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Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Long-Term Results of a
Daniel Keizman1, Moshe Frenkel2, Avivit Peer2
1Department of Oncology, Tel Aviv Sourasky Medical Center, School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Nutrients
|August 26, 2023
Summary
Modified citrus pectin (P-MCP) shows promise for treating non-metastatic biochemically relapsed prostate cancer (BRPC-M0). Extended treatment demonstrated durable efficacy and safety in patients, with significant improvements in PSA doubling time.
Area of Science:
- Oncology
- Nutritional Biochemistry
- Urology
Background:
- Optimal therapy for non-metastatic biochemically relapsed prostate cancer (BRPC-M0) remains undefined.
- There is a need for non-toxic therapeutic options for BRPC-M0 patients.
- Modified citrus pectin (P-MCP), a GRAS-categorized food supplement, inhibits galectin-3, a protein implicated in cancer progression.
Purpose of the Study:
- To evaluate the long-term efficacy and safety of P-MCP in BRPC-M0 patients.
- To assess the durability of P-MCP treatment beyond an initial 6-month period.
Main Methods:
- Phase 2 study extension involving 39 BRPC-M0 patients continuing P-MCP therapy (4.8 g × 3/day) for an additional 12 months.
- Patients were selected based on lack of disease progression during the initial 6 months of P-MCP treatment.
- Outcomes assessed included prostate-specific antigen (PSA) levels, PSA doubling time (PSADT), and imaging scans over a total of 18 months.
Main Results:
- 85% of patients achieved a durable long-term response after 18 months of P-MCP treatment.
- 62% experienced decreased or stable PSA levels, and 90% showed improved PSADT.
- All patients maintained negative imaging scans, and no grade 3/4 toxicity was reported.
Conclusions:
- P-MCP demonstrates potential for long-term, durable efficacy in managing BRPC-M0.
- P-MCP exhibits a favorable safety profile with no severe toxicities observed.
- Modified citrus pectin represents a safe and potentially effective therapeutic strategy for non-metastatic biochemically relapsed prostate cancer.

