Compatibility of MRI and Pathological Tumor Regression Grading in Patients with Locally Advanced Rectal Cancer After Undergoing Neoadjuvant Chemoradiotherapy

Compatibility of MRI and Pathological Tumor Regression Grading in Patients with Locally Advanced Rectal Cancer After Undergoing Neoadjuvant Chemoradiotherapy

OBJECTIVE The compatibility between magnetic resonance imaging tumor regression grade (mrTRG) and pathological tumor regression grade (pTRG) was examined in patients with locally advanced rectal cancer (LARC) who underwent neoadjuvant chemoradiotherapy (nCRT). The primary endpoint of the study was to evaluate the relationship between mrTRG and pTRG after nCRT. The secondary endpoint of the study was to evaluate the variables that affect mrTRG and pTRG. METHODS Forty-one patients with LARC treated with nCRT were analyzed. Magnetic resonance imaging (MRI) performed after nCRT was compared with MRI taken before nCRT. Changes in T and N stages and extramural vascular invasion positivity were investigated. TRG was divided into five groups in terms of pathological and MRI. The Dworak pTRG system was used for compatibility testing. MRI sensitivity and specificity were evaluated by comparing MRI-based response assessment with pathological assessment after nCRT. RESULTS Median patient age was 61 years (range, 26–79 years), and 18 (43.9%) were female. The relationship between mrTRG and pTRG was evaluated with the Cohen kappa coefficient. Significant compatibility was observed between pTRG and mrTRG (p=0.002), but the compatibility was low (kappa compatibility, 0.319). The sensitivity of mrTRG was 90% (18/20); specificity was 14.3% (3/21); positive predictive value was 85.7% (18/21); and negative predictive value was 90% (18/20). While pTRG was negatively affected by advanced age (p=0.037), mrTRG was adversely affected by advanced post-nCRT N stage (p=0.048). CONCLUSION As age increased, pTRG was negatively affected; as the post-nCRT N stage increased, mrTRG was negatively affected. There was compatibility between mrTRG and pTRG, as expected, but this compatibility was found to be low.

___

  • 1. Horvat N, Petkovska I, Gollub MJ. MR ımaging of rectal cancer. Radiol Clin N Am 2018;56:75.
  • 2. Gollub MJ, Arya S, Beets-Tan RG, DePrisco G, Gonen M, Jhaveri K, et al. Use of magnetic resonance imaging in rectal cancer patients: Society of Abdominal Radiology (SAR) rectal cancer disease-focused panel (DFP) recommendations 2017. Abdom Radiol 2018;43(11):2893–902.
  • 3. Horvat N, Rocha CC, Oliveira BC, Petkovska I, Gollub MJ. MRI of rectal cancer: Tumor staging, ımaging techniques, and management. Radiographics. 2019;39:367–87.
  • 4. Sauer R, Becker H, Hohenberger W, Rödel C, Wittekind C, Fietkau R, et al. Pre-operative versus postoperative chemoradiotherapy for rectal cancer. N Engl J Med 2004;351(17):1731–40.
  • 5. Lambregts DM, Boellaard TN, Beets-Tan RG. Response evaluation after neoadjuvant treatment for rectal cancer using modern MR imaging: A pictorial review. Insights Imaging 2019;10(1):15.
  • 6. Braun OM, Neumeister B, Popp W, Scherrer R, Dobrowsky E, Dobrowsky W, et al. Histologic tumor regression grades in squamous cell carcinoma of the head and neck after pre-operative radiochemotherapy. Cancer 1989;63(6):1097–100.
  • 7. Mandard AM, Dalibard F, Mandard JC, Marnay J, Henry‐Amar M, Petiot JF, et al. Pathologic assessment of tumor regression after pre-operative chemoradiotherapy of esophageal carcinoma. Clinicopathologic correlations. Cancer 1994;73(11):2680–6.
  • 8. Rödel C, Grabenbauer GG, Kühn R, Papadopoulos T, Dunst J, Meyer M, et al. Combined-modality treatment and selective organ preservation in invasive bladder cancer: Long-term results. J Clin Oncol 2002;20(14):3061–71.
  • 9. Becker K, Mueller JD, Schulmacher C, Ott K, Fink U, Busch R, et al. Histomorphology and grading of regression in gastric carcinoma treated with neoadjuvant chemotherapy. Cancer 2003;98(7):1521–30.
  • 10.Dhadda AS, Dickinson P, Zaitoun AM, Gandhi N, Bessell EM. Prognostic importance of Mandard tumor regression grade following pre-operative chemo/ radiotherapy for locally advanced rectal cancer. Eur J Cancer 2011;47(8):1138–45.
  • 11.Fokas E, Liersch T, Fietkau R, Hohenberger W, Beissbarth T, Hess C, et al. Tumor regression grading after pre-operative chemoradiotherapy for locally advanced rectal carcinoma revisited: Updated results of the CAO/ ARO/AIO-94 trial. J Clin Oncol 2014;32(15):1554–62.
  • 12.Rodel C, Martus P, Papadoupolos T. Prognostic significant for tumor regression after pre-operative chemoradiotherapy for rectal cancer. J Clin Oncol 2005;23(34):8688–96.
  • 13.Dworak O, Keilholz L, Hoffmann A. Pathological features of rectal cancer after pre-operative radiochemotherapy. Int J Colorectal Dis 1997;12(1):19– 23. 14.AJCC Cancer Stagıng Manual. 7th ed. Germany: Springer; 1997. p. 152.
  • 15.Patel UB, Blomqvist LK, Taylor F, George C, Guthrie A, Bees N, et al. MRI after treatment of locally advanced rectal cancer: How to report tumor response-the MERCURY experience. AJR Am J Roentgenol 2012;199(4):486–95.
  • 16.Sclafani F, Brown G, Cunningham D, Wotherspoon A, Mendes LS, Balyasnikova S, et al. Comparison between MRI and pathology in the assessment of tumor regression grade in rectal cancer. Br J Cancer 2017;117(10):1478–85.
  • 17.Rengo M, Picchia S, Marzi S, Bellini D, Caruso D, Caterino M, et al. Magnetic resonance tumor regression grade (MR-TRG) to assess pathological complete response following neoadjuvant radiochemotherapy in locally advanced rectal cancer. Oncotarget 2017;8(70):114746–55.
  • 18.Ko HM, Choi YH, Lee JE, Lee KH, Kim JY, Kim JS. Combination assessment of clinical complete response of patients with rectal cancer following chemoradiotherapy with endoscopy and magnetic resonance ımaging. Ann Coloproctol 2019;35(4):202–8.
  • 19.Betge J, Pollheimer MJ, Lindtner RA, Kornprat P, Schlemmer A, Rehak P, et al. Intramural and extramural vascular invasion in colorectal cancer: Prognostic significance and quality of pathology reporting. Cancer 2012;118(3):628–38.
  • 20.Smith NJ, Shihab O, Arnaout A, Swift RI, Brown G. MRI for detection of extramural vascular invasion in rectal cancer. AJR Am J Roentgenol 2008;191:1517– 22.
  • 21.Bugg WG, Andreou AK, Biswas D, Toms AP, Williams SM. The prognostic significance of MRI-detected extramural venous invasion in rectal carcinoma. Clin Radiol 2014;69(6):619–23.
  • 22.Sohn B, Lim JS, Kim H, Myoung S, Choi J, Kim NK, et al. MRI-detected extramural vascular invasion is an independent prognostic factor for synchronous metastasis in patients with rectal cancer. Eur Radiol 2015;25(5):1347–55.
  • 23.Sun Y, Li J, Shen L, Wang X, Tong T, Gu, Y. Predictive value of MRI-detected extramural vascular invasion in stage T3 rectal cancer patients before neoadjuvant chemoradiation. Diagn Interv Radiol 2018;24(3):128– 34.
  • 24.Balch GC, De Meo A, Guillem JG. Modern management of rectal canser: A 2006 update. World J Gastroenterol 2006;12(20):3186–95.
  • 25.Taylor FG, Swift RI, Blomqvist L, Brown G. A systematic approach to the interpretation of pre-operative staging MRI for rectal cancer. AJR 2008;191(6):1827–35.
  • 26.Huh JW, Lee JH, Kim HR, Kim YJ. Prognostic significance of lymphovascular or perineural invasion in patients with locally advanced colorectal cancer. Am J Surg 2013;206(5):758–63.
  • 27.Jhaveri KS, Hosseini-Nik H, Thipphavong S, Assarzadegan N, Menezes RJ, Kennedy ED, et al. MRI detection of extramural venous ınvasion in rectal cancer: Correlation with histopathology using Elastin Stain. AJR Am J Roentgenol 2016;206(4):747–55.
  • 28.Smith NJ, Barbachano Y, Norman AR, Swift RI, Abulafi AM, Brown G. Prognostic significance of magnetic resonance imaging-detected extramural vascular invasion in rectal cancer. Br J Surg 2008;95(2):229–36.
  • 29.Siddiqui MR, Gormly KL, Bhoday J, Balyansikova S, Battersby NJ, Chand M, et al. Interobserver agreement of radiologists assessing the response of rectal cancers to preoperative chemoradiation using the MRI tumour regression grading (mrTRG). Clin Radiol 2016;71(9):854–62.
Türk Onkoloji Dergisi-Cover
  • ISSN: 1300-7467
  • Başlangıç: 2015
  • Yayıncı: Ali Cangül
Sayıdaki Diğer Makaleler

Concurrent Use of Cyclin Dependent Kinase 4/6 (CDK4/6) Inhibitors with Palliative Radiotherapy for Metastatic Breast Cancer Patients: A Review of Toxicity

Özlem SÖNMEZ, Evrim TEZCANLI

Investigation of Methylation Status of Homeobox D3 (HOXD3) and Protocadherin 17 (PCDH17) in Patients with Prostate Cancer

Berna DEMİRCAN, Asıf YILDIRIM, Özgür EFİLOĞLU, Hatice İKİIŞIK, Burcu YÜCEL, Alper KAYA, Aslı KARAMAN, Ahsen Merve BAYRAK

Resection of a Giant Liposarcoma That Fills the Whole Retroperitoneal Area

İsmail SERT, Gülen GÜL, Korhan TUNCER, Semra DEMİRLİ ATICI, Ayberk DURSUN, Gizem KILINÇ

Prediction of Survival and Progression-free Survival Using Machine Learning in Stage III Lung Cancer: A Pilot Study

Güntülü AK, Melek YAKAR, Durmuş ETİZ, Muzaffer METİNTAŞ, Şenay YILMAZ, Özer ÇELİK

The Relationship of Ki-67 Over-expression with Clinicopathological Prognostic Parameters in Invasive Breast Carcinomas

Şennur İLVAN, Tülin ÖZTÜRK, Hale DEMİR, Buğra Taygun GÜLLE

Systemic Therapy in Recurrent or Metastatic Squamous Cell Head and Neck Cancer

Gökhan ÖZYİĞİT, Ivane KILADZE, Pavol DUBINSKY, Nenad FILIPOVIĆ, Branislav JEREMIĆ

The Effect of Henna in Nail Changes Due to Paclitaxel Treatment

Gülbeyaz CAN, Emel Emine KAYIKÇI

Increased Levels of Anxiety, Depression, and Secondary Trauma in Radiation Oncologists during COVID-19 Pandemic: A Preliminary Report from Turkey

Yasemin BÖLÜKBAŞI, Yakup ALBAYRAK, Uğur SELEK, Nülifer KILIÇ DURANKUŞ, Nihan POTAS, Duygu SEZEN, Eyüb Yaşar AKDEMİR, Erkan TOPKAN, Şükran ŞENYÜREK

Radiotherapy Equipment and Workforce in Turkey

Kadir YARAY, Tamer Oğuz GÜRSOY, Hatice Bilge BECERİR, Salih GÜRDALLI, Bülent YAPICI, Fadime ALKAYA, Aydın ÇAKIR

Therapeutic Benefit of Intracavitary-interstitial Brachytherapy in Cervical Cancer Patients with Small and Large High-risk Clinical Target Volume

Makbule TAMBAŞ