Evidence map›Paper›PMID 35994026›Full record

ArticleMedical physics2022

Direct incorporation of patient-specific efficacy and toxicity estimates in radiation therapy plan optimization.

Daniel F Polan, Marina A Epelman, Victor W Wu, Yilun Sun, Markus Varsta, Daniel R Owen, David Jarema, Charles K Matrosic, Shruti Jolly, Caitlin A Schonewolf and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Medical physics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Utility-Based Dose Selection for Stereotactic Body Radiation Therapy in Hepatocellular Carcinoma.International journal of radiation oncology, biology, physics · 2026
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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

12 authors at 2 institutions in 1 country.

Daniel F PolanDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Marina A EpelmanDepartment of Industrial and Operations Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Victor W WuDepartment of Industrial and Operations Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Yilun SunDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Markus VarstaVarian Medical Systems, Palo Alto, California, USA.
Daniel R OwenDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
David JaremaDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Charles K MatrosicDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Shruti JollyDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Caitlin A SchonewolfDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Matthew J SchipperDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
Martha M MatuszakDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
University of Michigan–Ann Arbor · USVarian Medical Systems (United States) · US

Funding

TREATMENT VERIFICATION AND TREATMENT PLAN REFINEMENTP01CA059827 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BALTER, JAMES M, LAWRENCE, THEODORE S · 1993 to 2018
$37.9M
NCI NIH HHS P01 CA059827
6 · The paper itself

Abstract

purposeCurrent radiation therapy (RT) treatment planning relies mainly on pre-defined dose-based objectives and constraints to develop plans that aim to control disease while limiting damage to normal tissues during treatment. These objectives and constraints are generally population-based, in that they are developed from the aggregate response of a broad patient population to radiation. However, correlations of new biologic markers and patient-specific factors to treatment efficacy and toxicity provide the opportunity to further stratify patient populations and develop a more individualized approach to RT planning. We introduce a novel intensity-modulated radiation therapy (IMRT) optimization strategy that directly incorporates patient-specific dose response models into the planning process. In this strategy, we integrate the concept of utility-based planning where the optimization objective is to maximize the predicted value of overall treatment utility, defined by the probability of efficacy (e.g., local control) minus the weighted sum of toxicity probabilities. To demonstrate the feasibility of the approach, we apply the strategy to treatment planning for non-small cell lung cancer (NSCLC) patients. METHODS AND MATERIALS: We developed a prioritized approach to patient-specific IMRT planning. Using a commercial treatment planning system (TPS), we calculate dose based on an influence matrix of beamlet-dose contributions to regions-of-interest. Then, outside of the TPS, we hierarchically solve two optimization problems to generate optimal beamlet weights that can then be imported back to the TPS. The first optimization problem maximizes a patient's overall plan utility subject to typical clinical dose constraints. In this process, we facilitate direct optimization of efficacy and toxicity trade-off based on individualized dose-response models. After optimal utility is determined, we solve a secondary optimization problem that minimizes a conventional dose-based objective subject to the same clinical dose constraints as the first stage but with the addition of a constraint to maintain the optimal utility from the first optimization solution. We tested this method by retrospectively generating plans for five previously treated NSCLC patients and comparing the prioritized utility plans to conventional plans optimized with only dose metric objectives. To define a plan utility function for each patient, we utilized previously published correlations of dose to local control and grade 3-5 toxicities that include patient age, stage, microRNA levels, and cytokine levels, among other clinical factors.

resultsThe proposed optimization approach successfully generated RT plans for five NSCLC patients that improve overall plan utility based on personalized efficacy and toxicity models while accounting for clinical dose constraints. Prioritized utility plans demonstrated the largest average improvement in local control (16.6%) when compared to plans generated with conventional planning objectives. However, for some patients, the utility-based plans resulted in similar local control estimates with decreased estimated toxicity.

conclusionThe proposed optimization approach, where the maximization of a patient's RT plan utility is prioritized over the minimization of standardized dose metrics, has the potential to improve treatment outcomes by directly accounting for variability within a patient population. The implementation of the utility-based objective function offers an intuitive, humanized approach to biological optimization in which planning trade-offs are explicitly optimized.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMicroRNAsRadiotherapy, Intensity-ModulatedCytokinesHumansRadiotherapy DosageRadiotherapy Planning, Computer-AssistedRetrospective StudiesCytokinesMicroRNAsHierarchical optimizationIMRTradiotherapy outcomes

Identifiers

PMID35994026
PMCPMC9826508
OpenAlexW4292647993

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.