Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:27 AM
Ignite Modification Date:
2025-12-25 @ 1:27 AM
NCT ID:
NCT02280694
Eligibility Criteria:
Inclusion Criteria:
1. Histological (or cytological) proof of colorectal carcinoma (CRC)
2. Measurable metastases
3. ECOG (Eastern Cooperative Oncology Group) performance status 0-2
4. Progressing disease following all available chemotherapy treatment lines (including chemotherapy, bevacizumab+/-ziv-aflibercept, and an epidermal growth factor receptor (EGFR) inhibitor \[if WT(wild type)-KRAS\]
5. The central-radiologist's confirmation of PD\* under the last (previous) line of "conventional treatment".
\* PD (progressive disease) by RECIST(Response Evaluation Criteria in Solid Tumors) criteria : a) there is 20% or more relative increment in the sum of diameters of target lesions in comparison with the base line sum, and their absolute increase is 5 mm. or more, or b) there appeared one or more new lesions, or c)there is substantial worsening in non-target disease
6. Age: between 18 and 85
7. Prior radiotherapy either as adjuvant treatment or for palliation is allowed, unless this was delivered to the only measurable lesion
8. Complete blood count reflecting adequate Bone Marrow:
Hb=/ \> 9 g/dL, ANC=/\> 1,500 Plt =/\> 75,000/mcL; 9. Adequate liver function:
1. Total Bilirubin always =/\<X1.5 ULN
2. ALT and AST and Alkaline Phosphatase =/ \< 2.5 X upper normal limit , although in patients with liver metastases these are acceptable if =/\< 5 X ULN; 11. Adequate renal function (serum creatinine): =/\< 1.5 X ULN. 12. Absence of any non-hematological toxicity at grade 2 or higher. 13.The patient is able to understand and ready to sign the informed consent
Exclusion Criteria:
1. Lack of confirmation of PD (under the pre-study treatment) by the central radiologist
2. Any concurrent other active cancer (except basal cell or squamous cell carcinoma of skin and early prostate cancer or DCIS- in situ breast cancer)
3. Inability to adhere to monthly visits to the oncological unit for evaluation
4. Presence of brain metastases
5. Continuous treatment with steroids or with NSAIDs or with anticoagulants during the last year (except micropirin)
6. Previous radiotherapy to the only site of measurable disease
7. Existence of active peptic ulcer or symptomatic coronary disease
8. Existence of chronic inflammatory diseases, such as ulcerative colitis or Crohn's disease or rheumatoid arthritis
9. Presence of ascites, and/or any other "third space" finding (eg. significant leg edema)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
85 Years
Study:
NCT02280694
Study Brief:
Protocol Section:
NCT02280694