4.5 Article

Sequential Versus Concurrent Chemoradiation Therapy by Surgical Margin Status in Resected Non-Small Cell Lung Cancer

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HARBORSIDE PRESS
DOI: 10.6004/jnccn.2018.7007

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  1. Elekta
  2. STCube Pharmaceuticals
  3. Peregrine
  4. Bayer
  5. Roche/Genentech

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Background: Postoperative chemoradiotherapy (CRT) for non-small cell lung cancer (NSCLC) can be delivered sequentially (sCRT) or concurrently (cCRT). Without high-volume data, current guidelines recommend either option for patients with negative margins (M-) and cCRT for those with positive margins (M+). In this study, survival was compared between sCRT versus cCRT for M-and M+ disease; survival in patients who underwent sCRT was also assessed with chemotherapy-first versus radiotherapy (RT)-first. Methods: The National Cancer Database was queried for patients with primary NSCLC undergoing surgery followed by CRT. Patients were excluded if they received neoadjuvant chemotherapy or RT. Both M-and M+ (including R1 and R2) subcohorts were evaluated. Multivariable logistic regression ascertained factors associated with cCRT delivery. Kaplan-Meier analysis evaluated overall survival (OS); Cox proportional hazards modeling determined variables associated with OS. Propensity score matching aimed to address group imbalances and indication biases. Results: Of 4,921 total patients, 3,475 (71%) were M-, 1,446 (29%) were M+, 2,271 (46%) received sCRT, and 2,650 (54%) underwent cCRT. Median OS among the sCRT and cCRT groups in patients who were M-was 54.6 versus 39.5 months, respectively (P<. 001); differences persisted following propensity score matching (P<. 001). In the overall M+ cohort, outcomes for sCRT and cCRT were 36.3 versus 30.5 months (P=. 011), but showed equipoise following matching (P=. 745). In the R1 and R2 subsets, no differences in OS were seen between cohorts (P=. 368 and.553, respectively). When evaluating the sCRT population, there were no OS differences between chemotherapy-first and RT-first after matching (P=. 229). Conclusions: Postoperative sCRT was associated with improved survival compared with cCRT in patients with M-disease, with statistical equipoise in those with M+ disease. Differential sequencing of sCRT does not appear to affect survival.

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