Evidence map›Paper›PMID 40923337›Full record

ArticleCancer medicine2025

Teleangiectatic Osteosarcoma Treated by Surgery and Chemotherapy: A Report of 223 Affected Patients From the Cooperative Osteosarcoma Study Group (COSS).

Stefan S Bielack, Vanessa Mettmann, Daniel Baumhoer, Andreas Beilken, Claudia Blattmann, Godehard Friedel, Jendrik Hardes, Wolf Hassenpflug, Leo Kager, Matthias Kevric and 8 more

Abstract read
In one paragraph

Article in Cancer medicine, 2025. 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
–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

2 citing papers in PubMed.

  1. [Pathological fractures in childhood].Unfallchirurgie (Heidelberg, Germany) · 2026
    Review
  2. Article
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

18 authors.

Stefan S BielackPädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.ORCID https://orcid.org/0000-0003-2144-3153
Vanessa MettmannPädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.ORCID https://orcid.org/0000-0002-4460-8830
Daniel BaumhoerKnochentumor- Referenzzentrum, Institut für Medizinische Genetik und Pathologie, Universitätsspital Beider Basel, und Basel Research Centre for Child Health, Basel, Switzerland.ORCID https://orcid.org/0000-0002-2137-7507
Andreas BeilkenKinder- und Jugendklinik, Städtisches Klinikum Braunschweig gGmbH, Braunschweig, Germany.ORCID https://orcid.org/0009-0004-3739-6093
Claudia BlattmannPädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.ORCID https://orcid.org/0000-0003-4045-5838
Godehard FriedelUniversitätsklinik für Thorax-, Herz- und Gefäßchirurgie - Sektion Thoraxchirurgie, Universitätsklinikum Tübingen, Tübingen, Germany.ORCID https://orcid.org/0000-0002-0340-4719
Jendrik HardesKlinik für Tumororthopädie und Sarkomchirurgie, Universitätsklinikum Essen, Essen, Germany.ORCID https://orcid.org/0000-0002-8408-2255
Wolf HassenpflugKlinik und Poliklinik für Pädiatrische Hämatologie und Onkologie, Zentrum für Geburtshilfe, Kinder- und Jugendmedizin, Universitätsklinikum Hamburg Eppendorf, Hamburg, Germany.ORCID https://orcid.org/0000-0002-4230-5828
Leo KagerSt. Anna Kinderspital, Universitätsklinik für Kinder- und Jugendheilkunde der Medizinischen Universität Wien, Vienna, Austria.ORCID https://orcid.org/0000-0003-4954-6488
Matthias KevricPädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.
Thekla von KalleRadiologisches Institut (Kinderradiologie), Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.ORCID https://orcid.org/0000-0001-8851-5014
Andreas KulozikAbteilung für Pädiatrische Onkologie, Hämatologie und Immunologie, Universitätsklinikum Heidelberg, Heidelberg, Germany.ORCID https://orcid.org/0000-0003-1953-0848
Markus MetzlerKinder- und Jugendklinik - Pädiatrische Onkologie und Hämatologie, Universitätsklinikum Erlangen, Erlangen, Germany.ORCID https://orcid.org/0000-0002-4523-1676
Michaela NathrathKlinik für Pädiatrische Hämatologie, Onkologie, Psychosomatik und Systemerkrankungen, Klinikum Kassel, Kassel, Germany.ORCID https://orcid.org/0000-0002-1584-1115
Claudia RossigKlinik für Kinder- und Jugendmedizin, Pädiatrische Hämatologie und Onkologie, Universitätsklinikum Münster, Münster, Germany.ORCID https://orcid.org/0000-0002-8672-5285
Benjamin SorgPädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.
Mathias WernerVivantes Netzwerk für Gesundheit GmbH, Fachbereich Pathologie, Osteopathologie - Referenzzentrum, Berlin, Germany.ORCID https://orcid.org/0000-0003-2393-3738
Stefanie Hecker-NoltingPädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.ORCID https://orcid.org/0000-0002-1815-138X

Funding

Förderkreis Krebskranke Kinder e.V. Stuttgart
6 · The paper itself

Abstract

purposeTeleangiectatic osteosarcoma is a histologic subtype of osteosarcoma that can mimic aneurysmal bone cysts and has so far been incompletely characterized. PATIENTS AND

methodsWe used the database of the Cooperative Osteosarcoma Study Group COSS (patient-registration 1980-2019) to better understand this rare histologic variant.

results223 eligible patients were identified, 164 having reference pathology (median age 15.9 (3.7-69.7) years; male 134, female 89; tumor sites limb 208 (201 metaphyses, 66 pathologic fractures), trunk 13, head & neck 2; 26 with primary metastases). Known tumor-predisposition syndromes were rare. Therapy included surgery in 215, radiotherapy in 10, and chemotherapy in all patients. Tumor response to preoperative treatment was good in 71% of 165 cases with available data. After a median follow-up of 7.1 (0.2-32.1) years for all patients and 10.5 (0.2-32.1) years for 152 survivors, 5-/10-year actuarial event-free and overall survival expectancies were 61%/57% and 73%/66%, respectively. Five unrelated malignancies occurred during this period. The presence of primary metastases, pathologic fracture, poor response to neoadjuvant chemotherapy, and not obtaining a complete macroscopic remission were associated with inferior outcomes for both event-free and overall survival (p < 0.01). DISCUSSION: This large analysis proves teleangiectatic osteosarcoma to be a disease predominantly of the metaphyses of the young. While detected only rarely, the true incidence of genetic tumor predispositions would require prospective assessments. Behaving like other osteosarcoma subtypes in many other ways, this variant may show greater chemosensitivity and hence somewhat better outcomes than other subtypes.

Indexed as

Bone NeoplasmsOsteosarcomaAdolescentAdultAgedChildChild, PreschoolCombined Modality TherapyFemaleHumansMaleMiddle AgedTreatment OutcomeYoung Adultchemotherapydemographicsosteosarcomaoutcomessurgeryteleangiectatic

Identifiers

PMID40923337
PMCPMC12418078

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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.