Preoperative MRI accuracy after neoadjuvant chemoradiation for locally advanced rectal cancer.

magnetic resonance imaging neoadjuvant chemoradiotherapy rectal neoplasms tumor response

Journal

Medicine and pharmacy reports
ISSN: 2668-0572
Titre abrégé: Med Pharm Rep
Pays: Romania
ID NLM: 101742144

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 16 05 2022
revised: 01 06 2022
accepted: 27 06 2022
medline: 14 8 2023
pubmed: 14 8 2023
entrez: 14 8 2023
Statut: ppublish

Résumé

To evaluate the performance of magnetic resonance imaging (MRI) in restaging locally advanced rectal cancers (LARC) after neoadjuvant chemoradiotherapy (nCRT), with pathologic correlation. 80 patients with LARC treated with neoadjuvant therapy, with restaging MRI and surgery, were enrolled and prospectively reviewed. The diagnostic accuracy of the restaging MRI was assessed for tumor (ymrT), nodal status (ymrN), circumferential resection margin (ymrCRM), extramural vascular invasion (ymrEMVI) and tumoral deposits (ymrN1c) by calculating the sensitivity (Se), specificity (Sp), negative predictive values (NPV) and positive predictive values (PPV). Response to treatment was classified as good response (complete/near complete) vs. poor response (poor/partial response). The agreement between the tumor regression grade at MRI (mrTRG) and pathology (pTRG) was reported, as well the performance of mrTRG to identify good responders. The correlation between restaging MRI and histopathology was assessed by Spearman correlation coefficient. The MRI accuracy ranged between 63.8% and 92.5% for T stage and was 81.3% for N stage. All MRI parameters evaluated at restaging were statistically significant correlated with histopathology evaluation, but EMVI. There was moderate correlation for N and N1c and a positive strong correlation for T, CRM and TRG (Spearman correlation coefficient of 0.390 for mrN1c-pN1c, 0.428 for mrN-pN, 0.522 for mrCRM-pCRM, 0.550 for mrT-pT and 0.731 for mrTRG-pTRG). Diagnostic accuracy of anal sphincter invasion was 91.3%, with a negative predictive value (NPV) of 100%. Accuracy rate varied between 70% for partial response to 93.75% for complete response after nCRT. MR imaging had good accuracy in restaging LARCs after nCRT. Our results showed high MRI accuracy in detecting anal sphincter involvement for low rectal tumors, with high NPV to exclude tumoral invasion. Restaging MRI predicted well the tumor regression grade, with good diagnostic performance in differentiating good responders from poor/partial responders. The accuracy was high for detecting complete response.

Sections du résumé

Background and aims UNASSIGNED
To evaluate the performance of magnetic resonance imaging (MRI) in restaging locally advanced rectal cancers (LARC) after neoadjuvant chemoradiotherapy (nCRT), with pathologic correlation.
Methods UNASSIGNED
80 patients with LARC treated with neoadjuvant therapy, with restaging MRI and surgery, were enrolled and prospectively reviewed. The diagnostic accuracy of the restaging MRI was assessed for tumor (ymrT), nodal status (ymrN), circumferential resection margin (ymrCRM), extramural vascular invasion (ymrEMVI) and tumoral deposits (ymrN1c) by calculating the sensitivity (Se), specificity (Sp), negative predictive values (NPV) and positive predictive values (PPV). Response to treatment was classified as good response (complete/near complete) vs. poor response (poor/partial response). The agreement between the tumor regression grade at MRI (mrTRG) and pathology (pTRG) was reported, as well the performance of mrTRG to identify good responders. The correlation between restaging MRI and histopathology was assessed by Spearman correlation coefficient.
Results UNASSIGNED
The MRI accuracy ranged between 63.8% and 92.5% for T stage and was 81.3% for N stage. All MRI parameters evaluated at restaging were statistically significant correlated with histopathology evaluation, but EMVI. There was moderate correlation for N and N1c and a positive strong correlation for T, CRM and TRG (Spearman correlation coefficient of 0.390 for mrN1c-pN1c, 0.428 for mrN-pN, 0.522 for mrCRM-pCRM, 0.550 for mrT-pT and 0.731 for mrTRG-pTRG). Diagnostic accuracy of anal sphincter invasion was 91.3%, with a negative predictive value (NPV) of 100%. Accuracy rate varied between 70% for partial response to 93.75% for complete response after nCRT.
Conclusions UNASSIGNED
MR imaging had good accuracy in restaging LARCs after nCRT. Our results showed high MRI accuracy in detecting anal sphincter involvement for low rectal tumors, with high NPV to exclude tumoral invasion. Restaging MRI predicted well the tumor regression grade, with good diagnostic performance in differentiating good responders from poor/partial responders. The accuracy was high for detecting complete response.

Identifiants

pubmed: 37577010
doi: 10.15386/mpr-2542
pii: cm-96-258
pmc: PMC10419690
doi:

Types de publication

Journal Article

Langues

eng

Pagination

258-268

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Auteurs

Anca-Raluca Popiţa (AR)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Medical Imaging Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Adriana Rusu (A)

Diabetes and Nutrition Diseases Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Valentin Muntean (V)

Surgery Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Patriciu Achimas Cadariu (PA)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Oncology Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Alexandru Irimie (A)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Oncology Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Cosmin Lisencu (C)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Oncology Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Bogdan Pop (B)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Anatomical Pathology Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Liliana Resiga (L)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.

Zsolt Fekete (Z)

"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Oncology Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Radu Badea (R)

Medical Imaging Department, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Classifications MeSH