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1 referred for management of a newly diagnosed rectal cancer.
2 weeks between the end of CRT and surgery, in rectal cancer.
3 similar, although C was slightly higher for rectal cancer.
4 Most symptoms were more present in rectal cancer.
5 chemoradiotherapy (CRT) in locally advanced rectal cancer.
6 e of pathological complete response (pCR) in rectal cancer.
7 apy in patients with resectable stage II-III rectal cancer.
8 e to conventional low anterior resection for rectal cancer.
9 motherapy with observation for patients with rectal cancer.
10 bdominal resection for patients with stage I rectal cancer.
11 r robotic compared to LLAR in the setting of rectal cancer.
12 counseling patients anticipating surgery for rectal cancer.
13 val after laparoscopic and open resection of rectal cancer.
14 rsus laparoscopic low anterior resection for rectal cancer.
15 local excision for patients with stage T2N0 rectal cancer.
16 and surgery for patients with non-metastatic rectal cancer.
17 after laparoscopic coloanal anastomosis for rectal cancer.
18 s of Excellence program for US patients with rectal cancer.
19 mains around 30% to 50% in patients with low rectal cancer.
20 aroscopic sphincter-saving resection for low rectal cancer.
21 paradigm shift, with only 12% ES rate in low rectal cancer.
22 important predictive factor in patients with rectal cancer.
23 oncologic safety of laparoscopic surgery for rectal cancer.
24 c safety of laparoscopy for the treatment of rectal cancer.
25 important step for personalized treatment of rectal cancer.
26 the conventional abdominal dissection in low rectal cancer.
27 al benefit in patients with locally advanced rectal cancer.
28 recurrence and a major factor in survival in rectal cancer.
29 ns and overall survival (OS) for early-stage rectal cancer.
30 rs better local control in the management of rectal cancer.
31 R0 margins and survival rates for recurrent rectal cancer.
32 cer was associated with an increased risk of rectal cancer.
33 ajor complications after rectal excision for rectal cancer.
34 l cancer, but inferior for T1-2 colon and T2 rectal cancer.
35 underwent sacrectomy, with 49 for recurrent rectal cancer.
36 tcomes of patients with colon cancer but not rectal cancer.
37 ectal excision is the mainstay treatment for rectal cancer.
38 and radiation therapy (CRT) in patients with rectal cancer.
39 (CRT) response is a predictor of survival in rectal cancer.
40 prove chemoradiotherapy for locally advanced rectal cancer.
41 tomy among patients undergoing resection for rectal cancer.
42 pelvic exenteration for primary or recurrent rectal cancer.
43 pic (LRR) vs open (ORR) rectal resection for rectal cancer.
44 is needed in patients with locally advanced rectal cancer.
45 arly postoperative outcomes in patients with rectal cancer.
46 strate intratumoral genetic heterogeneity in rectal cancer.
47 maging texture features derived from primary rectal cancer.
48 of germline alterations in the MMR genes in rectal cancer.
49 fter eAPR with preoperative radiotherapy for rectal cancer.
50 is the standard of care for locally advanced rectal cancer.
51 ged as a management option for patients with rectal cancer.
52 social functions were significantly worse in rectal cancer.
53 during preoperative CRT for locally advanced rectal cancer.
54 ive resection margins after resection of low rectal cancers.
55 ls metabolic differences between colonic and rectal cancers.
56 tumoral heterogeneity is present among naive rectal cancers.
57 inely tested, but little is known about dMMR rectal cancers.
58 is the optimal surgical technique for distal rectal cancers?
59 it on 2 consecutive days in 14 patients with rectal cancer (11 men [mean age, 61.7 years], three wome
62 nal bacteria, was positively associated with rectal cancer [3.38 (1.25-9.16); P trend = 0.02] and wit
63 53.8% [53.3-54.4] vs 60.4% [60.0-60.9]), and rectal cancer (52.1% [51.6-52.6] vs 57.6% [57.1-58.1]).
64 rapy (RT) is a mainstay in the management of rectal cancer, a tumor characterized by desmoplastic str
65 emoradiotherapy guidelines for patients with rectal cancer across geographic regions and institution
66 ing nonoperative management in patients with rectal cancer after chemoradiation is the inability to i
69 loratory data suggest local excision of T1-2 rectal cancer after neoadjuvant therapy may be safe.
70 lts of diagnostic performances for restaging rectal cancer after neoadjuvant treatment, but significa
71 e of adjuvant chemotherapy for patients with rectal cancer after preoperative (chemo)radiotherapy and
73 salvage surgery on survival in patients with rectal cancer after receiving multidisciplinary treatmen
82 l outcome after laparoscopic surgery for low rectal cancer and seems as a safe option to preserve the
83 tic leakage after low anterior resection for rectal cancer, and the proportion of leakages that devel
84 tations detected in different fragments from rectal cancers are frequently unique to a single fragmen
85 detection of local recurrence in the case of rectal cancer, as well as the place of CT colonography a
86 patients with stage II-III locally advanced rectal cancer at 17 institutions in the USA and Canada.
88 ive new surgical option in patients with low rectal cancer because laparotomy is not necessary due to
91 on or tumor-specific mesorectal excision for rectal cancer between April 2009 and April 2016 via a ro
92 l in the UK and Ireland was intermediate for rectal cancer, breast cancer, prostate cancer, skin mela
94 institutions and 11 subjects diagnosed with rectal cancer but with no clinical or MRI indications of
95 o major surgery for carcinoma in situ and T1 rectal cancer, but inferior for T1-2 colon and T2 rectal
96 comes/costs) of proctectomy in patients with rectal cancer by 3 approaches: open, laparoscopic, and r
97 precision in estimating the risk of colon or rectal cancer by reducing the impact of misclassificatio
98 and radiation therapy (CRT) in patients with rectal cancer by using histogram analysis derived from w
99 In this nationwide study, resection of low rectal cancers by ELAPE did not improve short-term oncol
102 as independent risk factors, and advances in rectal cancer care are necessary to approach the outcome
104 a mail survey with 8 questions pertaining to rectal cancer care was created, modified for content val
105 However, because of large evolvement in rectal cancer care, outcomes after APE may have improved
109 ests the need for specialized designation of rectal cancer centers to support ongoing regionalization
110 ests the need for specialized designation of rectal cancer centers to support ongoing regionalization
111 motherapy and radiation for locally advanced rectal cancer complete postoperative adjuvant systemic c
112 open surgery (n=142) for upper, mid, and low rectal cancer conducted at the Prince of Wales Hospital,
113 OM demonstrates promise for the treatment of rectal cancer; currently, however, the most appropriate
114 e, cetuximab, and ramucirumab for metastatic rectal cancer (diagnosed in November 2013 and treated th
116 of a pelvic drain after rectal excision for rectal cancer did not confer any benefit to the patient.
117 e laparoscopic surgery for colonic and upper rectal cancer, enrolled from October 2008 to October 201
120 t of adjuvant chemotherapy for patients with rectal cancer following radiotherapy or chemoradiation r
121 the National Cancer Data Base diagnosed with rectal cancer from 1998 to 2010 were initially included.
122 or all patients diagnosed as having colon or rectal cancer from January 1, 1975, through December 31,
123 57 patients diagnosed with stage IV colon or rectal cancer from January 1, 1988, through December 31,
124 ns will continue to advance the treatment of rectal cancer, further emphasizing the need for a multid
125 95% CI: 0.50, 0.96; P for trend = 0.06), and rectal cancer (>90 vs. </=30 minutes/day, HR = 0.59, 95%
126 tudy has shown poor compliance with national rectal cancer guidelines, but whether this finding is re
128 cess of neoadjuvant CRT for locally advanced rectal cancer has changed an already complex management
131 pearances of a vaginal metastasis from colon-rectal cancer have not been extensively investigated.
132 mprovements in the outcomes of patients with rectal cancer have occurred over the past 30 years.
133 comparing laparoscopic and open surgery for rectal cancer have reported long-term survival data.
136 lines (colon cancer: DLD-1, HCT116 and HT29; rectal cancer: HT55, SW837 and VACO4S) maintained in hyp
137 pared LRR with ORR for histologically proven rectal cancer in adult patients and reported pathologic
138 showed significant association with CRC and rectal cancer in Koreans, but not with colon cancer alon
139 rm accurate localization and segmentation of rectal cancer in MR imaging in the majority of patients.
140 s after rectal resection and anastomosis for rectal cancer in selected patients without clinical or r
143 ectional study of low anterior resection for rectal cancer in the Netherlands in 2011, with almost ro
145 ltidisciplinary approach to the patient with rectal cancer includes many health care professionals.
149 Laparoscopic sphincter preservation for low rectal cancer is challenging because of the high risk of
151 ut the efficacy of laparoscopic resection of rectal cancer is incomplete, particularly for patients w
155 The standard of care in locally advanced rectal cancer is preoperative, long course (5-fluorourac
156 ce to evidence-based treatment guidelines in rectal cancer is suboptimal in the United States, with s
159 ecurrence rates in clinical stages II to III rectal cancer, it delays administration of optimal chemo
162 had confirmed histopathological diagnosis of rectal cancer located within 15 cm from the anal verge,
163 Between 2008 and 2012, 100 patients with low rectal cancer (< 6 cm from the anal verge) suitable for
164 A substantial proportion of patients with rectal cancer managed by watch and wait avoided major su
166 Several clinical management decisions in rectal cancer may be influenced by pretreatment biopsy i
172 it is possible that the observed increase in rectal cancer mortality may be partly an artefact of cau
174 ectomy at 11 and 16 years, respectively, for rectal cancer; neither has developed recurrent disease.
175 cted patients with clinical stages II to III rectal cancer, neoadjuvant chemotherapy and selective ra
178 y evaluate the impact of robotic surgery for rectal cancer on sexual and urinary functions in male an
181 Clinical Complete Response in Patients with Rectal Cancer (OnCoRe) was a propensity-score matched co
183 objective was to examine the use of NOM for rectal cancer over time, as well as the patient- and fac
184 and in unmatched (interpatient) samples from rectal cancer patients after neoadjuvant chemoradiothera
186 mpared short-term oncologic outcomes between rectal cancer patients undergoing either RLAR or LLAR.
193 tal mesorectal excision for locally advanced rectal cancer, patients who experience local or systemic
194 udy was to evaluate the utility of reimaging rectal cancer post-CRT (chemoradiotherapy) with magnetic
198 nosed during 2005-09, survival for colon and rectal cancer reached 60% or more in 22 countries around
199 95% confidence interval: 1.07, 2.24) but not rectal cancer (relative risk = 1.07, 95% confidence inte
200 This follow-up study of 374 patients with rectal cancer reports the relationship between preoperat
201 of unselected consecutive patients with low rectal cancer requiring proctectomy and coloanal anastom
202 een elective open and laparoscopic colon and rectal cancer resection in a daily practice multicenter
203 at worse oncological outcomes after curative rectal cancer resection in patients receiving perioperat
205 237) or conventional (n = 234) laparoscopic rectal cancer resection, performed by either high (upper
208 pshot research project, data from registered rectal cancer resections in the Dutch Surgical Colorecta
211 Neoadjuvant chemoradiation for stage II/III rectal cancer results in up to 49% of patients with a cl
212 line tended to be positively associated with rectal cancer risk [OR (95% confidence interval, CI)(hig
217 ited Kingdom, patients with locally advanced rectal cancer routinely receive neoadjuvant chemoradioth
221 ancer susceptibility, but a possible role in rectal cancer should be further evaluated in larger coho
223 y (adjusted OR = 1.02; 95% CI: 0.83-1.25) or rectal cancer-specific mortality (adjusted OR = 1.10; 95
224 a median follow-up of 6.8 years, the 5-year rectal cancer-specific survival was 100% for stage I and
226 All consecutive patients with middle or low rectal cancer submitted to surgery were included into a
228 discharge VTE chemoprophylaxis if undergoing rectal cancer surgery [incidence rate ratio (IRR), 1.83;
230 ial resection margin (CRM) involvement after rectal cancer surgery in comparison with low anterior re
242 was to explore specific microRNAs (miRs) in rectal cancer that would predict response to radiation a
243 use of LE is also increasing for higher-risk rectal cancers that do not meet guideline criteria for L
244 arantee the quality of surgical treatment of rectal cancer, the Association of Surgeons of the Nether
247 ts (70 years or older) with locally advanced rectal cancers to image-guided radiotherapy (IGRT).
248 enters, a sizeable minority of patients with rectal cancer treated with curative-intent neoadjuvant c
249 patients with clinically staged T2N0 distal rectal cancer treated with neoadjuvant chemoradiotherapy
250 tive adjuvant chemotherapy for patients with rectal cancer treated with preoperative chemoradiation.
251 outcome of neoadjuvant chemoradiotherapy for rectal cancer treatment, in support of ongoing clinical
252 outcome of neoadjuvant chemoradiotherapy for rectal cancer treatment, in support of ongoing clinical
254 From 2005 to 2013, all patients with low rectal cancer undergoing laparoscopic total mesorectal e
257 Between 2000 and 2010, 220 patients with low rectal cancer underwent laparoscopic rectal excision wit
259 e and prognostic capability in patients with rectal cancer using histopathology as the gold standard.
263 fter eAPR with preoperative radiotherapy for rectal cancer was not improved when using a biological m
269 ents who underwent resection for stage I-III rectal cancer were identified from the 2010-2011 Nationa
271 d DWI) of 140 patients with locally advanced rectal cancer were included in our analysis, equally div
274 ients undergoing fully robotic resection for rectal cancer were prospectively included in the study.
275 ts operated on for clinical stage II and III rectal cancer were selected from the 2006-2011 National
277 R over time in either sex, or when colon and rectal cancers were considered separately; however the n
278 orectal, left-side colon, sigmoid colon, and rectal cancers were not associated with gallstone diseas
280 We prospectively studied 12 patients with rectal cancer who completed standardized neoadjuvant che
281 this retrospective study of 31 patients with rectal cancer who underwent magnetic resonance (MR) imag
282 rospective data from patients with recurrent rectal cancer who underwent pelvic exenteration involvin
283 of 13 elderly patients with locally advanced rectal cancer who underwent preoperative chemoradiation
284 sed to evaluate how frequently patients with rectal cancer who were treated with neoadjuvant chemothe
285 atients with locally advanced (cT3-4 or cN+) rectal cancer who were treated with preoperative chemora
288 , in 2030, the incidence rates for colon and rectal cancers will increase by 90.0% and 124.2%, respec
292 ed that show the ability to accurately stage rectal cancer with magnetic resonance (MR) imaging.
294 nd 1 year after the primary treatment of her rectal cancer with preoperative radiotherapy and low ant
295 interaction of location of tumor (colon vs. rectal cancer) with DM on OS (P = 0.009) and DFS (P = 0.
298 ative CRT increases the rate of pCR by 6% in rectal cancer, with similar outcomes and complication ra
299 f 486 patients with clinical stage II or III rectal cancer within 12 cm of the anal verge were random
300 observational cohort study of patients with rectal cancer within the National Cancer Data Base (2003
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