cT3N0 Rectal Cancer: Potential Overtreatment With Preoperative Chemoradiotherapy Is Warranted

Although combined-modality therapy (CMT) is the preferred treatment for T3 and/or lymph node (LN)-positive rectal cancer, the German rectal cancer study published in 2004 demonstrated that 18% of patients deemed suitable for preoperative CMT by endorectal ultrasound (ERUS) may be overstaged. Because...

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Published in:Journal of clinical oncology Vol. 26; no. 3; pp. 368 - 373
Main Authors: GUILLEM, José G, DIAZ-GONZALEZ, Juan A, RIEDEL, Elyn R, NITTI, Donato, WONG, W. Douglas, PUCCIARELLI, Salvatore, MINSKY, Bruce D, VALENTINI, Vincenzo, JEONG, Seung-Yong, RODRIGUEZ-BIGAS, Miguel A, COCO, Claudio, LEON, Rebecca, HERNANDEZ-LIZOAIN, José L, ARISTU, José J
Format: Journal Article
Language:English
Published: Baltimore, MD American Society of Clinical Oncology 20-01-2008
Lippincott Williams & Wilkins
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Abstract Although combined-modality therapy (CMT) is the preferred treatment for T3 and/or lymph node (LN)-positive rectal cancer, the German rectal cancer study published in 2004 demonstrated that 18% of patients deemed suitable for preoperative CMT by endorectal ultrasound (ERUS) may be overstaged. Because data also suggest that LN-negative rectal cancer after total mesorectal excision may not require radiotherapy, it is reasonable to consider omitting radiotherapy for the cT3N0 subset. We therefore determined the accuracy of pre-CMT ERUS or magnetic resonance imaging (MRI) staging, to explore the validity of a nonpreoperative CMT approach for cT3N0 disease. One hundred eighty-eight ERUS-/MRI-staged T3N0 rectal cancer patients received preoperative CMT (fluorouracil based and 45-50.4 Gy) followed by radical resection. Rates of pathologic complete response (pCR) and mesorectal LN involvement were determined. Tumors were located a median of 5 cm from the anal verge. Sphincter-preserving surgery was performed in 143 patients (76%). Overall pCR was 20%, and 41 patients (22%) had pathologically positive mesorectal LNs. The incidence of positive LNs significantly increased with T stage: ypT0, 3%; ypT1, 7%; ypT2, 20%; ypT3-4, 36% (P = .001). The accuracy of preoperative ERUS/MRI for staging mid to distal cT3N0 rectal cancer is limited because 22% of patients have undetected mesorectal LN involvement despite CMT. Therefore, ERUS-/MRI-staged T3N0 rectal cancer patients should continue to receive preoperative CMT. Although 18% may be overstaged and therefore overtreated, our data suggest that an even larger number would be understaged and require postoperative CMT, which is associated with significantly inferior local control, higher toxicity, and worse functional outcome.
AbstractList Although combined-modality therapy (CMT) is the preferred treatment for T3 and/or lymph node (LN)-positive rectal cancer, the German rectal cancer study published in 2004 demonstrated that 18% of patients deemed suitable for preoperative CMT by endorectal ultrasound (ERUS) may be overstaged. Because data also suggest that LN-negative rectal cancer after total mesorectal excision may not require radiotherapy, it is reasonable to consider omitting radiotherapy for the cT3N0 subset. We therefore determined the accuracy of pre-CMT ERUS or magnetic resonance imaging (MRI) staging, to explore the validity of a nonpreoperative CMT approach for cT3N0 disease. One hundred eighty-eight ERUS-/MRI-staged T3N0 rectal cancer patients received preoperative CMT (fluorouracil based and 45-50.4 Gy) followed by radical resection. Rates of pathologic complete response (pCR) and mesorectal LN involvement were determined. Tumors were located a median of 5 cm from the anal verge. Sphincter-preserving surgery was performed in 143 patients (76%). Overall pCR was 20%, and 41 patients (22%) had pathologically positive mesorectal LNs. The incidence of positive LNs significantly increased with T stage: ypT0, 3%; ypT1, 7%; ypT2, 20%; ypT3-4, 36% (P = .001). The accuracy of preoperative ERUS/MRI for staging mid to distal cT3N0 rectal cancer is limited because 22% of patients have undetected mesorectal LN involvement despite CMT. Therefore, ERUS-/MRI-staged T3N0 rectal cancer patients should continue to receive preoperative CMT. Although 18% may be overstaged and therefore overtreated, our data suggest that an even larger number would be understaged and require postoperative CMT, which is associated with significantly inferior local control, higher toxicity, and worse functional outcome.
Author Rebecca Leon
José J. Aristu
José L. Hernandez-Lizoain
Seung-Yong Jeong
José G. Guillem
Claudio Coco
Donato Nitti
Juan A. Díaz-González
Vincenzo Valentini
Bruce D. Minsky
Elyn R. Riedel
W. Douglas Wong
Salvatore Pucciarelli
Miguel A. Rodriguez-Bigas
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  fullname: DIAZ-GONZALEZ, Juan A
  organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States
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  fullname: VALENTINI, Vincenzo
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Issue 3
Keywords Rectal disease
Cancerology
Digestive diseases
Intestinal disease
Malignant tumor
Rectum cancer
Preoperative
Chemoradiotherapy
Anorectal disease
Cancer
Language English
License CC BY 4.0
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Snippet Although combined-modality therapy (CMT) is the preferred treatment for T3 and/or lymph node (LN)-positive rectal cancer, the German rectal cancer study...
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SubjectTerms Adenocarcinoma - drug therapy
Adenocarcinoma - pathology
Adenocarcinoma - radiotherapy
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Carboplatin - administration & dosage
Cisplatin - administration & dosage
Combined Modality Therapy
Endosonography
Female
Fluorouracil - administration & dosage
Gamma Rays
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Leucovorin - administration & dosage
Lymph Nodes - pathology
Magnetic Resonance Imaging
Male
Medical sciences
Middle Aged
Neoplasm Staging
Preoperative Care
Rectal Neoplasms - drug therapy
Rectal Neoplasms - pathology
Rectal Neoplasms - radiotherapy
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Tumors
Title cT3N0 Rectal Cancer: Potential Overtreatment With Preoperative Chemoradiotherapy Is Warranted
URI http://jco.ascopubs.org/content/26/3/368.abstract
https://www.ncbi.nlm.nih.gov/pubmed/18202411
Volume 26
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