Evidence map›Paper›PMID 42535416›Full record

ArticleActa oncologica (Stockholm, Sweden)2026

The Clinical outcomes following pencil beam scanning proton therapy for skull base chordoma and chondrosarcoma: a single-institution experience.

Tomasz Skóra, Kamila Rawoj C, Joanna Anioł, Tomasz Banaś, Anna Cepiga, Agnieszka Chrostowska, Adrianna Chudyba, Magdalena Garbacz, Eleonora Góra, Damian Kabat and 11 more

Abstract read
In one paragraph

Article in Acta oncologica (Stockholm, Sweden), 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

21 authors.

Tomasz SkóraMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Kamila Rawoj CMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland. kamila.rawojc@dworska.pl.
Joanna AniołMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Tomasz BanaśMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Anna CepigaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Agnieszka ChrostowskaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Adrianna ChudybaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Magdalena GarbaczCyclotron Centre Bronowice, The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Kraków, Poland.
Eleonora GóraMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Damian KabatMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Emilia KrzywonosMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Tomasz MikołajskiCyclotron Centre Bronowice, The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Kraków, Poland; Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.
Jadwiga Nowak-SadzikowskaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Anna PatlaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Elżbieta PlutaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Antoni RucinskiCyclotron Centre Bronowice, The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Kraków, Poland.
Konrad UrbanekMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Dominika Wojton-DziewońskaMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Mariusz WszołekMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.
Renata KopećCyclotron Centre Bronowice, The Henryk Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, Kraków, Poland.
Kamil KisielewiczMaria Skłodowska - Curie National Research Institute of Oncology, Kraków Branch, Kraków, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChordomas and chondrosarcomas of the skull base are rare, locally aggressive tumors that pose significant therapeutic challenges due to their proximity to critical anatomical structures. While maximal safe surgical resection remains the cornerstone of management, the infiltrative nature of these tumors often precludes radical excision, necessitating adjuvant radiotherapy. Given their relative radioresistance, high-dose radiotherapy exceeding 70 Gray Relative Biological Effectiveness (GyRBE) is required to achieve durable local control. This study evaluated long-term outcomes and toxicity following pencil beam scanning (PBS) proton therapy in patients with skull base chordoma and chondrosarcoma.

methodsWe retrospectively analyzed 76 patients (50 chordoma, 26 chondrosarcoma) treated with curative-intent PBS between 2016 and 2020. Median prescribed doses were 74.0 GyRBE for chordomas and 70.0 GyRBE for chondrosarcomas. Clinical endpoints included overall survival (OS), local failure-free survival (LFFS), distant metastasis-free survival (DMFS), and toxicity graded according to CTCAE v5.0.

resultsAt a median follow-up of 70.2 months, 5-year OS, LFFS, and DMFS for the entire cohort were 84.0, 86.9, and 92.7%, respectively. Local control was numerically higher in chondrosarcoma (96.1%) than in chordoma (81.9%; p = 0.116). Tumor contact with the optic apparatus or brainstem was associated with worse OS (p = 0.0034 and p = 0.0151, respectively) and proximity to the optic pathways correlated with poorer local control (p = 0.0182). Grade ≥ 3 late toxicity occurred in 9.2% of patients, predominantly hearing impairment and temporal lobe necrosis.

conclusionsPBS achieves excellent local control and survival with an acceptable safety profile in skull base chordoma and chondrosarcoma. Our findings align with ongoing efforts toward dose intensification, hypofractionation, and particle selection. Moreover, emerging integration of artificial intelligence for contouring, treatment adaptation, and toxicity prediction, along with augmented reality-assisted positioning and patient education, promises to further enhance treatment precision and outcomes. Through long-term follow-up and engagement with international research initiatives, our institution contributes to the global advancement of biologically guided, high-precision radiotherapy for rare skull base malignancies.

Indexed as

ChondrosarcomaChordomaProton TherapySkull Base NeoplasmsAdolescentAdultAgedAged, 80 and overFemaleFollow-Up StudiesHumansMaleMiddle AgedRadiotherapy DosageRetrospective StudiesTreatment Outcome

Identifiers

PMID42535416
PMCPMC13434534

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