Optimal waiting period to surgical treatment after neoadjuvant chemoradiotherapy for locally advanced rectum cancer: a retrospective observational study
- PMID: 37227524
- DOI: 10.1007/s00423-023-02930-4
Optimal waiting period to surgical treatment after neoadjuvant chemoradiotherapy for locally advanced rectum cancer: a retrospective observational study
Abstract
Background: The optimal waiting period after neoadjuvant treatment in patients with locally advanced rectal cancers is still controversial. The literature has different results regarding the effect of waiting periods on clinical and oncological outcomes. We aimed to investigate the effects of these different waiting periods on clinical, pathological, and oncological outcomes.
Methods: Between January 2014 and December 2018, a total of 139 consecutive patients with locally advanced rectal adenocarcinoma, who were treated in the Department of General Surgery at the Marmara University Pendik Training and Research Hospital, were enrolled in the study. The patients were split into three groups according to waiting time for surgery after neoadjuvant treatment: group 1 (n = 51) included patients that have 7 weeks and less (≤ 7 weeks) time interval, group 2 (n = 45) 8 to 10 weeks (8-10 weeks), group 3 (n = 43) 11 weeks and above (11 weeks ≤). Their database records, which were entered prospectively, were analyzed retrospectively.
Results: There were 83 (59.7%) males and 56 (40.3%) females. The median age was 60 years, and there was no statistical difference between the groups regarding age, gender, BMI, ASA score, ECOG performance score, tumor location, and preoperative CEA values. Also, we found no significant differences regarding operation times, intraoperative bleeding, length of hospital stay, and postoperative complications. According to the Clavien-Dindo (CD) classification, severe early postoperative complications (CD 3 and above) were observed in 9 patients. The complete pathological response (pCR, ypT0N0) was observed in 21 (15.1%) patients. The groups had no significant difference regarding 3-year disease-free and 3-year overall survival (p = 0.3, p = 0.8, respectively). Local recurrence was observed in 12 of 139 (8.6%) patients and distant metastases occurred in 30 of 139 (21.5%) patients during the follow-up period. There was no significant difference between the groups in terms of both local recurrence and distant metastasis (p = 0.98, p = 0.43, respectively).
Conclusion: The optimal time for postoperative complications and sphincter-preserving surgery in patients with locally advanced rectal cancer is 8-10 weeks. The different waiting periods do not affect disease-free and overall survival. While long-term waiting time does not make a difference in pathological complete response rates, it negatively affects the TME quality rate.
Keywords: Interval; Locally advanced rectal cancer; Neoadjuvant chemoradiotherapy; Waiting period.
© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Similar articles
-
[Rectum-preserving surgery after consolidation neoadjuvant therapy or totally neoadjuvant therapy for low rectal cancer: a preliminary report].Zhonghua Wei Chang Wai Ke Za Zhi. 2020 Mar 25;23(3):281-288. doi: 10.3760/cma.j.cn.441530-20200228-00096. Zhonghua Wei Chang Wai Ke Za Zhi. 2020. PMID: 32192308 Chinese.
-
[Short-term outcome of programmed cell death protein1 (PD-1) antibody combined with total neoadjuvant chemoradiotherapy in the treatment of locally advanced middle-low rectal cancer with high risk factors].Zhonghua Wei Chang Wai Ke Za Zhi. 2021 Nov 25;24(11):998-1007. doi: 10.3760/cma.j.cn441530-20210927-00386. Zhonghua Wei Chang Wai Ke Za Zhi. 2021. PMID: 34823301 Chinese.
-
[Analysis on efficacy and safety of total neoadjuvant therapy in patients with locally advanced rectal cancer with high risk factors].Zhonghua Wei Chang Wai Ke Za Zhi. 2019 Apr 25;22(4):349-356. doi: 10.3760/cma.j.issn.1671-0274.2019.04.007. Zhonghua Wei Chang Wai Ke Za Zhi. 2019. PMID: 31054549 Chinese.
-
Optimal Interval to Surgery After Neoadjuvant Chemoradiotherapy in Rectal Cancer: A Systematic Review and Meta-analysis.Clin Colorectal Cancer. 2018 Mar;17(1):13-24. doi: 10.1016/j.clcc.2017.10.012. Epub 2017 Nov 15. Clin Colorectal Cancer. 2018. PMID: 29153429
-
Changing patterns of neoadjuvant therapy for locally advanced rectal cancer: A narrative review.Crit Rev Oncol Hematol. 2023 Jan;181:103885. doi: 10.1016/j.critrevonc.2022.103885. Epub 2022 Dec 2. Crit Rev Oncol Hematol. 2023. PMID: 36464124 Review.
Cited by
-
Evaluation of pre-treatment F-18 FDG PET/CT according to Mandard classification in locally advanced rectal cancer patients undergoing neoadjuvant chemoradiotherapy.BMC Cancer. 2025 Aug 4;25(1):1262. doi: 10.1186/s12885-025-14659-y. BMC Cancer. 2025. PMID: 40760425 Free PMC article.
-
Recent advances in rectal cancer treatment - are we on the right track?Ups J Med Sci. 2024 Feb 21;129. doi: 10.48101/ujms.v129.10537. eCollection 2024. Ups J Med Sci. 2024. PMID: 38449909 Free PMC article. Review.
References
-
- Benson AB, Venook AP, Al-Hawary MM, Arain MA, Chen YJ, Ciombor KK (2020) NCCN guidelines insights: rectal cancer, Version 6.2020. J Natl Compr Canc Netw 18(7):806–815 - PubMed
-
- Oronsky B, Reid T, Larson C, Knox SJ (2020) Locally advanced rectal cancer: the past, present, and future. Semin Oncol 47(1):85–92 - PubMed
-
- Mohiuddin M, Winter K, Mitchell E, Hanna N et al (2006) Randomized phase II study of neoadjuvant combined-modality chemoradiation for distal rectal cancer: Radiation Therapy Oncology Group Trial 0012. J Clin Oncol 24(4):650–655 - PubMed
-
- Petrelli F, Sgroi G, Sarti E, Barni S (2016) Increasing the interval between neoadjuvant chemoradiotherapy and surgery in rectal cancer: a meta-analysis of published studies. Ann Surg 263(3):458–464 - PubMed
-
- Francois BY, Nemoz CJ, Beaulieu J, Vignal J, Grandjean JP, Partensky C, Souquet JC, Adeleine P, Gerard JP (1999) Influence of the interval between preoperative radiation therapy and surgery on downstaging and on the rate of sphincter-sparing surgery for rectal cancer: the Lyon R90-01 Randomized Trial. J Clin Oncol 17:2396–2402 - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources