Evidence map›Paper›PMID 37378079›Full record

ArticleDrugs in context2023

Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR

Barbara Tagliaferri, Ludovica Mollica, Raffella Palumbo, Claudia Leli, Alberto Malovini, Matteo Terzaghi, Erica Quaquarini, Cristina Teragni, Stefano Maccarone, Andrea Premoli and 1 more

Open access · goldAbstract read
In one paragraph

Article in Drugs in context, 2023. 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
0.5field-weighted citation impact, top 30% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

11 authors at 2 institutions in 1 country.

Barbara TagliaferriMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Ludovica MollicaMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Raffella PalumboMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Claudia LeliMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Alberto MaloviniLaboratory of Informatics and Systems Engineering for Clinical Research, ICS Maugeri IRCCS, Pavia, Italy.
Matteo TerzaghiLaboratory of Informatics and Systems Engineering for Clinical Research, ICS Maugeri IRCCS, Pavia, Italy.
Erica QuaquariniMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Cristina TeragniMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Stefano MaccaroneMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Andrea PremoliMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Federico SottotettiMedical Oncology Unit, ICS Maugeri IRCCS, Pavia, Italy.
Istituti Clinici Scientifici Maugeri · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Advanced breast cancer (ABC) is characterized by multidimensional clinical complexity that is usually not considered in randomized clinical trials. In the present real-life study, we investigated the link between clinical complexity and quality of life of patients with HR Methods: We evaluated multimorbidity burden assessed with the Cumulative Illness Rating Scale (CIRS), polypharmacy and patient-reported outcomes (PROs). PROs were assessed at baseline (T0), after 3 months of therapy (T1), and at disease progression (T2) using EORTC QLC-C30 and QLQ-BR23 questionnaires. Baseline PROs and changes between T0 and T1 were evaluated amongst patients with different multimorbidity burden (CIRS <5 and ≥5) and polypharmacy (<2 or ≥2 drugs). Results: From January 2018 to January 2022, we enrolled 54 patients (median age 66 years, IQR 59-74). The median CIRS score was 5 (IQR 2-7), whilst the median number of drugs taken by patients was 2 (IQR 0-4). No changes in QLQ-C30 final scoring between T0 and T1 were observed in the overall cohort ( Conclusion: Multimorbidity and polypharmacy increase the clinical complexity of patients with ABC and may affect baseline PROs. The safety profile of CDK4/6 inhibitors seems to be maintained in this population. Further studies are needed to assess clinical complexity in patients with ABC.This article is part of the

Indexed as

breast cancerCDK4/6 inhibitorsclinical complexitycomorbiditiespolypharmacyquality of lifereal-life population

Identifiers

PMID37378079
PMCPMC10291968
OpenAlexW4381191101

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.