Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
1.
Eur Radiol ; 27(3): 1012-1020, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27380902

ABSTRACT

OBJECTIVES: The purpose of this study was to investigate the ability of computed tomography texture analysis (CTTA) to provide additional prognostic information in patients with Hodgkin's lymphoma (HL) and high-grade non-Hodgkin's lymphoma (NHL). METHODS: This retrospective, pilot-study approved by the IRB comprised 45 lymphoma patients undergoing routine 18F-FDG-PET-CT. Progression-free survival (PFS) was determined from clinical follow-up (mean-duration: 40 months; range: 10-62 months). Non-contrast-enhanced low-dose CT images were submitted to CTTA comprising image filtration to highlight features of different sizes followed by histogram-analysis using kurtosis. Prognostic value of CTTA was compared to PET FDG-uptake value, tumour-stage, tumour-bulk, lymphoma-type, treatment-regime, and interim FDG-PET (iPET) status using Kaplan-Meier analysis. Cox regression analysis determined the independence of significantly prognostic imaging and clinical features. RESULTS: A total of 27 patients had aggressive NHL and 18 had HL. Mean PFS was 48.5 months. There was no significant difference in pre-treatment CTTA between the lymphoma sub-types. Kaplan-Meier analysis found pre-treatment CTTA (medium feature scale, p=0.010) and iPET status (p<0.001) to be significant predictors of PFS. Cox analysis revealed that an interaction between pre-treatment CTTA and iPET status was the only independent predictor of PFS (HR: 25.5, 95% CI: 5.4-120, p<0.001). Specifically, pre-treatment CTTA risk stratified patients with negative iPET. CONCLUSION: CTTA can potentially provide prognostic information complementary to iPET for patients with HL and aggressive NHL. KEY POINTS: • CT texture-analysis (CTTA) provides prognostic information complementary to interim FDG-PET in Lymphoma. • Pre-treatment CTTA and interim PET status were significant predictors of progression-free survival. • Patients with negative interim PET could be further stratified by pre-treatment CTTA. • Provide precision surveillance where additional imaging reserved for patients at greatest recurrence-risk. • Assists in risk-adapted treatment strategy based on interim PET and CTTA.


Subject(s)
Fluorodeoxyglucose F18 , Hodgkin Disease/diagnostic imaging , Lymphoma, Non-Hodgkin/diet therapy , Positron-Emission Tomography/methods , Tomography, X-Ray Computed/methods , Adult , Aged , Aged, 80 and over , Disease-Free Survival , Female , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Pilot Projects , Prognosis , Radiopharmaceuticals , Reproducibility of Results , Retrospective Studies , Risk Assessment , Young Adult
2.
Cancer Lett ; 121(1): 25-9, 1997 Dec 16.
Article in English | MEDLINE | ID: mdl-9459170

ABSTRACT

The number of Krebs II tumour cells recovered from the ascitic fluid of mice fed for 8 days on a lactalbumin (La) control diet was about three times higher than that in animals fed a phytohaemagglutinin-containing (PHA) diet. Feeding a PHA diet for less than 8 days after tumour cell injection also led to a reduction in tumour cell growth. There was an apparent inverse relationship between the total tumour cell count and the intracellular content of putrescine, spermidine and spermine. Hyperplasia of the small intestine occurred in the mice during the development of the ascites. A series of other organs were not affected in the same manner. The results indicate that the polyamine content of Krebs II ascites cells must increase by more than three-fold in order to achieve the intracellular concentration necessary to be able to enter the S-phase. A partial synchronization of the tumour cell population is suggested. Hyperplastic growth of the small intestine would appear to compete with tumour cells for polyamines from a common body pool.


Subject(s)
Lymphoma, Non-Hodgkin/pathology , Phytohemagglutinins/therapeutic use , Polyamines/analysis , Animals , Cell Division/drug effects , Female , Heart/drug effects , Heart/growth & development , Hyperplasia/chemically induced , Intestine, Small/drug effects , Intestine, Small/growth & development , Kidney/drug effects , Kidney/growth & development , Lymphoma, Non-Hodgkin/chemistry , Lymphoma, Non-Hodgkin/diet therapy , Mice , Mice, Inbred Strains , Muscle Development , Muscle, Skeletal/drug effects , Muscle, Skeletal/growth & development , Neoplasm Transplantation , Organ Size/drug effects , Putrescine/analysis , Spermidine/analysis , Spermine/analysis , Stomach/drug effects , Stomach/growth & development , Time Factors
3.
J Exp Ther Oncol ; 1(5): 273-7, 1996 Sep.
Article in English | MEDLINE | ID: mdl-9414414

ABSTRACT

The present study concerns the importance of the timing of feeding mice a PHA-containing diet (7 mg g-1 diet) on tumor formation. The major decrease in tumor weight occurred in mice fed on the PHA diet for 11 days. A marked reduction was also observed in animals pre-fed for 3 days with PHA before tumor cells were injected and the diet then changed to lactalbumin, La. A large decrease in tumor weight was also evident when a change of diet from La to PHA was made on the day of tumor cell inoculation. Despite the presence of the developing tumor PHA was able to induce hyperplasia of the small intestine in all groups of animals fed PHA during a part or the whole of the experiment. The dry weights of tumors attained in each of the experimental groups plotted as a function of duration of PHA feeding, and the percentage lipid content of the tumors, mirrored almost exactly one another, suggesting that the availability of essential lipid material is severely reduced by the lectin. This would appear to have a major effect on the observed reduction in tumor growth.


Subject(s)
Diet , Intestinal Neoplasms/diet therapy , Lymphoma, Non-Hodgkin/diet therapy , Phytohemagglutinins/therapeutic use , Animals , Body Fluids/drug effects , Body Fluids/physiology , Cell Line , Female , Intestinal Neoplasms/metabolism , Intestinal Neoplasms/pathology , Intestine, Small/pathology , Lipolysis/drug effects , Lymphoma, Non-Hodgkin/metabolism , Lymphoma, Non-Hodgkin/pathology , Mice , Organ Size/drug effects
4.
Acta Oncol ; 26(4): 301-5, 1987.
Article in English | MEDLINE | ID: mdl-3689583

ABSTRACT

Food intake and nutritional status were estimated in 34 cancer patients (14 patients with non-Hodgkin lymphoma and 20 patients with relapse of different cancers) and 25 healthy subjects (control group). A two-month dietary history based on Burke's method was used to estimate food intake. Nutritional status was expressed by weight, anthropometric parameters and hematologic parameters. The patients' intake of cheese, eggs, rye bread, and poultry was reduced compared to controls. The difference in food preferences resulted in a higher energy supply from carbohydrate and a lower intake of indigestible carbohydrate, vitamin B12, iron and iodine in patients than in controls. The groups did not differ in anthropometric parameters, but a decreased total serum protein, albumin and hemoglobin was observed in patients, whereas their alpha-globulin levels were increased. Thus, food preferences in cancer patients seem to be associated with insufficient intake of nutrients.


Subject(s)
Energy Intake , Food Preferences , Lymphoma, Non-Hodgkin/diet therapy , Nutritional Status , Body Weight , Diet , Female , Humans , Lymphoma, Non-Hodgkin/diagnosis , Male , Middle Aged
5.
Respiration ; 70(1): 107-9, 2003.
Article in English | MEDLINE | ID: mdl-12584402

ABSTRACT

Obstructive sleep apnea syndrome (OSAS) is characterized by repetitive episodes of upper airway obstruction during sleep that provoke an abnormal number of apneas and hypopneas, leading to arousals and, as a result, to an altered sleep architecture. Here we present a patient with clinical symptoms characteristic of OSAS. During follow-up, pharyngeal non-Hodgkin's lymphoma was diagnosed and treated, with a nearly complete normalization of polysomnography.


Subject(s)
Lymphoma, Non-Hodgkin/complications , Lymphoma, Non-Hodgkin/diagnosis , Pharyngeal Neoplasms/complications , Pharyngeal Neoplasms/diagnosis , Sleep Apnea, Obstructive/etiology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cyclophosphamide/therapeutic use , Doxorubicin/therapeutic use , Humans , Lymphoma, Non-Hodgkin/diet therapy , Male , Middle Aged , Pharyngeal Neoplasms/drug therapy , Prednisone/therapeutic use , Sleep Apnea, Obstructive/therapy , Vincristine/therapeutic use
6.
Support Care Cancer ; 11(4): 232-5, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12673461

ABSTRACT

The use of nutritional supplements in the general population and in cancer patients has become very popular. These supplements are not perceived as medications and are presumed to be safe by cancer patients, who may however be at risk for hypercalcemia. We note that many of our patients who have developed symptomatic hypercalcemia were taking vitamin D, calcium, or shark cartilage supplements. We report eight cases of hypercalcemia in cancer patients seen at the Cleveland Clinic Foundation in whom these nutritional supplements may have contributed to the prevalence or severity of hypercalcemia.


Subject(s)
Calcium/adverse effects , Dietary Supplements/adverse effects , Hypercalcemia/chemically induced , Neoplasms/diet therapy , Vitamin D/adverse effects , Aged , Animals , Breast Neoplasms/complications , Breast Neoplasms/diet therapy , Carcinoma, Renal Cell/complications , Carcinoma, Renal Cell/diet therapy , Carcinoma, Squamous Cell/complications , Carcinoma, Squamous Cell/diet therapy , Cartilage , Colonic Neoplasms/complications , Colonic Neoplasms/diet therapy , Female , Humans , Hypercalcemia/complications , Lymphoma, Non-Hodgkin/complications , Lymphoma, Non-Hodgkin/diet therapy , Male , Mesothelioma/complications , Mesothelioma/diet therapy , Middle Aged , Mouth Neoplasms/complications , Mouth Neoplasms/diet therapy , Multiple Myeloma/complications , Multiple Myeloma/diet therapy , Neoplasms/complications , Sharks , Treatment Outcome
SELECTION OF CITATIONS
SEARCH DETAIL