Evidence map›Paper›PMID 26797923›Full record

ArticlePediatric blood & cancer2016

Resource Utilization and Toxicities After Carboplatin/Etoposide/Melphalan and Busulfan/Melphalan for Autologous Stem Cell Rescue in High-Risk Neuroblastoma Using a National Administrative Database.

Ami V Desai, Alix E Seif, Yimei Li, Kelly Getz, Brian T Fisher, Vera Huang, Adjoa Mante, Richard Aplenc, Rochelle Bagatell

Open access · greenAbstract readComparative Study
In one paragraph

Article in Pediatric blood & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Ami V DesaiDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Alix E SeifDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Yimei LiDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Kelly GetzDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Brian T FisherDepartment of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Vera HuangDepartment of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Adjoa ManteDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Richard AplencDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Rochelle BagatellDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Toxicity Monitoring on Phase III Trials with Administrative DataR01CA165277 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI APLENC, RICHARD · 2012 to 2015
$1.8M
NCI NIH HHS 1 R01 CA165277NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA165277
6 · The paper itself

Abstract

backgroundHigh-dose chemotherapy with autologous stem cell rescue (ASCR) is a key component of high-risk neuroblastoma therapy. Resources required to support patients treated with ASCR conditioning regimens [carboplatin/etoposide/melphalan (CEM) and busulfan/melphalan (BuMel)] have not been directly compared. PROCEDURE: An administrative database was used to analyze resource utilization and outcomes in a cohort of high-risk neuroblastoma patients. Patients were followed for 60 days from start of conditioning or until death. Length of hospitalization, length of intensive care unit (ICU) level of care, incidence of sepsis and sinusoidal obstruction syndrome (SOS), and duration of use of specific supportive care resources were analyzed.

resultsSix of 171 CEM patients and zero of 59 BuMel patients died during the study period (P = 0.34). Duration of hospitalization was longer following BuMel (median 35 vs. 31 days; P = 0.01); however, there was no difference in duration of ICU-level care. Antibiotic use was longer following CEM (median 19 vs. 15 days; P = 0.01), as was antihypertensive use (median 5 vs. 1.6 days; P = 0.0024). Duration of opiate and nonnarcotic analgesic use was longer following CEM early in the study period. Resources consistent with a diagnosis of SOS were used in a higher proportion of BuMel patients. A higher proportion of BuMel treated patients required mechanical ventilation (17% vs. 6%; P = 0.03).

conclusionsWe used administrative billing data to compare resources associated with ASCR conditioning regimens. CEM patients required more extended use of analgesics, antibiotics, and antihypertensives, while duration of hospitalization was longer, and SOS and the use of mechanical ventilation were more frequent following BuMel.

Indexed as

Databases, FactualPeripheral Blood Stem Cell TransplantationStem CellsAdolescentAntineoplastic Combined Chemotherapy ProtocolsAutograftsBusulfanCarboplatinChildChild, PreschoolCritical CareEtoposideFemaleFollow-Up StudiesHumansIncidenceBusulfanCarboplatinEtoposideMelphalanneuroblastomaresource utilizationstem cell rescue

Identifiers

PMID26797923
PMCPMC5672623
OpenAlexW2252560577

What OpenQuestion holds

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Registered trials

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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.