Evidence map›Paper›PMID 40367007›Full record

Trial reportEinstein (Sao Paulo, Brazil)2025

Omission of dexamethasone in prophylaxis for highly emetogenic chemotherapy in patients with breast cancer.

Camilla Vieira de Rebouças, Rafaela de Brito Alves, Alayne Magalhães Trindade Domingues Yamada, Auro Del Giglio, Felipe José Silva Melo Cruz

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Einstein (Sao Paulo, Brazil), 2025. 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

5 authors.

Camilla Vieira de RebouçasNúcleo de Pesquisa e Ensino IBCC Oncologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-7333-398X
Rafaela de Brito AlvesNúcleo de Pesquisa e Ensino IBCC Oncologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-5416-1163
Alayne Magalhães Trindade Domingues YamadaNúcleo de Pesquisa e Ensino IBCC Oncologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-9778-6123
Auro Del GiglioCentro Universitário FMABC, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-2009-824X
Felipe José Silva Melo CruzNúcleo de Pesquisa e Ensino IBCC Oncologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-4558-4850

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA phase II study evaluated a corticosteroid-free regimen (olanzapine, netupitant, and palonosetron) for the treatment of chemotherapy-induced nausea and vomiting. The results showed control rates comparable to those of standard protocols, demonstrating its feasibility without dexamethasone. ■ Evaluation of a corticosteroid-free antiemetic regimen. ■ Primary endpoint: 46% nausea control. ■ Secondary endpoint: 68% emesis control. ■ Comparable to standard four-drug protocols.

objectiveChemotherapy-induced nausea and vomiting are highly prevalent adverse events that can lead to poor treatment adherence and a decreased quality of life. To the best of our knowledge, the complete omission of dexamethasone from any regimen for preventing nausea and vomiting has not yet been evaluated. This study aimed to evaluate the efficacy of a three-drug protocol without corticosteroids for preventing nausea and vomiting.

methodsThis prospective, single-arm, phase II study was designed to evaluate the efficacy of olanzapine, netupitant, and palonosetron in controlling nausea and vomiting induced by emetogenic chemotherapy. Patients were assigned to receive olanzapine on days 1-5 and netupitant and palonosetron on day 1. No corticosteroids were administered. The primary endpoint was complete nausea control during the first 5 days after chemotherapy. Secondary endpoints included complete emesis control (no emesis and no use of rescue medication) and overall complete control (no emesis, no rescue medication, and no nausea).

resultsThe complete nausea control rate was 46% (95% confidence interval [95%CI] 0.32-0.59). The emesis control rate was 68% (95%CI= 0.55-0.80), and the overall control rate was 46% (95%CI= 0.32-0.59).

conclusionThese findings suggest that omitting dexamethasone in highly emetogenic chemotherapy is feasible and results in nausea and vomiting control rates similar to those of the standard four-drug protocol. However, randomized controlled trials are required to confirm this hypothesis.

Indexed as

AntiemeticsAntineoplastic AgentsBreast NeoplasmsDexamethasoneNauseaVomitingAdultAgedBenzodiazepinesFemaleHumansIsoquinolinesMiddle AgedOlanzapinePalonosetronProspective StudiesAntiemeticsAntineoplastic AgentsBenzodiazepinesDexamethasoneIsoquinolinesOlanzapinePalonosetronPyridinesQuinuclidines

Identifiers

PMID40367007
PMCPMC12094673

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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.