Evidence map›Paper›PMID 33503971›Full record

ArticleCancers2021

A Mathematical Model to Estimate Chemotherapy Concentration at the Tumor-Site and Predict Therapy Response in Colorectal Cancer Patients with Liver Metastases.

Daniel A Anaya, Prashant Dogra, Zhihui Wang, Mintallah Haider, Jasmina Ehab, Daniel K Jeong, Masoumeh Ghayouri, Gregory Y Lauwers, Kerry Thomas, Richard Kim and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 23 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

20 authors at 6 institutions in 2 countries.

Daniel A AnayaDepartment of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Prashant DograMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX 77030, USA.ORCID 0000-0001-6722-7371
Zhihui WangMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX 77030, USA.ORCID 0000-0001-6262-700X
Mintallah HaiderDepartment of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Jasmina EhabDepartment of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Daniel K JeongDepartment of Diagnostic Imaging and Interventional Radiology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Masoumeh GhayouriDepartment of Diagnostic Imaging and Interventional Radiology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Gregory Y LauwersDepartment of Diagnostic Imaging and Interventional Radiology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Kerry ThomasDepartment of Diagnostic Imaging and Interventional Radiology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Richard KimDepartment of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Joseph D ButnerMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX 77030, USA.
Sara NizzeroMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX 77030, USA.
Javier Ruiz RamírezMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX 77030, USA.
Marija PlodinecBiozentrum and the Swiss Nanoscience Institute & ARTIDIS AG, University of Basel, 4056 Basel, Switzerland.
Richard L SidmanDepartment of Neurology, Harvard Medical School, Boston, MA 02115, USA.
Webster K CaveneeLudwig Institute for Cancer Research, University of California-San Diego, La Jolla, CA 92093, USA.
Renata PasqualiniRutgers Cancer Institute of New Jersey & Division of Cancer Biology, Department of Radiation Oncology, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.
Wadih ArapRutgers Cancer Institute of New Jersey & Division of Hematology/Oncology, Department of Medicine Rutgers New Jersey Medical School, Newark, NJ 07103, USA.
Jason B FlemingDepartment of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.ORCID 0000-0002-8796-5627
Vittorio CristiniMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX 77030, USA.
Moffitt Cancer Center · USHouston Methodist · USRutgers, The State University of New Jersey · USHarvard University · USUniversity of Basel · CHUniversity of California San Diego · US

Funding

Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WANG, RONGFU · 2016 to 2020
$9.3M
A Targeted Nanomedicine Prototype Against Enzalutamide-resistant Prostate CancerR01CA226537 · NCI · RBHS -CANCER INSTITUTE OF NEW JERSEY · PI ARAP, WADIH, BRINKER, C JEFFREY · 2018 to 2022
$3.2M
National Science Foundation DMS-1930583NCI NIH HHS R01 CA226537NIH HHS 1R01CA222007NIH HHS 1R01CA226537NIH HHS 1U01CA196403NIH HHS 1U01CA213759NIH HHS U54CA210181
6 · The paper itself

Abstract

Chemotherapy remains a primary treatment for metastatic cancer, with tumor response being the benchmark outcome marker. However, therapeutic response in cancer is unpredictable due to heterogeneity in drug delivery from systemic circulation to solid tumors. In this proof-of-concept study, we evaluated chemotherapy concentration at the tumor-site and its association with therapy response by applying a mathematical model. By using pre-treatment imaging, clinical and biologic variables, and chemotherapy regimen to inform the model, we estimated tumor-site chemotherapy concentration in patients with colorectal cancer liver metastases, who received treatment prior to surgical hepatic resection with curative-intent. The differential response to therapy in resected specimens, measured with the gold-standard Tumor Regression Grade (TRG; from 1, complete response to 5, no response) was examined, relative to the model predicted systemic and tumor-site chemotherapy concentrations. We found that the average calculated plasma concentration of the cytotoxic drug was essentially equivalent across patients exhibiting different TRGs, while the estimated tumor-site chemotherapeutic concentration (eTSCC) showed a quadratic decline from TRG = 1 to TRG = 5 (

Indexed as

chemotherapycolorectal cancerFOLFOXliver metastasesmathematical model

Identifiers

PMID33503971
PMCPMC7866038
OpenAlexW3124523826

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.