Evidence map›Paper›PMID 30742484›Full record

ArticleJCO clinical cancer informatics2019

The Immune Checkpoint Kick Start: Optimization of Neoadjuvant Combination Therapy Using Game Theory.

Jeffrey West, Mark Robertson-Tessi, Kimberly Luddy, Derek S Park, Drew F K Williamson, Cathal Harmon, Hung T Khong, Joel Brown, Alexander R A Anderson

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Immune-checkpoint inhibitor therapy response evaluation using oncophysics-based mathematical models.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2023
    Review
  3. Review
  4. Article
  5. The theory of tumor ecosystem.Cancer communications (London, England) · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Introduction to Mathematical Oncology.JCO clinical cancer informatics · 2019
    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

9 authors.

Jeffrey WestH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Mark Robertson-TessiH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Kimberly LuddyH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Derek S ParkH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Drew F K WilliamsonCleveland Clinic Foundation, Cleveland, OH.
Cathal HarmonTrinity College Dublin, Dublin, Ireland.
Hung T KhongH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Joel BrownH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Alexander R A AndersonH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.

Funding

"Research Supplement to Promote Diversity in Health-Related Research", as part of Moffitt PS-OC, "Cancer as a Complex adaptive System"U54CA193489 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, GATENBY, ROBERT A · 2015 to 2020
$12.5M
NCI NIH HHS U54 CA193489
6 · The paper itself

Abstract

purposeIn an upcoming clinical trial at the Moffitt Cancer Center for women with stage 2/3 estrogen receptor-positive breast cancer, treatment with an aromatase inhibitor and a PD-L1 checkpoint inhibitor combination will be investigated to lower a preoperative endocrine prognostic index (PEPI) that correlates with relapse-free survival. PEPI is fundamentally a static index, measured at the end of neoadjuvant therapy before surgery. We have developed a mathematical model of the essential components of the PEPI score to identify successful combination therapy regimens that minimize tumor burden and metastatic potential, on the basis of time-dependent trade-offs in the system.

methodsWe considered two molecular traits, CCR7 and PD-L1, which correlate with treatment response and increased metastatic risk. We used a matrix game model with the four phenotypic strategies to examine the frequency-dependent interactions of cancer cells. This game was embedded in an ecological model of tumor population-growth dynamics. The resulting model predicts evolutionary and ecological dynamics that track with changes in the PEPI score.

resultsWe considered various treatment regimens on the basis of combinations of the two therapies with drug holidays. By considering the trade off between tumor burden and metastatic potential, the optimal therapy plan was a 1-month kick start of the immune checkpoint inhibitor followed by 5 months of continuous combination therapy. Relative to a protocol giving both therapeutics together from the start, this delayed regimen resulted in transient suboptimal tumor regression while maintaining a phenotypic constitution that is more amenable to fast tumor regression for the final 5 months of therapy.

conclusionThe mathematical model provides a useful abstraction of clinical intuition, enabling hypothesis generation and testing of clinical assumptions.

Indexed as

Game TheoryAntineoplastic Combined Chemotherapy ProtocolsAromatase InhibitorsB7-H1 AntigenBiomarkers, TumorBreast NeoplasmsFemaleHumansImmunotherapyNeoadjuvant TherapyReceptors, CCR7Aromatase InhibitorsB7-H1 AntigenBiomarkers, TumorCCR7 protein, humanCD274 protein, humanReceptors, CCR7

Identifiers

PMID30742484
PMCPMC6873943

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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.