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http://hdl.handle.net/11452/30117
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DC Field | Value | Language |
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dc.contributor.author | Terzi, Cem | - |
dc.contributor.author | Bingül, Muhammet Bahattin | - |
dc.contributor.author | Arslan, Naciye Çiğdem | - |
dc.contributor.author | Canda, Aras Emre | - |
dc.contributor.author | Obuz, Funda | - |
dc.contributor.author | Görken, İlknur Birkay | - |
dc.contributor.author | Ünlü, Mehtat | - |
dc.contributor.author | Öztop, İlhan | - |
dc.date.accessioned | 2022-12-27T11:12:48Z | - |
dc.date.available | 2022-12-27T11:12:48Z | - |
dc.date.issued | 2019-09-30 | - |
dc.identifier.citation | Terzi, C. vd. (2019). ''Randomized controlled trial of 8 weeks' vs 12 weeks' interval between neoadjuvant chemoradiotherapy and surgery for locally advanced rectal cancer''. Colorectal Disease, 22(3), 279-288. | en_US |
dc.identifier.issn | 1462-8910 | - |
dc.identifier.issn | 1463-1318 | - |
dc.identifier.uri | https://doi.org/10.1111/codi.14867 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/codi.14867 | - |
dc.identifier.uri | http://hdl.handle.net/11452/30117 | - |
dc.description.abstract | Aim The aim was to compare the pathological complete response (pCR) rate at 8 compared to 12 weeks' interval between completion of neoadjuvant chemoradiotherapy (CRT) and surgery in patients with locally advanced rectal cancer. Method This was a randomized trial which included a total of 330 patients from two institutions. Patients with locally advanced (T3-4N0M0, TxN+M0) rectal cancer were randomized into 8- and 12-week interval groups. All the patients received long-course CRT (45 Gy in 1.8 Gy fractions and concomitant oral capecitabine or 5-fluorouracil infusion). Surgery was performed at either 8 or 12 weeks after CRT. The primary end-point was pCR. Secondary end-points were sphincter preservation, postoperative morbidity and mortality. Results Two-hundred and fifty-two patients (n = 125 in the 8-week group, n = 127 in the 12-week group) were included. Demographic and clinical characteristics were similar between groups. The overall pCR rate was 17.9% (n = 45): 12% (n = 15) in the 8-week group and 23.6% (n = 30) in the 12-week group (P = 0.021). Sphincter-preserving surgery was performed in 107 (85.6%) patients which was significantly higher than the 94 (74%) patients in the 12-week group (P = 0.016). Postoperative mortality was seen in three (1.2%) patients overall and was not different between groups (1.6% in 8 weeks vs 0.8% in 12 weeks, P = 0.494). Groups were similar in anastomotic leak (10.8% in 8 weeks vs 4.5% in 12 weeks, P = 0.088) and morbidity (30.4% in 8 weeks and 20.1% in 12 weeks, P = 0.083). Conclusion Extending the interval between CRT and surgery from 8 to 12 weeks resulted in a 2-fold increase in pCR rate without any difference in mortality and morbidity. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Gastroenterology & hepatology | en_US |
dc.subject | Surgery | en_US |
dc.subject | Rectal cancer | en_US |
dc.subject | Neoadjuvant chemoradiotherapy | en_US |
dc.subject | Interval | en_US |
dc.subject | Complete response | en_US |
dc.subject | Pathological complete response | en_US |
dc.subject | Radiation-therapy | en_US |
dc.subject | Adenocarcinoma | en_US |
dc.subject | Recommendations | en_US |
dc.subject | Resection | en_US |
dc.subject.mesh | Antineoplastic combined chemotherapy protocols | en_US |
dc.subject.mesh | Capecitabine | en_US |
dc.subject.mesh | Chemoradiotherapy | en_US |
dc.subject.mesh | Fluorouracil | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Neoadjuvant therapy | en_US |
dc.subject.mesh | Neoplasm staging | en_US |
dc.subject.mesh | Rectal neoplasms | en_US |
dc.subject.mesh | Rectum | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.title | Randomized controlled trial of 8 weeks' vs 12 weeks' interval between neoadjuvant chemoradiotherapy and surgery for locally advanced rectal cancer | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000491010400001 | tr_TR |
dc.identifier.scopus | 2-s2.0-85074361458 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Cerrahi Tıp Bilimleri/Genel Cerrahi Bölümü. | tr_TR |
dc.contributor.orcid | 0000-0002-9541-5035 | tr_TR |
dc.contributor.orcid | 0000-0002-9541-5035 | tr_TR |
dc.identifier.startpage | 279 | tr_TR |
dc.identifier.endpage | 288 | tr_TR |
dc.identifier.volume | 22 | tr_TR |
dc.identifier.issue | 3 | tr_TR |
dc.relation.journal | Colorectal Disease | en_US |
dc.contributor.buuauthor | Işık, Özgen | - |
dc.contributor.buuauthor | Yılmazlar, Tuncay | - |
dc.contributor.buuauthor | Uğraş, Nesrin | - |
dc.contributor.buuauthor | Kanat, Özkan | - |
dc.contributor.buuauthor | Öztürk, Ersin | - |
dc.contributor.buuauthor | Kurt, Malerie | - |
dc.contributor.researcherid | P-5779-2019 | tr_TR |
dc.contributor.researcherid | AAW-9602-2020 | tr_TR |
dc.contributor.researcherid | ABH-2238-2021 | tr_TR |
dc.contributor.researcherid | AAH-2716-2021 | tr_TR |
dc.identifier.pubmed | 31566843 | tr_TR |
dc.subject.wos | Gastroenterology & hepatology | en_US |
dc.subject.wos | Surgery | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q2 (Surgery) | en_US |
dc.wos.quartile | Q3 (Gastroenterology & hepatology) | en_US |
dc.contributor.scopusid | 36600543700 | tr_TR |
dc.contributor.scopusid | 6701800362 | tr_TR |
dc.contributor.scopusid | 55386535600 | tr_TR |
dc.contributor.scopusid | 55881548500 | tr_TR |
dc.contributor.scopusid | 35070171400 | tr_TR |
dc.contributor.scopusid | 8843050600 | tr_TR |
dc.subject.scopus | Rectum Tumor; Chemoradiotherapy; Neoadjuvant Therapy | en_US |
dc.subject.emtree | Capecitabine | en_US |
dc.subject.emtree | Fluorouracil | en_US |
dc.subject.emtree | Antineoplastic agent | en_US |
dc.subject.emtree | Adjuvant chemoradiotherapy | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Advanced cancer | en_US |
dc.subject.emtree | Anastomosis leakage | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Neoadjuvant chemotherapy | en_US |
dc.subject.emtree | Organ preservation | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Randomized controlled trial | en_US |
dc.subject.emtree | Rectum cancer | en_US |
dc.subject.emtree | Sigmoidoscopy | en_US |
dc.subject.emtree | Sphincter | en_US |
dc.subject.emtree | Surgical mortality | en_US |
dc.subject.emtree | Treatment duration | en_US |
dc.subject.emtree | Treatment response | en_US |
dc.subject.emtree | Tumor localization | en_US |
dc.subject.emtree | Cancer staging | en_US |
dc.subject.emtree | Chemoradiotherapy | en_US |
dc.subject.emtree | Neoadjuvant therapy | en_US |
dc.subject.emtree | Pathology | en_US |
dc.subject.emtree | Rectum | en_US |
dc.subject.emtree | Rectum tumor | en_US |
dc.subject.emtree | Treatment outcome | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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