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Endostar Combined With Corticosteroid for Treatment of Radiation-induced Brain Necrosis in Nasopharyngeal Carcinoma

J

Jiangxi Provincial Cancer Hospital

Status and phase

Enrolling
Phase 2

Conditions

Nasopharyngeal Carcinoma

Treatments

Drug: Endostar

Study type

Interventional

Funder types

Other

Identifiers

NCT05177237
NPC-RN-001

Details and patient eligibility

About

To evaluate the effectiveness and safety of Endostar combined with corticosteroids on Radiation-induced Brain Necrosis in Nasopharyngeal Carcinoma patients.

detailed description:

Full description

This was a single-arm, open-label study. We aimed to evaluate the effectiveness and safety of Endostar combined with corticosteroids on Radiation-induced Brain Necrosis in Nasopharyngeal Carcinoma patients. Magnetic resonance imaging (MRI) was performed pre- and post-treatment to define the radiographic response.The primary outcome was a 2-month response rate as determined by MRI and clinical symptoms. All of the patients were followed up with for 6 months.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cytologically or histologically proven Nasopharyngeal Carcinoma(WHO 2003 I-III) .
  • Presence of at least one measurable target lesion (RECIST rules) in a non irradiated region;
  • age ≥18 years;
  • radiation therapy history for histologically confirmed NPC administered≥6 months prior to study entry;
  • radiographic evidence to support the diagnosis of RN with out tumor recurrence or metastases;
  • patients had never received Antiangiogenic agents for RN treatment prior to the screening;
  • patients had never received corticosteroids for RN treatment prior to the screening;
  • no evidence of very high intracranial pressure suggestive of a brain hernia requiring surgery routine laboratory studies including urinalysis, complete blood count, liver function, renal function, and coagulation test within a normal range;
  • to understand and be willing to sign a written informed consent.

Exclusion criteria

  • Other types of Nasopharyngeal Carcinoma;
  • Recurrent nasopharyngeal carcinoma, resection of encephalopathy, metastasis, hepatitis, other malignant tumors, neurovascular diseases, or other diseases of the nervous system;
  • Inadequately controlled diabetes (FBG > 10mmol/L) and hypertension(systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg);
  • Other severe concurrent disorders that occurred before enrollment (severe or unstable angor, NYHA class 3 or 4 congestive heart failure, Myocardial infarction occurred within 6 months before enrollment;Aortic dissection aortic aneurysm.) active central nervous system hemorrhage;
  • pregnant or lactating women, women who have not undergone a pregnancy test (within 14 days prior to initial administration), and pregnant women;
  • Patients with a history of severe mental illness or communication disorders.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Endostar combined with Methylprednisolone
Experimental group
Description:
Endostar combined with Methylprednisolone lasts for 10 weeks
Treatment:
Drug: Endostar

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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