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Total neoadjuvant therapy with short-course radiotherapy Versus long-course neoadjuvant chemoradiotherapy in Locally Advanced Rectal cancer, Korean trial (TV-LARK trial): study protocol of a multicentre randomized controlled trial

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dc.contributor.authorKim, Min Jung-
dc.contributor.authorLee, Dae Won-
dc.contributor.authorKang, Hyun-Cheol-
dc.contributor.authorPark, Ji Won-
dc.contributor.authorRyoo, Seung-Bum-
dc.contributor.authorHan, Sae-Won-
dc.contributor.authorKim, Kyung Su-
dc.contributor.authorChie, Eui Kyu-
dc.contributor.authorOh, Jae Hwan-
dc.contributor.authorJeong, Woon Kyung-
dc.contributor.authorKim, Byoung Hyuck-
dc.contributor.authorNam, Eun Mi-
dc.contributor.authorJeong, Seung-Yong-
dc.date.accessioned2024-05-14T01:34:13Z-
dc.date.available2024-05-14T01:34:13Z-
dc.date.created2023-08-25-
dc.date.created2023-08-25-
dc.date.issued2023-08-
dc.identifier.citationBMC Cancer, Vol.23 No.1, p. 734-
dc.identifier.issn1471-2407-
dc.identifier.urihttps://hdl.handle.net/10371/201678-
dc.description.abstractBackgroundFor locally advanced rectal cancer (LARC), total neoadjuvant therapy (TNT) may enhance tumour response, reduce recurrence, and improve patient compliance compared to upfront surgery. Recent studies have shown that chemoradiotherapy (CRT) followed by consolidation chemotherapy leads to higher rate of pathologic complete response (pCR) than induction chemotherapy followed by CRT. However, an optimal TNT regimen that maximise the pCR rate and minimise toxicity has not been established. Therefore, the aim of this trial was to investigate whether preoperative short-course radiotherapy followed by chemotherapy with four cycles of CAPOX can double the pCR rate compared to a standard schedule of long-course preoperative CRT in patients with LARC.MethodsThis is a multi-centre, prospective, open label, randomised controlled trial. Patients with clinical primary tumour stage 3 and higher or regional node-involved rectal cancer located within 10 cm from the anal verge were randomly assigned equally to short-course radiotherapy (25 Gy in 5 fractions over 1 week) followed by four cycles of CAPOX (intravenous oxaliplatin [130 mg/m(2), once a day] on day 1 and capecitabine [1,000 mg/m(2), twice a day] from days 1 to 14) (TNT) or CRT (50.4 Gy in 28 fractions over 5 weeks, concurrently with concomitant oral capecitabine 825 mg/m(2) twice a day). After preoperative treatment, total mesorectal excision was performed 2-4 weeks in the TNT group and 6-10 weeks in the CRT group, followed by optional additional adjuvant chemotherapy. The primary endpoint is the pCR rate, and secondary endpoints include disease-related treatment failure, quality of life, and cost-effectiveness. Assuming a pCR rate of 28% and 15% in the TNT and CRT groups, respectively, and one-side alpha error rate of 0.025 and power of 80%, 348 patients will be enrolled considering 10% dropout rate.DiscussionThe TV-LARK trial will evaluate the superiority of employed TNT regimen against the standard CRT regimen for patients with LARC. We aimed to identify a TNT regimen that will improve the pCR rate and decrease systemic recurrence in these patients.-
dc.language영어-
dc.publisherBioMed Central-
dc.titleTotal neoadjuvant therapy with short-course radiotherapy Versus long-course neoadjuvant chemoradiotherapy in Locally Advanced Rectal cancer, Korean trial (TV-LARK trial): study protocol of a multicentre randomized controlled trial-
dc.typeArticle-
dc.identifier.doi10.1186/s12885-023-11177-7-
dc.citation.journaltitleBMC Cancer-
dc.identifier.wosid001044418100001-
dc.identifier.scopusid2-s2.0-85167370316-
dc.citation.number1-
dc.citation.startpage734-
dc.citation.volume23-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorLee, Dae Won-
dc.contributor.affiliatedAuthorChie, Eui Kyu-
dc.contributor.affiliatedAuthorKim, Byoung Hyuck-
dc.contributor.affiliatedAuthorJeong, Seung-Yong-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusTOTAL MESORECTAL EXCISION-
dc.subject.keywordPlusADJUVANT CHEMOTHERAPY-
dc.subject.keywordPlusPREOPERATIVE CHEMORADIOTHERAPY-
dc.subject.keywordPlusPOSTOPERATIVE CHEMORADIOTHERAPY-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusCHEMORADIATION-
dc.subject.keywordPlusFLUOROURACIL-
dc.subject.keywordPlusRECURRENCE-
dc.subject.keywordPlusLEUCOVORIN-
dc.subject.keywordPlusVALIDATION-
dc.subject.keywordAuthorTotal neoadjuvant therapy-
dc.subject.keywordAuthorRectal cancer-
dc.subject.keywordAuthorChemoradiotherapy-
dc.subject.keywordAuthorRadiotherapy-
dc.subject.keywordAuthorChemotherapy-
dc.subject.keywordAuthorPathologic complete response-
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Kim, Byoung hyuck김병혁
(기금)조교수
  • College of Medicine
  • Department of Medicine
Research Area 소화기암, 육종, 폐암

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