- 1Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States
- 2McGovern Medical School at University of Texas Health Houston, Houston, TX, United States
- 3Division of Diagnostic Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX, United States
- 4Department of Rehabilitation Services, The University of Texas MD Anderson Cancer Center, Houston, TX, United States
- 5St Charles Health System, Bend, OR, United States
- 6Department of Gastrointestinal Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States
Background: Nonoperative management is increasingly offered to patients who achieve a complete clinical response to neoadjuvant therapy for rectal cancer. However, long-term bowel dysfunction and fecal incontinence can occur, potentially due in part to post-radiation fibrosis and atrophy of the pelvic floor muscles. In this pilot study, we investigated post-radiation changes in the levator ani muscles and their association with long-term patient-reported bowel dysfunction and incontinence scores.
Methods: Fifteen patients with rectal cancer treated with definitive chemoradiation followed by non-operative management were included. 2D and volumetric measurements of the levator ani were made on pre-treatment and 1-year post-radiation MRI. The changes in levator ani width and volume were correlated with the Low Anterior Resection Syndrome (LARS) and Fecal Incontinence Quality of Life (FiQOL) scores at least 1-year post treatment.
Results: The 2D and volumetric measurements of the levator ani decreased between pre-treatment and 1-year post-radiation. (-21.0% and –21.7%, respectively; both P<0.01). The decrease in 2D levator ani measurements was positively associated with LARS score (Pearson r(13) = 0.55; P = .03) but not FiQOL score. The decrease in volumetric levator ani measurements was not significantly correlated with LARS or FiQOL scores.
Conclusions: Decrease in 2D measurements of the levator ani from pre-treatment to 1-year post-radiation is correlated with higher LARS scores, indicating worse bowel function, perhaps due to radiation fibrosis and atrophy. This imaging biomarker may help to identify patients who could most benefit from pelvic floor physical therapy interventions. Further studies with larger cohorts are required to validate these findings.
1 Introduction
For decades, surgery with pre- or postoperative radiation and/or chemotherapy has been the mainstay of treatment for patients with locally advanced rectal cancer (LARC). However, the use of a nonoperative management strategy is increasing for patients who attain a complete clinical response (cCR) after radiation and/or chemotherapy (1). Interest in nonoperative management is driven by a desire to avoid surgery requiring a permanent ostomy or expected poor bowel function with sphincter-preserving surgery (2). Rates of Major Low Anterior Resection Syndrome (LARS), a constellation of symptoms that includes problems with frequency, urgency, and control of bowel movements, are nearly 50% when surgery requires a low anastomosis (3).
Although LARS was originally described as altered and problematic bowel function that occurs after rectal resection (4), studies suggest that approximately 25-33% of patients treated with definitive radiation and nonoperative management for rectal cancer can also develop Major LARS (5, 6). Bowel dysfunction, particularly fecal incontinence, after pelvic radiation is likely multifactorial (7). In the acute setting, radiation causes inflammation that leads to the development of fibrosis. This can result in issues with large bowel wall compliance, small bowel absorption, and persistent dysbiosis, causing diarrhea and urgency (8). Additionally, radiation-induced fibrosis, vascular changes, and nerve damage can lead to muscle atrophy within the pelvic floor muscles and sphincter complex (9).
Interventions such as pelvic floor physical therapy may improve post-treatment bowel dysfunction by isolating and strengthening pelvic floor muscles (10). However, tools for accurately assessing pelvic floor atrophy or damage remain limited. Magnetic resonance imaging (MRI) offers detailed visualization of soft tissues, including the pelvic floor, and may serve as a quantitative biomarker to detect radiation-induced atrophy (11). In this pilot study, we seek to evaluate 2D and volumetric levator ani measurements on pre- and 1-year post-treatment MRI among patients treated with radiation as a component of nonoperative management and correlate post-radiation MRI changes with LARS and patient-reported Fecal Incontinence Quality of Life (FIQoL) scores.
2 Methods
2.1 Patient population
This study was approved by the Institutional Review Board at The University of Texas MD Anderson Cancer Center (2020-0513). All patients provided informed consent to participate. We conducted a survey study of patients who completed pelvic radiation for rectal adenocarcinoma at our institution between 1/1/2017 and 12/31/2020 and were alive and without evidence of disease at the time of the survey administration in January 2022. Of 202 patients surveyed, 124 (61.4%) responded, and the results of their patient-reported quality of life outcomes have been reported elsewhere (12). For this pilot analysis of levator ani measurements, we selected the 15 patients from this cohort who had attained a cCR to chemoradiation and were treated with nonoperative management.
2.2 Treatment details
All patients were treated with long-course chemoradiation to a total dose of either 50.4Gy in 28 fractions or 50Gy in 25 fractions. Chemoradition was given alone or as a component of total neoadjuvant therapy depending on the stage and discretion of the multidisciplinary tumor board. Volumetric-modulated arc therapy (VMAT) or 3D conformal techniques were chosen at the discretion of the treating radiation oncologist. Concurrent capecitabine was given on the days of radiation. If patients were treated with induction chemotherapy followed by chemoradiation or by upfront chemoradiation, patients were assessed 6–8 weeks after chemoradiation by clinical exam, endoscopic examination, and pelvic MRI. Patients who were treated with upfront chemoradiation were observed if they had a cCR. Patients who had a near cCR were given consolidative chemotherapy and reassessed 2–6 weeks after the final cycle of chemotherapy. Once a cCR was confirmed endoscopically and radiogracphically, clinical and endoscopic exams were typically performed every 3 months, pelvic MRIs every 6 months, and CT abdomen and pelvis every 12 months for the first two years. Then, clinical exams, endoscopic exams, and pelvic MRIs were performed every 6 months until year 5, with CT abdomen and pelvis performed every 12 months until year 5.
2.3 Patient-reported bowel function
All patients in this study filled out a post-treatment patient-reported outcomes survey at least 18 months after completion of chemoradiation. The survey included two validated, patient-reported outcome measures of bowel function. First, the LARS score is calculated from five questions about incontinence, frequency, clustering, and urgency of bowel movements. LARS score ranges from 0-42, with higher scores indicating worse function. A score of 30–42 indicates the patient meets major LARS criteria (13). Second, the FIQoL score is calculated from 29 questions about lifestyle, coping/behavior, depression/self-perception, and embarrassment related to fecal incontinence. FIQoL score ranges from 4-20, with higher scores indicating better QoL (14).
2.4 Levator ani measurements
The levator ani muscles were assessed on pre-treatment and 12-month post-radiation MRI scans. MRIs were obtained on a 1.5 Tesla MRI scanner. T2-weighted coronal and axial sequences with 5mm slice thickness were used for measurements. 2D measurements (in mm) were made at the widest portion of the left and right levator ani muscles in the coronal plane by a specialized gastrointestinal and genitourinary diagnostic radiologist (SP) on both the pre-treatment and 12-month post-radiation scans (Figure 1). 2D measurements were standardized by following previously published measurement protocols for 2D levator ani assessment in the coronal plane (15). Volumetric measurements (in cc) of the levator ani were generated by importing the pre-treatment and 12-month post-radiation scans into RayStation version 12A (RaySearch Laboratories, 2022). The levator ani muscles were contoured in the axial plane by a radiation oncologist expert in lower gastrointestinal malignancies (EH) as a single structure that included the three paired muscle components: the iliococcygeus muscles originating from the ischial spine and attaching to the coccyx and anococcygeal raphe’, the pubococcygeus muscles originating from the back of the pubis extending along the anal canal and attaching to the coccyx and sacrum and the puboanalis muscles originating from the pubic bone, looping around the anorectal junction and inserting into the perineal body and rectum (Figure 2). 3D delineation of the levator ani muscles in the axial plane was performed by following previously published protocols and atlases as well (16, 17).
2.5 Statistical analysis
The Wilcoxon signed-rank test was used to assess potential differences in 2D and volumetric measurements pre-radiation versus post-radiation. The median and interquartile range (IQR) percent change were reported. The Pearson correlation coefficient was used to assess the strength and direction of the relationship between 2D and volumetric measurements, as well as between the levator ani measurements and both LARS and FIQoL scores. Significance was set at p<0.05.
3 Results
3.1 Demographic information
Fifteen patients were included in this pilot analysis. Nine men and six women. All patients were treated with long-course chemoradiation and were followed with close observation after attaining a complete clinical response. Demographic and clinical characteristics are outlined in Table 1.
Table 1. Demographic and clinical characteristics of patients treated with definitive radiation for locally advanced rectal adenocarcinoma.
3.2 Patient-reported bowel function
Post-treatment LARS and FiQOL scores represent long-term bowel function as the questionnaires were filled out a median [IQR] of 31.8 [19.2-47.9] months after completion of chemoradiation. No patient had an ostomy at the time of survey completion. No patient had experienced recurrent disease or had received any other cancer-directed therapy after chemoradiation. The median [IQR] LARS score was 24 [20-32]; seven (46.7%) patients met the criteria for Major LARS (score of 30-42). The median [IQR] FiQOL score was 15.3 [11.6-15.7]. Item-level survey responses for LARS and FiQoL are outlined in Table 2 and Supplementary Table, respectively.
Table 2. Low Anterior Resection Syndrome questionnaire item responses for patients treated with definitive radiation for locally advanced rectal adenocarcinoma.
3.3 Levator ani measurements
The 2D and volumetric measurements of the levator ani decreased from pretreatment to 12 months post-treatment. The median [IQR] pretreatment and 12-month post-treatment 2D measurements of the right levator ani are 7.1 [5.1-8.0] mm and 4.8 [4.1-5.75] mm, respectively (P<.01). The median [IQR] pretreatment and 12-month post-treatment 2D measurements of the left levator ani are 5.2 [4.3-7.2] mm and 3.8 [3.25-6.1] mm, respectively (P<.01). The median [IQR] volume of the bilateral levator ani muscles pretreatment vs 12 months post-treatment are 44.3 [37.2- 54.1] cc vs 32.6 [29.1-42.7] cc, respectively (P<.01).
The median [IQR] percent difference between pretreatment and 12-month post-treatment 2D measurements (taken of the average between the right and left measurements) and volumetric measurements are -21.0% [-13.9--30.7%] and -21.7% [-9.5--28.0%], respectively. The 2D and volumetric measurements were moderately positively correlated (Pearson r(13) = 0.71; P<.01).
3.4 Association between levator ani measurements and patient-reported bowel function
The 2D (Pearson r(13) = 0.13; P = .63) and volumetric (Pearson r(13) = -0.18; P = .53) pretreatment levator ani measurements were not significantly correlated with the post-treatment LARS score. The decrease in 2D levator ani measurements between pretreatment and 12-month post-treatment MRI was moderately positively correlated with a larger (or worse) LARS score (Pearson r(13) = 0.55; P = .03) and not significantly correlated with the FiQOL score (Pearson r(13) = -0.37; P = 0.17). The decrease in volumetric levator ani measurements between pretreatment and 12-month post-treatment MRI was not significantly correlated with LARS score (Pearson r(13)= 0.25; P = .37) or FiQOL score (Pearson (r13) = -0.27; P = .33).
4 Discussion
In this pilot study, we show a decrease in 2D and volumetric measurements of the levator ani one year after definitive pelvic radiation for rectal adenocarcinoma. The demonstrated correlation between 2D levator ani measurements and LARS suggests MRI may be a useful biomarker for bowel dysfunction and incontinence. By integrating structural imaging with patient-reported outcomes, this work provides preliminary support for advancing personalized survivorship care strategies and will serve as the foundation for future studies.
We found significant reductions in both 2D and volumetric levator ani measurements at 12 months post-treatment, suggesting a lasting effect of radiation on pelvic floor atrophy. Radiation exposure is known to induce transforming growth factor-β (TGF-β) release and chronic inflammation, leading to sustained fibroblast activation and extracellular matrix deposition that replace normal tissue architecture with fibrotic tissue (18). Additionally, oxidative stress and DNA damage results in depletion of myogenic stem cells, impacting regenerative capacity and further propagating muscle atrophy (19). These pathophysiological mechanisms induced by radiation therapy result in structural changes in pelvic floor muscles (20, 21). While the optimal levator ani quantification strategy is unknown, the strong positive correlation between 2D and volumetric measurements in our study supports the potential utility of simplified linear assessments as a practical alternative to volumetric analysis. Notably, given that the changes were detected through routine baseline and surveillance imaging, clinical implementation may be feasible without additional imaging burden.
Among this cohort of 15 patients treated with definitive, long-course chemoradiation +/- chemotherapy for locally advanced rectal cancer, 7 (46.7%) had symptoms consistent with Major LARS at least 18 months from completion of therapy. This is somewhat higher than other reported series (5, 6). In a cohort of 221 patients treated with radiation and nonoperative management, the rate of major LARS was 25% (5). This variation may be attributed to the cumulative multimodal treatment burden associated with long-term chemoradiation in comparison to selective nonoperative strategies such as short-course radiotherapy. In a cohort of 33 patients similarly treated, the rate of major LARS was 33%. This study also included a dosimetric analysis, but there were no significant associations between dose to the anal sphincter complex and LARS score (6).
With respect to functional outcomes, a moderate correlation was observed between reductions in 2D measurements and worsening LARS scores, suggesting a trend towards clinically relevant functional decline in patients with a high degree of pelvic atrophy. In contrast, correlation with volumetric change and FiQOL scores were weaker and non-significant. These trends may reflect the multifactorial nature of post-treatment dysfunction. Differences between volumetric and 2D correlations may be attributed to greater sensitivity of single plane 2D measurements to focal levator ani thinning in regions most relevant with anorectal support. In contrast, volumetric measurements integrate multiple dimensions and may dilute localized atrophy measurements with functional implications. As evidenced by the questionnaires, patient-reported outcomes are influenced not only by structural factors but also by psychosocial and behavioral components. Notably, the FiQOL outcome assesses broader quality of life aspects, such as emotional and social well-being, which may not be directly linked to structural alterations compared to questions regarding stool leakage and urgency. These variations emphasize the need for multimodal assessments alongside imaging to evaluate both functional and psychosocial quality of life.
Therapeutic interventions, such as pelvic floor physical therapy, have demonstrated efficacy in managing radiation-induced dysfunctions such as incontinence, pain, and sexual dysfunction in pelvic cancer survivors (22, 23). Leveraging MRI findings to guide these interventions with early risk stratification could enhance their effectiveness, particularly for patients with significant muscle atrophy. Emerging tools with MRI through predictive models and radiomics may enhance the predictive value of imaging alongside functional response to guide and personalize treatment options (24, 25). While pretreatment levator ani width and volume were not significantly correlated with post-treatment LARS score, change post treatment may predict worse function. By identifying pelvic floor atrophy prior to symptom onset, clinicians may mitigate chronic pelvic dysfunction and the associated patient outcomes.
While this study provides promising insights, several limitations should be acknowledged. The small cohort size limits the statistical power and generalizability, and the lack of pre-treatment patient-reported functional assessments restricts the ability to assess functional changes over time. Furthermore, the absence of dosimetric data limits the evaluation of dose-response relationships with muscle volume loss. Finally, although we utilized published guidelines and atlases for the 2D and volumetric measurements in this pilot study, we only had one expert diagnostic radiologist recording 2D measurements and one expert radiation oncologist recording volumetric measurements. Measurements were recorded one time per patient and timepoint. Therefore, intra- and interobserver variability were not formally assessed. Future research should also explore advanced imaging techniques, such as diffusion tensor imaging, to assess microstructural changes in pelvic musculature. Establishing an MRI-based threshold for clinically significant atrophy would be helpful in defining criteria for risk stratification and early therapeutic intervention. Additionally, longitudinal studies are needed to understand the progression of atrophy and its relationship to functional outcomes and quality of life. We plan to use these pilot data to design future studies to risk-stratify patients for early therapeutic interventions for bowel dysfunction and assess response to treatment.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by Institutional Review Board at University of Texas MD Anderson Cancer Center (2020-0513). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
RT: Writing – original draft, Writing – review & editing, Methodology, Investigation. SD: Writing – review & editing, Formal Analysis, Writing – original draft, Visualization. SP: Conceptualization, Methodology, Writing – original draft, Data curation, Investigation. NS: Writing – review & editing. LA: Investigation, Conceptualization, Writing – original draft, Methodology, Data curation. EH: Resources, Formal Analysis, Project administration, Writing – review & editing, Validation, Conceptualization, Methodology, Writing – original draft, Supervision, Investigation, Data curation, Visualization.
Funding
The author(s) declared that financial support was not received for this work and/or its publication.
Conflict of interest
The authors declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declared that generative AI was not used in the creation of this manuscript.
Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2025.1656898/full#supplementary-material
References
1. Lee KC, Zhao B, Pianka K, Liu S, Eisenstein S, Ramamoorthy S, et al. Current trends in nonoperative management for rectal adenocarcinoma: An unequal playing field? J Surg Oncol. (2022) 126:1504–11. doi: 10.1002/jso.27082
2. Kennedy ED, Borowiec AM, Schmocker S, Cho C, Brierley J, Li S, et al. Patient and physician preferences for nonoperative management for low rectal cancer: is it a reasonable treatment option? Dis Colon Rectum. (2018) 61:1281–9. doi: 10.1097/DCR.0000000000001166
3. Croese AD, Lonie JM, Trollope AF, Vangaveti VN, and Ho YH. A meta-analysis of the prevalence of Low Anterior Resection Syndrome and systematic review of risk factors. Int J Surg. (2018) 56:234–41. doi: 10.1016/j.ijsu.2018.06.031
4. Keane C, Fearnhead NS, Bordeianou LG, Christensen P, Basany EE, Laurberg S, et al. International consensus definition of low anterior resection syndrome. Dis Colon Rectum. (2020) 63:274–84. doi: 10.1097/DCR.0000000000001583
5. Custers PA, van der Sande ME, Grotenhuis BA, Peters FP, van Kuijk SMJ, Beets GL, et al. Long-term quality of life and functional outcome of patients with rectal cancer following a watch-and-wait approach. JAMA Surg. (2023) 158:e230146. doi: 10.1001/jamasurg.2023.0146
6. van der Sande ME, Hupkens BJP, Berbée M, van Kuijk SMJ, Maas M, Melenhorst J, et al. Impact of radiotherapy on anorectal function in patients with rectal cancer following a watch and wait programme. Radiother Oncol. (2019) 132:79–84. doi: 10.1016/j.radonc.2018.11.017
7. Morris KA and Haboubi NY. Pelvic radiation therapy: Between delight and disaster. World J Gastrointest Surg. (2015) 7:279–88. doi: 10.4240/wjgs.v7.i11.279
8. Ferreira MR, Sands CJ, Li JV, Andreyev JN, Chekmeneva E, Gulliford S, et al. Impact of pelvic radiation therapy for prostate cancer on global metabolic profiles and microbiota-driven gastrointestinal late side effects: A longitudinal observational study. Int J Radiat Oncol Biol Phys. (2021) 111:1204–13. doi: 10.1016/j.ijrobp.2021.07.1713
9. Bernard S, Ouellet MP, Moffet H, Roy JS, and Dumoulin C. Effects of radiation therapy on the structure and function of the pelvic floor muscles of patients with cancer in the pelvic area: a systematic review. J Cancer Surviv. (2016) 10:351–62. doi: 10.1007/s11764-015-0481-8
10. Ansar M, Boddeti S, Noor K, Malireddi A, Abera M, Suresh SB, et al. A systematic review of comparative effectiveness of interventions for low anterior resection syndrome: impacts on bowel function and quality of life. Cureus. (2024) 16:e72772. doi: 10.7759/cureus.72772
11. Woodfield CA, Krishnamoorthy S, Hampton BS, and Brody JM. Imaging pelvic floor disorders: trend toward comprehensive MRI. AJR Am J Roentgenol. (2010) 194:1640–9. doi: 10.2214/AJR.09.3670
12. Rooney MK, De B, Corrigan K, Smith GL, Taniguchi C, Minsky BD, et al. Patient-reported bowel function and bowel-related quality of life after pelvic radiation for rectal adenocarcinoma: the impact of radiation fractionation and surgical resection. Clin Colorectal Cancer. (2023) 22:211–21. doi: 10.1016/j.clcc.2023.02.003
13. Emmertsen KJ and Laurberg S. Low anterior resection syndrome score: development and validation of a symptom-based scoring system for bowel dysfunction after low anterior resection for rectal cancer. Ann Surg. (2012) 255:922–8. doi: 10.1097/SLA.0b013e31824f1c21
14. Rockwood TH, Church JM, Fleshman JW, Kane RL, Mavrantonis C, Thorson AG, et al. Fecal Incontinence Quality of Life Scale: quality of life instrument for patients with fecal incontinence. Dis Colon Rectum. (2000) 43:9–16; discussion 16-17. doi: 10.1007/BF02237236
15. Shek KL and Dietz HP. Coronal plane assessment for levator trauma. J Ultrasound Med. (2024) 43:1627–33. doi: 10.1002/jum.16484
16. Margulies RU, Hsu Y, Kearney R, Stein T, Umek WH, and DeLancey JOL. Appearance of the levator ani muscle subdivisions in magnetic resonance images. Obstet Gynecol. (2006) 107:1064–9. doi: 10.1097/01.AOG.0000214952.28605.e8
17. Lakhoo J, Khatri G, Elsayed RF, Chernyak V, Olpin J, Steiner A, et al. MRI of the male pelvic floor. Radiographics. (2019) 39:2003–22. doi: 10.1148/rg.2019190064
18. Kreuder L, Bissey PA, Yip KW, and Liu FF. Exploring radiation-induced fibrosis: biological mechanisms and new frontiers in research and therapeutics. Int J Radiat Biol. (2025), 1–16. doi: 10.1080/09553002.2025.2540353
19. Collao N, Johannsen EB, Just J, and De Lisio M. Single-cell transcriptomic analysis reveals alterations to cellular dynamics and paracrine signaling in radiation-induced muscle pathology. Am J Physiol Cell Physiol. (2025) 328:C1995–2012. doi: 10.1152/ajpcell.00115.2025
20. Huh JW, Tanksley J, Chino J, Willett CG, and Dewhirst MW. Long-term consequences of pelvic irradiation: toxicities, challenges, and therapeutic opportunities with pharmacologic mitigators. Clin Cancer Res. (2020) 26:3079–90. doi: 10.1158/1078-0432.CCR-19-2744
21. Wo JY, Anker CJ, Ashman JB, Bhadkamkar NA, Bradfield L, Chang DT, et al. Radiation therapy for rectal cancer: executive summary of an ASTRO clinical practice guideline. Pract Radiat Oncol. (2021) 11:13–25. doi: 10.1016/j.prro.2020.08.004
22. Barcellini A, Dominoni M, Dal Mas F, Biancuzzi H, Venturini SC, Gardella B, et al. Sexual health dysfunction after radiotherapy for gynecological cancer: role of physical rehabilitation including pelvic floor muscle training. Front Med (Lausanne). (2021) 8:813352. doi: 10.3389/fmed.2021.813352
23. Brennen R, Lin KY, Denehy L, and Frawley HC. The effect of pelvic floor muscle interventions on pelvic floor dysfunction after gynecological cancer treatment: A systematic review. Phys Ther. (2020) 100:1357–71. doi: 10.1093/ptj/pzaa081
24. Del Vescovo R, Piccolo CL, Della Vecchia N, Giurazza F, Cazzato RL, Grasso RF, et al. MRI role in morphological and functional assessment of the levator ani muscle: use in patients affected by stress urinary incontinence (SUI) before and after pelvic floor rehabilitation. Eur J Radiol. (2014) 83:479–86. doi: 10.1016/j.ejrad.2013.11.021
Keywords: imaging biomarker, pelvic floor dysfunction, incontinence, radiation late effects, fibrosis
Citation: Thomas RJ, Derasari S, Palmquist SM, Samms N, Andring L and Holliday EB (2026) Post-radiation levator ani atrophy is associated with worse Low Anterior Resection Syndrome score after nonoperative management for locally advanced rectal cancer: a potential MRI biomarker. Front. Oncol. 15:1656898. doi: 10.3389/fonc.2025.1656898
Received: 30 June 2025; Accepted: 16 December 2025; Revised: 23 November 2025;
Published: 12 January 2026.
Edited by:
Timothy James Kinsella, Brown University, United StatesReviewed by:
Ritchell Van Dams, Dana-Farber/Brigham and Women’s Cancer Center, United StatesTayfun Bisgin, Dokuz Eylul University, Türkiye
Copyright © 2026 Thomas, Derasari, Palmquist, Samms, Andring and Holliday. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Emma B. Holliday, RWJob2xsaWRheUBtZGFuZGVyc29uLm9yZw==
†These authors have contributed equally to this work
Sarah M. Palmquist3