Abstract
Simple SummaryRadiotherapy is the standard treatment for locally advanced rectal cancer with a high risk of local recurrence, if treated with surgery alone. The two regimens accepted are preoperative long-course radiotherapy with concomitant chemotherapy and preoperative short-course radiotherapy. The aim of our retrospective study is to provide a comprehensive morphological description of radiation-induced changes in rectal cancer specimens. We compared 2 groups of 95 rectal cancer patients treated preoperatively with either short-course (45 patients) or long-course radiotherapy (50 patients). Interestingly, in the non-neoplastic mucosa we identified features closely mimicking dysplasia/pre-neoplasia only in the group treated with short-course radiotherapy. Pathologists awareness of radiation-induced abnormalities is essential, as the misinterpretation may lead to patient’s overtreatment. In our study, next generation sequencing analysis supported the morphological concept that short-course radiotherapy-induced abnormalities do not represent true dysplasia, as somatic mutations were not identified in “dysplastic-like” tissues.Preoperative radiotherapy is a widely accepted treatment procedure in rectal cancer. Radiation-induced changes in the tumor are well described, whereas less attention has been given to the non-neoplastic mucosa. Our aim is to provide a detailed analysis of the morphological features present in non-neoplastic mucosa that pathologists need to be familiar with, in order to avoid misdiagnosis, when evaluating rectal cancer specimens of patients preoperatively treated with radiotherapy, especially with short-course regimen. We compared 2 groups of 95 rectal cancer patients treated preoperatively with either short-course (45 patients) or long-course radiotherapy (50 patients). Depending on the type of protocol, different histopathological features, in terms of inflammation, glandular abnormalities and endocrine differentiation were seen in the non-neoplastic mucosa within the irradiated volume. Of note, features mimicking dysplasia, such as crypt distortion, nuclear and cytoplasmic atypia of glandular epithelium, were identified only in the short-course group. DNA mutation analysis, using a panel of 56 genes frequently mutated in cancer, and p53 immunostaining were performed on both tumor and radiation-damaged mucosa in a subset of short course cases. Somatic mutations were identified only in tumors, supporting the concept that tissues with radiation-induced “dysplastic-like” features are not genetically transformed. Pathologists should be aware of the characteristic morphological changes induced by radiation. The presence of features simulating dysplasia in the group treated with short-course radiotherapy may lead to serious diagnostic mistakes, if erroneously interpreted. Next generation sequencing (NGS) analysis further validated the morphological concept that radiation-induced abnormalities do not represent pre-neoplastic lesions.
Highlights
IntroductionRadiotherapy represents the standard treatment for locally advanced rectal cancer with a high risk of local recurrence, if treated with surgery alone
Rectal cancer is one of the most common malignant tumors in western countries [1,2].Radiotherapy represents the standard treatment for locally advanced rectal cancer with a high risk of local recurrence, if treated with surgery alone
Radiation-induced changes in the tumor are well described, tumor down-staging as a consequence of long-term radiotherapy [16]
Summary
Radiotherapy represents the standard treatment for locally advanced rectal cancer with a high risk of local recurrence, if treated with surgery alone. Two neoadjuvant regimens are accepted: preoperative long-course radiotherapy (PLRT) with concomitant chemotherapy and preoperative short-course radiotherapy (PSRT). PLRT is preferred for either low-seated or bulky, unresectable tumors which should benefit from radiation-induced down staging [3,4,5,6,7,8]. PLRT protocol consists of 45–50 gray (Gy) in 4–6 weeks, followed by surgery four weeks later. PSRT consists of 25 Gy administered in five consecutive days, followed by surgery a few days after. PSRT is not associated with significant tumor regression, as the interval from the end of radiotherapy to surgery is too short to allow tumor down-staging
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