The Journal of Thoracic and Cardiovascular Surgery

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Accepted Manuscript Rightsizing Lung Cancer Surveillance Farhood Farjah, MD, MPH, Larry Kessler, ScD PII: S0022-5223(18)32803-4 DOI: https://doi.org/10.1016/j.jtcvs.2018.10.046 Reference: YMTC 13618 To appear in: The Journal of Thoracic and Cardiovascular Surgery Received Date: 10 October 2018 Accepted Date: 10 October 2018 Please cite this article as: Farjah F, Kessler L, Rightsizing Lung Cancer Surveillance, The Journal of Thoracic and Cardiovascular Surgery (2018), doi: https://doi.org/10.1016/j.jtcvs.2018.10.046. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

1 Rightsizing Lung Cancer Surveillance 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 Farhood Farjah, MD, MPH 1, and Larry Kessler, ScD 2 1 Department of Surgery, University of Washington, Seattle, WA 2 Department of Health Services, University of Washington, Seattle, WA Conflicts of Interest: None Corresponding Author: Farhood Farjah, MD MPH University of Washington 1959 NE Pacific Street Box 356310 Seattle, WA 98195 Email: ffarjah@uw.edu Central Message A pragmatic trial comparing varying intensities of surveillance among lung cancer survivors can overcome the limitations of observational studies and potentially lead to more efficient use of imaging. 24 25 Central Picture Farhood Farjah, MD, MPH and Larry Kessler, ScD 1

1 2 Among operated lung cancer patients, the risk of recurrence peaks in the first two years after surgery and the risk of a new primary lung cancer is substantially higher than the general 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 population. 1 The intent of surveillance imaging is to detect both recurrent and new lung cancers early when the disease is curable. Two investigations published in this month s Journal provide evidence that surveillance imaging may be beneficial. Both studies report 1) high rates of early-detection; 2) high rates of treatment for recurrence or new primary lung cancer; and 3) high 5-year survival rates for treated patients. 2-3 Wang s study also provides a novel description of prevalent (i.e. synchronous) lung cancers among survivors undergoing surveillance. 2 However, Subramanian s investigation using a unique data source consisting of tumor registry (not administrative) data supplemented by human chart abstraction reveals no relationship between survival and the intensity of surveillance. 3 This finding sounds a cautionary note about the possible benefits of intense imaging surveillance. Despite the strengths of these two carefully conducted investigations, the evidence base supporting lung cancer surveillance remains weak owing to the limitations of observational study designs. Limitations such as lead and length time bias, confounding, and time-varying surveillance imaging are examples of potential threats to the validity of observational studies. 4-5 A randomized trial can overcome these limitations if we can agree on the most important question to answer. Preliminary findings from a French trial randomizing subjects to CT versus chest x-ray surveillance showed no effect of surveillance on survival. 6-7 There is likely no appetite for repeating a similar trial given prevailing, strong beliefs in North America in favor of surveillance imaging with CT. Even though there is no evidence to date that surveillance imaging causes patient harm, it is possible that we overutilize imaging without any benefit to the 24 25 26 patient. A trial could be conducted to compare outcomes across two extremes of surveillance intensity (e.g. CT every 3 versus 12 months; 8 versus 2 scans over a two-year surveillance period, with annual follow-up imaging thereafter in both groups). Contrasting two extremes is 1

27 28 more likely to reveal an effect of surveillance imaging on survival if one really exists. Such a trial would close a significant knowledge gap over the optimal intensity of surveillance imaging, and 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 therefore make a large impact on the delivery of lung cancer care. However, this trial would be expensive. A value-of-information analysis estimates the return on investment from conducting such a study 8 and may provide the justification to move forward with a large, multi-center pragmatic trial. Given how much we have learned from investigations such as the National Lung Screening Trial and the National Emphysema Treatment Trial 9-10, thoracic surgeons should provide the leadership and advocacy necessary to pursue a lung cancer surveillance trial. 50 51 52 2

53 54 References 1. Lou F, Huang J, Sima CS, Dycoco J, Rusch V, Bach PB. Patterns of recurrence and second 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 primary lung cancer in early-stage lung cancer survivors followed with routine computed tomography surveillance. J Thorac Cardiovasc Surg. 2013 Jan;145(1):75-81. 2. Wang Y, Yeung J, Hanna WC, Allison F, Paul NS, Waddell TK, et. al. Metachronous or synchronous primary lung cancer in the era of computed tomography surveillance. J Thorac Cardiovasc Surg (in press 2018). 3. Subramanian M, Liu J, Greenberg C, Schumacher J, Chang GJ, McMurry TL, et. al. Imaging surveillance for surgically resected stage 1 I non-small cell lung cancer: is more always better? J Thorac Cardiovasc Surg (in press 2018). 4. Weiss NS, Rossing MA. Healthy screened bias in epidemiologic studies of cancer incidence. 1996 May;7(3):319-22. 5. Chubak J, Boudreau DM, Wirtz HS, McKnight B, Weiss NS. Threats to validity of nonrandomized studies of postdiagnosis exposures on cancer recurrence and survival. J Natl Cancer Inst. 2013 Oct 2;105(19):1456-62. 6. Westeel V, Lebitasy MP, Mercier M, Girard P, Barlesi F, Blanchon F, et. al. IFCT-0302 trial: randomised study comparing two follow-up schedules in completely resected non-small cell lung cancer. Rev Mal Respir. 2007 May;24(5):645-52. 7. ESMO 2017 Press Release: IFCT-0302 results question role of CT-scan in NSCLC postsurgery follow-up. Available at: https://www.esmo.org/conferences/past- Conferences/ESMO-2017-Congress/Press-Media/Press-Releases/IFCT-0302-results- question-role-of-ct-scan-in-nsclc-post-surgery-follow-up. 8. Ramsey SD, Blough DK, Sullivan SD. A forensic evaluation of the National Emphysema 76 77 Treatment Trial using the expected value of information approach. Med Care. 2008 May;46(5):542-8. 3

78 79 9. National Lung Screening Trial Research Team, Aberle DR, Adams AM, Berg CD, Black WC, Clapp JD, et. al. Reduced lung-cancer mortality with low-dose computed tomographic 80 81 82 83 84 85 86 screening. N Engl J Med. 2011 Aug 4;365(5):395-409. 10. Fishman A, Martinez F, Naunheim K, Piantadosi S, Wise R, Ries A, Weinmann G, Wood DE; National Emphysema Treatment Trial Research Group. A randomized trial comparing lung-volume-reduction surgery with medical therapy for severe emphysema. N Engl J Med. 2003 May 22;348(21):2059-73. 4