Evidence map›Paper›PMID 30792968›Full record

ArticleFrontiers in oncology2019

Bevacizumab Combined With Oxaliplatin/Capecitabine in Patient With Refractory and Recurrent Mucinous Adenocarcinoma of the Appendix: A Case Report.

Wenzhi Liu, Lili Liu, Ruoyu Wang, Guanyu Gong, Xinjia Ding, Bin Yang, Yun Bao, Zhiqiang Wang, Bo Zhang, Dewei Zhao and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
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

12 authors at 4 institutions in 2 countries.

Wenzhi LiuThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Lili LiuDepartment of Oncology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Ruoyu WangThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Guanyu GongThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Xinjia DingDepartment of Neurosurgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Bin YangGenomic Future Inc., Lexington, MA, United States.
Yun BaoThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Zhiqiang WangThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Bo ZhangDepartment of Neurosurgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Dewei ZhaoThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Fei WuThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Yan DingThe Institute for Translational Medicine, The Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Affiliated Zhongshan Hospital of Dalian University · CNBoston Children's Hospital · USDalian Medical University · CNSecond Affiliated Hospital of Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary appendiceal adenocarcinoma with peritoneal pseudomyxoma (PPM) has a high recurrence rate and refractory to medical interventions such as repetitive debulking surgery and systemic chemotherapy. Genome-based targeted therapy for such cases has not been well-documented. Here we present a 63-years-old women, who was diagnosed with recurrent mucinous adenocarcinoma of the appendix with local invasions and peritoneal carcinomatosis, was refractory to systemic chemotherapy after surgery. We used a regime developed using whole exome sequencing. Somatic mutations in the genes encoding VEGFR2, FGFR1, FGFR2, FGFR3, and KRAS were identified in the patient's tumor tissue. The patient was then treated with bevacizumab plus oxaliplatin. After 4 months of treatment, pelvic CT showed dramatic reduction of pseudomyoma and a decline of CA199 level from 5436.7 to 1121.4 U/ml. Continual treatment with bevacizumab-capecitabine remained effective and the patient's CA199 level further decreased to 401.26 U/ml according to the follow-up examination on Aug 15th, 2018. Results from this study show the evidence of gene mutations involving VEGF signal activation in the recurrence of appendiceal adenocarcinoma. Our results also suggest the association of these mutations with the effectiveness of anti-VEGF treatment using bevacizumab. Therefore, the screening of gene mutations involved in VEGF signaling and targeted therapy with anti-VEGF drugs may provide a new option to manage refractory/recurrent advanced-stage appendiceal adenocarcinoma.

Indexed as

appendiceal adenocarcinomabevacizumabnext generation sequencingperitoneal carcinomatosistargeted therapy

Identifiers

PMID30792968
PMCPMC6374296
OpenAlexW2912130378

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.