Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey

被引:4
|
作者
Mraz, Kathryn A. [1 ,2 ]
Hodan, Rachel [3 ]
Rodgers-Fouche, Linda [4 ]
Arora, Sanjeevani [5 ]
Balaguer, Francesc [6 ]
Guillem, Jose G. [7 ]
Jeter, Joanne M. [8 ]
Kanth, Priyanka [9 ]
Li, Dan [10 ]
Liska, David [11 ,12 ]
Melson, Joshua [13 ]
Perez, Kimberly [14 ]
Ricker, Charite [15 ]
Shirts, Brian H. [16 ]
Vilar, Eduardo [17 ]
Katona, Bryson W. [18 ]
Dominguez-Valentin, Mev [19 ]
机构
[1] Grey Genet, Dept Genet, Brooklyn, NY USA
[2] Ctr Genom Interpretat, Res Dept, Sandy, UT USA
[3] Stanford Hlth Care, Canc Genet, Palo Alto, CA USA
[4] Massachusetts Gen Hosp, Ctr Canc Risk Assessment, Boston, MA USA
[5] Fox Chase Canc Ctr, Canc Prevent & Control Program, Philadelphia, PA USA
[6] Univ Barcelona, Hosp Clin Barcelona, Inst Invest Biomed August Pi i Sunyer IDIBAPS, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Barcelona, Spain
[7] Univ North Carolina Chapel Hill, Div Gastrointestinal Surg, Chapel Hill, NC USA
[8] Univ Utah, Huntsman Canc Inst, Dept Internal Med, Salt Lake City, UT USA
[9] MedStar Georgetown Univ Hosp, Dept Gastroenterol, Washington, DC USA
[10] Kaiser Permanente Med Ctr, Dept Gastroenterol, Santa Clara, CA USA
[11] Cleveland Clin, Dept Colorectal Surg, Cleveland, OH USA
[12] Cleveland Clin, Digest Dis & Surg Inst, Sanford R Weiss MD Ctr Hereditary Colorectal Neop, Cleveland, OH USA
[13] Univ Arizona, Canc Ctr, Div Gastroenterol, Tucson, AZ USA
[14] Harvard Med Sch, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[15] Univ Southern Calif, Keck Sch Med, Dept Med, Div Med Oncol, Los Angeles, CA USA
[16] Univ Washington, Dept Lab Med & Pathol, Seattle, WA USA
[17] Univ Texas MD Anderson Canc Ctr, Dept Clin Canc Prevent, Houston, TX USA
[18] Univ Penn, Perelman Sch Med, Div Gastroenterol & Hepatol, Philadelphia, PA USA
[19] Norwegian Radium Hosp, Inst Canc Res, Dept Tumor Biol, Oslo, Norway
来源
FRONTIERS IN ONCOLOGY | 2023年 / 13卷
关键词
chemoprevention; CRC; Lynch syndrome; Familial adenomatous polyposis; FAP; barriers; aspirin; HEREDITARY COLORECTAL-CANCER; GASTROINTESTINAL CANCER; EUROPEAN-SOCIETY; TASK-FORCE; ASPIRIN; MANAGEMENT; PREVENTION; GUIDELINES; RECOMMENDATIONS; EFFICACY;
D O I
10.3389/fonc.2023.1141810
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundInternational chemoprevention preferences and approaches in Lynch syndrome (LS) and APC-associated polyposis, including Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP) have not been previously explored. AimTo describe current chemoprevention strategies for patients with LS or FAP/AFAP (referred to collectively as FAP) practiced by members of four international hereditary cancer societies through administration of a survey. ResultsNinety-six participants across four hereditary gastrointestinal cancer societies responded to the survey. Most respondents (91%, 87/96) completed information regarding their demographics and practice characteristics relating to hereditary gastrointestinal cancer and chemoprevention clinical practices. Sixty-nine percent (60/87) of respondents offer chemoprevention for FAP and/or LS as a part of their practice. Of the 75% (72/96) of survey respondents who were eligible to answer practice-based clinical vignettes based off of their responses to ten barrier questions regarding chemoprevention, 88% (63/72) of those participants completed at least one case vignette question to further characterize chemoprevention practices in FAP and/or LS. In FAP, 51% (32/63) would offer chemoprevention for rectal polyposis, with sulindac - 300 mg (18%, 10/56) and aspirin (16%, 9/56) being the most frequently selected options. In LS, 93% (55/59) of professionals discuss chemoprevention and 59% (35/59) frequently recommend chemoprevention. Close to half of the respondents (47%, 26/55) would recommend beginning aspirin at time of commencement of the patient's first screening colonoscopy (usually at age 25yrs). Ninety-four percent (47/50) of respondents would consider a patient's diagnosis of LS as an influential factor for aspirin use. There was no consensus on the dose of aspirin (<= 100 mg, >100 mg - 325 mg or 600 mg) to offer patients with LS and there was no agreement on how other factors, such as BMI, hypertension, family history of colorectal cancer, and family history of heart disease, would affect the recommendation for aspirin use. Possible harm among older patients (>70 years) was identified as the most common reason to discourage aspirin use. ConclusionAlthough chemoprevention is widely discussed and offered to patients with FAP and LS by an international group of hereditary gastrointestinal cancer experts, there is significant heterogeneity in how it is applied in clinical practice.
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页数:15
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