2016
DOI: 10.1093/jjco/hyw086
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Therapeutic approaches for patients with coexisting familial adenomatous polyposis and colorectal cancer

Abstract: In patients with familial adenomatous polyposis and colorectal cancer, primary surgery, metastasectomy and chemotherapy could be compatible with standard surgical approaches for familial adenomatous polyposis . However, modifying surgical procedures for familial adenomatous polyposis might help multimodality therapy for Stage IV colorectal cancer to prolong survival.

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Cited by 9 publications
(3 citation statements)
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“…In our study, metachronous rectal cancer was the most common cause of death. In previous studies, the surveillance period was approximately 5-10 years, and long-term prognosis of metachronous rectal cancer remains unknown (11,(14)(15)(16)(17). In our study, the median surveillance period was 169 months.…”
Section: Discussionmentioning
confidence: 61%
See 1 more Smart Citation
“…In our study, metachronous rectal cancer was the most common cause of death. In previous studies, the surveillance period was approximately 5-10 years, and long-term prognosis of metachronous rectal cancer remains unknown (11,(14)(15)(16)(17). In our study, the median surveillance period was 169 months.…”
Section: Discussionmentioning
confidence: 61%
“…The findings of this study can be expected to substantially impact the recommendations of surveillance for FAP. In the past, CRC was the most common reason for death in patients with FAP (14,15). Metachronous rectal cancer after IRA was reported to account for nearly one-fifth of FAP-related causes of death (16).…”
Section: Discussionmentioning
confidence: 99%
“…FAP was classified into the following three types according to the number of colorectal adenomas: profuse type (>1,000), sparse type (between 100 and 1,000), and attenuated type (between 10 and 99) [8]. The details of the treatment were reported previously [16]; the most common procedure for FAP was restorative proctocolectomy with ileal pouch anal anastomosis, irrespective of the phenotype.…”
Section: Original Data Sources and Patient Selectionmentioning
confidence: 99%