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Parotid-sparing IMRT for Nasopharyngeal Cancer

Phase II Study of Parotid Sparing IMRT for Nasopharyngeal Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02149641
Enrollment
42
Registered
2014-05-29
Start date
2006-02-28
Completion date
2012-04-30
Last updated
2014-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensity Modulated Radiotherapy With Chemotherapy, Nasopharyngeal Cancers

Brief summary

In the treatment of nasopharyngeal cancers, to determine the incidence of high grade (≥G2) subjective xerostomia at 1 year.

Detailed description

The purpose of this study was to determine the feasibility in delivering induction chemotherapy and concomitant chemotherapy with IMRT in the treatment of locally advanced nasopharyngeal cancers and to determine the incidence of high grade (≥G2) subjective xerostomia at 1 year.

Interventions

RADIATIONIntensity modulated radiotherapy with chemotherapy

Sponsors

Royal Marsden NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* nasopharyngeal cancers

Exclusion criteria

* Patients \<16 years old or with a previous malignancy other than non-melanomatous skin cancer were excluded

Design outcomes

Primary

MeasureTime frame
the incidence of ≥G2 xerostomia at 1 year using the subjective component LENTSOMA12 months

Secondary

MeasureTime frame
Acute radiation toxicities0-3 months
Late radiation toxicities3-24 months
loco-regional disease-free survival (LRDFS), progression-free survival (PFS) and overall survival (OS)2 years
chemotherapy compliance and toxicities0-12 weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026