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 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: José G surname: GUILLEM fullname: GUILLEM, José G organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 2 givenname: Juan A surname: DIAZ-GONZALEZ fullname: DIAZ-GONZALEZ, Juan A organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 3 givenname: Elyn R surname: RIEDEL fullname: RIEDEL, Elyn R organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 4 givenname: Donato surname: NITTI fullname: NITTI, Donato organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 5 givenname: W. Douglas surname: WONG fullname: WONG, W. Douglas organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 6 givenname: Salvatore surname: PUCCIARELLI fullname: PUCCIARELLI, Salvatore organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 7 givenname: Bruce D surname: MINSKY fullname: MINSKY, Bruce D organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 8 givenname: Vincenzo surname: VALENTINI fullname: VALENTINI, Vincenzo organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 9 givenname: Seung-Yong surname: JEONG fullname: JEONG, Seung-Yong organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 10 givenname: Miguel A surname: RODRIGUEZ-BIGAS fullname: RODRIGUEZ-BIGAS, Miguel A organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 11 givenname: Claudio surname: COCO fullname: COCO, Claudio organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 12 givenname: Rebecca surname: LEON fullname: LEON, Rebecca organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 13 givenname: José L surname: HERNANDEZ-LIZOAIN fullname: HERNANDEZ-LIZOAIN, José L organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States – sequence: 14 givenname: José J surname: ARISTU fullname: ARISTU, José J organization: Memorial Sloan-Kettering Cancer Center, New York, NY, United States |
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Keywords | Rectal disease Cancerology Digestive diseases Intestinal disease Malignant tumor Rectum cancer Preoperative Chemoradiotherapy Anorectal disease Cancer |
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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 |
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