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Optimization of Erlotinib Plus Sulindac Dosing Regimens for Intestinal Cancer Prevention in an Apc-Mutant Model of Familial Adenomatous Polyposis (FAP).
Ulusan, Ahmet M; Rajendran, Praveen; Dashwood, Wan Mohaiza; Yavuz, Omer F; Kapoor, Sabeeta; Gustafson, Trace A; Savage, Michelle I; Brown, Powel H; Sei, Shizuko; Mohammed, Altaf; Vilar, Eduardo; Dashwood, Roderick H.
Afiliación
  • Ulusan AM; Center for Epigenetics and Disease Prevention, Texas A&M Health Science Center, Houston, Texas.
  • Rajendran P; Internal Medicine, Hackensack University Medical Center, Hackensack, New Jersey.
  • Dashwood WM; Center for Epigenetics and Disease Prevention, Texas A&M Health Science Center, Houston, Texas. rdashwood@tamu.edu prajendran@tamu.edu evilar@mdanderson.org.
  • Yavuz OF; Center for Epigenetics and Disease Prevention, Texas A&M Health Science Center, Houston, Texas.
  • Kapoor S; Center for Epigenetics and Disease Prevention, Texas A&M Health Science Center, Houston, Texas.
  • Gustafson TA; Center for Epigenetics and Disease Prevention, Texas A&M Health Science Center, Houston, Texas.
  • Savage MI; Center for Epigenetics and Disease Prevention, Texas A&M Health Science Center, Houston, Texas.
  • Brown PH; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Sei S; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Mohammed A; Chemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Rockville, Maryland.
  • Vilar E; Chemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Rockville, Maryland.
  • Dashwood RH; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas. rdashwood@tamu.edu prajendran@tamu.edu evilar@mdanderson.org.
Cancer Prev Res (Phila) ; 14(3): 325-336, 2021 03.
Article en En | MEDLINE | ID: mdl-33277315
ABSTRACT
A clinical trial in patients with familial adenomatous polyposis (FAP) demonstrated that sulindac plus erlotinib (SUL+ERL) had good efficacy in the duodenum and colon, but toxicity issues raised concerns for long-term prevention. We performed a biomarker study in the polyposis in rat colon (Pirc) model, observing phosphorylated Erk inhibition in colon polyps for up to 10 days after discontinuing ERL+SUL administration. In a follow-up study lasting 16 weeks, significant reduction of colon and small intestine (SI) tumor burden was detected, especially in rats given 250 ppm SUL in the diet plus once-a-week intragastric dosing of ERL at 21 or 42 mg/kg body weight (BW). A long-term study further demonstrated antitumor efficacy in the colon and SI at 52 weeks, when 250 ppm SUL was combined with once-a-week intragastric administration of ERL at 10, 21, or 42 mg/kg BW. Tumor-associated matrix metalloproteinase-7 (Mmp7), tumor necrosis factor (Tnf), and early growth response 1 (Egr1) were decreased at 16 weeks by ERL+SUL, and this was sustained in the long-term study for Mmp7 and Tnf. Based on the collective results, the optimal dose combination of ERL 10 mg/kg BW plus 250 ppm SUL lacked toxicity, inhibited molecular biomarkers, and exhibited effective antitumor activity. We conclude that switching from continuous to once-per-week ERL, given at one-quarter of the current therapeutic dose, will exert good efficacy with standard-of-care SUL against adenomatous polyps in the colon and SI, with clinical relevance for patients with FAP before or after colectomy. PREVENTION RELEVANCE This investigation concludes that switching from continuous to once-per-week erlotinib, given at one-quarter of the current therapeutic dose, will exert good efficacy with standard-of-care sulindac against adenomatous polyps in the colon and small intestine, with clinical relevance for patients with FAP before or after colectomy.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Pólipos del Colon / Genes APC / Neoplasias del Colon / Poliposis Adenomatosa del Colon / Neoplasias Intestinales / Mutación Tipo de estudio: Observational_studies / Prognostic_studies Límite: Animals Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Pólipos del Colon / Genes APC / Neoplasias del Colon / Poliposis Adenomatosa del Colon / Neoplasias Intestinales / Mutación Tipo de estudio: Observational_studies / Prognostic_studies Límite: Animals Idioma: En Año: 2021 Tipo del documento: Article