Evidence map›Paper›PMID 32803720›Full record

ArticlePharmacoEconomics2020

Simulating Progression-Free and Overall Survival for First-Line Doublet Chemotherapy With or Without Bevacizumab in Metastatic Colorectal Cancer Patients Based on Real-World Registry Data.

Koen Degeling, Hui-Li Wong, Hendrik Koffijberg, Azim Jalali, Jeremy Shapiro, Suzanne Kosmider, Rachel Wong, Belinda Lee, Matthew Burge, Jeanne Tie and 7 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in PharmacoEconomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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

17 authors at 12 institutions in 2 countries.

Koen DegelingHealth Technology and Services Research Department, Faculty of Behavioural, Management and Social Sciences, Technical Medical Centre, University of Twente, Enschede, The Netherlands. koen.degeling@unimelb.edu.au.ORCID http://orcid.org/0000-0001-7487-2491
Hui-Li WongPersonalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-3803-2107
Hendrik KoffijbergHealth Technology and Services Research Department, Faculty of Behavioural, Management and Social Sciences, Technical Medical Centre, University of Twente, Enschede, The Netherlands.ORCID http://orcid.org/0000-0002-1753-0652
Azim JalaliPersonalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Jeremy ShapiroDepartment of Medical Oncology, Cabrini Health, Melbourne, VIC, Australia.
Suzanne KosmiderDepartment of Medical Oncology, Western Health, Melbourne, VIC, Australia.
Rachel WongPersonalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-4926-5689
Belinda LeePersonalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Matthew BurgeDepartment of Medical Oncology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Jeanne TiePersonalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Desmond YipDepartment of Medical Oncology, The Canberra Hospital, Canberra, ACT, Australia.
Louise NottDepartment of Medical Oncology, Royal Hobart Hospital, Hobart, TAS, Australia.
Adnan KhattakDepartment of Medical Oncology, Fiona Stanley Hospital, Perth, WA, Australia.
Stephanie LimDepartment of Medical Oncology, Campbelltown Hospital, Campbelltown, NSW, Australia.ORCID http://orcid.org/0000-0001-5940-7137
Susan CairdDepartment of Medical Oncology, Gold Coast University Hospital, Gold Coast, QLD, Australia.ORCID http://orcid.org/0000-0002-3125-704X
Peter Gibbs *Personalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-1423-4484
Maarten IJzerman *Health Technology and Services Research Department, Faculty of Behavioural, Management and Social Sciences, Technical Medical Centre, University of Twente, Enschede, The Netherlands.ORCID http://orcid.org/0000-0001-5788-5805
Walter and Eliza Hall Institute of Medical Research · AUThe University of Melbourne · AUCabrini Hospital · AUCamden and Campbelltown Hospitals · AUCanberra Hospital · AUFiona Stanley Hospital · AUGold Coast Hospital · AUNorthern Health · AURoyal Brisbane and Women's Hospital · AURoyal Hobart Hospital · AUUniversity of Twente · NLWestern Health · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSimulation models utilizing real-world data have potential to optimize treatment sequencing strategies for specific patient subpopulations, including when conducting clinical trials is not feasible. We aimed to develop a simulation model to estimate progression-free survival (PFS) and overall survival for first-line doublet chemotherapy with or without bevacizumab for specific subgroups of metastatic colorectal cancer (mCRC) patients based on registry data.

methodsData from 867 patients were used to develop two survival models and one logistic regression model that populated a discrete event simulation (DES). Discrimination and calibration were used for internal validation of these models separately and predicted and observed medians and Kaplan-Meier plots were compared for the integrated DES. Bootstrapping was performed to correct for optimism in the internal validation and to generate correlated sets of model parameters for use in a probabilistic analysis to reflect parameter uncertainty.

resultsThe survival models showed good calibration based on the regression slopes and modified Hosmer-Lemeshow statistics at 1 and 2 years, but not for short-term predictions at 0.5 years. Modified C-statistics indicated acceptable discrimination. The simulation estimated that median first-line PFS (95% confidence interval) of 219 (25%) patients could be improved from 175 days (156-199) to 269 days (246-294) if treatment would be targeted based on the highest expected PFS.

conclusionsExtensive internal validation showed that DES accurately estimated the outcomes of treatment combination strategies for specific subpopulations, with outcomes suggesting treatment could be optimized. Although results based on real-world data are informative, they cannot replace randomized trials.

Indexed as

Colorectal NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsBevacizumabDisease-Free SurvivalHumansKaplan-Meier EstimateRegistriesTreatment OutcomeBevacizumab

Identifiers

PMID32803720
OpenAlexW3049732599

What OpenQuestion holds

Textmetadata
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.