PMID- 35307270 OWN - NLM STAT- MEDLINE DCOM- 20220517 LR - 20220520 IS - 1938-0690 (Electronic) IS - 1525-7304 (Linking) VI - 23 IP - 3 DP - 2022 May TI - Active Surveillance for Early Stage Lung Cancer. PG - 226-235 LID - S1525-7304(22)00012-2 [pii] LID - 10.1016/j.cllc.2022.01.001 [doi] AB - OBJECTIVES: Data describing outcomes for patients with early stage lung cancer who undergo expectant management is lacking, despite evidence of a sub-population with indolent malignancies. We used the National Cancer Data Base (NCDB) to identify factors associated with active surveillance for early stage lung cancer. Additionally, we sought to describe outcomes of three different care plans: active surveillance, no treatment, and Stereotactic Body Radiation Therapy (SBRT). METHODS: Patients diagnosed in 2010 to 2017 with early stage lung cancer who underwent active surveillance, no treatment, and SBRT were retrospectively identified in the NCDB. Multinomial logistic regression was used to assess care plan selection. Kaplan Meier analysis was used to assess overall survival (OS). RESULTS: We identified 30,107 patients that met our inclusion criteria: 838 (3%) underwent active surveillance, 6388 patients (21%) received no treatment, and 22,881 (76%) underwent SBRT. Black race (relative risk ratio (RRR): 1.66) and older age (RRR: 1.02) were significant positive predictors of active surveillance selection. Conversely, higher tumor stage (RRR: 0.26) and squamous cell carcinoma (RRR: 0.35) were significant negative predictors of active surveillance selection. Kaplan Meier analysis revealed a longer median OS associated with active surveillance compared to no treatment at 49.3 months versus 26.5 months, respectively. SBRT OS was 43.1 months. CONCLUSIONS: We identified a population of lung cancer patients who underwent expectant management with favorable outcomes. Additionally, we identified factors associated with active surveillance selection. The selection of active surveillance over no treatment was associated with significantly longer OS. CI - Copyright (c) 2022 Elsevier Inc. All rights reserved. FAU - Payne, Ryan G AU - Payne RG AD - University of Massachusetts Medical School, Worcester, MA. FAU - Anker, Christopher J AU - Anker CJ AD - University of Vermont Larner College of Medicine, Burlington, VT. FAU - Sprague, Brian L AU - Sprague BL AD - University of Vermont Larner College of Medicine, Burlington, VT. FAU - No, Hyunsoo J AU - No HJ AD - Stanford University, Radiation Oncology, Stanford, CA. FAU - Lin, Steven H AU - Lin SH AD - University of Texas MD Anderson Cancer Center, Houston, TX. FAU - Lester-Coll, Nataniel H AU - Lester-Coll NH AD - University of Vermont Larner College of Medicine, Burlington, VT. Electronic address: nataniel.lester-coll@med.uvm.edu. LA - eng PT - Journal Article DEP - 20220212 PL - United States TA - Clin Lung Cancer JT - Clinical lung cancer JID - 100893225 SB - IM MH - *Carcinoma, Non-Small-Cell Lung/pathology MH - Humans MH - *Lung Neoplasms/diagnosis/therapy MH - Neoplasm Staging MH - *Radiosurgery/adverse effects MH - Retrospective Studies MH - Treatment Outcome MH - Watchful Waiting OTO - NOTNLM OT - Cancer outcomes OT - Expectant Management OT - National Cancer Data Base OT - Non-Small Cell Lung Cancer OT - Stereotactic Body Radiation Therapy EDAT- 2022/03/22 06:00 MHDA- 2022/05/18 06:00 CRDT- 2022/03/21 05:33 PHST- 2021/09/24 00:00 [received] PHST- 2021/11/30 00:00 [revised] PHST- 2022/01/18 00:00 [accepted] PHST- 2022/03/22 06:00 [pubmed] PHST- 2022/05/18 06:00 [medline] PHST- 2022/03/21 05:33 [entrez] AID - S1525-7304(22)00012-2 [pii] AID - 10.1016/j.cllc.2022.01.001 [doi] PST - ppublish SO - Clin Lung Cancer. 2022 May;23(3):226-235. doi: 10.1016/j.cllc.2022.01.001. Epub 2022 Feb 12.