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1 ients were treated, and 13 received the full preoperative chemotherapy.
2 re registered in the study, and 138 received preoperative chemotherapy.
3 e operative morbidity and mortality by using preoperative chemotherapy.
4 Each patient was treated with four cycles of preoperative chemotherapy.
5 ncer who underwent resection of CCLM without preoperative chemotherapy.
6 T10 protocol and therapy with more intensive preoperative chemotherapy.
7 ix patients with stage IIIB disease received preoperative chemotherapy.
8 28% displayed a good histologic response to preoperative chemotherapy.
9 sectable gastric adenocarcinoma who received preoperative chemotherapy.
10 calendar period of surgery, and response to preoperative chemotherapy.
11 ing and histologic assessment of response to preoperative chemotherapy.
12 mber and diameter, extrahepatic disease, and preoperative chemotherapy.
13 ng system, lack validation in the setting of preoperative chemotherapy.
14 59.8% of patients received preoperative chemotherapy.
15 ge of the primary, and the administration of preoperative chemotherapy.
16 er resection for colorectal metastases after preoperative chemotherapy.
17 a is possible in many patients after initial preoperative chemotherapy.
18 physicians prefer a short course of systemic preoperative chemotherapy.
19 ve histologically positive lymph nodes after preoperative chemotherapy.
20 f Pediatric Oncology in Europe in regards to preoperative chemotherapy.
21 the time of diagnosis patients' response to preoperative chemotherapy.
22 s (727 after excluding patients who received preoperative chemotherapy, 202 after 1:1 PS-matching).
24 6.4%; P=0.037), as well as lower response to preoperative chemotherapy (63.9% vs 85.2%; P=0.006).
27 tricted to "benchmark" patients, selected on preoperative chemotherapy administration and response.
28 carcinoma in situ (DCIS) after completion of preoperative chemotherapy affects the outcome of patient
30 e excluded, two because they were undergoing preoperative chemotherapy and 11 because of the presence
31 l: 14.9 months for the patients who received preoperative chemotherapy and 16.1 months for those who
32 adequate data , 213 were assigned to receive preoperative chemotherapy and 227 to undergo immediate s
33 was 78% for the regimen with more intensive preoperative chemotherapy and 73% for the control arm.
35 linical stage II or III disease treated with preoperative chemotherapy and curative-intent resection,
36 rbB-2 expression with histologic response to preoperative chemotherapy and event-free survival in thi
37 utcomes for 378 patients treated with modern preoperative chemotherapy and hepatectomy were analyzed.
38 e residual disease at surgery after standard preoperative chemotherapy and HER2-targeted therapy shou
39 nt, and the relationship between response to preoperative chemotherapy and outcome were also evaluate
40 APC and PIK3CA predicts inferior response to preoperative chemotherapy and poor survival in patients
41 Although EPP as part of trimodality therapy (preoperative chemotherapy and postoperative radiation) i
42 of newer chemotherapeutic agents, the use of preoperative chemotherapy and radiotherapy, and the use
43 and PIK3CA mutations in patients undergoing preoperative chemotherapy and resection for colorectal l
45 chemotherapy predicts patient survival after preoperative chemotherapy and resection of colorectal li
47 y scans of consecutive patients who received preoperative chemotherapy and/or (chemo)radiation before
49 in the surgery-only arm and 62 months in the preoperative chemotherapy arm (hazard ratio, 0.79; 95% C
50 h AJCC stage IIIB extremity STS treated with preoperative chemotherapy between 1986 and 1990 at The U
51 vascular or biliary invasion) are reduced by preoperative chemotherapy, but their impact on survival
52 ic radiation therapy (50 to 60 Gy; arm A) or preoperative chemotherapy (cisplatin/etoposide [PE]; thr
54 hile preserving renal tissue by intensifying preoperative chemotherapy, completing definitive surgery
56 nts (6 months to 18 years) were treated with preoperative chemotherapy consisting of 6 weeks of vincr
57 tion was to administer up to five courses of preoperative chemotherapy consisting of fluorouracil (50
59 ptor status, histologic grade, and number of preoperative chemotherapy cycles had good discrimination
60 The success of breast conservation after preoperative chemotherapy depends on careful patient sel
61 le gastric cancer were randomized to receive preoperative chemotherapy followed by adequate gastrecto
62 OS for chemotherapy alone, cystectomy alone, preoperative chemotherapy followed by cystectomy, and cy
63 is made with a biopsy, treatment consists of preoperative chemotherapy followed by definitive surgery
64 lti-institutional randomized trial comparing preoperative chemotherapy followed by surgery with surge
65 ents with primary breast cancer treated with preoperative chemotherapy followed by surgery; have avai
70 l vein embolization (5%, 9%, 9%, P = 0.001), preoperative chemotherapy for colorectal liver metastase
73 opsy can be performed either before or after preoperative chemotherapy for patients with clinical N0
75 ients whose tumour showed a poor response to preoperative chemotherapy (>/=10% viable tumour) improve
77 ents who had initial tumor size < or = 2 cm, preoperative chemotherapy had no impact on volume of bre
78 al tumor size >2.0 cm, patients who received preoperative chemotherapy had significantly smaller volu
80 larger breast tumors, patients treated with preoperative chemotherapy have less extensive resection,
81 0 months for surgery alone and 33 months for preoperative chemotherapy (hazard ratio, 0.80; 95% CI, 0
82 NBC patients treated with anthracycline-only preoperative chemotherapy, high CD73 gene expression was
84 tal neoadjuvant therapy (TNT) protocols (ie, preoperative chemotherapy in addition to radiotherapy) m
86 ally assess benefits and risks of the use of preoperative chemotherapy in patients presenting with co
87 value of an optimal morphologic response to preoperative chemotherapy in patients undergoing chemoth
88 OEO2 is a randomized, controlled trial of preoperative chemotherapy in patients undergoing radical
89 ET is valuable for monitoring the effects of preoperative chemotherapy in patients with locally advan
91 The degree of tumor necrosis in response to preoperative chemotherapy is a reliable prognostic facto
92 localized esophageal cancer, whether or not preoperative chemotherapy is administered, only an R0 re
95 ms' tumour when the histological response to preoperative chemotherapy is incorporated into the risk
97 resected primary tumor following a period of preoperative chemotherapy is predictive of subsequent ev
99 ts with LA/BR PDAC, which includes prolonged preoperative chemotherapy, is associated with a high inc
100 ectomy between 2010 and 2018 after receiving preoperative chemotherapy (n = 36; 12%), (chemo)radiatio
101 th good histologic response with intensified preoperative chemotherapy, no improvement in EFS was obs
103 g those that occurred during the interval of preoperative chemotherapy (one of the five also had a su
105 rcinoma specimens from patients treated with preoperative chemotherapy or chemoradiation therapy, we
107 ephrectomy from 1989 to 2006 did not receive preoperative chemotherapy or radiation therapy and under
112 ith fluorine-18 fluorodeoxyglucose (FDG) for preoperative chemotherapy response in patients with loca
114 tment approach including standardized 3-drug preoperative chemotherapy, surgical resection within 12
115 tients who underwent hepatic resection after preoperative chemotherapy that included bevacizumab at a
117 lly advanced breast carcinoma (LABC) receive preoperative chemotherapy to provide early systemic trea
120 h of liver resection, malignant indications, preoperative chemotherapy treatment, elements of metabol
121 ilar demographics, diagnoses, comorbidities, preoperative chemotherapy treatments, and extent of part
122 .99; 95% CI, 0.97-1.00), less sensitivity to preoperative chemotherapy (very sensitive vs refractory
123 ological response (> 90% tumour necrosis) to preoperative chemotherapy was about 29% with both regime
131 ted with oxaliplatin and/or irinotecan-based preoperative chemotherapy were eligible for the study.
132 surgically resected CLM patients without any preoperative chemotherapy were included with a median fo
135 red fifty-eight patients (38.9%) received no preoperative chemotherapy, whereas 248 patients (61.1%)
138 atients started and 89% (85 of 95) completed preoperative chemotherapy with grade 3-4 gastrointestina
140 trials have again demonstrated tolerance to preoperative chemotherapy with no increase in operative
142 in 26 countries who had received 4 weeks of preoperative chemotherapy with vincristine and actinomyc
144 his study was to determine if more intensive preoperative chemotherapy would increase the proportion