Evidence map›Paper›PMID 41587947›Full record

ArticleThe oncologist2026

Clinical characteristics and drug-drug interactions in human epidermal growth factor receptor 2-positive breast cancer treated with trastuzumab deruxtecan: real-world data from the DE-REAL study.

Simona Pisegna, Simone Scagnoli, Gabriella Gentile, Antonella Chiavassa, Roberta Caputo, Michelino De Laurentiis, Giuseppe Curigliano, Matteo Lambertini, Francesco Pantano, Armando Orlandi and 15 more

Abstract read
In one paragraph

Article in The oncologist, 2026. 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

25 authors.

Simona PisegnaDepartment of Experimental Medicine, Sapienza University of Rome, Rome, 00161, Italy.ORCID 0000-0002-6910-9528
Simone ScagnoliDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, 00161, Italy.ORCID 0000-0003-4943-5622
Gabriella GentileDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, 00161, Italy.
Antonella ChiavassaDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, 00161, Italy.
Roberta CaputoDepartment of Breast and Thoracic Oncology, Division of Breast Medical Oncology, Istituto Nazionale Tumori IRCCS "Fondazione Pascale, Naples, 80131, Italy.ORCID 0000-0003-4231-1184
Michelino De LaurentiisDepartment of Breast and Thoracic Oncology, Division of Breast Medical Oncology, Istituto Nazionale Tumori IRCCS "Fondazione Pascale, Naples, 80131, Italy.ORCID 0000-0001-9009-1572
Giuseppe CuriglianoEuropean Institute of Oncology, IRCCS, Milan, 20141, Italy.ORCID 0000-0003-1781-2518
Matteo LambertiniDepartment of Internal Medicine and Medical Specialties (DiMI), School of Medicine, University of Genova, Genoa, 16132, Italy.ORCID 0000-0003-1797-5296
Francesco PantanoMedical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, 00128, Italy.
Armando OrlandiComprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, 00168, Italy.ORCID 0000-0001-5253-4678
Antonella PalazzoComprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, 00168, Italy.ORCID 0000-0002-8371-7087
Ida ParisDepartment of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, 00168, Italy.ORCID 0000-0002-7445-3366
Claudio VernieriDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, 20133, Italy.
Beatrice TedescoMedical Oncology Unit, "S. Carlo" Hospital, Potenza, 85100 , Italy.
Marianna GiampagliaMedical Oncology Unit, "S. Carlo" Hospital, Potenza, 85100 , Italy.
Michela PalleschiMedical Oncology, Breast & GYN Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, 47014, Italy.
Zelmira BallatoreMedical Oncology Unit, AST Pesaro Urbino, 61121, Italy.
Daniele AlesiniUOSD Centro Oncologico S. Spirito e Nuovo Regina Margherita, Ospedale Santo Spirito in Sassia, Rome, 00193, Italy.
Giuliana D'AuriaDepartment of Medical Oncology, Sandro Pertini Hospital, Rome, 00157, Italy.
Maria Agnese FabbriDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Santa Rosa Hospital, Viterbo, 01100, Italy.
Luigi RossiMultispeciality Department of Oncology, ASL Latina, "Sapienza" University of Rome, Formia, 04011, Italy.
Giulia FisconDepartment for the Promotion of Human Science and Quality of Life, San Raffaele Open University, Rome, 00166, Italy.
Paolo MarchettiDepartment of Oncology, Istituto Dermopatico dell'Immacolata IDI-IRCCS, Rome, 00167, Italy.
Alessandra FabiPrecision Medicine in Senology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, 00168, Italy.ORCID 0000-0002-0758-8033
Andrea BotticelliDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, 00161, Italy.ORCID 0000-0002-6425-9893

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrastuzumab deruxtecan (T-DXd) reshaped clinical practice in human epidermal growth factor receptor 2-positive (HER2+) metastatic breast cancer (mBC). The impact of clinical characteristics and drug-drug interactions (DDIs) on outcomes in patients receiving T-DXd is still under investigation.

methodsWe retrospectively analyzed data of patients from the Italian DE-REAL study. Clinical features including age, body mass index (BMI), toxicity and DDIs were assessed and correlated with clinical outcomes. The Drug-PIN software was used to evaluate DDIs.

resultsAmong 143 patients, age did not significantly affect progression-free survival (PFS) but influenced overall survival (OS), with younger patients (<65 years) showing better outcomes (median overall survival [mOS]: 12 vs. 10 months, P = 0.02). Patients with BMI >25 demonstrated significantly longer PFS (11 vs. 9 months, P = 0.04), which was confirmed as independent predictor of better PFS at multivariate analysis (P ≤0.05), but experienced higher toxicity rates, particularly nausea (P = 0.019). Drug-PIN classification showed no impact on survival outcomes, although patients with high-risk DDIs experienced more nausea and asthenia compared to those with low-risk interactions (P = 0.0018 and P = 0.003, respectively).

conclusionT-DXd efficacy appears consistent across different age groups, although elderly patients showed reduced OS. Higher BMI was associated with improved PFS but increased toxicity. While DDIs did not affect survival outcomes, they influenced specific adverse events. Our results reinforce the efficacy and favorable safety profile of T-DXd in a broad real-world population, including patients with polypharmacy or comorbidities, while highlighting that personalized monitoring and supportive care strategies may be particularly beneficial for elderly patients and those with higher BMI.

Indexed as

Breast NeoplasmsCamptothecinErb-b2 Receptor Tyrosine KinasesImmunoconjugatesTrastuzumabAdultAgedAged, 80 and overDrug InteractionsFemaleHumansMiddle AgedRetrospective StudiesCamptothecinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmunoconjugatesTrastuzumabtrastuzumab deruxtecanbody mass indexdrug–drug interactionselderly patientsHER2-positive breast cancerreal-world datatrastuzumab deruxtecan

Identifiers

PMID41587947
PMCPMC12848230

What Socratic holds

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LicenceCC BY
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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.