Evidence map›Paper›PMID 34101934›Full record

Trial reportThe oncologist2021

Dexamethasone-Sparing Regimens with Oral Netupitant and Palonosetron for the Prevention of Emesis Caused by High-Dose Cisplatin: A Randomized Noninferiority Study.

Luigi Celio, Diego Cortinovis, Alessio Aligi Cogoni, Luigi Cavanna, Olga Martelli, Simona Carnio, Elena Collovà, Federica Bertolini, Fausto Petrelli, Alessandra Cassano and 11 more

2 registry-linked trialsOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled TrialEquivalence Trial
In one paragraph

Trial report in The oncologist, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 5 pooled it
4.2field-weighted citation impact, top 5% 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.

NCT07699276 phase2recruitingnot on this mapstarted 2026, after this paper: background citation

Steroid-sparing Regimen With Olanzapine and Ondansetron to Prevent Emesis Caused by High Dose Cisplatin in Solid Cancer Patient : A Single Arm Phase II Study

TypeinterventionalSponsorMahidol UniversityRan2026 to 2027Enrolled95ConditionsCancer (Solid Tumors), Vomiting, Cisplatin, OlanzapineArmsdexamethasone sparing
NCT07743827 narecruitingnot on this mapstarted 2026, after this paper: background citation

Efficacy of an Olanzapine Based Dexamethasone-sparing Regimen in Breast Cancer Patients With Metabolic-risk Factors: A Randomized, Controlled Trial

TypeinterventionalSponsorAlexandria UniversityRan2026 to 2027Enrolled90ConditionsOlanzapine, Breast Cancer, DexamethasoneArmsPantoprazole, olanzapine, Dexamethasone
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 5 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. 2023 updated MASCC/ESMO consensus recommendations: prevention of nausea and vomiting following high-emetic-risk antineoplastic agents.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Pooled it
  5. Pooled it
  6. Trial
  7. Trial
  8. Trial
  9. Global inequitable distribution of seminal studies of chemotherapy-induced nausea and vomiting.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Review
  10. Article
  11. Review
  12. Article
  13. Reply to L. Celio et al.British journal of cancer · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
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

21 authors at 17 institutions in 1 country.

Luigi CelioOncology Unit, Azienda Socio Sanitaria Territoriale del Garda, Desenzano del Garda Hospital, Brescia, Italy.ORCID 0000-0001-6849-9838
Diego CortinovisMedical Oncology Department, Azienda Socio Sanitaria Territoriale Monza San Gerardo Hospital, Monza, Italy.
Alessio Aligi CogoniMedical Oncology Department, Azienda Ospedaliero-Universitaria di Sassari, Sassari, Italy.
Luigi CavannaOncology Department, Azienda Ospedaliera di Piacenza, Piacenza, Italy.
Olga MartelliMedical Oncology, San Giovanni-Addolorata Hospital, Rome, Italy.
Simona CarnioDepartment of Oncology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Turin, Italy.
Elena CollovàCancer Centre Department, Oncology Unit, Azienda Socio Sanitaria Territoriale Ovest Milanese, Legnano Hospital, Legnano, Milan, Italy.
Federica BertoliniDepartment of Oncology and Hematology, Azienda Ospedaliero-Universitaria Policlinico di Modena, Modena, Italy.
Fausto PetrelliMedical Oncology Unit, Azienda Socio Sanitaria Territoriale Bergamo Ovest, Treviglio, Bergamo, Italy.ORCID 0000-0001-9639-4486
Alessandra CassanoMedical Oncology, Università Cattolica del Sacro Cuore, Rome, Italy.
Rita ChiariOncology Unit, AULSS6 Euganea, Padova, Italy.
Francesca ZanelliMedical Oncology Unit, Istituto di Ricovero e Cura a Carattere Scientifico Santa Maria Nuova, Reggio Emilia, Italy.
Salvatore PiscontiMedical Oncology Department, San Giuseppe Moscati Hospital, Statte, Taranto, Italy.
Isabella VittimbergaDepartment of Oncology, Azienda Socio Sanitaria Territoriale Lecco, Lecco, Italy.
Antonietta LetiziaDepartment of Pneumology and Oncology, Azienda Ospedaliera di Rilievo Nazionale dei Colli-Ospedale Monaldi, Naples, Italy.
Andrea MisinoMedical Oncology, Clinical Cancer Center "Giovanni Paolo II," Istituto di Ricovero e Cura a Carattere Scientifico, Bari, Italy.
Angela GernoneMedical Oncology Unit, University of Bari, Policlinico di Bari, Bari, Italy.
Erminio BonizzoniDepartment of Clinical Science and Community. Section of Medical Statistics, Biometry and Epidemiology "G.A. Maccacaro," Faculty of Medicine and Surgery, University of Milan, Milan, Italy.
Sara PilottoSection of Oncology, Department of Medicine, University and Hospital Trust of Verona, Verona, Italy.
Sabino De PlacidoClinical Medicine and Surgery Department, University of Naples "Federico II," Naples, Italy.
Emilio BriaMedical Oncology, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-2333-704X
Azienda Socio Sanitaria Territoriale Lariana · ITUniversità Cattolica del Sacro Cuore · ITAzienda Ospedaliera Ospedale Civile di Legnano · ITAzienda Ospedaliera San Gerardo · ITAzienda Ospedaliera San Giovanni Addolorata · ITAzienda Ospedaliera S.Giuseppe Moscati · ITAzienda Ospedaliero-Universitaria di Modena · ITAzienda Ospedaliero Universitaria di Sassari · ITCasa di Cura Villa Garda · ITOspedale Monaldi · ITOspedale San Luigi Gonzaga · ITOspedaliera di Piacenza · ITSanta Maria Nuova Hospital · ITUniversity of Bari Aldo Moro · ITUniversity of Milan · ITUniversity of Naples Federico II · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo reduce the overall exposure to dexamethasone (DEX) in patients receiving cisplatin-based chemotherapy, we evaluated the noninferiority of DEX on day 1, with or without low-dose DEX on days 2 and 3, combined with an oral fixed-dose combination of netupitant and palonosetron (NEPA), compared with the guideline-consistent use of 4-day DEX. PATIENTS AND

methodsIn this open-label, multicenter study, chemotherapy-naïve patients undergoing high-dose cisplatin (≥70 mg/m

resultsTwo-hundred twenty-eight patients, 76 in each arm, were assessable. Noninferiority was met for both DEX-sparing regimens and the reference arm, with overall phase CR rates of 76.3% in each of the DEX1 and DEX3 arms and 75.0% in the DEX4 arm (95% confidence interval, -12.3% to 15% for each comparison). During the overall phase, CP rates were similar between groups.

conclusionA simplified regimen of NEPA plus single-dose DEX offers comparable chemotherapy-induced nausea and vomiting prevention throughout 5 days post-chemotherapy with the advantage of sparing patients additional doses of DEX in the high-emetic-risk setting of cisplatin-based chemotherapy. IMPLICATIONS FOR PRACTICE: Dexamethasone (DEX) has traditionally played an integral role in the management of chemotherapy-induced emesis. Although generally considered safe, even short-term DEX use is associated with various side effects, and some evidence suggests that concurrent steroids may reduce the efficacy of immunotherapies. This study demonstrates comparable antiemetic control during the 5 days post-chemotherapy with a simplified regimen of netupitant/palonosetron plus single-dose DEX versus the standard 4-day DEX reference treatment in high-dose cisplatin. This represents a clinically relevant achievement as it not only simplifies antiemetic prophylaxis but also offers an opportunity to appropriately use in patients where caution with corticosteroid use is advised.

Indexed as

AntiemeticsCisplatinAntineoplastic Combined Chemotherapy ProtocolsBenzeneacetamidesDexamethasoneHumansPalonosetronPiperazinesPyridinesQuinuclidinesVomitingAntiemeticsBenzeneacetamidesCisplatinDexamethasonenetupitantPalonosetronPiperazinesPyridinesQuinuclidinesChemotherapy-induced nausea and vomitingCisplatinDexamethasoneNetupitantPalonosetron

Identifiers

PMID34101934
PMCPMC8488764
OpenAlexW3167136754

What OpenQuestion holds

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Registered trials

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.