{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,31]],"date-time":"2026-08-31T01:25:55Z","timestamp":1788139555237,"version":"build-2803163510"},"reference-count":13,"publisher":"American Medical Association (AMA)","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec>\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>The impact of patient-specific, disease-related, and social factors on outcomes in limited-stage small cell lung cancer (LS-SCLC) is not well defined. A post hoc secondary analysis of such factors from the Cancer and Leukemia Group B (CALGB) 30610\u2013Radiation Therapy Oncology Group (RTOG) 0538 trial may impact future trial design.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To assess the comprehensive demographic, disease-related, treatment-related, and social factors for potential associations with survival outcomes and understand whether specific subpopulations may benefit from radiotherapy (RT) dose escalation in LS-SCLC.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This post hoc secondary analysis of a randomized clinical trial included 638 adults with LS-SCLC treated at 186 unique treatment sites with at least 1 accrual for all patients from March 15, 2008, to December 1, 2019; 313 patients were randomized to receive RT twice daily to a dosage of 45 Gy for 3 weeks and 325 to receive RT once daily to a dosage of 70 Gy for 7 weeks. Data were locked February 28, 2022, and analyzed from November 28, 2022, to June 4, 2024.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interventions<\/jats:title>\n                    <jats:p>Twice-daily RT or once-daily RT.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Multivariable Cox proportional hazards models evaluated the association of treatment groups and other risk factors with progression-free survival (PFS) and overall survival (OS). Patient-specific factors included age, sex, and Eastern Cooperative Oncology Group performance status. Disease-related factors included tumor, nodal, and overall cancer stages. Treatment-related factors included type of chemotherapy, timing of concurrent RT, RT technique, and prophylactic cranial irradiation. Social factors included marital status and treatment center accrual volume.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among 507 patients (260 [51.3%] female and 247 [48.7%] male; mean [SD] age, 62.6 [7.9] years) included in the multivariate survival analysis, with a median follow-up of 4.7 (IQR, 3.7-7.1) years, female sex was associated with improved OS (hazard ratio [HR],\u20090.73 [95% CI, 0.58-0.91];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.006), while being 70 years or older was associated with decreased OS (HR,\u20091.50 [95% CI, 1.14-1.98];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.004). Neither age nor sex was associated with PFS. When compared with those with N1 disease, OS and PFS were worse in patients with N2 (HRs,\u20091.64 [95% CI, 1.19-2.26];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.002 and 1.36 [95% CI, 1.02-1.81];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.04, respectively) and N3 (HRs,\u20092.03 [95% CI, 1.40-2.93];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001 and 1.63 [95% CI, 1.17-2.26];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.004) disease. Compared with stage II cancer, OS was worse for stage IIIA (HR,\u20091.65 [95% CI, 1.17-2.31];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.004) and stage IIIB (HR,\u20091.94 [95% CI, 1.34-2.83];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). Compared with high-volume accrual centers, treatment at low- or middle-volume accrual centers was associated with worse PFS (HRs,\u20091.94 [95% CI, 1.33-2.82;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001] and 1.44 [95% CI, 1.15-1.82;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.002], respectively) and worse OS (HRs,\u20091.55 [95% CI, 1.03-2.32;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.03] and 1.33 [95% CI, 1.04-1.70;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.02], respectively).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>This secondary analysis of the CALGB 30610\u2013RTOG 0538 randomized clinical trial of patients with LS-SCLC found associations between female sex or being younger than 70 years and improved overall survival and between advanced nodal stage or treatment at low- or middle-volume accrual centers and worse outcomes. These findings suggest that stratification by nodal stage, clinical stage, and age should be considered in future randomized trials.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Trial Registration<\/jats:title>\n                    <jats:p>\n                      ClinicalTrials.gov Identifier:\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/www.clinicaltrials.gov\/study\/NCT00632853\">NCT00632853<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2024.40673","type":"journal-article","created":{"date-parts":[[2024,10,24]],"date-time":"2024-10-24T11:32:04Z","timestamp":1729769524000},"page":"e2440673","source":"Crossref","is-referenced-by-count":13,"title":["Prognostic Factors in Limited-Stage Small Cell Lung Cancer"],"prefix":"10.1001","volume":"7","author":[{"given":"Michael K.","family":"Farris","sequence":"first","affiliation":[{"name":"Department of Radiation Oncology, Wake Forest Medical University, Winston-Salem, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael D.","family":"Mix","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, SUNY Upstate Medical University, Syracuse, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaofei","family":"Wang","sequence":"additional","affiliation":[{"name":"Alliance Statistics and Data Management Center, Duke University, Durham, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brandy","family":"Jaszewski","sequence":"additional","affiliation":[{"name":"Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nathan","family":"Foster","sequence":"additional","affiliation":[{"name":"Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gregory A.","family":"Masters","sequence":"additional","affiliation":[{"name":"Helen F. Graham Cancer Center, Newark, Delaware"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fran","family":"Laurie","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, University of Massachusetts Chan Medical School, Worcester, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Koren","family":"Smith","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, University of Massachusetts Chan Medical School, Worcester, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Niema B.","family":"Razavian","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, Wake Forest Medical University, Winston-Salem, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ryan S.","family":"Alden","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, SUNY Upstate Medical University, Syracuse, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ritsuko","family":"Komaki","sequence":"additional","affiliation":[{"name":"University of Texas M. 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Anderson Cancer Center, Houston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas E.","family":"Stinchcombe","sequence":"additional","affiliation":[{"name":"Division of Medical Oncology, Duke Cancer Institute, Duke University, Durham, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jeffrey D.","family":"Bradley","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Everett E.","family":"Vokes","sequence":"additional","affiliation":[{"name":"Department of Medicine, University of Chicago, Chicago, Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jeffrey","family":"Bogart","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, SUNY Upstate Medical University, Syracuse, New 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