Literature DB >> 18046561

Predictive clinicopathologic factors for limited response of T3 rectal cancer to combined modality therapy.

Anne Y Lin1, W Douglas Wong, Jinru Shia, Bruce D Minsky, Larissa K Temple, José G Guillem, Philip B Paty, Martin R Weiser.   

Abstract

PURPOSE: The response of T3 rectal cancer to combined modality therapy (CMT) is highly predictive of long-term outcome following surgery. The aim of this study was to identify pretreatment factors associated with poor tumor response to neoadjuvant chemoradiation.
METHODS: A prospective institutional database at Memorial Sloan-Kettering Cancer Center was queried for endorectal ultrasound (ERUS) stage T3N0-2 rectal cancer patients, treated with CMT followed by surgical resection, between 1998 and 2003. Preoperative clinicopathologic factors determined by biopsy, ERUS, proctoscopy, and digital rectal examination were correlated with the degree of downstaging of the primary mural lesion (tumor downstaging) in response to neoadjuvant therapy. Associations were analyzed by chi-square, Kaplan-Meier, and logistic regression.
RESULTS: Of 274 patients, 51% obtained tumor downstaging in response to preoperative treatment, i.e., lower pathologic T-stage compared with pretreatment ERUS. Five-year recurrence-free survival was 89% in the cohort that obtained tumor downstaging compared with only 45% in the cohort that obtained no tumor downstaging. Factors significantly associated with limited or lack of tumor downstaging after CMT included: fixed tumor on digital rectal examination (p < 0.021), near-circumferential tumor (p < 0.011), tumor stenosis (p < 0.025), metastatic disease (p < 0.012), biopsy-proven poorly differentiated pathology (p < 0.002), and radial extension >2.5 mm on ERUS (p < 0.031). On multivariate analysis, deep radial extension on ERUS, metastatic disease, and poorly differentiated pathology were in each, independently associated with limited or lack of tumor downstaging.
CONCLUSIONS: Pretreatment evaluation with biopsy, proctoscopy, and ERUS can identify T3 rectal cancer patients unlikely to respond well to CMT. These patients may be considered for alternative protocols and their tumors studied to ascertain the molecular events responsible for resistance to chemoradiation.

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Year:  2007        PMID: 18046561     DOI: 10.1007/s00384-007-0406-8

Source DB:  PubMed          Journal:  Int J Colorectal Dis        ISSN: 0179-1958            Impact factor:   2.571


  20 in total

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Authors:  Andrew X Zhu; Christopher G Willett
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3.  Long-term oncologic outcome following preoperative combined modality therapy and total mesorectal excision of locally advanced rectal cancer.

Authors:  Jose G Guillem; David B Chessin; Alfred M Cohen; Jinru Shia; Madhu Mazumdar; Warren Enker; Philip B Paty; Martin R Weiser; David Klimstra; Leonard Saltz; Bruce D Minsky; W Douglas Wong
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Authors:  H Ueno; H Mochizuki; S Tamakuma
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5.  Neoadjuvant therapy for adenocarcinoma of the rectum: tumor response and acute toxicity.

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Journal:  Dis Colon Rectum       Date:  2001-04       Impact factor: 4.585

6.  A pathologic complete response of rectal cancer to preoperative combined-modality therapy results in improved oncological outcome compared with those who achieve no downstaging on the basis of preoperative endorectal ultrasonography.

Authors:  Francesco Stipa; David B Chessin; Jinru Shia; Philip B Paty; Martin Weiser; Larissa K F Temple; Bruce D Minsky; W Douglas Wong; Jose G Guillem
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Review 7.  Preoperative staging of rectal cancer.

Authors:  H Kwok; I P Bissett; G L Hill
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9.  Levamisole and fluorouracil for adjuvant therapy of resected colon carcinoma.

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Authors:  U Hildebrandt; G Feifel
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Review 3.  Treatment of locally advanced rectal cancer: controversies and questions.

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4.  YKL-40/c-Met expression in rectal cancer biopsies predicts tumor regression following neoadjuvant chemoradiotherapy: a multi-institutional study.

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5.  Pretreatment Inflammatory-Nutritional Biomarkers Predict Responses to Neoadjuvant Chemoradiotherapy and Survival in Locally Advanced Rectal Cancer.

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