Evidence map›Paper›PMID 32652753›Full record

ArticleThe oncologist2020

Successful Treatment of Patients with Refractory High-Grade Serous Ovarian Cancer with GOPC-ROS1 Fusion Using Crizotinib: A Case Report.

Dapeng Dong, Ge Shen, Yong Da, Ming Zhou, Gang Yang, Mingming Yuan, Rongrong Chen

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 12 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

7 authors at 1 institution in 1 country.

Dapeng DongDepartment of Oncology, Beijing Hui 'an Hospital of Integrated Traditional Chinese and Western Medicine, Beijing, People's Republic of China.
Ge ShenDepartment of Oncology, Beijing Hui 'an Hospital of Integrated Traditional Chinese and Western Medicine, Beijing, People's Republic of China.
Yong DaDepartment of Oncology, Beijing Hui 'an Hospital of Integrated Traditional Chinese and Western Medicine, Beijing, People's Republic of China.
Ming ZhouDepartment of Oncology, Beijing Hui 'an Hospital of Integrated Traditional Chinese and Western Medicine, Beijing, People's Republic of China.
Gang YangDepartment of Oncology, Beijing Hui 'an Hospital of Integrated Traditional Chinese and Western Medicine, Beijing, People's Republic of China.
Mingming YuanGeneplus-Beijing Ltd., Beijing, People's Republic of China.
Rongrong ChenGeneplus-Beijing Ltd., Beijing, People's Republic of China.
Beijing Chang'an Integrated Traditional Chinese and Western Medicine Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently, multiple poly (ADP-ribose) polymerase (PARP) inhibitors have demonstrated excellent efficacy among patients with ovarian cancer with or without BRCA mutations. However, alternative therapeutic options are urgently required for patients who cannot benefit from conventional chemotherapy or PARP inhibitors. CASE PRESENTATION: A patient with high-grade serous ovarian carcinoma presented to our clinic after developing resistance to chemotherapy. Paired tumor-normal next-generation sequencing (NGS) was performed using peripheral blood to identify potential actionable mutations. NGS revealed the patient harboring a GOPC-ROS1 fusion, which was subsequently verified using a reverse transcription polymerase chain reaction assay. No germline or somatic mutation in BRCA1/2 or mismatch repair genes was detected. Therefore, the patient received crizotinib treatment. A rapid, favorable clinical response (partial response at 1 month) was observed, with further pathological response monitored and evaluated in follow-up interrogation.

conclusionThis study suggested that crizotinib was an off-the-shelf, practical, and ostensibly effective treatment option for patients with ovarian cancer with ROS1 rearrangement. NGS-based genetic testing may guide to plan therapeutic paradigms, and render precision medicine promising in ovarian cancer treatment. IMPLICATIONS FOR PRACTICE: Despite the previous report of ROS1 fusion in patients with ovarian cancer, it remains unknown whether patients can benefit from targeted therapeutic drugs. This study reports a GOPC-ROS1 fusion identified by next-generation sequencing in a patient with chemotherapy-resistant ovarian cancer. The patient was administered crizotinib and showed rapid, remarkable response. This study suggests that comprehensive sequencing should be offered for patients with ovarian cancer without effective therapeutic strategies, and crizotinib can be used to treat ROS1-rearranged ovarian carcinomas.

Indexed as

Carcinoma, Non-Small-Cell LungCrizotinibOvarian NeoplasmsAdaptor Proteins, Signal TransducingFemaleGolgi Matrix ProteinsHumansOncogene Proteins, FusionProtein-Tyrosine KinasesProto-Oncogene ProteinsAdaptor Proteins, Signal TransducingCrizotinibGolgi Matrix ProteinsGOPC protein, humanOncogene Proteins, FusionProtein-Tyrosine KinasesProto-Oncogene ProteinsROS1 protein, humanCrizotinibNext-generation sequencingOvarian cancerROS1 fusion

Identifiers

PMID32652753
PMCPMC7648329
OpenAlexW3041582734

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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.