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 | |
| dc.contributor.author | Patel, Mallika P | |
| dc.contributor.author | Severance, Erin K | |
| dc.contributor.author | Loughlin, Charles | |
| dc.contributor.author | Bradbury, Claire | |
| dc.contributor.author | Herndon, James E | |
| dc.contributor.author | Boyd, Kendra | |
| dc.contributor.author | Lipp, Eric S | |
| dc.contributor.author | Friedman, Henry S | |
| dc.contributor.author | Desjardins, Annick | |
| dc.contributor.author | Johnson, Margaret O | |
| dc.contributor.author | 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 | BackgroundNausea 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.MethodsThis 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.ResultsForty-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.ConclusionsNo 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 | ||
| 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 | ||
| dc.subject | antiemesis | |
| dc.subject | emesis | |
| dc.subject | gliomas | |
| dc.subject | nausea | |
| dc.subject | 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 | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | School of Nursing | |
| pubs.organisational-group | Nursing | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Biostatistics & Bioinformatics | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Pathology | |
| pubs.organisational-group | Medicine, Medical Oncology | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | Neurology | |
| pubs.organisational-group | Neurology, General & Community Neurology | |
| pubs.organisational-group | Neurosurgery | |
| pubs.organisational-group | 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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