Risk and location of distant metastases in patients with locally advanced rectal cancer after total neoadjuvant treatment or chemoradiotherapy in the RAPIDO trial

被引:36
作者
Bahadoer, Renu R. [1 ]
Hospers, Geke A. P. [2 ,9 ]
Marijnen, Corrie A. M. [3 ,4 ]
Peeters, Koen C. M. J. [1 ]
Putter, Hein [5 ]
Dijkstra, Esmee A. [2 ]
Kranenbarg, Elma Meershoek-Klein [1 ]
Roodvoets, Annet G. H. [1 ]
van Etten, Boudewijn [6 ]
Nilsson, Per J. [7 ]
Glimelius, Bengt [8 ]
van de Velde, Cornelis J. H. [1 ]
机构
[1] Leiden Univ, Dept Surg, Med Ctr, Albinusdreef 2,Postbus 9600, NL-2300 RC Leiden, Netherlands
[2] Univ Med Ctr Groningen, Dept Med Oncol, Hanzepl 1,Postbus 30-001, NL-9700 RB Groningen, Netherlands
[3] Netherlands Canc Inst, Dept Radiat Oncol, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[4] Leiden Univ, Dept Radiat Oncol, Med Ctr, Albinusdreef 2,Postbus 9600, NL-2300 RC Leiden, Netherlands
[5] Leiden Univ, Dept Med Stat & Bioinformat, Med Ctr, Albinusdreef 2,Postbus 9600, NL-2300 RC Leiden, Netherlands
[6] Univ Med Ctr Groningen, Dept Surg, Hanzepl 1,Postbus 30-001, NL-9700 RB Groningen, Netherlands
[7] Karolinska Univ Hosp, Dept Surg, Anna Stecksensg 30A D2 05171 76, Stockholm, Sweden
[8] Uppsala Univ, Dept Immunol Genet & Pathol, Dag Hammarskjold Vag 20, S-75185 Uppsala, Sweden
[9] Univ Med Ctr Groningen, Dept Med Oncol, Hanzepl 1,Postbus 30-001, NL-9700 RB Groningen, Netherlands
基金
瑞典研究理事会;
关键词
Rectal cancer; Total neoadjuvant therapy; Distant metastases; Metastatic pattern; TOTAL MESORECTAL EXCISION; RANDOMIZED PHASE-III; PREOPERATIVE RADIOTHERAPY; POSTOPERATIVE CHEMORADIOTHERAPY; COMPETING RISKS; CHEMOTHERAPY; MULTICENTER; RECURRENCE; SURVIVAL; THERAPY;
D O I
10.1016/j.ejca.2023.02.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Although optimising rectal cancer treatment has reduced local recurrence rates, many patients develop distant metastases (DM). The current study investigated whether a total neoadjuvant treatment strategy influences the development, location, and timing of metastases in patients diagnosed with high-risk locally advanced rectal cancer included in the Rectal cancer And Pre-operative Induction therapy followed by Dedicated Operation (RAPIDO) trial. Material and methods: Patients were randomly assigned to short-course radiotherapy fol-lowed by 18 weeks of CAPOX or FOLFOX4 before surgery (EXP), or long-course che-moradiotherapy with optional postoperative chemotherapy (SC-G). Assessments for metastatic disease were performed pre-and post-treatment, during surgery, and 6, 12, 24, 36, and 60 months postoperatively. From randomisation, differences in the occurrence of DM and first site of metastasis were evaluated. Results: In total, 462 patients were evaluated in the EXP and 450 patients in the SC-G groups. The cumulative probability of DM at 5 years after randomisation was 23% [95% CI 19-27] and 30% [95% CI 26-35] (HR 0.72 [95% CI 0.56-0.93]; P = 0.011) in the EXP and SC -G, respectively. The median time to DM was 1.4 (EXP) and 1.3 years (SC-G). After diagnosis of DM, median survival was 2.6 years [95% CI 2.0-3.1] in the EXP and 3.2 years [95% CI 2.3-4.1] in the SC-G groups (HR 1.39 [95% CI 1.01-1.92]; P = 0.04). First occurrence of DM was most often in the lungs (60/462 [13%] EXP and 55/450 [12%] SC-G) or the liver (40/462 [9%] EXP and 69/450 [15%] SC-G). A hospital policy of postoperative chemotherapy did not influence the development of DM. Conclusions: Compared to long-course chemoradiotherapy, total neoadjuvant treatment with short-course radiotherapy and chemotherapy significantly decreased the occurrence of me-tastases, particularly liver metastases. (c) 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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收藏
页码:139 / 149
页数:11
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