ASO Author Reflections: Neoadjuvant Treatment Does not Increase Postoperative Complications Compared with Upfront Surgery in Esophageal Cancer
Ville E. J. Sirviö, Jari V. Räsänen, Olli Helminen, Mika Helmiö, Heikki Huhta, Raija Kallio, Vesa Koivukangas, Arto Kokkola, Elina Lietzen, Sanna Meriläinen, Vesa-Matti Pohjanen, Tuomo Rantanen, Ari Ristimäki, Juha Saarnio, Eero Sihvo, Tuula Tyrväinen, Mikko Uimonen

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
- —http://dx.doi.org/10.13039/100010129Maud Kuistilan Muistosäätiö
- —http://dx.doi.org/10.13039/501100007083Orionin Tutkimussäätiö
- —http://dx.doi.org/10.13039/501100006306Sigrid Juséliuksen Säätiö
- —http://dx.doi.org/10.13039/501100010711Syöpäsäätiö
- —http://dx.doi.org/10.13039/501100004212Päivikki ja Sakari Sohlbergin Säätiö
- —University of Helsinki (including Helsinki University Central Hospital)
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Taxonomy
TopicsEsophageal Cancer Research and Treatment · Gastric Cancer Management and Outcomes · Esophageal and GI Pathology
Past
The role of neoadjuvant treatment (nT) and its modalities (chemotherapy [nCT], chemoradiotherapy [nCRT]) in the risk of complications after esophagectomy for cancer is unclear outside clinical trial settings. Randomized studies to date have not reported that nT increases surgical complications, however meta-analyses and the only existing nationwide study have had opposing results.^1,2^ The latest randomized data comparing nCRT and nCT in surgical risk have also had mixed results.^3,4^ Further large, population-based studies are warranted.
Present
We compared postoperative complications and 90-day mortality after nT and upfront surgery, and after chemoradiotherapy and chemotherapy, in an unselected, population-based, nationwide cohort using standardized outcome definitions.^5^ There were no meaningful differences in postoperative outcomes in patients undergoing nT versus upfront surgery or patients undergoing nCRT versus nCT. Outcomes were also similar in patients with aborted or dose-reduced neoadjuvant regimens versus patients tolerating full intended neoadjuvant regimens.
Future
In the present study, the choice of preoperative treatment strategy did not affect the risk of postoperative complications or mortality. These results support the use of preoperative oncologic treatment, with the choice of modality guided primarily by oncologic and survival outcomes, without concerns of said choice affecting surgical risk. Patients experiencing adverse events during nT are often considered to be of higher surgical risk and can be denied surgery. Similarly, nT may be withheld from patients with reduced performance status due to fear of complications. Our results suggest these concerns are unwarranted and such patients should not be excluded from surgery or nT if otherwise eligible.
Further population-based studies using widely accepted, standardized outcome definitions are needed for international comparison, identification of potential pitfalls, and to facilitate quality-improvement efforts. Future studies should monitor more recently introduced neoadjuvant regimens such as fluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT), and emerging neoadjuvant immunotherapies in surgical safety.
