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1 l carcinoma undergoing radiotherapy alone or concurrent chemoradiotherapy.
2 nts undergoing radiotherapy or sequential or concurrent chemoradiotherapy.
3 e consistent with toxicities associated with concurrent chemoradiotherapy.
4 early postoperative chemotherapy followed by concurrent chemoradiotherapy.
5 on chemotherapy did not preclude delivery of concurrent chemoradiotherapy.
6 o achieved more than 50% response went on to concurrent chemoradiotherapy.
8 and randomly assigned to receive twice-daily concurrent chemoradiotherapy (274 patients) or once-dail
9 The addition of induction chemotherapy to concurrent chemoradiotherapy added toxicity and provided
10 rrent chemoradiotherapy with cisplatin-based concurrent chemoradiotherapy alone in patients with loca
11 rapy with either docetaxel or carboplatin or concurrent chemoradiotherapy alone with two cycles of bo
13 nt studies have suggested the superiority of concurrent chemoradiotherapy and the efficacy of paclita
14 atients did not receive more than 2 weeks of concurrent chemoradiotherapy and were not assessable for
15 ve a role for patients who initially receive concurrent chemoradiotherapy, and further study in this
16 ntified, and this has led to the adoption of concurrent chemoradiotherapy as a standard of care for t
17 ith advanced T-stage OPSCC who had completed concurrent chemoradiotherapy, bioradiotherapy, or radiot
20 PET/CT scan before adjuvant radiotherapy or concurrent chemoradiotherapy (CCRT) could meaningfully i
22 hibitor, added to, and in maintenance after, concurrent chemoradiotherapy (CCRT) in locally advanced
24 oesophageal cancer (EC) patients undergoing concurrent chemoradiotherapy (CCRT) remains uncertain.
26 ies have demonstrated the safety of adjuvant concurrent chemoradiotherapy (CRT) for locally advanced
27 d safety of palifermin in patients receiving concurrent chemoradiotherapy for advanced head and neck
28 cancer, or prevention of esophagitis during concurrent chemoradiotherapy for non-small-cell lung can
29 study of induction chemotherapy followed by concurrent chemoradiotherapy for organ preservation in p
31 gative (18)F-FDG PET or PET/CT results after concurrent chemoradiotherapy have a high negative predic
32 hedule of induction chemotherapy followed by concurrent chemoradiotherapy have been encouraging, and
34 -intent treatment of locally advanced NSCLC, concurrent chemoradiotherapy improves local control and
35 Limited-stage disease should be treated with concurrent chemoradiotherapy in patients with good perfo
36 ot differ between twice-daily and once-daily concurrent chemoradiotherapy in patients with limited-st
37 9) demonstrated efficacy and tolerability of concurrent chemoradiotherapy in poor-risk stage III non-
38 daily gefitinib with radiation alone or with concurrent chemoradiotherapy in previously untreated pat
42 ad and neck squamous cell carcinoma (HNSCC), concurrent chemoradiotherapy is a widely accepted treatm
48 of HART, mucosal toxicity, and the fact that concurrent chemoradiotherapy now seems more effective th
49 s more pronounced with the administration of concurrent chemoradiotherapy on study arms 2 and 3 (19%
50 based chemotherapies with or without upfront concurrent chemoradiotherapy or radiotherapy with curati
52 in/etoposide [PE]; three cycles) followed by concurrent chemoradiotherapy (PE plus 45 Gy; 1.5 Gy twic
53 ute mucositis is a dose-limiting toxicity of concurrent chemoradiotherapy regimens for locally advanc
55 carcinoma trial showed that cisplatin-based concurrent chemoradiotherapy resulted in a significantly
56 appropriate, standard treatment option, and concurrent chemoradiotherapy therapy is the most widely
57 Chemotherapy soon after surgery followed by concurrent chemoradiotherapy therapy was feasible; toler
63 assigned to arm A, which involved immediate concurrent chemoradiotherapy with carboplatin area under
64 cil (TPF) induction chemotherapy followed by concurrent chemoradiotherapy with cisplatin-based concur
65 therapy with three cycles of TPF followed by concurrent chemoradiotherapy with either docetaxel or ca
68 1998, many randomized studies that compared concurrent chemoradiotherapy with radiotherapy alone hav
70 luated whether induction chemotherapy before concurrent chemoradiotherapy would result in improved su
71 d that tirapazamine (TPZ) when combined with concurrent chemoradiotherapy yielded a promising median
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