Evidence map›Paper›PMID 31555453›Full record

ArticleNeuro-oncology practice2019

Second primary cancers in long-term survivors of glioblastoma.

Jung-Young Kim, Jennifer G Jackman, Sarah Woodring, Frances McSherry, James E Herndon, Annick Desjardins, Henry S Friedman, Katherine B Peters

Open access · greenAbstract read
In one paragraph

Article in Neuro-oncology practice, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 15 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

8 authors at 2 institutions in 1 country.

Jung-Young KimDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.
Jennifer G JackmanDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.
Sarah WoodringDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.
Frances McSherryDepartment of Biostatistics, Duke University School of Medicine, Durham, NC, USA.
James E HerndonDepartment of Biostatistics, Duke University School of Medicine, Durham, NC, USA.
Annick DesjardinsDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.
Henry S FriedmanDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-7588-032X
Katherine B PetersDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-5110-3868
Duke Medical Center · USDuke University · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
NCI NIH HHS P30 CA014236
6 · The paper itself

Abstract

backgroundOverall survival (OS) in glioblastoma (GBM) is poor at an average of 14 to 18 months, and long-term survivors (LTS) of GBM are rare. LTS of GBM, defined as surviving >5 years postdiagnosis, represent only 2% to 10% of all GBM patients. LTS of cancer are at high risk of developing second primary neoplasms. This study looks at occurrences of second primary neoplasms in LTS of GBM.

methodsRecords from adult patients newly diagnosed with GBM between January 1, 1998 and February 8, 2010, were retrospectively reviewed to identify LTS, defined as patients who survived ≥5 years. We focused on the identification of a new diagnosis of cancer occurring at least 2 years after the initial GBM diagnosis.

resultsWe identified 155 LTS of GBM, with a median OS of 11.0 years (95% CI: 9.0 to 13.1 years) and a median follow-up of 9.6 years (95% CI: 8.7 to 10.7 years). In this cohort of patients, 13 (8.4%) LTS of GBM developed 17 secondary cancers. Eight could potentially be attributed to previous radiation and chemotherapy (skin cancer in radiation field [n = 4], leukemia [n = 2], low-grade glioma [n = 1], and sarcoma of the scalp [n = 1]). The other 9 cases included melanoma (n = 2), prostate cancer (n = 2), bladder cancer (n = 1), endometrioid adenocarcinoma (n = 1), basal cell carcinoma (n = 1), and renal cell carcinoma (n = 1).

conclusionsAlthough second primary cancers are rare in GBM LTS, providers should continue close monitoring with appropriate oncologic care. Moreover, this highlights the need for survivorship care of patients with GBM.

Indexed as

chemotherapyglioblastomalong-term survivorsradiation therapysecond primary neoplasm

Identifiers

PMID31555453
PMCPMC6753354
OpenAlexW2913686595

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.