TY - JOUR
T1 - Modified citrus pectin treatment in non-metastatic biochemically relapsed prostate cancer
T2 - Results of a prospective phase ii study
AU - Keizman, Daniel
AU - Frenkel, Moshe
AU - Peer, Avivit
AU - Kushnir, Igal
AU - Rosenbaum, Eli
AU - Sarid, David
AU - Leibovitch, Ilan
AU - Mano, Roy
AU - Yossepowitch, Ofer
AU - Margel, David
AU - Wolf, Ido
AU - Geva, Ravit
AU - Dresler, Hadas
AU - Rouvinov, Keren
AU - Rapoport, Noa
AU - Eliaz, Isaac
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12
Y1 - 2021/12
N2 - Optimal therapy of biochemically relapsed prostate cancer (BRPC) after local treatment is elusive. An established modified citrus pectin (PectaSol®, P-MCP), a dietary polysaccharide, is an established antagonist of galectin-3, a carbohydrate-binding protein involved in cancer pathogenesis. Based on PSA dynamics, we report on the safety and the primary outcome analysis of a prospective phase II study of P-MCP in non-metastatic BRPC based. Sixty patients were enrolled, and one patient withdrew after a month. Patients (n = 59) were given P-MCP, 4.8 grams X 3/day, for six months. The primary endpoint was the rate without PSA progression and improved PSA doubling time (PSADT). Secondary endpoints were the rate without radiologic progression and toxicity. Patients that did not progress by PSA and radiologically at six months continued for an additional twelve months. After six months, 78% (n = 46) responded to therapy, with a decreased/stable PSA in 58% (n = 34), or improvement of PSADT in 75% (n = 44), and with negative scans, and entered the second twelve months treatment phase. Median PSADT improved significantly (p = 0.003). Disease progression during the first 6 months was noted in only 22% (n = 13), with PSA progression in 17% (n = 10), and PSA and radiologic progression in 5% (n = 3). No patients developed grade 3 or 4 toxicity.
AB - Optimal therapy of biochemically relapsed prostate cancer (BRPC) after local treatment is elusive. An established modified citrus pectin (PectaSol®, P-MCP), a dietary polysaccharide, is an established antagonist of galectin-3, a carbohydrate-binding protein involved in cancer pathogenesis. Based on PSA dynamics, we report on the safety and the primary outcome analysis of a prospective phase II study of P-MCP in non-metastatic BRPC based. Sixty patients were enrolled, and one patient withdrew after a month. Patients (n = 59) were given P-MCP, 4.8 grams X 3/day, for six months. The primary endpoint was the rate without PSA progression and improved PSA doubling time (PSADT). Secondary endpoints were the rate without radiologic progression and toxicity. Patients that did not progress by PSA and radiologically at six months continued for an additional twelve months. After six months, 78% (n = 46) responded to therapy, with a decreased/stable PSA in 58% (n = 34), or improvement of PSADT in 75% (n = 44), and with negative scans, and entered the second twelve months treatment phase. Median PSADT improved significantly (p = 0.003). Disease progression during the first 6 months was noted in only 22% (n = 13), with PSA progression in 17% (n = 10), and PSA and radiologic progression in 5% (n = 3). No patients developed grade 3 or 4 toxicity.
KW - Modified citrus pectin
KW - Non-metastatic biochemically relapsed prostate cancer
KW - PSA doubling time
KW - PectaSol
UR - http://www.scopus.com/inward/record.url?scp=85120038899&partnerID=8YFLogxK
U2 - 10.3390/nu13124295
DO - 10.3390/nu13124295
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C2 - 34959847
AN - SCOPUS:85120038899
SN - 2072-6643
VL - 13
JO - Nutrients
JF - Nutrients
IS - 12
M1 - 4295
ER -