Evidence map›Paper›PMID 39651705›Full record

ArticleCancer medicine2024

Novel Systemic Anticancer Therapy and Healthcare Utilization at the End of Life: A Retrospective Cohort Study.

Vikas Garg, Alejandra Ruiz Buenrostro, Katrina Heuniken, Rebecca Bagnarol, Mohamed Yousef, Katrina Sajewicz, Suman Dhanju, Kirsten Wentlandt, John Kuruvilla, Stephanie Lheureux and 2 more

Abstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Vikas GargDepartment of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0009-0009-0336-2107
Alejandra Ruiz BuenrostroDepartment of Supportive Care, University Health Network, Toronto, Ontario, Canada.
Katrina HeunikenDepartment of Biostatistics, University Health Network, Toronto, Ontario, Canada.
Rebecca BagnarolDepartment of Supportive Care, University Health Network, Toronto, Ontario, Canada.
Mohamed YousefDepartment of Supportive Care, University Health Network, Toronto, Ontario, Canada.
Katrina SajewiczTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Suman DhanjuRegional Cancer Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Kirsten WentlandtDepartment of Supportive Care, University Health Network, Toronto, Ontario, Canada.
John KuruvillaDepartment of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Stephanie LheureuxDepartment of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0003-4405-5890
Camilla ZimmermannDivision of Medical Oncology, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Breffni HannonDepartment of Supportive Care, University Health Network, Toronto, Ontario, Canada.

Funding

High Definition Therapeutics Program, Princess Margaret Cancer CentreRose Family Chair in Palliative Medicine and Supportive Care
6 · The paper itself

Abstract

backgroundNovel systemic anticancer therapies (SACT) in the form of targeted and immunotherapies are increasingly replacing traditional chemotherapy. Little is known about the impact of novel SACT on healthcare resource utilization (HCRU) at the end of life. METHODOLOGY: A retrospective review of patients attending a tertiary cancer center in Toronto, Canada, with advanced solid or hematological malignancies who died in 2019. Demographic and cancer data, SACT use, HCRU (emergency room [ER] visits, acute/intensive care unit [ICU] admission, and place of death) were retrieved and compared between those who received SACT in their last 30 days of life and those who did not. Chi-squared tests or Quasi-Poisson regression calculated HCRU expressed as percentages or rate ratios (RR). Univariate and multivariable logistic regression identified factors independently associated with SACT use.

resultsOf 443 patients included, 88 (20%) received SACT in the last 30 days of life, with 42 (48%) receiving targeted therapies and 10 (11%) immunotherapy. Factors associated with SACT use included younger age (p = 0.016), breast (p < 0.001), lung (p = 0.047), hematological malignancies (p = 0.002), fewer comorbidities (p = 0.039), and novel SACT (p = 0.006). Receipt of SACT was associated with a higher frequency of ER visits (55% vs. 36% who did not receive SACT, p = 0.001), acute hospitalizations (68% vs. 47%, p < 0.001), ICU admissions (18% vs. 7%, p = 0.003), and death in hospital (45% vs. 30%, p = 0.008).

conclusionNovel SACT use at the end of life is high and is strongly associated with HCRU. Future studies should explore the impact of advance care planning and palliative care referrals on SACT use.

Indexed as

NeoplasmsPatient Acceptance of Health CareTerminal CareAgedAged, 80 and overAntineoplastic AgentsFemaleHumansImmunotherapyMaleMiddle AgedMolecular Targeted TherapyRetrospective StudiesAntineoplastic Agentsend‐of‐life carehealthcare resource utilizationimmunotherapysystemic anticancer therapy

Identifiers

PMID39651705
PMCPMC11626481

What Socratic 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 Socratic graph.