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Currently, no formal recommendations exist for lung cancer screening in PJS. This structured narrative review compares lung cancer risk in PJS with lung cancer risk in individuals currently eligible for screening based on age and smoking history. PubMed and Web of Science were searched from 1\/1\/1980 to 9\/11\/2023 using the terms \u201cPeutz-Jeghers Syndrome\u201d AND \u201cCancer.\u201d Studies reporting lung cancer risk in PJS were included. Reported lung cancer risks were compared to 5-year, 10-year, and lifetime lung cancer risks in the general population based on age and pack-years of smoking. Seventeen studies were included. Across the studies, the incidence of lung cancer ranged from 0.8 to 13.3%. Studies that included lung cancer risk relative to the general population reported a relative risk range of 2.9\u201322.9. Cumulative risk was reported in 5 studies and surpassed 5% by age 60 (range 7 to 17%). Guidelines for low-dose CT (LDCT) lung cancer screening for individuals aged 50\u201380 with a smoking history of at least 20 pack-years are associated with a similar or higher threshold for lung cancer risk. The lifetime lung cancer risk for individuals with PJS is similar to current guideline-based risk thresholds for screening based on age and smoking status. Given their elevated lifetime risk, individuals with PJS may be candidates for LDCT for lung cancer screening and should be formally studied to elucidate the risks, benefits, and optimal implementation in this patient population.\n                  <\/jats:p>","DOI":"10.1007\/s10689-026-00587-8","type":"journal-article","created":{"date-parts":[[2026,7,3]],"date-time":"2026-07-03T05:58:05Z","timestamp":1783058285000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Peutz-Jeghers Syndrome and lung cancer: does the risk meet the threshold for lung cancer screening?"],"prefix":"10.1007","volume":"25","author":[{"given":"Faizah","family":"Shareef","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mounica","family":"Konjeti","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Samir","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer M.","family":"Weiss","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2026,7,3]]},"reference":[{"key":"587_CR1","doi-asserted-by":"publisher","first-page":"442","DOI":"10.1097\/MPG.0000000000002248","volume":"68","author":"A Latchford","year":"2019","unstructured":"Latchford A, Cohen S, Auth M, Scaillon M, Viala J, Daniels R et al (2019) Management of Peutz-Jeghers Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group. 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