Evidence map›Paper›PMID 28940863›Full record

Trial reportPediatric blood & cancer2018

A phase II study of radioimmunotherapy with intraventricular

Kim Kramer, Neeta Pandit-Taskar, John L Humm, Pat B Zanzonico, Sofia Haque, Ira J Dunkel, Suzanne L Wolden, Maria Donzelli, Debra A Goldman, Jason S Lewis and 10 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Pediatric blood & cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Intensive Multimodality Therapy for Extraocular Retinoblastoma: A Children's Oncology Group Trial (ARET0321).Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Trial
  3. Review
  4. Programmable shunt valves with a "virtual off" for intrathecal chemotherapy delivery in children with high-grade CNS tumors and hydrocephalus.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. Immunotherapy in central nervous system tumors.International journal of surgery (London, England) · 2025
    Review
  9. Article
  10. Review
  11. Medulloblastoma: biology and immunotherapy.Frontiers in immunology · 2025
    Review
  12. Review
  13. Review
  14. Article
  15. Mechanistic insights into medulloblastoma relapse.Pharmacology & therapeutics · 2024
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
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

20 authors at 2 institutions in 1 country.

Kim KramerDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Neeta Pandit-TaskarDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
John L HummDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Pat B ZanzonicoDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Sofia HaqueDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Ira J DunkelDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Suzanne L WoldenDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York.
Maria DonzelliDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Debra A GoldmanDepartment of Epidemiology & Biostatistics, Weill Cornell Medical College, New York.
Jason S LewisDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Serge K LyashchenkoDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Yasmin KhakooDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Jorge A CarrasquilloDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Mark M SouweidaneDepartment of Neurosurgery, Weill Cornell Medical College, New York.
Jeffrey P GreenfieldDepartment of Neurosurgery, Weill Cornell Medical College, New York.
David LydenDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Kevin D De BragancaDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Stephen W GilheeneyDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Steven M LarsonDepartment of Radiology (Molecular Imaging and Therapy Service), Memorial Sloan Kettering Cancer Center, New York.
Nai-Kong V CheungDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Memorial Sloan Kettering Cancer Center · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundHigh-risk and recurrent medulloblastoma (MB) is associated with significant mortality. The murine monoclonal antibody 3F8 targets the cell-surface disialoganglioside GD2 on MB. We tested the efficacy, toxicity, and dosimetry of compartmental radioimmunotherapy (cRIT) with intraventricular

methodsPatients with histopathologically confirmed high-risk or recurrent MB were eligible for cRIT. After determining adequate cerebrospinal fluid (CSF) flow, patients received 2 mCi (where Ci is Curie)

resultsForty-three patients received a total of 167 injections; 42 patients were evaluable for outcome. No treatment-related deaths occurred. Toxicities related to drug administration included acute bradycardia with somnolence, headache, fatigue, and CSF pleocytosis consistent with chemical meningitis and dystonic reaction. Total CSF absorbed dose was 1,453 cGy (where Gy is Gray; 350.0-2,784). Median overall survival from first dose of cRIT was 24.9 months (95% confidence interval [CI]:16.3-55.8). Patients treated in radiographic and cytologic remission were at a lower risk of death compared to patients with radiographically measurable disease (hazard ratio: 0.40, 95% CI: 0.18-0.88, P = 0.024).

conclusionscRIT with

Indexed as

RadioimmunotherapyAdolescentAdultAntibodies, Monoclonal, Murine-DerivedAntineoplastic Agents, ImmunologicalCerebellar NeoplasmsChildChild, PreschoolDisease-Free SurvivalFemaleHumansInfantInjections, IntraventricularIodine RadioisotopesMaleMedulloblastomaAntibodies, Monoclonal, Murine-DerivedAntineoplastic Agents, ImmunologicalIodine Radioisotopes3F8CNS tumorsintrathecal therapymedulloblastomaradioimmunotherapy

Identifiers

PMID28940863
PMCPMC6692907
OpenAlexW2759328813

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.