Evidence map›Paper›PMID 42741182›Full record

ArticleOncology letters2026

Pazopanib treatment for primary cardiovascular sarcoma: A retrospective observational study and literature review.

Shintaro Yamanaka, Yoshihiro Yakushijin, Shinji Hasebe, Shoichiro Yamamoto, Tomomi Fujii, Riko Kitazawa, Taketsugu Fujibuchi, Teruki Kidani, Masaki Maruta

Abstract read
In one paragraph

Article in Oncology letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Shintaro YamanakaCancer Center, Ehime University Hospital, Toon, Ehime 791-0295, Japan.
Yoshihiro YakushijinCancer Center, Ehime University Hospital, Toon, Ehime 791-0295, Japan.
Shinji HasebeCancer Center, Ehime University Hospital, Toon, Ehime 791-0295, Japan.
Shoichiro YamamotoCancer Center, Ehime University Hospital, Toon, Ehime 791-0295, Japan.
Tomomi FujiiPalliative Care Center, Ehime University Hospital, Toon, Ehime 791-0295, Japan.
Riko KitazawaDepartment of Diagnostic Pathology, Ehime University Hospital, Toon, Ehime 791-0295, Japan.
Taketsugu FujibuchiDepartment of Orthopedic Surgery, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan.
Teruki KidaniDepartment of Orthopedic Surgery, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan.
Masaki MarutaCancer Center, Ehime University Hospital, Toon, Ehime 791-0295, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cardiovascular sarcoma (PCS) is a rare, aggressive malignancy with a poor prognosis. The present study describes a single-center experience with pazopanib, an oral multikinase inhibitor, for the outpatient management of unresectable PCS. A retrospective review was conducted of consecutive patients with sarcoma involving the heart and/or pulmonary artery treated with pazopanib at Ehime University Hospital (Toon, Japan) between January 2015 and December 2025. Pazopanib was initiated at 200-400 mg daily and escalated to 600-800 mg according to tolerability. Five patients aged 56-81 years were identified, with angiosarcoma (n=1), intimal sarcoma (n=2) or leiomyosarcoma (n=2). Two patients achieved durable stable disease for >500 days. A case of right atrial angiosarcoma with lung metastasis remained stable for 33 months when treated with 800 mg pazopanib; the patient later died of recurrent cerebral infarction. A case of pulmonary artery intimal sarcoma remained stable for 22 months when treated with 400-600 mg pazopanib; however, treatment was discontinued because of fatigue. Two additional patients stopped treatment because dose escalation led to intolerable toxicities. One patient continued therapy with 800 mg pazopanib as of 8 months, with stable disease, despite requiring a pericardial window for malignant pericardial effusion during treatment. In conclusion, pazopanib can provide meaningful disease control and long-term stabilization for selected patients with unresectable PCS. As treatment-related toxicities frequently limit therapy, individualized dose management and proactive supportive care are essential to maintain treatment continuity and to maximize clinical benefit.

Indexed as

angiosarcomaintimal sarcomaleiomyosarcomapazopanibPCStyrosine kinase inhibitor

Identifiers

PMID42741182
PMCPMC13572868

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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.