Evidence map›Paper›PMID 38369555›Full record

ArticleJournal of cancer research and clinical oncology2024

A retrospective study on the mechanism underlying quick transfer from response to resistance in a repeated recurrent chordoma patient with molecular alterations treated with Palbociclib.

Nanzhe Zhong, Dong Yu, Minglei Yang, Xingyi Lu, Qiangzu Zhang, Wei Wei, Jian Jiao, Xinghai Yang, Zhi Zhu, Su Chen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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

11 authors at 3 institutions in 1 country.

Nanzhe Zhong *Department of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Dong Yu *Center of Translational Medicine, Naval Medical University, Shanghai, China.
Minglei Yang *Department of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Xingyi LuState Key Laboratory of Computer Architecture, Institute of Computing Technology, Chinese Academy of Sciences, Beijing, China.
Qiangzu ZhangState Key Laboratory of Computer Architecture, Institute of Computing Technology, Chinese Academy of Sciences, Beijing, China.
Wei Wei *Department of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Jian JiaoDepartment of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Xinghai YangDepartment of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Zhi ZhuDepartment of Pathology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Su ChenDepartment of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China. chensudx@126.com.
Jianru XiaoDepartment of Orthopedic Oncology, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China. jianruxiao83@163.com.
Shanghai Changzheng Hospital · CNChinese Academy of Sciences · CNSecond Military Medical University · CN

Funding

he National Natural Science Fund Project of China 81902731The National Natural Science Fund Project of China 82141105
6 · The paper itself

Abstract

purposeThere is no approved targeted therapy for chordoma at present. Although several preclinical studies have implied the potential applicability of CDK4/6 inhibitor for this rare tumor, no clinical evidence has been documented so far. The purpose of this study was to elucidate the therapeutic efficacy of CDK4/6 inhibitor for chordoma.

methodsThe next generation sequencing (as for whole-exome sequencing, WES assay) and immunohistochemical (IHC) staining of the chordoma tissue from a patient with an advanced lesion were performed before treatment. Then, the patient was treated with Palbociclib for 4 months until progression occurred in the 5th month. Surgical resection was implemented and the tumor tissue was obtained postoperatively for assessment of molecular alterations.

resultsMolecular features of the tumor before medical treatment suggested applicability of CDK4/6 inhibitor and the patient showed partial response (PR) according to Choi Criteria after 4 months treating with Palbociclib until progression occurred. Then, a drastic molecular alteration of the tumor as represented by emergence of dramatic E2F amplification, which is known to induce CDK4/6 independent cell-cycle entry and progression after treatment, was detected. The findings in this patient demonstrated tumor evolution under drug pressure.

conclusionThe findings of the present study suggest the feasibility of Palbociclib for the clinical treatment of chordoma, and imply the necessity of combination therapies rather single drug administration due to the quick resistance of the tumor to Palbociclib treatment.

Indexed as

ChordomaPiperazinesCyclin-Dependent Kinase 4HumansNeoplasm Recurrence, LocalProtein Kinase InhibitorsPyridinesRetrospective StudiesCyclin-Dependent Kinase 4palbociclibPiperazinesProtein Kinase InhibitorsPyridinesChordomaDrug resistanceGenomic featuresPalbociclib

Identifiers

PMID38369555
PMCPMC10874909
OpenAlexW4391944593

What OpenQuestion 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 OpenQuestion graph.