Evidence map›Paper›PMID 35490579›Full record

ArticleESMO open2022

Patient-reported outcomes predict survival and adverse events following anticancer treatment initiation in advanced HER2-positive breast cancer.

N D Modi, N O Danell, R N A Perry, A Y Abuhelwa, A Rathod, S Badaoui, R A McKinnon, M Haseloff, A Shahnam, S M Swain and 3 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 17 citations in OpenAlex.

  1. Prognostic associations between patient-reported outcomes and overall survival among patients with advanced squamous non-small cell lung cancer: results from the RATIONALE-307 trial.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2026
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  11. Patient-Reported Quality of Life at Diagnosis in Adolescent and Young Adults With Cancer.Journal of the National Comprehensive Cancer Network : JNCCN · 2024
    Article
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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

13 authors at 4 institutions in 3 countries.

N D ModiCollege of Medicine and Public Health, Flinders University, South Australia.
N O DanellCollege of Medicine and Public Health, Flinders University, South Australia.
R N A PerryCollege of Medicine and Public Health, Flinders University, South Australia.
A Y AbuhelwaCollege of Medicine and Public Health, Flinders University, South Australia.
A RathodCollege of Medicine and Public Health, Flinders University, South Australia.
S BadaouiCollege of Medicine and Public Health, Flinders University, South Australia.
R A McKinnonCollege of Medicine and Public Health, Flinders University, South Australia.
M HaseloffCollege of Medicine and Public Health, Flinders University, South Australia.
A ShahnamCrown Princess Mary Cancer Centre, Westmead Hospital, New South Wales, Australia.
S M SwainUniversity of Georgetown Medical Center, Washington DC, USA.
M WelslauOnkologie Aschaffenburg, Aschaffenburg, Germany.
M J SorichCollege of Medicine and Public Health, Flinders University, South Australia.
A M HopkinsCollege of Medicine and Public Health, Flinders University, South Australia. Electronic address: ashley.hopkins@flinders.edu.au.
Flinders University · AUGeorgetown University Medical Center · USKlinikum Aschaffenburg · DEWestmead Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognostic value of patient-reported outcomes (PROs) has been minimally explored in advanced breast cancer (BC), and their comparative prognostic performance against Eastern Cooperative Oncology Group performance status (ECOG PS) is largely unknown. PATIENTS AND

methodsThis study pooled individual participant data from clinical trials CLEOPATRA, EMILIA, and MARIANNE. Pre-treatment PRO associations with overall survival (OS), progression-free survival (PFS), and grade ≥3 adverse events were evaluated via Cox proportional hazards regression. Prognostic performance was assessed with the C-statistic (c). PRO values were collected via the Functional Assessment of Cancer Therapy-Breast (FACT-B) questionnaire. All analyses were stratified by study and treatment arms. Analyses adjusted for known prognostic variables were conducted. Exploratory analysis of the prognostic performance of PROs compared to ECOG PS was undertaken.

resultsThe study included data from 2894 patients initiated on contemporary therapies including pertuzumab (n = 765), trastuzumab (n = 1173), trastuzumab emtansine (n = 1225), taxanes (n = 1173), lapatinib (n = 496), and capecitabine (n = 496). On univariable and adjusted analysis, patient-reported physical well-being, functional well-being, and BC subscale were all identified to be associated with OS, PFS, and grade ≥3 adverse events (P < 0.05). Patient-reported physical well-being was the most prognostic PRO for all assessed outcomes. The OS prognostic performance of physical well-being (c = 0.58) was superior to ECOG PS (c = 0.56) (P < 0.05), with multivariable analysis indicating that both provide independent information (P < 0.0001).

conclusionsPROs were identified as independent prognostic factors for OS, PFS, and grade ≥3 adverse events in patients with human epidermal growth factor receptor 2 (HER2)-positive advanced BC initiating contemporary treatment options. Further, patient-reported physical well-being was more prognostic of OS than ECOG PS and contained independent information. PROs have value as prognostic and stratification factors for clinical use and research trials of anticancer treatment in HER2-positive ABC.

Indexed as

Breast NeoplasmsAdo-Trastuzumab EmtansineFemaleHumansLapatinibPatient Reported Outcome MeasuresTrastuzumabAdo-Trastuzumab EmtansineLapatinibTrastuzumabadvanced breast cancercontemporary therapyEastern Cooperative Oncology Group performance statuspatient-reported outcomessurvival outcomestoxicity outcomes

Identifiers

PMID35490579
PMCPMC9271483
OpenAlexW4225081785

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.