Phase II randomized glioma study to evaluate efficacy and satisfaction of rolapitant plus ondansetron in preventing chemoradiation-induced nausea and vomiting.

dc.contributor.author

Affronti, Mary Lou

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Patel, Mallika P

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Severance, Erin K

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Loughlin, Charles

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Bradbury, Claire

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Herndon, James E

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Boyd, Kendra

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Lipp, Eric S

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Friedman, Henry S

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Desjardins, Annick

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Johnson, Margaret O

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Peters, Katherine B

dc.date.accessioned

2026-04-02T16:56:29Z

dc.date.available

2026-04-02T16:56:29Z

dc.date.issued

2025-08

dc.description.abstract

Background

Nausea and vomiting remain feared cancer treatment-related side effects. Antiemetic guideline trials exclude malignant glioma patients. In patients receiving radiation with concurrent temozolomide, chemoradiation-induced nausea; vomiting (cRINV) rates are 35% and 26%, respectively, which reduce quality of life, treatment adherence, and cancer control.

Methods

This randomized phase-II open-label trial, evaluated efficacy, patient preference, and satisfaction of ondansetron (short-acting 5HT3-RA; 3 h-half-life) monotherapy versus rolapitant (long-acting NK1-RA; 180 h-half-life) plus ondansetron in preventing cRINV during 6 weeks of temozolomide (75 mg/m2/day × 42 day) with radiation. Fifty-three eligible patients were randomized to Sequence-A (ondansetron-8 mg days: 1-42, day 22 rolapitant-180 mg) or Sequence-B (rolapitant day 1 plus daily ondansetron). Primary endpoint was percentage achieving cRINV-complete response (no vomiting/antiemetic rescue) during the first 2 weeks of radiation. Secondary endpoints: cRIN/cRIV rates, preference/satisfaction for rolapitant/ondansetron, toxicity, and adherence.

Results

Forty-eight (Sequence-A: 25; Sequnce-B: 23) initiated chemoradiation. Mean age = 53, 58% male, 73% Karnofsky performance status (KPS) > 90%, and 73% glioblastoma. During first 2 weeks of radiation, cRINV-CR was 57% with ondansetron and 74% receiving rolapitant/ondansetron (P = .27). Patient-reported 6-week cRINV-CR was 55% for both arms. First 2-week cRIN rates (38% Sequence-A; 32% Sequence-B) were more than cRIV rates (19% Sequence-A; 0% Sequence-B). Patients receiving ondansetron alone vomited more during the first 2 weeks and overall (26%) than with rolapitant/ondansetron (11%). Among 35 completers, 20% preferred rolapitant/ondansetron, 60% preferred ondansetron, and 20% had no preference (P = .0004). Adverse-events attributable to antiemetics were grade 1-2.

Conclusions

No difference was found in cRINV-CRs between the first 2-week treatments or overall satisfaction. Although not a positive study, less vomiting occurred with rolapitant/ondansetron. While patients prefer ondansetron monotherapy, most perceived better effectiveness with rolapitant/ondansetron.
dc.identifier

npaf014

dc.identifier.issn

2054-2577

dc.identifier.issn

2054-2585

dc.identifier.uri

https://hdl.handle.net/10161/34361

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Neuro-oncology practice

dc.relation.isversionof

10.1093/nop/npaf014

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

antiemesis

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emesis

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gliomas

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nausea

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radiation-induced-nausea/vomiting

dc.title

Phase II randomized glioma study to evaluate efficacy and satisfaction of rolapitant plus ondansetron in preventing chemoradiation-induced nausea and vomiting.

dc.type

Journal article

duke.contributor.orcid

Friedman, Henry S|0000-0001-7588-032X

duke.contributor.orcid

Johnson, Margaret O|0000-0003-1208-622X|0009-0005-5596-3407

pubs.begin-page

618

pubs.end-page

630

pubs.issue

4

pubs.organisational-group

Duke

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School of Medicine

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School of Nursing

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Nursing

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Biostatistics & Bioinformatics

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Medicine

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Pathology

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Medicine, Medical Oncology

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Duke Cancer Institute

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Neurology

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Neurology, General & Community Neurology

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Neurosurgery

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Neurosurgery, Neuro-Oncology

pubs.organisational-group

Biostatistics & Bioinformatics, Division of Biostatistics

pubs.organisational-group

Neurosurgery

pubs.publication-status

Published

pubs.volume

12

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