Evidence map›Paper›PMID 34125480›Full record

ArticlePediatric blood & cancer2021

Multi-institutional analysis of treatment modalities in basal ganglia and thalamic germinoma.

Richard T Graham, Mohammad H Abu-Arja, Joseph R Stanek, Andrea Cappellano, Christina Coleman, Susan Chi, Tabitha Cooney, Girish Dhall, Jacob G Ellen, Jonathan L Finlay and 20 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Pediatric blood & cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Pineal Tumors and Pineal Region Tumors.Advances and technical standards in neurosurgery · 2026
    Review
  5. Article
  6. 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

30 authors at 19 institutions in 4 countries.

Richard T GrahamDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.ORCID 0000-0002-8566-5970
Mohammad H Abu-ArjaDepartment of Pediatrics, New York-Presbyterian Brooklyn Methodist Hospital, Weill-Cornell College of Medicine, Brooklyn, New York, USA.
Joseph R StanekDivision of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, Ohio, USA.
Andrea CappellanoInstituto de Oncologia Pediátrica GRAACC/UNIFESP, Division of Neuroncology, Sao Paulo, Brazil.
Christina ColemanDepartments of Pediatrics, Neurology, and Neurological Surgery, University of California San Francisco, San Francisco, California, USA.
Susan ChiDana Farber/Boston Children's Cancer and Blood Disorder Center, Pediatric Neuro-Oncology, Boston, Massachusetts, USA.
Tabitha CooneyDana Farber/Boston Children's Cancer and Blood Disorder Center, Pediatric Neuro-Oncology, Boston, Massachusetts, USA.
Girish DhallDivision of Hematology and Oncology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jacob G EllenDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Jonathan L FinlayDivision of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0002-8312-6586
Michael J FisherDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Gregory K FriedmanDivision of Hematology and Oncology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0000-0002-6653-7420
Amar GajjarDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0001-5019-0699
Karen GauvainWashington University School of Medicine, St. Louis Children's Hospital, St. Louis, Missouri, USA.
Lindsey M HoffmanDivision of Hematology/Oncology, Phoenix Children's Hospital, Phoenix, Arizona, USA.
Juliette HukinDivision of Hematology and Oncology, Children's and Women's Health Centre of B.C., University of British Columbia, Vancouver, British Columbia, Canada.
John T LucasDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Sabine MuellerDepartments of Pediatrics, Neurology, and Neurological Surgery, University of California San Francisco, San Francisco, California, USA.
Pournima NavalkeleDepartment of Pediatrics, SSM Cardinal Glennon Children's Hospital, Saint Louis University, Saint Louis, Missouri, USA.
Rebecca RonsleyDivision of Hematology and Oncology, Children's and Women's Health Centre of B.C., University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0003-3961-3042
Christopher TinkleDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0001-5552-2664
Stephanie VilleneuveDivision of Hematology/Oncology, Izaak Walton Killam Hospital for Children, Halifax, Nova Scotia, Canada.
Kee Kiat YeoDana Farber/Boston Children's Cancer and Blood Disorder Center, Pediatric Neuro-Oncology, Boston, Massachusetts, USA.ORCID 0000-0003-0713-6384
Jack M SuTexas Children's Cancer Center, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
Ashley MargolCancer and Blood Disease Institute and Division of Hematology-Oncology, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Nicholas G GottardoDepartment of Paediatric and Adolescent Oncology/Haematology, Perth Children's Hospital, Nedlands, Western Australia, Australia.
Jeffrey AllenDepartment of Pediatrics, NYU Langone Health, New York, New York, USA.
Roger PackerCenter for Neuroscience and Behavioral Medicine, Brain Tumor Institute, Children's National Health System, Washington, District of Columbia, USA.
Ute BartelsDivision of Hematology/Oncology, Pediatric Neuro-Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Mohamed S AbdelbakiDivision of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio, USA.
Nationwide Children's Hospital · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USSt. Jude Children's Research Hospital · USChildren's Hospital of Philadelphia · USUniversity of Alabama at Birmingham · USUniversity of British Columbia · CAUniversity of California, San Francisco · USBaylor College of Medicine · USCardinal Glennon Children’s Medical Center · USChildren's National · USCincinnati Children's Hospital Medical Center · USHospital for Sick Children · CAIzaak Walton Killam Health Centre · CANYU Langone Health · USPhoenix Children's Hospital · USPrincess Margaret Hospital for Children · AUSt. Louis Children's Hospital · USSupport group for adolescents and children with cancer · BRUniversity of Southern California · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

backgroundCentral nervous system (CNS) germinomas are treatment-sensitive tumors with excellent survival outcomes. Current treatment strategies combine chemotherapy with radiotherapy (RT) in order to reduce the field and dose of RT. Germinomas originating in the basal ganglia/thalamus (BGTGs) have proven challenging to treat given their rarity and poorly defined imaging characteristics. Craniospinal (CSI), whole brain (WBI), whole ventricle (WVI), and focal RT have all been utilized; however, the best treatment strategy remains unclear.

methodsRetrospective multi-institutional analysis has been conducted across 18 institutions in four countries.

resultsFor 43 cases of nonmetastatic BGTGs, the 5- and 10-year event-free survivals (EFS) were 85.8% and 81.0%, respectively, while the 5- and 10-year overall survivals (OS) were 100% and 95.5%, respectively (one patient fatality from unrelated cause). Median RT doses were as follows: CSI: 2250 cGy/cGy(RBE) (1980-2400); WBI: 2340 cGy/cGy(RBE) (1800-3000); WVI: 2340 cGy/cGy(RBE) (1800-2550); focal: 3600 cGy (3060-5400). Thirty-eight patients (90.5%) received chemotherapy. There was no statistically significant difference in the EFS based on initial field extent (p = .84). Nevertheless, no relapses were reported in patients who received CSI or WBI. Chemotherapy alone had significantly inferior EFS compared to combined therapy (p = .0092), but patients were salvageable with RT.

conclusionPatients with BGTGs have excellent outcomes and RT proved to be an integral component of the treatment plan. This group of patients should be included in future prospective clinical trials and the best RT field should be investigated further.

Indexed as

Brain NeoplasmsCentral Nervous System NeoplasmsGerminomaBasal GangliaHumansNeoplasm Recurrence, LocalRadiotherapy DosageRetrospective StudiesThalamusbasal gangliachemotherapygerminomapure germinomaradiation therapythalamus

Identifiers

PMID34125480
PMCPMC9639702
OpenAlexW3172564483

What OpenQuestion holds

Textmetadata
LicenceTDM
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.