In this issue of Cancer, Desai et al have described the financial conflict of interest (FCOI) disclosures among panelists on the National Comprehensive Cancer Network (NCCN) clinical practice guidelines committees. 1 Not surprisingly, they documented that the vast majority of panelists complete their FCOI disclosures as required, but that nearly one-half, including chairs, have declared FCOIs. The authors also clearly demonstrated how NCCN processes are not fully compliant with recommendations regarding FCOI management for guideline committees as promulgated by the Institute of Medicine (IOM). 1 None of this should be surprising, and many of these findings have been described previously for guideline committees, 2,3 clinical trial publications, 4 and educational speakers 5 in oncology as well as other fields. 6,7 What perhaps is notable for this publication is the set of specific suggestions made by the authors regarding how NCCN guideline committees could come into closer alignment with IOM recommendations. More specifically, Desai et al suggested that chairs and vice chairs should be free of all FCOIs, that committee members with FCOIs play a limited role in the rating process and be restricted from any formal voting on guidelines, and that the guidelines be rated according to standardized criteria (see for example https://www.leitl inien watch.de/engli sh-crite ria/). 1 This brings us to 4 important questions: 1) Are FCOIs significant within the context of clinical recommendations? 2) Are FCOIs the only important conflicts? 3) Is disclosure as the principal approach for FCOI sufficient? 4) Are the recommendations pragmatic? Although a full discourse herein could be the subject of a weighty tome, or an entire academic career, a few comments, observations, and opinions may be helpful. First, there is an extensive literature demonstrating that even trivial remunerations introduce bias, and in fact a multibillion dollar pharmaceutical marketing industry has successfully used pens, lunches, tote bags, and other "trivial" gifts to induce the use of their products. More important is how this bias impacts NCCN or other guideline recommendations. There likely is minimal impact on guidelines based on data from phase 3 clinical trials with clinically validated, accepted endpoints despite the usual debates regarding the quality of the study and appropriateness of the control. However, NCCN guidelines describe "category 1" evidence as "based upon high-level evidence, [and] there is uniform NCCN consensus that the intervention is appropriate." Notably, only approximately 16% of NCCN recommendations are based on a randomized phase 3 trial. 8 Although it essentially is impossible to base all oncology treatment decisions on phase 3 data, and recommendations often must be based on lower level evidence, there is an inescapable conclusion that FCOIs influence NCCN recommendations. The vast majority of the literature and public discourse regarding COIs is focused on FCOIs. However, it is important to point out that academic resear...