Evidence map›Paper›PMID 35413852›Full record

ArticleWorld journal of surgical oncology2022

The number of cycles of adjuvant chemotherapy in stage III and high-risk stage II rectal cancer: a nomogram and recursive partitioning analysis.

Wei-Wei Chen, Wen-Ling Wang, Hong-Min Dong, Gang Wang, Xiao-Kai Li, Guo-Dong Li, Wang-Hua Chen, Juan Chen, Sai-Xi Bai

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Wei-Wei ChenDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China. chen_ww523@21cn.com.
Wen-Ling WangDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Hong-Min DongDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Gang WangDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Xiao-Kai LiDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Guo-Dong LiDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Wang-Hua ChenDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Juan ChenDepartment of Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, China.
Sai-Xi BaiDepartment of Abdominal Oncology, Affiliated Cancer Hospital of Guizhou Medical University, Guiyang, 550000, China.
Guiyang Medical University · CNAffiliated Hospital of Guizhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe prognostic role of the number of cycles of adjuvant chemotherapy (ACT) after total mesorectal excision in stage III and high-risk stage II rectal cancer is unknown. As a result of this, our study was designed to assess the effect of the number of cycles of ACT on the prediction of cancer-specific survival.

methodsFour hundred patients that were diagnosed as stage III and high-risk stage II rectal cancer from January 2012 to January 2018 and who had received total mesorectal excision were enrolled in this study. A nomogram incorporating the number of cycles of ACT was also developed in this study. For internal validation, the bootstrap method was used and the consistency index was used to evaluate the accuracy of the model. The patients were stratified into risk groups according to their tumor characteristics by recursive partitioning analysis.

resultsWe found that the risk of death was decreased by 26% (HR = 0.74, 95% CI: 0.61-0.89, P = 0.0016) with each increasing ACT cycle. The N stage, positive lymph node ratio (PLNR), carcinoembryonic antigen, neutrophil-to-lymphocyte ratio, and the number of cycles of ACT were chosen and entered into the nomogram model. Recursive partitioning analysis-based risk stratification revealed a significant difference in the prognosis in rectal cancer patients with high-risk, intermediate-risk, and low-risk (3-year cancer-specific survival: 0.246 vs. 0.795 vs. 0.968, P < 0.0001). Seven or more cycles of ACT yielded better survival in patients with PLNR ≥ 0.28 but not in patients with PLNR < 0.28.

conclusionIn conclusion, the nomogram prognosis model based on the number of cycles of ACT predicted individual prognosis in rectal cancer patients who had undergone total mesorectal excision. These findings further showed that in patients with PLNR ≥ 0.28, no fewer than 7 cycles of ACT are needed to significantly reduce the patient's risk of death.

Indexed as

Rectal NeoplasmsTesticular NeoplasmsChemotherapy, AdjuvantHumansMaleNeoplasm StagingNomogramsPrognosisRetrospective StudiesAdjuvantChemotherapyNomogramPrognosisRectal neoplasmRecursive partitioning analysis

Identifiers

PMID35413852
PMCPMC9003995
OpenAlexW4223548300

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.