Induction chemotherapy followed by neoadjuvant chemoradiotherapy and surgery for patients with locally advanced rectal cancer: a systematic review and meta-analysis.


Journal

International journal of colorectal disease
ISSN: 1432-1262
Titre abrégé: Int J Colorectal Dis
Pays: Germany
ID NLM: 8607899

Informations de publication

Date de publication:
Aug 2020
Historique:
accepted: 14 05 2020
pubmed: 4 6 2020
medline: 24 6 2021
entrez: 4 6 2020
Statut: ppublish

Résumé

Controversy persists about whether additional induction chemotherapy (ICT) before neoadjuvant chemoradiation (NCRT) yields improved oncological outcomes. We performed a systematic review and meta-analysis to compare ICT+ NCRT+ surgery(S) with NCRT+ S in patients with locally advanced rectal cancer (LARC). We searched the PubMed, EMBASE, Cochrane Library, and China Biology Medicine (CBM) databases. The data were analyzed with Stata version 12.0 software. We identified 9 relevant trials that enrolled 1538 patients. We detected no significant difference in the 5-year overall survival (OS) (OR 1.50, 95% CI 0.48-4.64), disease-free survival (DFS) (OR 1.03, 95% CI 0.73-1.46), local recurrence (LR) (OR 0.80, 95% CI 0.45-1.43), and distant metastasis (DM) rates (OR 1.03, 95% CI 0.55-1.93) between patients who did and did not receive ICT. The addition of ICT before NCRT had a similar pathological complete response rate compared to NCRT (OR 1.26, 95% CI 0.90-1.77). Our findings suggest that between the ICT + NCRT+S and NCRT+S groups, ICT improved the incidence of grade 3 to 4 toxicity effects (OR 4.81, 95% CI 2.38-9.37), but between the ICT + NCRT+S and NCRT+S+ adjuvant chemotherapy (ACT) groups, ICT might reduce toxicity (OR 0.19, 95% CI 0.08-0.50). ICT had no significant impact on surgical complications (OR 0.97, 95% CI 0.63-1.51). The addition of ICT before NCRT seemingly shows no survival benefit on patients with LARC, and might increase the toxicity.

Sections du résumé

BACKGROUND BACKGROUND
Controversy persists about whether additional induction chemotherapy (ICT) before neoadjuvant chemoradiation (NCRT) yields improved oncological outcomes. We performed a systematic review and meta-analysis to compare ICT+ NCRT+ surgery(S) with NCRT+ S in patients with locally advanced rectal cancer (LARC).
METHODS METHODS
We searched the PubMed, EMBASE, Cochrane Library, and China Biology Medicine (CBM) databases. The data were analyzed with Stata version 12.0 software.
RESULTS RESULTS
We identified 9 relevant trials that enrolled 1538 patients. We detected no significant difference in the 5-year overall survival (OS) (OR 1.50, 95% CI 0.48-4.64), disease-free survival (DFS) (OR 1.03, 95% CI 0.73-1.46), local recurrence (LR) (OR 0.80, 95% CI 0.45-1.43), and distant metastasis (DM) rates (OR 1.03, 95% CI 0.55-1.93) between patients who did and did not receive ICT. The addition of ICT before NCRT had a similar pathological complete response rate compared to NCRT (OR 1.26, 95% CI 0.90-1.77). Our findings suggest that between the ICT + NCRT+S and NCRT+S groups, ICT improved the incidence of grade 3 to 4 toxicity effects (OR 4.81, 95% CI 2.38-9.37), but between the ICT + NCRT+S and NCRT+S+ adjuvant chemotherapy (ACT) groups, ICT might reduce toxicity (OR 0.19, 95% CI 0.08-0.50). ICT had no significant impact on surgical complications (OR 0.97, 95% CI 0.63-1.51).
CONCLUSIONS CONCLUSIONS
The addition of ICT before NCRT seemingly shows no survival benefit on patients with LARC, and might increase the toxicity.

Identifiants

pubmed: 32488419
doi: 10.1007/s00384-020-03621-y
pii: 10.1007/s00384-020-03621-y
doi:

Types de publication

Journal Article Meta-Analysis Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1355-1369

Subventions

Organisme : Lanzhou Innovation and Entrepreneurship Talent Project
ID : 2017- RC-23

Auteurs

Shuangwu Feng (S)

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.

Peijing Yan (P)

Department of Clinical Research Management, West China Hospital, Sichuan University, Chengdu, 610041, China.

Qiuning Zhang (Q)

Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, 730000, China.
Lanzhou Heavy Ions Hospital, Lanzhou, 730000, China.

Zheng Li (Z)

Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, 730000, China.

Chengcheng Li (C)

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.

Yichao Geng (Y)

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.

Lina Wang (L)

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.

Xueshan Zhao (X)

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.

Zhen Yang (Z)

School of Basic Medical Sciences, Lanzhou University, Lanzhou, 730000, China.

Hongyi Cai (H)

Department of Radiation Oncology, Gansu Province People's Hospital, Lanzhou, 730000, China.

Xiaohu Wang (X)

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China. xhwanggansu@163.com.
Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, 730000, China. xhwanggansu@163.com.
Lanzhou Heavy Ions Hospital, Lanzhou, 730000, China. xhwanggansu@163.com.

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