Status:
UNKNOWN
First-line Combination of Capecitabine and Oxaliplatin Plus Bevacizumab in Elderly Patients With Metastatic Colorectal Cancer
Lead Sponsor:
Istituto Oncologico Veneto IRCCS
Conditions:
Elderly Metastatic Colorectal Cancer Patients
Eligibility:
All Genders
70+ years
Brief Summary
* Oxaliplatin-based doublets plus bevacizumab are standard first-line therapy options for patients (pts) with metastatic colorectal cancer (mCRC). Slight adjustments in chemo-dosage are commonly appli...
Eligibility Criteria
Inclusion
- Histologically proven diagnosis of colorectal cancer.
- Initially unresectable metastatic colorectal cancer not previously treated with chemotherapy for metastatic disease.
- Indication to oxaliplatin, capecitabine and bevacizumab as first line treatment.
- At least one measurable lesion according to RECIST1.1 criteria.
- Availability of a tumoral sample (primary and/or metastatic sites).
- Age ≥ 70 years.
- ECOG PS (Eastern Cooperative Oncology Group - Performance Status) 1 or 2 for pts aged 70 to 75 years; ECOG PS 0 or 1 for pts aged \> 75 years.
- Life expectancy of at least 12 weeks.
- Previous adjuvant chemotherapy allowed only if with fluoropyrimidine monotherapy and more than 6 months elapsed between the end of adjuvant and first relapse.
- Laboratory Requirements:
- Neutrophils ≥1.5 x 109/L,
- Platelets ≥100 x 109/L,
- Hgb ≥ 9 g/dl.
- Total bilirubin ≤ 1.5 time the upper-normal limits (UNL) of the normal values and ASAT (SGOT) and/or ALAT (SGPT) ≤ 2.5 x UNL (or \<5 x UNL in case of liver metastases),
- Alkaline phosphatase ≤ 2.5 x UNL (or \<5 x UNL in case of liver metastases),
- Creatinine clearance ≥ 50 mL/min or serum creatinine ≤1.5 x UNL,
- Urine dipstick of proteinuria \<2+. Pts discovered to have 2+ proteinuria on dipstick urinalysis at baseline, should undergo a 24-hour urine collection and must demonstrate \<1 g of protein/24 hr.
- Male subjects with female partners of childbearing potential must be willing to use adequate contraception as approved by the investigator (i.e. barrier contraceptive measure or oral contraception, total abstinence) during the study and until 6 months after the last treatment.
- Geriatric assessment by means of G8 screening tool and CRASH score.
- Written informed consent to study procedures and to molecular analyses before pts registration.
- Will and ability to comply with the protocol.
Exclusion
- criteria
- Previous adjuvant oxaliplatin-containing chemotherapy.
- Previous treatment with bevacizumab.
- Previous systemic treatment for the metastatic disease.
- Previous radiotherapy treatment to any site within 4 weeks before the study.
- Evidence of untreated brain metastases or spinal cord compression or primary brain tumours.
- History or evidence upon physical examination of CNS disease unless adequately treated.
- Symptomatic peripheral neuropathy \> 1 grade NCIC-CTG criteria.
- Serious, non-healing wound, ulcer, or bone fracture.
- Evidence of bleeding diathesis or coagulopathy.
- Uncontrolled hypertension and prior history of hypertensive crisis or hypertensive encephalopathy.
- Clinically significant (i.e. active) cardiovascular disease for example cerebrovascular accidents (≤6 months), myocardial infarction (≤6 months), unstable angina, New York Heart Association (NYHA) grade II or greater congestive heart failure (CHF), serious cardiac arrhythmia requiring medication.
- Any previous venous thromboembolism \> NCI CTCAE Grade 3.
- History of abdominal fistula, GI perforation, intra-abdominal abscess or active GI bleeding within 6 months prior to the first study treatment.
- Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to study treatment start, or anticipation of the need for major surgical procedure during the course of the study.
- Current ongoing treatment with anticoagulants for therapeutic purposes.
- Chronic, daily treatment with high-dose aspirin (\>325 mg/day).
- Active uncontrolled infections or other clinically relevant concomitant illness contraindicating chemotherapy administration or putting the patient at high risk for treatment-related toxicities.
- Other co-existing malignancies or malignancies diagnosed within the last 5 years with the exception of localized basal and squamous cell carcinoma or cervical cancer in situ.
- Lack of physical integrity of the upper gastrointestinal tract, malabsorption syndrome, or inability to take oral medication.
- Contraindications for the use of corticosteroids and antihistamines as premedication or known hypersensitivity to any other component of the study drugs.
- Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.
Key Trial Info
Start Date :
November 1 2017
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2024
Estimated Enrollment :
121 Patients enrolled
Trial Details
Trial ID
NCT03451370
Start Date
November 1 2017
End Date
December 1 2024
Last Update
November 29 2023
Active Locations (1)
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1
Istituto Oncologico Veneto IRCCS
Padua, Italy, 35128