MétaCan
Menu
Back to cohort

Abstract 4915: Optimal frequency of follow up scans on systemictherapy for advanced malignancies

2019· article· en· W2955594557 on OpenAlexaff
David J. Stewart, Blair Macdonald, Sasha van Katwyk, Arif Awan, Kednapa Thavorn

Bibliographic record

VenueClinical Research (Excluding Clinical Trials) · 2019
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCancer Genomics and Diagnostics
Canadian institutionsUniversity of OttawaOttawa Hospital
Fundersnot available
KeywordsMedicineNuclear medicineRegimenProgression-free survivalConfidence intervalSurgeryInternal medicineOverall survival

Abstract

fetched live from OpenAlex

Background: Frequency of follow-up scans is specified in trials but there is little evidence to guide optimal frequency in standard therapy. Progression-free survival (PFS) generally follows first order kinetics and PFS half-lives (calculated by nonlinear regression analysis of more than 300 published PFS curves) correlated strongly with PFS medians (Stewart, AACR 2018).Method: We used the Excel formula EXP(-tn*0.693/t1/2) to calculate proportion of residual patients remaining progression-free at different time intervals, where tn is the potential time of follow-up scans (eg, every 3 weeks, 6 weeks, etc), * indicates multiplication, 0.693 is the natural logarithm of 2, and t1/2 is the PFS half-life in weeks.Results: Proportion of remaining patients expected to still remain progression-free at each subsequent scan varied with time interval between scans and with PFS half-life for the individual regimen. For example, with a PFS half-life of 4 months (17.3 weeks) and scans repeated every 6 weeks, 21% of the patients would have progressed by the first scan, 21% of the remaining patients would have progressed by the second scan at 12 weeks, etc. With PFS half-lives of 2, 4, 6, 12 and 20 months (for example), the proportion of remaining patients progressing by the time of each subsequent follow up scan if the scans were repeated every 3 weeks would be 21%, 11%, 8%, 4% and 2%, respectively, while with scans repeated every 6 weeks the proportion progressing would be 38%, 21%, 15%, 8% and 5%, by 12 weeks it would be 62%, 38%, 27%, 15% and 9%, and by 15 weeks it would be 70%, 45%, 33%, 18% and 11%, respectively.Conclusions: For therapies with short PFS half-lives, scanning every 6 weeks may not be often enough, while with long PFS half-lives, less frequent scans may be warranted. We plan analyses to estimate economic implications of varying scan frequency based on PFS half-life, drug and toxicity costs, opportunity costs (where other effective therapies might be offered if progression is detected), etc. We will also assess how this approach might be adapted for PFS curves that follow exponential 2-phase decay due to presence of distinct good vs poor prognosis subgroups, and we are in the process of using published PFS curves to assess the PFS half-lives for multiple different cancer therapies.Citation Format: David J. Stewart, Blair Macdonald, Sasha Van Katwyk, Arif Awan, Kednapa Thavorn. Optimal frequency of follow up scans on systemictherapy for advanced malignancies [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 4915.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.004
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.007
Threshold uncertainty score0.025

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.004
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0070.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.458
GPT teacher head0.575
Teacher spread0.117 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2019
Admission routes1
Has abstractyes

Explore more

Same venueClinical Research (Excluding Clinical Trials)Same topicCancer Genomics and DiagnosticsFrench-language works237,207