{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T15:42:49Z","timestamp":1792510969811,"version":"4.5.0"},"reference-count":46,"publisher":"American Medical Association (AMA)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi260179-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Taxane-induced peripheral neuropathy (TIPN) affects quality of life and ability to complete cancer treatment and has limited effective interventions for prevention and treatment.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260179-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To develop and validate a TIPN risk prediction model.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260179-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>SWOG S1714 was a prospective observational cohort study conducted at sites in the National Cancer Institute National Community Oncology Research Program between March 1, 2019, and November 15, 2021, with 3 years of follow-up. The study included evaluable participants 18 years or older with stage I to III lung, breast, or ovarian, fallopian tube, or primary peritoneal cancer who were starting taxane-based treatment. Statistical analysis was conducted from December 2023 to June 2024.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260179-7\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>Taxane-based regimens including paclitaxel or docetaxel.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260179-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>\n                      The primary end point was occurrence of TIPN by 24 weeks. TIPN was assessed using the patient-reported European Organization of Research and Treatment of Cancer Quality of Life Questionnaire\u2013Chemotherapy-Induced Peripheral Neuropathy 20-item scale (CIPN-20) at baseline and weeks 4, 8, 12, and 24. Occurrence of TIPN was defined as an increase of 8 points or more over baseline in the CIPN-20 sensory subscale score. With a 60% random sample of evaluable participants, best-subset selection using logistic regression and\n                      <jats:italic toggle=\"yes\">k<\/jats:italic>\n                      -fold cross-validation identified a best model based on demographic factors, baseline comorbid conditions, and treatment factors. Adverse risk factors were summed, generating a score, split at the median and tested in the remaining 40% of evaluable participants. The target difference was 12% between high-risk vs low-risk groups.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260179-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>A total of 1336 participants enrolled in S1714. Of 1278 evaluable participants (median age, 55.0 years [range, 23.0-84.0 years]; 1264 women [98.9%]; 1164 with breast cancer [91.1%]), 804 (62.9%) experienced TIPN by week 24. Using the training set of 768 participants, a risk prediction model for TIPN was developed that included 5 adverse risk factors: receipt of paclitaxel; stage II or III disease; planned taxane duration of more than 12 weeks; diabetes, autoimmune disease, moderate kidney disease, or a neurologic condition; and self-identified race and ethnicity (Black, Hispanic, Native American, Pacific Islander, multiple races, or unknown race or ethnicity). In the test set of 510 participants, TIPN was more common in high-risk (235 of 345 [68.1%]) vs low-risk (84 of 165 [50.9%]) groups (absolute difference, 17.2%), exceeding the 12% target.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260179-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this cohort study of participants with early-stage cancer receiving a taxane regimen, a set of baseline risk factors stratified TIPN risk. A risk prediction model may guide treatment decision-making, symptom monitoring, and enrollment in interventional trials for TIPN prevention and treatment.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2026.4901","type":"journal-article","created":{"date-parts":[[2026,4,10]],"date-time":"2026-04-10T15:30:56Z","timestamp":1775835056000},"page":"e264901","source":"Crossref","is-referenced-by-count":3,"title":["Risk Prediction Model for Taxane-Induced Peripheral Neuropathy in Early-Stage Cancer"],"prefix":"10.1001","volume":"9","author":[{"given":"Meghna S.","family":"Trivedi","sequence":"first","affiliation":[{"name":"Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joseph M.","family":"Unger","sequence":"additional","affiliation":[{"name":"SWOG Cancer Research Network Statistics and Data Management Center, Seattle, Washington"},{"name":"Fred Hutch Cancer Center, Seattle, Washington"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N. 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