Evidence map›Paper›PMID 29094224›Full record

Trial reportMedical oncology (Northwood, London, England)2017

Primary metastatic osteosarcoma: results of a prospective study in children given chemotherapy and interleukin-2.

Cristina Meazza, Graziella Cefalo, Maura Massimino, Primo Daolio, Ugo Pastorino, Paolo Scanagatta, Carlo Morosi, Marta Podda, Andrea Ferrari, Monica Terenziani and 12 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Medical oncology (Northwood, London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  13. Recent and Ongoing Research into Metastatic Osteosarcoma Treatments.International journal of molecular sciences · 2022
    Review
  14. Article
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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

22 authors at 3 institutions in 1 country.

Cristina MeazzaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy. cristina.meazza@istitutotumori.mi.it.ORCID http://orcid.org/0000-0002-1875-9563
Graziella CefaloPediatric Department, ASST Santi Paolo e Carlo, Milan, Italy.
Maura MassiminoPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Primo DaolioC.O.O., Azienda Socio Sanitaria Territoriale Gaetano Pini, Milan, Italy.
Ugo PastorinoDivision of Thoracic Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Paolo ScanagattaDivision of Thoracic Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Carlo MorosiRadiology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Marta PoddaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Andrea FerrariPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Monica TerenzianiPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Filippo SpreaficoPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Michela CasanovaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Antonina ParafioritiPathology Department, Azienda Socio Sanitaria Territoriale Gaetano Pini, Milan, Italy.
Paola ColliniPathology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Lorenza GandolaRadiology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Stefano BastoniC.O.O., Azienda Socio Sanitaria Territoriale Gaetano Pini, Milan, Italy.
Veronica BiassoniPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Elisabetta SchiavelloPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Stefano ChiaravalliPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Nadia PumaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Luca BergamaschiPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Roberto LukschPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian, 20133, Milan, MI, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITAzienda Socio Sanitaria Territoriale Lariana · ITAzienda Socio Sanitaria Territoriale Santi Paolo e Carlo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To improve the poor prognosis for children with metastatic osteosarcoma (OS), interleukin-2 (IL-2) was added to the standard treatment due to its capacity to activate lymphocytes and differentiate lymphocyte subsets into lymphokine-activated killer (LAK) cells that are capable of recognizing and killing various tumor cells. This study concerns a cohort of unselected patients aged < 18 years with metastatic OS, who were treated with IL-2, high-dose methotrexate, doxorubicin, cisplatin, ifosfamide, LAK reinfusion, and surgery, between 1995 and 2010. Thirty-five patients aged 4-17 years were involved. Thirty-two of the 35 patients underwent surgery on their primary tumor, and 25 had surgery on lung metastases too. Twenty-seven patients received IL-2 plus LAK reinfusion. The median follow-up was 130 months (77-228), and the 3-year event-free and overall survival rates were 34.3 and 45.0%, respectively. Eleven patients remained alive, all of whom achieved a complete surgical removal of the primary tumor and lung metastases (1 patient did not receive lung resections due to complete lung metastases remission). Patients who had a complete surgical remission of the primary and metastatic sites and who responded well to chemotherapy had a better event-free survival. These results confirm the importance of complete surgical remission and point to a noteworthy (though still be ameliorate) survival rate in our series of patients, underling a potential role for immunotherapy with IL-2 and LAK/NK cell activation.

Indexed as

AdolescentAntineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsChildChild, PreschoolCisplatinDoxorubicinFemaleHumansIfosfamideImmunotherapyInterleukin-2Lung NeoplasmsMaleOsteosarcomaProspective StudiesCisplatinDoxorubicinIfosfamideInterleukin-2ChemotherapyChildrenIL-2Lung metastasesOsteosarcomaSurgery

Identifiers

PMID29094224
OpenAlexW2765706741

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.