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1 Each patient was treated with four cycles of preoperative chemotherapy.
2 ing and histologic assessment of response to preoperative chemotherapy.
3 T10 protocol and therapy with more intensive preoperative chemotherapy.
4 ix patients with stage IIIB disease received preoperative chemotherapy.
5 28% displayed a good histologic response to preoperative chemotherapy.
6 mber and diameter, extrahepatic disease, and preoperative chemotherapy.
7 59.8% of patients received preoperative chemotherapy.
8 ge of the primary, and the administration of preoperative chemotherapy.
9 er resection for colorectal metastases after preoperative chemotherapy.
10 a is possible in many patients after initial preoperative chemotherapy.
11 ncer who underwent resection of CCLM without preoperative chemotherapy.
12 physicians prefer a short course of systemic preoperative chemotherapy.
13 ve histologically positive lymph nodes after preoperative chemotherapy.
14 calendar period of surgery, and response to preoperative chemotherapy.
15 f Pediatric Oncology in Europe in regards to preoperative chemotherapy.
16 the time of diagnosis patients' response to preoperative chemotherapy.
17 ients were treated, and 13 received the full preoperative chemotherapy.
18 re registered in the study, and 138 received preoperative chemotherapy.
19 e operative morbidity and mortality by using preoperative chemotherapy.
21 6.4%; P=0.037), as well as lower response to preoperative chemotherapy (63.9% vs 85.2%; P=0.006).
23 carcinoma in situ (DCIS) after completion of preoperative chemotherapy affects the outcome of patient
25 e excluded, two because they were undergoing preoperative chemotherapy and 11 because of the presence
26 l: 14.9 months for the patients who received preoperative chemotherapy and 16.1 months for those who
27 adequate data , 213 were assigned to receive preoperative chemotherapy and 227 to undergo immediate s
28 was 78% for the regimen with more intensive preoperative chemotherapy and 73% for the control arm.
30 rbB-2 expression with histologic response to preoperative chemotherapy and event-free survival in thi
31 utcomes for 378 patients treated with modern preoperative chemotherapy and hepatectomy were analyzed.
32 nt, and the relationship between response to preoperative chemotherapy and outcome were also evaluate
33 APC and PIK3CA predicts inferior response to preoperative chemotherapy and poor survival in patients
34 Although EPP as part of trimodality therapy (preoperative chemotherapy and postoperative radiation) i
35 of newer chemotherapeutic agents, the use of preoperative chemotherapy and radiotherapy, and the use
36 and PIK3CA mutations in patients undergoing preoperative chemotherapy and resection for colorectal l
38 chemotherapy predicts patient survival after preoperative chemotherapy and resection of colorectal li
41 in the surgery-only arm and 62 months in the preoperative chemotherapy arm (hazard ratio, 0.79; 95% C
42 h AJCC stage IIIB extremity STS treated with preoperative chemotherapy between 1986 and 1990 at The U
43 vascular or biliary invasion) are reduced by preoperative chemotherapy, but their impact on survival
44 ic radiation therapy (50 to 60 Gy; arm A) or preoperative chemotherapy (cisplatin/etoposide [PE]; thr
46 hile preserving renal tissue by intensifying preoperative chemotherapy, completing definitive surgery
48 nts (6 months to 18 years) were treated with preoperative chemotherapy consisting of 6 weeks of vincr
49 tion was to administer up to five courses of preoperative chemotherapy consisting of fluorouracil (50
51 ptor status, histologic grade, and number of preoperative chemotherapy cycles had good discrimination
52 The success of breast conservation after preoperative chemotherapy depends on careful patient sel
53 OS for chemotherapy alone, cystectomy alone, preoperative chemotherapy followed by cystectomy, and cy
54 is made with a biopsy, treatment consists of preoperative chemotherapy followed by definitive surgery
55 lti-institutional randomized trial comparing preoperative chemotherapy followed by surgery with surge
56 ents with primary breast cancer treated with preoperative chemotherapy followed by surgery; have avai
63 opsy can be performed either before or after preoperative chemotherapy for patients with clinical N0
65 ients whose tumour showed a poor response to preoperative chemotherapy (>/=10% viable tumour) improve
67 ents who had initial tumor size < or = 2 cm, preoperative chemotherapy had no impact on volume of bre
68 al tumor size >2.0 cm, patients who received preoperative chemotherapy had significantly smaller volu
70 larger breast tumors, patients treated with preoperative chemotherapy have less extensive resection,
71 0 months for surgery alone and 33 months for preoperative chemotherapy (hazard ratio, 0.80; 95% CI, 0
72 NBC patients treated with anthracycline-only preoperative chemotherapy, high CD73 gene expression was
75 ally assess benefits and risks of the use of preoperative chemotherapy in patients presenting with co
76 value of an optimal morphologic response to preoperative chemotherapy in patients undergoing chemoth
77 OEO2 is a randomized, controlled trial of preoperative chemotherapy in patients undergoing radical
78 ET is valuable for monitoring the effects of preoperative chemotherapy in patients with locally advan
80 The degree of tumor necrosis in response to preoperative chemotherapy is a reliable prognostic facto
81 localized esophageal cancer, whether or not preoperative chemotherapy is administered, only an R0 re
84 ms' tumour when the histological response to preoperative chemotherapy is incorporated into the risk
86 resected primary tumor following a period of preoperative chemotherapy is predictive of subsequent ev
88 ts with LA/BR PDAC, which includes prolonged preoperative chemotherapy, is associated with a high inc
89 th good histologic response with intensified preoperative chemotherapy, no improvement in EFS was obs
91 g those that occurred during the interval of preoperative chemotherapy (one of the five also had a su
94 ephrectomy from 1989 to 2006 did not receive preoperative chemotherapy or radiation therapy and under
99 ith fluorine-18 fluorodeoxyglucose (FDG) for preoperative chemotherapy response in patients with loca
101 tment approach including standardized 3-drug preoperative chemotherapy, surgical resection within 12
102 tients who underwent hepatic resection after preoperative chemotherapy that included bevacizumab at a
104 lly advanced breast carcinoma (LABC) receive preoperative chemotherapy to provide early systemic trea
107 h of liver resection, malignant indications, preoperative chemotherapy treatment, elements of metabol
108 ilar demographics, diagnoses, comorbidities, preoperative chemotherapy treatments, and extent of part
109 ological response (> 90% tumour necrosis) to preoperative chemotherapy was about 29% with both regime
116 ted with oxaliplatin and/or irinotecan-based preoperative chemotherapy were eligible for the study.
119 red fifty-eight patients (38.9%) received no preoperative chemotherapy, whereas 248 patients (61.1%)
122 atients started and 89% (85 of 95) completed preoperative chemotherapy with grade 3-4 gastrointestina
124 trials have again demonstrated tolerance to preoperative chemotherapy with no increase in operative
126 in 26 countries who had received 4 weeks of preoperative chemotherapy with vincristine and actinomyc
127 his study was to determine if more intensive preoperative chemotherapy would increase the proportion
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