiation response and progression in solid tumors.
Radiation itself induces transient tumor hypoxia, which in turn stimulates VEGF production and VEGFR-2 expression what may also serve as a paracrine proliferative stimulus that promotes out-of-field growth.
The combination of radiotherapy with an antiangiogenic agent (e.g.
bevacizumab) thus offers the potential to enhance the effect of radiation, and avoid further spread of disease.
Furthermore, targeting tumor vasculature improves the delivery of cytotoxic drugs (e.g.
capecitabine) leading to increased efficacy of chemoradiation.
Combination with cytotoxic drugs could additionally limit treatment-induced hypoxia (Senan and Smit 2007; Mazeron, Anderson et al. 2011).
Studietype
Intervensjonell
Registrering (Faktiske)
1
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
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Hamburg, Tyskland
- University Hospital Hamburg-Eppendorf
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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:
- 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.
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: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: 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)
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Progression free survival rate
Tidsramme: 12 months
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Progression free survival rate at 12 months after start of induction treatment (PFSR@12)
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12 months
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Total overlevelse (OS)
Tidsramme: 36 måneder
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36 måneder
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|
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Time to progression (TTP) in 2 cohorts
Tidsramme: 24 months
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Time to progression (TTP) in 2 cohorts:
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24 months
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Overall Response Rate
Tidsramme: 12 months
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Efficacy of the investigational therapy shown by the Overall Response Rate (CR and PR) according to RECIST v1.1
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12 months
|
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Quality of life (QoL)
Tidsramme: 12 months
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Quality of life using the EORTC QLQ-C30 and the module CR29
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12 months
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Prognostic and predictive value of PET scan
Tidsramme: at baseline and 2 months after chemoradiation
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Prognostic and predictive value of PET scan at baseline and at 2 months after chemoradiation
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at baseline and 2 months after chemoradiation
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Toxicity
Tidsramme: 12 months
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Number of adverse events, according to NCI CTCAE v4.0)
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12 months
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Etterforskere
- Hovedetterforsker: Cordula Petersen, Prof., Universitätsklinikum Hamburg-Eppendorf
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
1. mai 2013
Primær fullføring (Faktiske)
1. oktober 2014
Studiet fullført (Faktiske)
1. oktober 2014
Datoer for studieregistrering
Først innsendt
17. desember 2012
Først innsendt som oppfylte QC-kriteriene
2. januar 2013
Først lagt ut (Anslag)
3. januar 2013
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
1. juli 2022
Siste oppdatering sendt inn som oppfylte QC-kriteriene
29. juni 2022
Sist bekreftet
1. juni 2022
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i fordøyelsessystemet
- Patologiske prosesser
- Neoplasmer
- Neoplasmer etter nettsted
- Gastrointestinale neoplasmer
- Neoplasmer i fordøyelsessystemet
- Gastrointestinale sykdommer
- Kolonsykdommer
- Tarmsykdommer
- Intestinale neoplasmer
- Rektale sykdommer
- Neoplastiske prosesser
- Kolorektale neoplasmer
- Neoplasma Metastase
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Antimetabolitter, antineoplastisk
- Antimetabolitter
- Antineoplastiske midler
- Antineoplastiske midler, immunologiske
- Angiogenese-hemmere
- Angiogenesemodulerende midler
- Vekststoffer
- Veksthemmere
- Capecitabin
- Bevacizumab
Andre studie-ID-numre
- OLGA
- 2011-005296-16 (EudraCT-nummer)
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