Total Neoadjuvant Therapy (TNT) versus Standard Neoadjuvant Chemoradiotherapy for Locally Advanced Rectal Cancer: A Systematic Review and Meta‐Analysis
Background Total neoadjuvant therapy (TNT) is a novel approach for locally advanced rectal cancer (LARC), which attempts to deliver both systemic chemotherapy and neoadjuvant chemoradiotherapy prior to surgery. However, its efficacy and safety remain controversial in randomized controlled trials (RC...
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Published in | The oncologist (Dayton, Ohio) Vol. 26; no. 9; pp. e1555 - e1566 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.09.2021
Oxford University Press |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Total neoadjuvant therapy (TNT) is a novel approach for locally advanced rectal cancer (LARC), which attempts to deliver both systemic chemotherapy and neoadjuvant chemoradiotherapy prior to surgery. However, its efficacy and safety remain controversial in randomized controlled trials (RCTs). We conducted this meta‐analysis to assess such concerns.
Materials and Methods
Head‐to‐head phase II/III RCTs were searched in Embase, PubMed, Web of Science, and the Cochrane Library, as well as other sources. The primary endpoint was pathologic complete response (pCR). Secondary endpoints were disease‐free survival (DFS), overall survival (OS), local recurrence‐free survival, distant metastasis‐free survival, and the R0 resection rate.
Results
Eight phase II/III RCTs involving 2,196 patients with LARC were assessed. The primary analysis demonstrated a statistically significant improvement in the pCR rate for TNT treatment (odds ratio, 1.77; 95% confidence interval [CI], 1.28–2.45; p = .0005). TNT treatment also showed improvements in DFS and OS outcomes compared with standard chemoradiotherapy (hazard ratio [HR], 0.83; 95% CI, 0.72–0.96; p = .03 and HR, 0.88; 95% CI, 0.74–1.05; p = .15). In addition, TNT treatment showed significant efficacy in reducing the risk of distant metastasis (HR, 0.81; 95% CI, 0.68–0.95; p = .012).
Conclusion
The overall pCR rate may be improved with TNT compared with standard treatment. The TNT strategy may also improve DFS and OS and reduce the risk of distant metastasis.
Implications for Practice
Locally advanced rectal cancer (LARC) is a relatively common disease, with a poor prognosis because of its high metastatic potential. The role of total neoadjuvant therapy (TNT) has always been controversial. This meta‐analysis found that TNT in LARC is associated with a significant improvement in overall pathologic complete response rate, disease‐free survival, overall survival, and distant metastasis‐free survival compared with standard treatment. TNT is a promising strategy for LARC, especially for patients who have little desire for surgery.
Total neoadjuvant therapy (TNT) is a novel therapeutic approach for locally advanced rectal cancer that delivers both systemic chemotherapy and neoadjuvant chemoradiotherapy before surgery; however, this approach remains controversial. This article reports the results of a meta‐analysis comparing TNT with standard chemotherapy. |
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Bibliography: | commercialreprints@wiley.com No part of this article may be reproduced, stored, or transmitted in any form or for any means without the prior permission in writing from the copyright holder. For information on purchasing reprints contact Disclosures of potential conflicts of interest may be found at the end of this article Contributed equally. For permission information contact permissions@wiley.com . ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 Disclosures of potential conflicts of interest may be found at the end of this article. No part of this article may be reproduced, stored, or transmitted in any form or for any means without the prior permission in writing from the copyright holder. For information on purchasing reprints contact commercialreprints@wiley.com. For permission information contact permissions@wiley.com. |
ISSN: | 1083-7159 1549-490X 1549-490X |
DOI: | 10.1002/onco.13824 |