Deeper sections reveal residual tumor cells in rectal cancer specimens diagnosed with pathological complete response following neoadjuvant treatment.

Autor: Slumstrup L; Department of Pathology, Zealand University Hospital, Roskilde, Denmark. lassl@regionsjaelland.dk.; Center for Surgical Science, Zealand University Hospital, Køge, Denmark. lassl@regionsjaelland.dk., Eiholm S; Department of Pathology, Zealand University Hospital, Roskilde, Denmark., Bennedsen ALB; Center for Surgical Science, Zealand University Hospital, Køge, Denmark., Jepsen DNM; Department of Pathology, Zealand University Hospital, Roskilde, Denmark.; Center for Surgical Science, Zealand University Hospital, Køge, Denmark., Gögenur I; Center for Surgical Science, Zealand University Hospital, Køge, Denmark.; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark., Fiehn AK; Department of Pathology, Zealand University Hospital, Roskilde, Denmark.; Center for Surgical Science, Zealand University Hospital, Køge, Denmark.; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Jazyk: angličtina
Zdroj: Virchows Archiv : an international journal of pathology [Virchows Arch] 2022 May; Vol. 480 (5), pp. 1041-1049. Date of Electronic Publication: 2022 Jan 31.
DOI: 10.1007/s00428-022-03287-7
Abstrakt: Guidelines and requirements for diagnosing pathological complete response (pCR) in rectal adenocarcinoma following neoadjuvant treatment vary, and there is currently no consensus on the appropriate number of sections to examine per formalin-fixed, paraffin-embedded (FFPE) tissue block. The consequences of systematic use of deeper sections on the diagnostic accuracy and prognosis for patients classified as ypT0 rectal cancer were investigated. In this retrospective study, 23 out of 155 patients who underwent neoadjuvant therapy and surgical resection between 2015 and 2020 were diagnosed with ypT0 rectal cancer. Three additional deeper sections were cut from each FFPE block from the primary tumor site and reviewed for presence of residual tumor cells. Additional sections revealed residual viable tumor cells in seven patients (30.4%), reducing the rate of pCR in the cohort from 14.8 to 10.3%. Of the seven patients, three patients later had local recurrence or distant metastasis during the follow-up period, compared with one patient with no residual tumor cells in deeper sections (p = 0.07). A nonsignificant reduction in disease-free survival (p = 0.08) was observed in the patients with residual tumor. Systematic use of deeper sections in evaluation of tumor regression in rectal cancer reveals the presence of residual tumor cells in a subset of patients originally diagnosed with pCR based on a single section per FFPE block. Although the results are not statistically significant, it cannot be excluded that accurately distinguishing complete from near-complete response may be clinically relevant for prognostic prediction.
(© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
Databáze: MEDLINE
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