Evidence map›Paper›PMID 40236790›Full record

ArticlePathology oncology research : POR2025

Real-world experience with pazopanib in locally advanced and metastatic soft tissue sarcomas: a Hungarian retrospective single-center study.

Nóra Ecker, Marietta Aranyi, Edina Kiss, Nóra Kiss, Erika Lahm, Zsófia Nagy, Márta Sikter, Ádám Szabó, Anikó Szászné Szentesi, Klára Takács and 4 more

Abstract read
In one paragraph

Article in Pathology oncology research : POR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

14 authors.

Nóra EckerDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Marietta AranyiDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Edina KissDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Nóra KissDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Erika LahmDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Zsófia NagyDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Márta SikterDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Ádám SzabóDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Anikó Szászné SzentesiDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Klára TakácsDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Andrea UhlyarikDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
József VachajaDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Barbara SebőkDepartment of Pediatric Traumatology, Dr. Manninger Jenő Accident Center, Budapest, Hungary.
Zsuzsanna PápaiDepartment of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pazopanib is a tyrosine-kinase inhibitor also used for the treatment of advanced soft tissue sarcomas. Our retrospective study analyzed real-world data of stage 4 sarcoma patients treated with pazopanib in our department in the past 10 years. Data were collected from the Medworks medical system, which is used for daily work in our center. A total of 99 patients were included: 46 men and 53 women The median age at the diagnosis was 49.8 years. The most common histological subtypes were leiomyosarcoma and synovial sarcoma. All patients received 800 mg of pazopanib per day, which was reduced to 400 mg in the event of toxicity. Treatment was continued until disease progression or unmanageable toxicity. The primary endpoint of the study was progression-free survival and the secondary endpoints were overall survival, overall response rate and disease control rate. The results in relation to demographic data, previous treatments, localizations of primary tumors and metastasis and histological subtypes were analyzed. In our center pazopanib was most frequently used in the third line. In total, 61 patients received perioperative therapy; the most common regimen used in the metastatic setting was VIP. Median PFS and OS were 3 months and 7 months, respectively. ORR was 14% and DCR was 40.45%. Dose reductions were necessary during the treatment of 56 patients. Hematological toxicity was detected in 23% of cases, with the most frequent events being grade 1 thrombocytopenia and grade 2 leukocytopenia. Non-hematological adverse events were documented in half of the patients. Pazopanib was more effective in earlier lines of treatment. Compared to the PALETTE phase 3 trial more patients received perioperative therapy, median PFS and OS were shorter (3 months vs. 4.6 months and 7 months vs. 11.9 months) and ORR was higher (14% vs. 9%) in our patient population. Dose reductions were more frequent in our center. Pazopanib is a therapeutic option for the treatment of advanced soft tissue sarcoma, also according to real-world data. Further investigations are needed to select patients who can benefit the most from pazopanib and to determine the most appropriate sequence of therapy.

Indexed as

Angiogenesis InhibitorsPyrimidinesSarcomaSulfonamidesAdultAgedAged, 80 and overFemaleFollow-Up StudiesHumansHungaryIndazolesMaleMiddle AgedPrognosisRetrospective StudiesAngiogenesis InhibitorsIndazolespazopanibPyrimidinesSulfonamidesHungarypazopanibreal-worldSTStyrosine-kinase inhibitor

Identifiers

PMID40236790
PMCPMC11996657

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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.