Background/Aim: Neoadjuvant concurrent chemoradiotherapy (nCCRT) is the standard of care for locally advanced rectal cancer (LARC) patients treated with neoadjuvant concurrent chemoradiotherapy (nCCRT). The aim of this study was to compare intensity-modulated radiotherapy (IMRT) to 3D conformal radiotherapy (3DCRT) in nCCRT patients. Patients and Methods: We identified LARC patients diagnosed from 2007 to 2015 through the Taiwan cancer registry (TCR) and we constructed a propensity score matched cohort to compare IMRT to 3DCRT after balancing observable potential confounders. We compared the hazard ratio (HR) of death as well as other endpoints between the IMRT and 3DCRT. We performed supplementary analysis (SA) when additional potential confounders were considered. Results: Our study population consisted of 696 patients. There was no statistical difference when IMRT was compared to 3DCRT (HR for death=1.01, 95%confidence interval(CI)=0. 76-1.35, p=0.93). There were also no statistical differences for the other endpoints or SA. Conclusion: For LARC patients treated with nCCRT, the treatment outcome has no statistically significant benefit between those treated with IMRT or 3DCRT.Rectal cancer is one of the leading cancers responsible for mortality worldwide (1). Radiotherapy is an important tool for locally advanced rectal cancer (LARC), while neoadjuvant concurrent chemoradiotherapy (nCCRT) has been the common standard of care for decades (2-4).Intensity-modulated radiotherapy (IMRT) is a 2nd generation advanced radiotherapy technology that allows highly conformal dose distribution (5). IMRT has been advocated for many cancer types, such as head-and-neck cancer, lung cancer, and prostate cancer (6-8), however, its role in rectal cancer was still debated in the current guidelines (9). A review paper published in 2016 stated: "There were no randomized control trials or prospective studies comparing IMRT with three-dimensional conformal radiotherapy (3DCRT) in rectal cancer", and none of the eight clinical studies mentioned in this review were population-based (10). Another systematic review published in 2018 also stated "Due to the sensitivity of IMRT to geometric errors, one might be concerned of the risk of missing the target volume, which can consequently affect oncologic outcomes" (11). This systematic review reported lower toxicity with IMRT (11). However, a landmark single arm phase II study (Radiation Therapy Oncology Group 0822) had reported that the use of IMRT in neoadjuvant chemoradiation for rectal cancer does not reduce the rate of GI toxicity (12). We have found only one relevant population-based study reporting the survival outcome of rectal cancer patients from North America (13). Due to the controversy of IMRT and the lack of population-based studies for rectal cancer, we aimed to compare the outcomes of locally advanced rectal cancer patients treated with neoadjuvant concurrent chemoradiotherapy (with IMRT versus 3DCRT) in this large population-based propensity score-matched analysis.