Evidence map›Paper›PMID 37046450›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Application of Drug Testing Platforms in Circulating Tumor Cells and Validation of a Patient-Derived Xenograft Mouse Model in Patient with Primary Intracranial Ependymomas with Extraneural Metastases.

Muh-Lii Liang, Ting-Chi Yeh, Man-Hsu Huang, Pao-Shu Wu, Shih-Pei Wu, Chun-Chao Huang, Tsung-Yu Yen, Wei-Hsin Ting, Jen-Yin Hou, Jia-Yun Huang and 6 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Review
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

16 authors.

Muh-Lii LiangDepartment of Neurosurgery, MacKay Memorial Hospital, Taipei 104, Taiwan.ORCID 0000-0002-5923-9812
Ting-Chi YehDepartment of Medicine, MacKay Medical College, New Taipei City 252, Taiwan.ORCID 0000-0003-0437-3130
Man-Hsu HuangDepartment of Pathology, Shuang-Ho Hospital, Taipei Medical University, New Taipei City 235, Taiwan.
Pao-Shu WuDepartment of Pathology, MacKay Memorial Hospital, Taipei 104, Taiwan.ORCID 0000-0003-4823-9582
Shih-Pei WuCancerFree Biotech, Ltd., Taipei 114, Taiwan.
Chun-Chao HuangDepartment of Medicine, MacKay Medical College, New Taipei City 252, Taiwan.ORCID 0000-0003-0757-6486
Tsung-Yu YenDepartment of Radiation Oncology, MacKay Memorial Hospital, Taipei 104, Taiwan.ORCID 0000-0002-5348-9183
Wei-Hsin TingDepartment of Medicine, MacKay Medical College, New Taipei City 252, Taiwan.
Jen-Yin HouDivision of Pediatric Hematology-Oncology, Department of Pediatrics, Mackay Children's Hospital, Taipei 104, Taiwan.ORCID 0000-0002-0716-0838
Jia-Yun HuangDivision of Pediatric Neurology, Department of Pediatrics, MacKay Children's Hospital, Taipei 104, Taiwan.
Yi-Huei DingDepartment of Medical Research, Mackay Memorial Hospital, Tamshui Branch, New Taipei City 251, Taiwan.
Jia-Huei ZhengJoint Biobank, Office of Human Research, Taipei Medical University, Taipei 110, Taiwan.
Hsi-Che LiuDepartment of Medicine, MacKay Medical College, New Taipei City 252, Taiwan.
Che-Sheng HoDepartment of Medicine, MacKay Medical College, New Taipei City 252, Taiwan.
Shiu-Jau ChenDepartment of Neurosurgery, MacKay Memorial Hospital, Taipei 104, Taiwan.ORCID 0000-0002-4263-527X
Tsung-Han HsiehJoint Biobank, Office of Human Research, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0002-2268-9246

Funding

Mackay Memorial Hospital MMH-110-83Mackay Memorial Hospital MMH-112-70Ministry of Science and Technology of the Republic of China MOST110-2314-B-195-027
6 · The paper itself

Abstract

Primary intracranial ependymoma is a challenging tumor to treat despite the availability of multidisciplinary therapeutic modalities, including surgical resection, radiotherapy, and adjuvant chemotherapy. After the completion of initial treatment, when resistant tumor cells recur, salvage therapy needs to be carried out with a more precise strategy. Circulating tumor cells (CTCs) have specifically been detected and validated for patients with primary or recurrent diffused glioma. The CTC drug screening platform can be used to perform a mini-invasive liquid biopsy for potential drug selection. The validation of potential drugs in a patient-derived xenograft (PDX) mouse model based on the same patient can serve as a preclinical testing platform. Here, we present the application of a drug testing model in a six-year-old girl with primary ependymoma on the posterior fossa, type A (EPN-PFA). She suffered from tumor recurrence with intracranial and spinal seeding at 2 years after her first operation and extraneural metastases in the pleura, lung, mediastinum, and distant femoral bone at 4 years after initial treatment. The CTC screening platform results showed that everolimus and entrectinib could be used to decrease CTC viability. The therapeutic efficacy of these two therapeutic agents has also been validated in a PDX mouse model from the same patient, and the results showed that these two therapeutic agents significantly decreased tumor growth. After precise drug screening and the combination of focal radiation on the femoral bone with everolimus chemotherapy, the whole-body bone scan showed significant shrinkage of the metastatic tumor on the right femoral bone. This novel approach can combine liquid biopsy, CTC drug testing platforms, and PDX model validation to achieve precision medicine in rare and challenging tumors with extraneural metastases.

Indexed as

circulating tumor cellsdrug screeningependymomaextraneural metastasispatient-derived xenograft

Identifiers

PMID37046450
PMCPMC10093690

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.