Clinical trial · Interventional
Genistein in Treatment of Metastatic Colorectal Cancer
Genistein Combined With FOLFOX or FOLFOX-Avastin for Treatment of Metastatic Colorectal Cancer: Phase I/II Pilot Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Colorectal neoplasms are the third most common malignancies in the United States. Patients with metastatic (stage IV) colorectal cancer have a median life expectancy of 2 years. The response rates to chemotherapy range from 35-40%. Epidemiologic evidence suggests that soy compounds may reduce the incidence of colorectal cancers. Laboratory analyses demonstrate that genistein, a soy-derived compound, may inhibit Wnt signaling, a pathway activated in majority of colorectal cancers. Laboratory observations also demonstrate that genistein may augment growth inhibition when combined with chemotherapeutic agents of 5-Fluorouracil and platinum compounds. Based on pre-clinical data the investigators hypothesize that combining genistein with the standard of care chemotherapeutic regimens will reduce chemotherapy resistance and improve response rates in patients. The aim of the study is to add genistein to the regimens of FOLFOX or FOLFOX-Avastin in patients with newly diagnosed stage IV colon or rectal neoplasms.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colon Cancer | Malignant Colon Neoplasm | CURATED_EXACT | 0.92 |
| Colorectal Cancer | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
| Rectal Cancer | Malignant Rectal Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Genistein | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Genistein
- description
- Genistein combined with FOLFOX or FOLFOX-Avastin Genistein 60mg/day orally for 7 days every 2 weeks. Genistein will be administered beginning 4 days prior to FOLFOX or FOLFOX-Avastin and continuing the 3 days of chemotherapy.
- interventionNames
- Drug: Genistein
Primary outcomes (2)
- measure
- Number of Adverse Events
- timeFrame
- up to 6 months
- description
- Number of adverse events to assess tolerability of genistein treatment. Evaluation of side effects conducted every 14 days before each chemotherapy/genistein cycle.
- measure
- Percent Change in Tumor Size
- timeFrame
- end of Cycle 6
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria:
* Adult male and female patients ≥18 years old
* Have pathologically confirmed colon or rectal carcinoma
* Have metastatic (stage IV) disease
* Have a plan by treating physician to receive FOLFOX or FOLFOX-Avastin
* Have an Eastern Cooperative Oncology Group (ECOG) performance status ≤2
* Have adequate hematopoietic, hepatic and renal function
1. Hematopoietic function
* Hemoglobin ≥10g/dL
* Absolute Neutrophil Count(ANC) ≥1,500cells/mm2
* Platelet Count ≥100,000/µL
2. Hepatic Function
* Total bilirubin ≤ 1.5x the upper limit of normal
* ALT and AST must each be ≤2,5x the upper limits of normal
3. Renal Function
* Estimated creatinine clearance (Clcr) ≥30 mL/minute
* Are not pregnant and do not plan to become pregnant
Exclusion Criteria:
* Prior systemic chemotherapy for metastatic disease
* History of breast cancer, endometrial cancer or ovarian cancer or taking aromatase inhibitors or selective estrogen receptor modulators
* Patients taking MAO-inhibitors
* History of myocardial infarctions or cardiac stent placement less than 1 year before recruitment into the study
* Unable to give informed consent or comply with clinical trial requirements
* Uncontrolled hypertension
* History of clinically significant GI bleeding within prior 2 months prior to enrollment
* Presence of GI fistula
* Prior history of bowel perforation
* History of CNS thrombotic/embolic or ischemic events
* Have past or current, acute or chronic concurrent medical condition/illness or therapy that, in the opinion of the investigator, would make the subject unsuitable for the clinical trial or unable to comply with the follow up visits.References
Publications (26)
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- BACKGROUNDHu JF, Liu YY, Yu YK, Zhao TZ, Liu SD, Wang QQ. Diet and cancer of the colon and rectum: a case-control study in China. Int J Epidemiol. 1991 Jun;20(2):362-7. doi: 10.1093/ije/20.2.362. PMID 1917235
- BACKGROUNDNishi M, Yoshida K, Hirata K, Miyake H. Eating habits and colorectal cancer. Oncol Rep. 1997 Sep-Oct;4(5):995-8. doi: 10.3892/or.4.5.995. PMID 21590181
- BACKGROUNDKono S, Imanishi K, Shinchi K, Yanai F. Relationship of diet to small and large adenomas of the sigmoid colon. Jpn J Cancer Res. 1993 Jan;84(1):13-9. doi: 10.1111/j.1349-7006.1993.tb02777.x. PMID 8449821
- BACKGROUNDWitte JS, Longnecker MP, Bird CL, Lee ER, Frankl HD, Haile RW. Relation of vegetable, fruit, and grain consumption to colorectal adenomatous polyps. Am J Epidemiol. 1996 Dec 1;144(11):1015-25. doi: 10.1093/oxfordjournals.aje.a008872. PMID 8942431
- BACKGROUNDPereira MA, Barnes LH, Rassman VL, Kelloff GV, Steele VE. Use of azoxymethane-induced foci of aberrant crypts in rat colon to identify potential cancer chemopreventive agents. Carcinogenesis. 1994 May;15(5):1049-54. doi: 10.1093/carcin/15.5.1049.