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Dietary, Herbal and Alternative Medicine in Glioblastoma Multiforme

Yalnız qeydiyyatdan keçmiş istifadəçilər məqalələri tərcümə edə bilərlər
Giriş / Qeydiyyatdan keçin
Bağlantı panoya saxlanılır
StatusXitam verilib
Sponsorlar
Ali Altunkaya
Əməkdaşlar
National Cancer Institute (NCI)

Açar sözlər

Mücərrəd

RATIONALE: Giving the herb Boswellia serrata after surgery and radiation therapy may slow the growth of any remaining tumor cells. It is not yet known whether giving Boswellia serrata together with standard treatment is more effective than standard treatment alone in treating high-grade gliomas.
PURPOSE: This randomized phase II trial is the study of a combination of complementary and alternative medicine (CAM) herbal supplement intervention as an adjuvant to standard treatment of patients with newly diagnosed and recurrent high-grade gliomas (HGG). The central hypothesis of this application is that a herbal preparation that inhibits 5-LO activity, will produce measurable biologically meaningful decrease in 5-LO eicosanoid production and brain edema that will be associated with improved survival and quality of life in patients with HGG.

Təsvir

OBJECTIVES:

Primary

- To determine whether a herbal approach to decreasing 5-LO eicosanoid production reduces peritumoral brain edema in patients with HGG.

Secondary

- To determine if this adjuvant approach improves the quality of life and progression free and overall survival of patients with HGG.

OUTLINE: This a randomized, controlled study. Patients are randomized to 1 of 2 treatment arms.

- Arm I (intervention): Patients receive oral Boswellia serrata herbal extract 4 times a day and oral cyanocobalamin (vitamin B-12) once a day for 6 months in the absence of unacceptable toxicity.

- Arm II (control): Patients receive oral vitamin B-12 once a day for 6 months. All patients are encouraged to eat a regular balanced diet (as recommended by the American Cancer Society for cancer prevention) with limited consumption of red and processed meats.

Quality of life will be assessed at baseline and then at 2, 4, 6, 12, and 24 months.

After completion of study treatment, patients will be followed every 6 months.

PROJECTED ACCRUAL: A total of 70 patients (35 per treatment arm) will be accrued for this study.

Tarixlər

Son Doğrulandı: 03/31/2019
İlk təqdim: 10/19/2005
Təxmini qeydiyyat təqdim edildi: 10/19/2005
İlk Göndərmə: 10/20/2005
Son Yeniləmə Göndərildi: 04/20/2019
Son Yeniləmə Göndərildi: 04/29/2019
İlk təqdim edilmiş nəticələrin tarixi: 10/10/2012
İlk təqdim edilmiş QC nəticələrinin tarixi: 06/20/2013
İlk göndərilən nəticələrin tarixi: 07/29/2013
Həqiqi Təhsilin Başlama Tarixi: 08/31/2004
Təxmini İlkin Tamamlanma Tarixi: 02/28/2010
Təxmini İşin Tamamlanma Tarixi: 02/28/2011

Vəziyyət və ya xəstəlik

Brain and Central Nervous System Tumors
Cerebral Edema

Müdaxilə / müalicə

Drug: Arm I (intervention)

Dietary Supplement: cyanocobalamin

Faza

Faza 2

Qol Qrupları

QolMüdaxilə / müalicə
Experimental: Arm I (intervention)
Patients receive oral Boswellia serrata extract 4 times a day and oral cyanocobalamin (vitamin B 12) once a day for 6 months in the absence of unacceptable toxicity.
Drug: Arm I (intervention)
given orally
Active Comparator: Arm II (control)
Patients in the control arm receive oral cyanocobalamin (vitamin B 12) once a day for 6 months.

Uyğunluq Kriteriyaları

Təhsil üçün uyğun yaşlar 18 Years Üçün 18 Years
Təhsilə Uyğun CinslərAll
Sağlam Könüllüləri qəbul edirBəli
Kriteriyalar

INCLUSION CRITERIA:

- Patients after surgical removal of histologically confirmed World Health Organization high-grade gliomas, including astrocytomas grade III (anaplastic astrocytoma), astrocytoma grade IV (glioblastoma multiforme, GBM), anaplastic oligodendroglioma and oligoastrocytoma

- Karnofsky performance status of greater or equal 60

- Patients who signed informed consent

- Patients can be receiving standard or investigational chemotherapy , hormonal therapy, immunotherapy or biologic agents as the primary treatment for their tumor

- Glucocorticoid therapy is allowed

- Bone marrow function (absolute neutrophil count [ANC] >=1500/mm^3 and platelet count >=75,000/mm^3); in the event of plate count dropping below 50,000/ mm^3 the Boswellia will be withdrawn until plate count reaches 75,000 mm^3 and above

- Liver function (bilirubin and alkaline phosphatase =< 2 x normal and serum glutamic oxaloacetic transaminase [SGOT] =< 3 x normal)

- Renal function (blood urea nitrogen [BUN] or creatinine =< 1.5 x normal)

- Patients suffering from mild to moderate asthma, liver and kidney disease; an assessment of the condition will be made to establish a baseline and monitor progress at 4 weekly intervals to start with for the first two months and thereafter at the usual study intervals of 4 and 6 months; if there is any significant deterioration in their condition the Boswellia will be withdrawn until these parameters are restored to their pre-treatment levels

EXCLUSION CRITERIA:

- Any medical condition that could interfere with eating and oral administration of B. serrata

- Patients already taking herbal preparations that contain 5-LO inhibitors

- Any previous (within the past 3 years) or concurrent malignancies at other sites, with the exception of surgically cured carcinoma-in-situ of the cervix and non-melanoma skin cancer

- Pregnancy and breastfeeding

- Active infection

- Inability to be followed closely at the Cleveland Clinic Foundation

Nəticə

İlkin nəticə tədbirləri

1. Change From Pooled Baseline in Peritumoral Brain Edema [at 2 months]

The relative change from baseline will be assessed longitudinally, however, the main comparison of interest is the relative change at the 4-month evaluation. For each patient change = edema at follow up - baseline edema

2. Change From Baseline in Peritumoral Brain Edema [at 4 months]

The relative change from baseline will be assessed longitudinally, however, the main comparison of interest is the relative change at the 4-month evaluation.For each patient change = edema at follow up - baseline edema.

3. Change From Baseline in Peritumoral Brain Edema [at 6 months]

The relative change from baseline will be assessed longitudinally, however, the main comparison of interest is the relative change at the 4-month evaluation. For each patient change = edema at follow up - baseline edema.

İkincili Nəticə Tədbirləri

1. Quality of Life at 6 Months [At 2, 4, 6, 12, and 24 months]

Quality of life as assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 Items (EORTC QLQ-C30)

2. Time-to-tumor-progression: Percentage of Patients With Tumor Progression at 6 Months [6 months]

Percentage of participants with tumor progression (>25% increase in tumor volume compared to time 0) will be measured from enrollment to documented progression or death whichever comes first. The method used to calculate the time to tumor progression was Kaplan Meier test method to define the 95% confidence levels.

3. Time-to-tumor-progression: Percentage of Patients With Tumor Progression at 1 Year [1 year]

Percentage of participants with tumor progression (>25% increase in tumor volume compared to time 0) will be measured from enrollment to documented progression or death whichever comes first. The method used to calculate the time to tumor progression was Kaplan Meier test method to define the 95% confidence levels.

4. Overall Survival: Percentage of Patients That Were Alive at 1 Year [1 year.]

Overall survival will be measured from the date of enrollment to date of death or last contact. Survival will be evaluated by the Kaplan Meier method to evaluate the median survival and 1 year survival rates.

Digər nəticə tədbirləri

1. Food Intake as Assessed by the Block 98 Food Frequency Questionnaire and a 3-day Food Record [At 2, 4, 6, 12, and 24 months]

The 3-day food diary will be used to assess the dietary intake and to increase eating awareness of patients.

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