Evidence map›Paper›PMID 25209056›Full record

ArticleCancer2015

Provider-based research networks may improve early access to innovative colon cancer treatment for African Americans treated in the community.

Dolly C Penn, YunKyung Chang, Anne-Marie Meyer, Christina DeFilippo Mack, Hanna K Sanoff, Karyn B Stitzenberg, William R Carpenter

Open access · greenAbstract read
In one paragraph

Article in Cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. 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

7 authors at 1 institution in 1 country.

Dolly C PennDepartment of Social Medicine, Preventive Medicine Residency, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
YunKyung Chang
Anne-Marie Meyer
Christina DeFilippo Mack
Hanna K Sanoff
Karyn B Stitzenberg
William R Carpenter
University of North Carolina at Chapel Hill · US

Funding

Implementing Systemic Interventions to Close the Discovery-Delivery GapR01CA124402 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEINER, BRYAN J. · 2007 to 2012
$2.8M
Research Training:Health Care Quality &Patient OutcomesT32NR008856 · NINR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MARK, BARBARA A · 2004 to 2013
$2.7M
Academic Training in Oncology at the University of North Carolina at Chapel HillT32CA128590 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CAREY, LISA A · 2008 to 2012
$1.2M
NCI NIH HHS 5R01CA124402NCI NIH HHS 5T32CA128590-04NCI NIH HHS HHSN261200800726PNCI NIH HHS R01 CA124402NCI NIH HHS T32 CA128590NINR NIH HHS 2T32NR008856NINR NIH HHS T32 NR008856PHS HHS HHSN-261200800726P
6 · The paper itself

Abstract

backgroundAfrican American (AA) patients with colon cancer (CC) experience worse outcomes than whites partly due to differential treatment. The National Cancer Institute's Community Clinical Oncology Program (CCOP), a provider-based research network, adopts and diffuses innovative CC treatments quickly. The authors hypothesized that CCOP participation would lessen racial differences in the receipt of oxaliplatin, an innovative treatment for CC, among patients with stage III CC in the community.

methodsUsing Surveillance, Epidemiology, and End Results (SEER)-Medicare data, the authors performed a population-based retrospective cohort study of AA and white individuals aged ≥66 years who were diagnosed with AJCC stage III CC from 2003 through 2005. Generalized estimating equations were used to calculate the odds of receiving an oxaliplatin-containing regimen. Predicted probabilities of oxaliplatin receipt for race-CCOP combinations were calculated. The absolute difference in oxaliplatin receipt between races was estimated using the interaction contrast ratio.

resultsOf 2971 included individuals, 36% received oxaliplatin, 29.5% were CCOP-affiliated, and 7.6% were AA. On multivariate analysis, early diffusion of oxaliplatin was not found to be associated with race or CCOP participation. The probability of receiving oxaliplatin for AAs participating in a CCOP (0.46) was nearly double that of AAs who were not participating in a CCOP (0.25; P <.05). For white individuals, the probabilities of receiving oxaliplatin did not differ by CCOP participation. For oxaliplatin receipt, the joint effects assessment suggested a greater benefit of CCOP participation among AAs (interaction contrast ratio, 1.7).

conclusionsAmong older patients with stage III CC, there is a differential impact of race on oxaliplatin receipt depending on CCOP participation. AAs treated by CCOPs were more likely to receive oxaliplatin than AAs treated elsewhere. Provider-based research networks may facilitate early access to innovative treatment for AAs with stage III CC.

Indexed as

Black or African AmericanNational Cancer Institute (U.S.)AgedAged, 80 and overAntineoplastic AgentsCohort StudiesColonic NeoplasmsCommunity NetworksFemaleHealthcare DisparitiesHealth Services AccessibilityHumansMaleOrganoplatinum CompoundsOxaliplatinRetrospective StudiesAntineoplastic AgentsOrganoplatinum CompoundsOxaliplatinagedcolon cancercolonic neoplasms/therapycommunity-institutional relationsEnd Results (SEER) programhealth care disparitiesoxaliplatinSurveillance, Epidemiology

Identifiers

PMID25209056
PMCPMC4270819
OpenAlexW1916703295

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.