Evidence map›Paper›PMID 31464611›Full record

ArticleBMC cancer2019

Sites of metastasis and association with clinical outcome in advanced stage cancer patients treated with immunotherapy.

Mehmet Asim Bilen, Julie M Shabto, Dylan J Martini, Yuan Liu, Colleen Lewis, Hannah Collins, Mehmet Akce, Haydn Kissick, Bradley C Carthon, Walid L Shaib and 10 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 4 pooled it
6.9field-weighted citation impact, top 2% 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

82 citing papers in PubMed, 4 syntheses or guidelines pooled it, 122 citations in OpenAlex.

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  16. Broad Utility of Ultrasensitive Analysis of ctDNA Dynamics across Solid Tumors Treated with Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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22 more citing papers are in PubMed but not listed here.

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.

Mehmet Asim BilenDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA. mehmet.a.bilen@emory.edu.ORCID http://orcid.org/0000-0003-4003-1103
Julie M ShabtoDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Dylan J MartiniDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Yuan LiuDepartments of Biostatistics and Bioinformatics, Emory University, 1518 Clifton Rd, Atlanta, GA, USA.
Colleen LewisDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, 1365 Clifton Rd, Atlanta, GA, USA.
Hannah CollinsDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, 1365 Clifton Rd, Atlanta, GA, USA.
Mehmet AkceDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Haydn KissickDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, 1365 Clifton Rd, Atlanta, GA, USA.
Bradley C CarthonDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Walid L ShaibDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Olatunji B AleseDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Conor E SteuerDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Christina WuDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
David H LawsonDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Ragini KudchadkarDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Viraj A MasterDepartment of Urology, Emory University, 5673 Peachtree, Dunwoody Rd, Atlanta, GA, USA.
Bassel El-RayesDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Suresh S RamalingamDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Taofeek K OwonikokoDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
R Donald HarveyDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Emory University · USEmory Healthcare · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
NCI NIH HHS P30 CA138292Winship Cancer Institute P30CA138292
6 · The paper itself

Abstract

backgroundSelecting the appropriate patients to receive immunotherapy (IO) remains a challenge due to the lack of optimal biomarkers. The presence of liver metastases has been implicated as a poor prognostic factor in patients with metastatic cancer. We investigated the association between sites of metastatic disease and clinical outcomes in patients receiving IO.

methodsWe conducted a retrospective review of 90 patients treated on IO-based phase 1 clinical trials at Winship Cancer Institute of Emory University between 2009 and 2017. Overall survival (OS) and progression-free survival (PFS) were measured from the first dose of IO to date of death or hospice referral and clinical or radiographic progression, respectively. Clinical benefit (CB) was defined as a best response of complete response (CR), partial response (PR), or stable disease (SD). Univariate analysis (UVA) and Multivariate analysis (MVA) were carried out using Cox proportional hazard model or logistic regression model. Covariates included age, whether IO is indicated for the patient's histology, ECOG performance status, Royal Marsden Hospital (RMH) risk group, number of metastatic sites, and histology.

resultsThe median age was 63 years and 53% of patients were men. The most common histologies were melanoma (33%) and gastrointestinal cancers (22%). Most patients (73.3%) had more than one site of distant metastasis. Sites of metastasis collected were lymph node (n = 58), liver (n = 40), lung (n = 37), bone (n = 24), and brain (n = 8). Most patients (80.7%) were RMH good risk. Most patients (n = 62) had received 2+ prior lines of systemic treatment before receiving IO on trial; 27 patients (30.0%) received prior ICB. Liver metastases were associated with significantly shorter OS (HR: 0.38, CI: 0.17-0.84, p = 0.017). Patients with liver metastasis also trended towards having shorter PFS (HR: 0.70, CI: 0.41-1.19, p = 0.188). The median OS was substantially longer for patients without liver metastases (21.9 vs. 8.1 months, p = 0.0048).

conclusionsLiver metastases may be a poor prognostic factor in patients receiving IO on phase 1 clinical trials. The presence of liver metastases may warrant consideration in updated prognostic models if these findings are validated in a larger prospective cohort.

Indexed as

AgedClinical Trials, Phase I as TopicFemaleHumansImmunotherapyLiver NeoplasmsMaleMiddle AgedNeoplasmsNeoplasm StagingRetrospective StudiesRisk FactorsSurvival AnalysisTreatment OutcomeClinical outcomesImmune checkpoint blockadeImmunotherapyLiver metastasisPhase 1 clinical trialsSites of metastasisTumor immunologyTumor microenvironment

Identifiers

PMID31464611
PMCPMC6716879
OpenAlexW2971136376

What OpenQuestion holds

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LicenceCC BY
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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.