Evidence map›Paper›PMID 35982957›Full record

ArticleFrontiers in oncology2022

Neoadjuvant Anlotinib and chemotherapy followed by minimally invasive esophagectomy in patients with locally advanced esophageal squamous cell carcinoma: Short-term results of an open-label, randomized, phase II trial.

Ying-Jian Wang, Kun-Kun Li, Xian-Feng Xie, Tao Bao, Zhi-Peng Hao, Jiang Long, Shuai Wang, Zhao-Yang Zhong, Wei Guo

Abstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
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.

Ying-Jian WangDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Kun-Kun LiDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Xian-Feng XieDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Tao BaoDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Zhi-Peng HaoDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Jiang LongDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Shuai WangDepartment of Cancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Zhao-Yang ZhongDepartment of Cancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Wei GuoDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Clinical benefits of neoadjuvant Anlotinib for locally advanced esophageal squamous cell carcinoma (ESCC) remains unclear. This study evaluated the efficacy and safety of neoadjuvant Anlotinib plus chemotherapy followed by minimally invasive esophagectomy (MIE) for the treatment of patients with locally advanced ESCC. Methods: Patients with locally advanced ESCC were randomly assigned to neoadjuvant Anlotinib combined with chemotherapy (Anlotinib group) or neoadjuvant chemoradiotherapy alone (nCRT group) with an allocation ratio of 1:1. The primary endpoint was the R0 surgical resection rate. Secondary endpoints included postoperative pathologic stage, complete response (CR) rate, and safety. Safety was assessed by adverse events (AEs) and postoperative complications. Results: From August 2019 to August 2021, 93 patients were assigned to the nCRT or Anlotinib group. Of the 93 patients, 79 underwent MIE and were finally included in the per-protocol set (nCRT group: n=39; Anlotinib group: n=40). The R0 resection rate was 97.4% for nCRT versus 100.0% for Anlotinib group ( Conclusions: Neoadjuvant Anlotinib plus chemotherapy had a similar safety profile and pathologic response, but better surgical outcomes than nCRT for locally advanced ESCC.

Indexed as

Anlotinibchemoradiotherapychemotherapyesophageal squamous cell carcinomaminimally invasive esophagectomyneoadjuvant therapy

Identifiers

PMID35982957
PMCPMC9380438

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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.