Evidence map›Paper›PMID 38584192›Full record

Observational studyBreast cancer research and treatment2024

Body composition measures as a determinant of Alpelisib related toxicity.

Eliya Shachar, Ari Raphael, Uriel Katz, Rivka Kessner, Shlomit Strulov Shachar

Abstract readObservational Study
In one paragraph

Observational study in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Eliya Shachar *Oncology Department, Tel Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv, Israel.
Ari Raphael *Oncology Department, Tel Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv, Israel.
Uriel KatzFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Rivka KessnerFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Shlomit Strulov ShacharOncology Department, Tel Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv, Israel. Shlomitss@tlvmc.gov.il.

Funding

Conquer Cancer-Israel Cancer Research Fund Career Development Award 2021CC-ICRFCDA-5807223889 2021CC-ICRFCDA-5807223889
6 · The paper itself

Abstract

backgroundBody composition has emerged as an important prognostic factor in patients treated with cancer. Severe depletion of skeletal muscle, sarcopenia, has been associated with poor performance status and worse oncological outcomes. We studied patients with metastatic breast cancer receiving alpelisib, to determine if sarcopenia and additional body composition measures accounting for muscle and adiposity are associated with toxicity.

methodsA retrospective observational analysis was conducted, including 38 women with metastatic breast cancer and a PIK3CA mutation, treated with alpelisib as advanced line of therapy. Sarcopenia was determined by measuring skeletal muscle cross-sectional area at the third lumbar vertebra using computerized tomography. Various body composition metrics were assessed along with drug toxicity, dose reductions, treatment discontinuation, hospitalizations, time to treatment failure and overall survival.

resultsSarcopenia was observed in half of the patients (n = 19, 50%), spanning normal weight, overweight, and obese individuals. Among the body composition measures, lower skeletal muscle density (SMD) was associated with an increased risk of treatment-related hyperglycaemia (P = 0.03). Additionally, lower visceral adipose tissue (VAT) was associated with alpelisib-induced rash (P = 0.04) and hospitalizations (P = 0.04). Notably, alpelisib treatment discontinuation was not impacted by alpelisib toxicity.

conclusionBody composition measures, specifically SMD and VAT may provide an opportunity to identify patients at higher risk for severe alpelisib related hyperglycemia, and cutaneous toxicity. These findings suggest the potential use of body composition assessment to caution toxicity risk, allowing for personalized therapeutic observation and intervention.

Indexed as

Body CompositionBreast NeoplasmsSarcopeniaAdultAgedAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesFemaleHumansMiddle AgedMuscle, SkeletalMutationPrognosisRetrospective StudiesThiazolesAlpelisibAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesPIK3CA protein, humanThiazolesAdipose tissueAlpelisibHyperglycemiaMetastatic breast cancerMuscle attenuationSarcopeniaSkeletal muscle gaugeSkeletal muscle indexSurvivalToxicity

Identifiers

PMID38584192
PMCPMC11182811

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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 OpenQuestion graph.