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1.
Stud Health Technol Inform ; 308: 396-403, 2023 Nov 23.
Article in English | MEDLINE | ID: mdl-38007765

ABSTRACT

Primary splenic angiosarcoma is a very rare disease that causes the development of malignant tumors in the vascular endothelium of the splenic sinuses. Moreover, the disease maintains a very low survival rate for patients to live over 5 years, which is relatively low when compared to another splenic cancer, splenic lymphomas. The treatment options for splenic angiosarcoma narrow down to surgical removal or radiation combined with chemotherapy, but both cost a lot, so discovering potential alternative treatments may eventually increase the possible survival rate. Ginseng and Zhi Gan Cao are both common herbs in Traditional Chinese Medicine (TCM); however, the price of Ginseng is much higher than that of Zhi Gan Cao. A possible reason could be the frequent studies and researches over Ginseng's active ingredient, ginsenoside rh2 or rg3 as they are both potent cancer treatments. The reason to study Zhi Gan Cao and predict its possible potential in cancer treatment is due to the similarity between its active ingredient and the active ingredient in Ginseng, namely, ginsenoside rh2 and licorice saponins. Both TCM contain the active ingredient, triterpenoid saponin, as their main composition, and the further text will predict the possible research and results that may be taken in vitro to reveal the question of whether licorice saponin has the potential to become a major treatment for splenic angiosarcoma or not.


Subject(s)
Glycyrrhiza uralensis , Hemangiosarcoma , Saponins , Splenic Neoplasms , Humans , Medicine, Chinese Traditional , Splenic Neoplasms/drug therapy , Hemangiosarcoma/drug therapy , Vascular Endothelial Growth Factors
2.
Rev Med Interne ; 43(10): 608-616, 2022 Oct.
Article in French | MEDLINE | ID: mdl-35691756

ABSTRACT

Some common clinical situations, such as splenomegaly or lymphocytosis, or less common, such as autoimmune hemolytic anemia, cold agglutinin disease, or cryoglobulinemia can lead to the diagnosis of splenic lymphoma. Splenic lymphoma is rare, mainly of non-hodgkinian origin, encompassing very different hematological entities in their clinical and biological presentation from an aggressive form such as hepato-splenic lymphoma to indolent B-cell lymphoma not requiring treatment such as marginal zone lymphoma, the most frequent form of splenic lymphoma. These entities can be challenging to diagnose and differentiate. This review presents different clinical and biological manifestations suspicious of splenic lymphoma and proposes a diagnosis work-up. We extended the strict definition of splenic lymphoma (lymphoma exclusively involving the spleen) to lymphoma thant can be revealed by a splenomegaly and we discuss the differential diagnosis of splenomegaly.


Subject(s)
Anemia, Hemolytic, Autoimmune , Lymphocytosis , Lymphoma, B-Cell, Marginal Zone , Splenic Neoplasms , Anemia, Hemolytic, Autoimmune/diagnosis , Anemia, Hemolytic, Autoimmune/therapy , Diagnosis, Differential , Humans , Lymphocytosis/pathology , Lymphoma, B-Cell, Marginal Zone/diagnosis , Lymphoma, B-Cell, Marginal Zone/pathology , Lymphoma, B-Cell, Marginal Zone/therapy , Splenic Neoplasms/diagnosis , Splenic Neoplasms/pathology , Splenic Neoplasms/therapy , Splenomegaly/diagnosis , Splenomegaly/etiology
3.
Vet Comp Oncol ; 20(3): 688-696, 2022 Sep.
Article in English | MEDLINE | ID: mdl-35442554

ABSTRACT

Canine splenic hemangiosarcoma (HSA) is an aggressive tumour of vascular endothelium that carries a grave prognosis following standard of care treatment with surgery and doxorubicin. A previous pilot study revealed potential anti-tumour activity of I'm-Yunity polysaccharopeptide (PSP) for canine HSA. The aim of this prospective study was to assess patient outcome when treated with PSP alone or in combination with doxorubicin post-splenectomy compared to patients treated with surgery and doxorubicin that received a placebo in place of PSP. Dogs undergoing splenectomy for splenic HSA were eligible. Following splenectomy, owners were offered treatment with PSP alone or adjuvant doxorubicin chemotherapy (unblinded). Patients with owners that selected to proceed with doxorubicin chemotherapy were blindly randomized to receive placebo or PSP. Dogs were evaluated weekly for 15 weeks, then scheduled for monthly visits until death. One hundred and one dogs were included in the final analysis: 51 PSP alone, 25 doxorubicin/placebo, and 25 combination PSP/doxorubicin. On multivariate analysis, dogs treated with single agent PSP, female dogs, decreased haematocrit at diagnosis, and stage III disease were negatively significantly associated with outcome; however, an interaction between treatment group and sex was documented. Gender-specific outcomes revealed no significant difference in survival between treatment groups for male dogs, but female dogs treated with PSP alone had significantly reduced survival compared to females receiving doxorubicin/placebo (HR 0.21; p = .004). Anaemia (HR 5.28; p < .001) and stage III disease (HR 2.9; p = .014) remained negatively associated with survival when controlling for sex and treatment group. The addition of PSP to doxorubicin post-splenectomy did not improve survival in dogs with splenic HSA.


Subject(s)
Dog Diseases , Hemangiosarcoma , Splenic Neoplasms , Animals , Dog Diseases/drug therapy , Dogs , Doxorubicin/therapeutic use , Drugs, Chinese Herbal , Female , Hemangiosarcoma/drug therapy , Hemangiosarcoma/veterinary , Male , Pilot Projects , Polyporaceae , Prospective Studies , Proteoglycans , Splenic Neoplasms/drug therapy , Splenic Neoplasms/veterinary
4.
Clin Lymphoma Myeloma Leuk ; 21(11): e839-e844, 2021 11.
Article in English | MEDLINE | ID: mdl-34326035

ABSTRACT

INTRODUCTION: Treatment of Splenic (SMZL) and Nodal (NMZL) Marginal Zone Lymphoma is not consensual. Histologic transformation (HT) to aggressive lymphoma is a poorly understood event, with an unfavorable outcome. OBJECTIVES: Describe the clinical characteristics, treatment, outcomes and incidence of HT. METHODS: Characteristics of patients with SMZL and NMZL consecutively diagnosed in 8 Portuguese centers were retrospectively reviewed. Endpoints were overall survival (OS), time to first systemic treatment (TTFST), frequency of HT and time to transformation (TTT). RESULTS: This study included 122 SMZL and 68 NMZL, most of them received systemic treatment: 55.4% and 76.5%, respectively. Splenectomy was performed in 58.7% of patients with SMZL. Different treatment protocols were used. OS or TTFST did not differ significantly according to treatments. Given the small sample size, no conclusion can be made concerning the role of Rituximab in the treatment of NMZL and SMZL based in these results. HT was documented in 18 patients, mainly in SMZL, with a cumulative incidence at 5 years of 4.2%. We confirmed that age is a prognostic factor. CONCLUSION: Randomized prospective trials are needed to standardize treatment in MZL. Patients with HT did appear to have shorter OS in comparison with those who did not experience HT (OS 5 years of 68.4% vs. 80.4%), but the number of HT was too small to reach statistical significance.


Subject(s)
Lymphoma, B-Cell, Marginal Zone/therapy , Splenic Neoplasms/therapy , Adult , Aged , Aged, 80 and over , Female , Humans , Incidence , Lymphoma, B-Cell, Marginal Zone/epidemiology , Male , Middle Aged , Portugal , Prospective Studies , Retrospective Studies , Splenic Neoplasms/epidemiology , Treatment Outcome
5.
J Ethnopharmacol ; 267: 113522, 2021 Mar 01.
Article in English | MEDLINE | ID: mdl-33127562

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Locally known as 'pecah batu', 'bayam karang', 'keci beling' or 'batu jin', the Malaysian medicinal herb, Strobilanthes crispus (S. crispus), is traditionally used by the local communities as alternative or adjuvant remedy for cancer and other ailments and to boost the immune system. S. crispus has demonstrated multiple anticancer therapeutic potential in vitro and in vivo. A pharmacologically active fraction of S. crispus has been identified and termed as F3. Major constituents profiled in F3 include lutein and ß-sitosterol. AIM OF THE STUDY: In this study, the effects of F3, lutein and ß-sitosterol on tumor development and metastasis were investigated in 4T1-induced mouse mammary carcinoma model. MATERIALS AND METHODS: Tumor-bearing mice were fed with F3 (100 mg/kg/day), lutein (50 mg/kg/day) and ß-sitosterol (50 mg/kg/day) for 30 days (n = 5 each group). Tumor physical growth parameters, animal body weight and development of secondary tumors were investigated. The safety profile of F3 was assessed using hematological and histomorphological changes on the major organs in normal control mice (NM). RESULTS: Our findings revealed significant reduction of physical tumor growth parameters in all tumor-bearing mice treated with F3 (TM-F3), lutein (TM-L) or ß-sitosterol (TM-ß) as compared with the untreated group (TM). Statistically significant reduction in body weight was observed in TM compared to the NM or treated (TM-F3, TM-L and TM-ß) groups. Histomorphological examination of tissue sections from the F3-treated group showed normal features of the vital organs (i.e., liver, kidneys, lungs and spleen) which were similar to those of NM. Administration of F3 to NM mice (NM-F3) did not cause significant changes in full blood count values. CONCLUSION: F3 significantly reduced the total tumor burden and prevented secondary tumor development in metastatic breast cancer without significant toxicities in 4T1-induced mouse mammary carcinoma model. The current study provides further support for therapeutic development of F3 with further pharmacokinetics studies.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Breast Neoplasms/drug therapy , Kidney Neoplasms/prevention & control , Liver Neoplasms/prevention & control , Lung Neoplasms/prevention & control , Plant Extracts/pharmacology , Splenic Neoplasms/prevention & control , Acanthaceae/chemistry , Animals , Antineoplastic Agents, Phytogenic/isolation & purification , Breast Neoplasms/blood , Breast Neoplasms/pathology , Cell Line, Tumor , Female , Kidney Neoplasms/blood , Kidney Neoplasms/secondary , Liver Neoplasms/blood , Liver Neoplasms/secondary , Lung Neoplasms/blood , Lung Neoplasms/secondary , Lutein/pharmacology , Mice, Inbred BALB C , Plant Extracts/isolation & purification , Sitosterols/pharmacology , Splenic Neoplasms/blood , Splenic Neoplasms/secondary , Tumor Burden/drug effects
6.
Hematol Oncol Stem Cell Ther ; 14(2): 153-155, 2021 Jun.
Article in English | MEDLINE | ID: mdl-31306619

ABSTRACT

We report the case of a patient diagnosed with a splenic marginal zone lymphoma with a simultaneous finding of hepatitis B virus infection, who responded to antiviral treatment and splenectomy. We highlighted this association described in the literature and its possible causal role, as well as the available therapeutic choices.


Subject(s)
Hepatitis B/complications , Lymphoma, B-Cell, Marginal Zone/complications , Splenic Neoplasms/complications , Antiviral Agents/therapeutic use , Hepatitis B/therapy , Hepatitis B virus/drug effects , Hepatitis B virus/isolation & purification , Humans , Lymphoma, B-Cell, Marginal Zone/therapy , Male , Middle Aged , Splenectomy , Splenic Neoplasms/therapy
7.
BMC Cancer ; 20(1): 717, 2020 Aug 03.
Article in English | MEDLINE | ID: mdl-32746790

ABSTRACT

BACKGROUND: Splenic marginal zone lymphoma (SMZL) is a rare lymphoid B-cell malignant neoplasm with primary involvement of the spleen. It is a chronic disease, of indolent behavior and prolonged survival. However, 25% of cases have higher biological aggressiveness, propensity for histological transformation to high grade B-cell non-Hodgkin lymphoma and shortened survival. Recognition of these cases of reserved outcome is important for selecting a risk-adapted therapeutic approach in a resource-poor settings. METHODS: We described clinical and epidemiological characteristics, survival analysis and prognostic factors in a retrospective cohort of 39 SMZL patients, treated in Latin America. RESULTS: We observed a predominance of female (71.8%), median age of 63 years and higher incidence of B symptoms (56.4%) and extra-splenic involvement (87.1%) than in European and North-American series. With a median follow-up of 8.7 years (0.6-20.2 years), estimated 5-year overall survival (OS) and progression-free survival (PFS) were 76.9% and 63.7%, respectively. Factors with adverse prognostic impact on OS and PFS were Hb < 100 g/L, platelet count < 100 x 109/L, albumin < 3.5 g/dL, LDH > 480 U/L and high-risk Arcaini and SMZL/WG scores. Despite a relative low number of patients, no superiority was observed among the therapeutic regimens used including rituximab monotherapy, splenectomy and cytotoxic chemotherapy. CONCLUSION: Therefore, in resource-poor settings, where access to immunotherapy is not universal for all SMZL patients, we suggest that first-line should consist on rituximab therapy for elderly patients or with high surgical risk or with at least 1 risk factor identified in our study. Remainders can be safely managed with splenectomy.


Subject(s)
Antineoplastic Agents, Immunological/therapeutic use , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Developing Countries , Lymphoma, B-Cell, Marginal Zone/therapy , Rituximab/therapeutic use , Splenectomy , Adult , Aged , Analysis of Variance , Antineoplastic Agents, Immunological/administration & dosage , Brazil/epidemiology , Cancer Care Facilities , Cyclophosphamide/therapeutic use , Developing Countries/statistics & numerical data , Drug Administration Schedule , Female , Health Resources , Humans , Lymphoma, B-Cell, Marginal Zone/blood , Lymphoma, B-Cell, Marginal Zone/mortality , Male , Middle Aged , Prednisone/therapeutic use , Prognosis , Progression-Free Survival , Retrospective Studies , Rituximab/administration & dosage , Splenic Neoplasms , Symptom Assessment , Vincristine/therapeutic use , Watchful Waiting
8.
Expert Rev Hematol ; 12(12): 1011-1022, 2019 12.
Article in English | MEDLINE | ID: mdl-31619091

ABSTRACT

Introduction: Marginal zone lymphoma (MZL) accounts for approximately 10% of all cases of non-Hodgkin lymphoma and includes 3 clinically distinct subtypes: extranodal (MALT), splenic (SMZL), and nodal (NMZL). Though commonly grouped in trials of iNHL the clinical behavior, molecular features, and response to therapy of MZL is distinct from other iNHL subtypes and varies among MZL subtypes.Areas covered: This review focuses on the contemporary management of NMZL and SMZL. Treatment with monoclonal antibodies, chemoimmunotherapy, BTK inhibitors, PI3K/mTOR inhibitors, Bcl2 inhibitors, lenalidomide, and CAR-T cell therapy will be covered.Expert opinion: In the era of targeted medicine, the need to develop MZL specific clinicogenetic models with prognostic and predictive value in both the frontline and relapsed/refractory setting is becoming increasingly apparent. Due to the relative rarity of each MZL subtype, the use of novel trial design with correlative studies is imperative to advance the field.


Subject(s)
Immunotherapy, Adoptive , Lenalidomide/therapeutic use , Lymphoma, B-Cell, Marginal Zone/therapy , Models, Biological , Splenic Neoplasms/therapy , Humans , Lymphoma, B-Cell, Marginal Zone/metabolism , Lymphoma, B-Cell, Marginal Zone/pathology , Splenic Neoplasms/metabolism , Splenic Neoplasms/pathology
9.
Eur J Surg Oncol ; 45(11): 2096-2102, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31227342

ABSTRACT

OBJECTIVE: To describe accurately the oncological outcomes after hepatic resection (HR) in recurrent ovarian carcinoma (ROC) evaluating clinic-pathological variables and mutational status of BRCA1/2. Although HR is considered a challenging situation in ROC patients, assessment of BRCA1/2 mutational status seems to have a relevant clinical value to guide surgical therapy. METHODS: Patients who underwent HR for ROC at the Catholic University of Rome, between June 2012 and October 2017 were included. Exclusion criteria were represented by extra-abdominal disease and presence of diffuse peritoneal carcinomatosis requiring more than 2 bowel resections. Details relative to HR were collected and BRCA analysis was performed. Predictive factors of post-HR progression free survival (PHR-PFS) were assessed by univariate analyses using Cox-proportional hazard regression models. RESULTS: Thirty-four patients undewent HR within secondary cytoreductive surgery (SCS). Six patients (17.6%) presented with hepatic relapse only, while the remaining 28 patients (82.4%) had concomitant extra-hepatic disease. In the whole series, the 3-yr PHR-PFS was 49.1% and the 3-yr post-HR overall survival was 72.9%. Univariate analysis of variables conditioning PHR-PFS showed that only BRCA mutational status played a statistically significant favourable role: the 3-yr PHR-PFS rate was 81.0% in BRCA mutated patient compared to 15.2% in wild type ones (p value: 0.001). CONCLUSIONS: Our clinical analyses suggest that in ROC patients with liver disease the assessment of germline and somatic BRCA mutational status can help to select patients elegible for SCS.


Subject(s)
BRCA1 Protein/genetics , BRCA2 Protein/genetics , Carcinoma, Ovarian Epithelial/genetics , Liver Neoplasms/genetics , Ovarian Neoplasms/genetics , Adult , Aged , Carcinoma, Endometrioid/genetics , Carcinoma, Endometrioid/secondary , Carcinoma, Endometrioid/therapy , Carcinoma, Ovarian Epithelial/secondary , Carcinoma, Ovarian Epithelial/therapy , Chemotherapy, Adjuvant , Cytoreduction Surgical Procedures , Female , Germ-Line Mutation , Hepatectomy , Humans , Liver Neoplasms/secondary , Liver Neoplasms/therapy , Lymph Node Excision , Metastasectomy , Middle Aged , Mutation , Neoplasms, Cystic, Mucinous, and Serous/genetics , Neoplasms, Cystic, Mucinous, and Serous/secondary , Neoplasms, Cystic, Mucinous, and Serous/therapy , Ovarian Neoplasms/pathology , Peritoneal Neoplasms/genetics , Peritoneal Neoplasms/secondary , Peritoneal Neoplasms/therapy , Phthalazines/therapeutic use , Piperazines/therapeutic use , Platinum Compounds/therapeutic use , Poly(ADP-ribose) Polymerase Inhibitors/therapeutic use , Prognosis , Progression-Free Survival , Proportional Hazards Models , Splenic Neoplasms/genetics , Splenic Neoplasms/secondary , Splenic Neoplasms/therapy
10.
Eur J Surg Oncol ; 45(7): 1225-1231, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30879932

ABSTRACT

AIM: To evaluate the pattern of tumor relapse of pathological complete response (pCR) patients with locally advanced rectal cancer (LARC) following neoadjuvant chemoradiotherapy (nCRT) and total mesorectal excision (TME), and to identify predictive factors of distant metastasis in pCR patients after nCRT. METHOD: This was a retrospective analysis of 118 LARC patients who achieved a pCR following nCRT and TME from 2008 to 2015. Clinicopathological and therapeutic parameters were evaluated as possible predictors of distant metastasis-free survival (DMFS), and COX regression analysis was performed. RESULTS: After a median follow-up of 57 months, the 5-year overall and disease-free survival rates were 94.7% and 88.1%, respectively. Overall, 6 patients (5.1%) died, no local recurrence occurred, 13 patients (11%) developed distant metastases, including lung (n = 5), liver (n = 2), bone (n = 3), lung and brain (n = 1), peritoneal (n = 1), and spleen (n = 1) metastasis. On univariate analysis, tumor distance from the anal verge (HR = 0.706, P = 0.039), acellular mucin pools (HR = 6.687, P = 0.002), and MUC1 expression (HR = 8.280, P < 0.001) were independently associated with DMFS. COX regression demonstrated that MUC1 expression (HR = 3.812, P = 0.041) remained to be an independent predictor of DMFS in pCR patients. CONCLUSION: Distant metastasis still remained a major concern in pCR patients following nCRT and TME. Tumor distance from the anal verge, acellular mucin pools, and MUC1 expression were associated with distant metastasis in patients with pCR. MUC1 staining remained to be an independent risk factor for DMFS. Such information could facilitate treatment decision in these patients, such as adjuvant chemotherapy and follow-up.


Subject(s)
Adenocarcinoma/therapy , Bone Neoplasms/epidemiology , Liver Neoplasms/epidemiology , Lung Neoplasms/epidemiology , Rectal Neoplasms/therapy , Adenocarcinoma/epidemiology , Adenocarcinoma/secondary , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bone Neoplasms/secondary , Brain Neoplasms/epidemiology , Brain Neoplasms/secondary , Capecitabine/administration & dosage , Chemoradiotherapy , Chemotherapy, Adjuvant , Disease-Free Survival , Female , Fluorouracil/therapeutic use , Humans , Incidence , Leucovorin/therapeutic use , Liver Neoplasms/secondary , Lung Neoplasms/secondary , Male , Mesentery/surgery , Middle Aged , Mucin-1/metabolism , Mucins/metabolism , Neoadjuvant Therapy , Neoplasm Metastasis , Organoplatinum Compounds/therapeutic use , Oxaliplatin/administration & dosage , Peritoneal Neoplasms/epidemiology , Peritoneal Neoplasms/secondary , Proctectomy , Proportional Hazards Models , Rectal Neoplasms/metabolism , Rectal Neoplasms/pathology , Remission Induction , Retrospective Studies , Splenic Neoplasms/epidemiology , Splenic Neoplasms/secondary
11.
Eur J Radiol ; 110: 60-65, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30599874

ABSTRACT

PURPOSE: To estimate the performances of computed tomography (CT) and magnetic resonance imaging (MRI) and those of the combination of CT with MRI in the identification of splenic involvement in patients with peritoneal carcinomatosis (PC). MATERIAL AND METHOD: CT and MRI examinations of 26 patients with PC with splenic involvement and 26 patients with PC and no splenic involvement treated by total cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) were reviewed. There were 32 women and 20 men with a mean age of 53.44 ± 12.22 (SD) years (range: 20-73 years). Imaging examinations were reviewed separately as three independent imaging sets (CT only, MRI only and CT with MRI) by two independent readers. A consensus was reached during a joint reading session and these results were used for determining the performances of the three imaging sets in the diagnosis of splenic involvement using surgical and histopathological findings as standard of reference. RESULTS: Splenic involvement was histologically proven in 26/52 patients (50%). There were no significant differences in sensitivity, specificity and accuracy for the diagnosis of splenic involvement between CT, MRI and CT + MRI, with respectively 84.62%, 96.15% and 90.00% for CT, 84.62%, 84.62% and 85.00% for MRI and 92.31%, 92.31% and 92.00% for CT + MRI. CONCLUSION: CT and MRI have similar sensitivities, specificites and accuracies for the diagnosis of splenic involvement in patients with PC. The combination of CT and MRI does not significantly improve the preoperative diagnosis of splenic involvement in patients with PC compared to CT only.


Subject(s)
Carcinoma/pathology , Peritoneal Neoplasms/pathology , Splenic Neoplasms/pathology , Adult , Aged , Carcinoma/therapy , Cytoreduction Surgical Procedures/methods , Female , Humans , Hyperthermia, Induced/methods , Magnetic Resonance Imaging/methods , Male , Middle Aged , Peritoneal Neoplasms/therapy , Preoperative Care/methods , Sensitivity and Specificity , Spleen/pathology , Tomography, X-Ray Computed/methods , Young Adult
12.
Medicine (Baltimore) ; 97(51): e13867, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30572559

ABSTRACT

RATIONALE: Malignant struma ovarii is extremely rare in the clinic. The diagnosis and modalities of treatment are still controversial. Here we describe a case of extensive peritoneal implant metastasis originating from malignant struma ovarii discovered 14 years after ovariectomy and chemotherapy. PATIENT CONCERNS: A 48-year-old female was admitted to our clinic due to hematochezia with a past history of left malignant struma ovarii. Enhanced computed tomography (CT) examination suggested multiple metastasis nodules in the abdomen and pelvic cavity. DIAGNOSES: Laparoscopy biopsy results of intraperitoneal nodules showed a metastasis of papillary thyroid carcinoma. While pathological examination after total thyroidectomy showed no definite malignant tumor component in the thyroid tissue. Finally, combined with the patient's past history of malignant struma ovarii, peritoneal implantation metastasis derived from the malignant struma ovarii was diagnosed. INTERVENTIONS: The patient was treated by total thyroidectomy and iodine 131 (I) therapy. Post-therapy iodine scan and the single-photon emission computed tomography/computed tomography (SPECT/CT) fusion image showed iodine uptake in the distal descending colon, sigmoid colon, rectal lesions, and a larger lesion in the liver. OUTCOME: After treatment, although the thyroid globulin remained at a high level 3 months after treatment, the patient's hematochezia was relieved. LESSONS: Therefore, thyroidectomy followed by adjuvant I treatment should be recommended in patients with malignant struma ovarii as metastatic risk is difficult to predict based on histopathologic examination.


Subject(s)
Carcinoid Tumor/pathology , Liver Neoplasms/secondary , Ovarian Neoplasms/pathology , Splenic Neoplasms/secondary , Struma Ovarii/secondary , Thyroid Cancer, Papillary/secondary , Thyroid Neoplasms/pathology , Female , Humans , Iodine Radioisotopes/therapeutic use , Liver Neoplasms/diagnostic imaging , Liver Neoplasms/therapy , Middle Aged , Splenic Neoplasms/diagnostic imaging , Splenic Neoplasms/therapy , Struma Ovarii/therapy , Thyroid Cancer, Papillary/diagnostic imaging , Thyroid Cancer, Papillary/therapy , Thyroid Neoplasms/diagnostic imaging , Thyroid Neoplasms/therapy , Tomography, X-Ray Computed
13.
Best Pract Res Clin Haematol ; 31(1): 65-72, 2018 03.
Article in English | MEDLINE | ID: mdl-29452668

ABSTRACT

BACKGROUND: SMZL is a relatively rare low grade B-cell lymphoma, characterized usually by an indolent clinical behavior. Since there is no prospective randomized trials to establish the best treatment approach, decision on therapeutic management should be based on the available retrospective series. Based on these data, rituximab and splenectomy appear to be the most effective. Splenectomy represented the standard treatment modality until early 2000s. More than 90% of the patients present quick amelioration of splenomegaly related symptoms along with improvement of cytopenias related to hypersplenism. The median progression free survival was 8.25 years in the largest series of patients published so far, while the median 5- and 10- year OS were 84% and 67%, respectively. Responses to splenectomy are not complete since extrasplenic disease persists. Patients with heavy bone marrow infiltration, lymphadenopathy or other disease localization besides the spleen are not good candidates for splenectomy. Furthermore splenectomy is a major surgical procedure accompanied by acute perioperative complications as well as late toxicities mainly due to infections. For that reasons splenectomy is not appropriate for elderly patients or patients with comorbidities with a high surgical risk. On the other hand rituximab monotherapy displays high efficacy with minimal toxicity. Several published series have shown an ORR more than 90%, with high CR rates (∼50%). The 10-year PFS and OS were 63% and 85%, respectively in a series of 104 SMZL patients. The role of rituximab maintenance has been investigated by only one group. Based on these data, maintenance with rituximab further improved the quality of responses by increasing significantly the CR rates (from 42% at the end of induction to 71% at the end of maintenance treatment), as well as the duration of responses: 7-year PFS was 75% for those patients who received maintenance vs 39% for those who did not (p < 0.0004). However no difference in OS has been noticed between the two groups, so far. Summarizing the above data, it is obvious that Rituximab monotherapy is associated with high response rates, long response duration and favorable safety profile, rendering it as the treatment of choice in SMZL.


Subject(s)
Lymphoma, B-Cell, Marginal Zone/therapy , Rituximab/therapeutic use , Splenectomy , Splenic Neoplasms/therapy , Humans , Lymphoma, B-Cell, Marginal Zone/metabolism , Lymphoma, B-Cell, Marginal Zone/mortality , Lymphoma, B-Cell, Marginal Zone/pathology , Splenic Neoplasms/metabolism , Splenic Neoplasms/mortality , Splenic Neoplasms/pathology , Splenomegaly/metabolism , Splenomegaly/mortality , Splenomegaly/pathology , Splenomegaly/therapy
14.
Rev. bras. hematol. hemoter ; 39(2): 146-154, Apr.-June 2017. tab, ilus
Article in English | LILACS | ID: biblio-898917

ABSTRACT

ABSTRACT Splenic marginal zone lymphoma (SMZL) is a low-grade B-cell non-Hodgkin's lymphoma characterized by massive splenomegaly, moderate lymphocytosis with or without villous lymphocytes, rare involvement of peripheral lymph nodes and indolent clinical course. As a rare disease, with no randomized prospective trials, there is no standard of care for SMZL so far. Splenectomy has been done for many years as an attempt to control disease, but nowadays it has not been encouraged as first line because of new advances in therapy as rituximab, that are as effective with minimal toxicity. Facing these controversies, this review highlights advances in the literature regarding diagnosis, prognostic factors, treatment indications and therapeutic options.


Subject(s)
Prognosis , Splenic Neoplasms , Splenomegaly , Lymphoma, Non-Hodgkin , Lymphoma, B-Cell, Marginal Zone/diagnosis , Lymphoma, B-Cell, Marginal Zone/therapy
15.
Best Pract Res Clin Haematol ; 30(1-2): 139-148, 2017.
Article in English | MEDLINE | ID: mdl-28288709

ABSTRACT

Splenic marginal zone lymphoma (SMZL) is a distinct lymphoma entity characterized by an indolent clinical course and prolonged survival. Treatment is not standardized, since there are no prospective randomized trials in large series of SMZL patients. Splenectomy and rituximab represent the most effective treatment strategies used so far. The addition of chemotherapy to rituximab has not further improved the outcome, although this issue requires further investigation. Rituximab monotherapy has been associated with high response rates (∼90%), with approximately half of these responses being complete, even at the molecular level. More importantly, many of these responses are long-lasting, with a reported 7-year progression-free survival (PFS) at the rate of 69%. Maintenance rituximab treatment has been associated with further improvement of the quality of response as well as longer response duration in studies derived from one group of investigators. Based on its high efficacy and the good safety profile, rituximab represent one of the best treatment options for SMZL patients. Moreover, rituximab retains its efficacy in the relapse setting in most cases. Splenectomy is a meaningful alternative to rituximab in patients with bulky splenomegaly and cytopenias, without extensive bone marrow infiltration, who are fit for surgery. However splenectomy cannot completely eradicate the disease and it is also associated with greater morbidity or even mortality compared to rituximab. The choice of one of these two treatment approaches (rituximab or splenectomy) should mainly be based on patient's characteristics and on the disease burden. Novel agents are currently testing in low grade lymphomas including a small number of SMZL patients with promising results.


Subject(s)
Lymphoma, B-Cell, Marginal Zone/therapy , Rituximab/therapeutic use , Splenectomy , Disease-Free Survival , Humans , Lymphoma, B-Cell, Marginal Zone/diagnosis , Lymphoma, B-Cell, Marginal Zone/mortality , Prospective Studies , Randomized Controlled Trials as Topic , Splenic Neoplasms , Survival Rate
16.
Food Funct ; 8(1): 151-166, 2017 Jan 25.
Article in English | MEDLINE | ID: mdl-27924972

ABSTRACT

The previous study evaluated the antitumor activity and the underlying mechanism of the purified polyphenols from pinecones of Pinus koraiensis (PPP-40) using a tumor-bearing S180 mice model. This study was designed to evaluate the protective effects of PPP-40 on spleen tissues of S180 mice in vivo. Pretreatment with PPP-40 (150 mg per kg BW per D) could significantly inhibit tumor growth, enhance spleen index and prevent the decline of haematological parameters of S180 mice induced by the tumor microenvironment. Moreover, the treatment with PPP-40 was shown to significantly inhibit splenocyte apoptosis by TUNEL staining and flow cytometry, characterized by the inhibition of splenocyte cycle (G0/G1) arrest, increase in the percentages of splenic T lymphocytes (CD3+ T cells) and T cell subsets (CD3+CD4+ and CD3+CD8+ T cells), as well as the production of T cell-related cytokines (IL-2, IL-12, and TNF-α) in splenocytes exposed to the tumor microenvironment. These effects were associated with a decrease in oxidative stress, as evidenced by the changes in the SOD, GSH-Px, GSH and MDA levels of liver and spleen tissues of S180 mice. Furthermore, the protective effect of PPP-40 on spleen tissues was deeply analyzed by detecting apoptosis-related proteins using immunohistochemistry staining. The results indicated that the protective multi-mechanisms of action also were associated with the inhibition of apoptosis through down-regulation protein expressions of Bax, caspase-9, caspase-8 caspase-3, Fas and up-regulation of the expressions of Bcl-2. These results suggested that PPP-40 is a natural antitumor agent and possesses strong immunomodulatory activities by protecting the spleen tissues of tumor-bearing S180 mice.


Subject(s)
Antineoplastic Agents, Phytogenic/administration & dosage , Pinus/chemistry , Plant Extracts/administration & dosage , Polyphenols/administration & dosage , Protective Agents/administration & dosage , Splenic Neoplasms/prevention & control , Animals , Apoptosis/drug effects , Caspases/genetics , Caspases/metabolism , Cell Cycle/drug effects , Cell Line, Tumor , Humans , Interleukin-12/genetics , Interleukin-12/metabolism , Interleukin-2/genetics , Interleukin-2/metabolism , Male , Mice , Oxidative Stress/drug effects , Splenic Neoplasms/genetics , Splenic Neoplasms/metabolism , Splenic Neoplasms/physiopathology , T-Lymphocytes/drug effects , T-Lymphocytes/metabolism , Tumor Burden/drug effects , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/metabolism
17.
Leuk Res ; 44: 53-60, 2016 May.
Article in English | MEDLINE | ID: mdl-27030961

ABSTRACT

Splenic marginal zone lymphoma (SMZL) is an indolent lymphoma in which watch and wait (W&W) approach as well as splenectomy and chemo-immunotherapy are usually recommended. The role of the different approaches in relation to risk factors was evaluated. One hundred patients with SMZL were retrospectively studied. Median age was 65 years. HCV positivity was 3.1%. The 10-year overall-survival was 95.1% (CI: 90-100%). Sixty-two asymptomatic, low tumour burden patients were submitted to W&W. A low-risk group not requiring treatment was identified. Patients requiring treatment received splenectomy (36), chemotherapy-alone (27) and rituximab ± chemotherapy (16). In multivariate analysis, negative predictors for starting treatment were female-sex, splenomegaly, ECOG ≥ 1. Patients with low IIL-Score had a better 5-year TFT (24%). The median TFT of the W&W cohort was 58.5 months; at 10 years, 17% of patients were still on W&W. Splenectomy and rituximab ± chemotherapy showed similar results, while chemotherapy alone proved inferior. This real-life single-centre study of SMZL confirmed its very good prognosis with a survival likelihood overlapping that of general population. The prognostic role of IIL-Score was confirmed. The W&W approach allowed a median PFS longer than in follicular lymphoma. Finally, our data confirm the inferiority of chemotherapy compared to splenectomy and rituximab±chemotherapy.


Subject(s)
Antineoplastic Agents/therapeutic use , Lymphoma, B-Cell, Marginal Zone/therapy , Rituximab/therapeutic use , Splenectomy/mortality , Splenic Neoplasms/therapy , Adult , Aged , Aged, 80 and over , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Lymphoma, B-Cell, Marginal Zone/mortality , Lymphoma, B-Cell, Marginal Zone/pathology , Male , Middle Aged , Neoplasm Staging , Prognosis , Retrospective Studies , Splenic Neoplasms/mortality , Splenic Neoplasms/pathology , Survival Rate
18.
Exp Toxicol Pathol ; 67(9): 435-41, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26095745

ABSTRACT

The role of Balanites aegyptiaca (B. aegyptiaca) on development and growth of Ehrlich Ascitic carcinoma (EAC) and metastasis (liver and spleen) was evaluated. Balanite (400mg/kg; 10mg in 0.1ml/mouse) was given daily over a period of two weeks started 24h before intraperitoneal injection of EAC (2×10(6)/once). The present study deals with the effect of B. aegyptiaca on the growth of transplantable ascetic tumor, life span of EAC-bearing mice, hepatocellular and splenic histology. Antioxidant and biochemical changes as well as p53 genes expression were recorded. B. aegyptiaca extracts inhibited tumor growth and proliferation in ascetic fluid through a significant decrease in tumor volume, total cell volume, and viable cell count and prolonged the life span of mice. Also, it significantly decreased the levels of lipid peroxidation and increased SOD, CAT levels and P53 expression. Also, balanite inhibited either tumor invaded/or affected hepatic and splenic tissue. This result gives a new insight on beneficial effect of B. aegyptiaca in primary and secondary loci of Ehrlich Ascitic tumor through its antioxidant effect.


Subject(s)
Antineoplastic Agents, Phytogenic/therapeutic use , Balanites/chemistry , Carcinoma, Ehrlich Tumor/drug therapy , Liver Neoplasms/drug therapy , Plant Extracts/therapeutic use , Splenic Neoplasms/drug therapy , Animals , Antineoplastic Agents, Phytogenic/administration & dosage , Antineoplastic Agents, Phytogenic/isolation & purification , Carcinoma, Ehrlich Tumor/pathology , Cell Line, Tumor , Cell Proliferation/drug effects , Female , Fruit/chemistry , Liver Neoplasms/secondary , Mice , Plant Extracts/administration & dosage , Plant Extracts/isolation & purification , Splenic Neoplasms/secondary , Treatment Outcome , Tumor Suppressor Protein p53/genetics
19.
World J Surg Oncol ; 12: 107, 2014 Apr 23.
Article in English | MEDLINE | ID: mdl-24755405

ABSTRACT

There are few reported cases of colorectal metastasis from cancers of other organs, particularly other segments of the colon. Here we describe the long-term survival of a 68-year-old male patient with metachronous rectal metastasis from cecal cancer who underwent repetitive resection and chemotherapy. The patient underwent ileocecal resection and hepatectomy for cecal cancer with liver metastasis (T3, N1a, M1a, Stage IVA) in 2006. The patient subsequently underwent splenectomy for splenic metastasis in 2007. In August 2008, barium enema revealed compression of the rectal wall, and abdominal computed tomography (CT) detected a mass along the rectum extending into the pelvis. Rectal metastasis from cecal cancer was suspected and Hartmann's operation with bilateral seminal vesicle dissection was performed. Histological examination of the excised tumor revealed moderately differentiated adenocarcinoma formed in the muscularis propria of the rectum and infiltrating the connective tissue between the seminal vesicle and rectum. However, no tumor was detected in the rectal mucosa or submucosa. These histological findings supported the diagnosis of rectal metastasis from cecal cancer. The patient has been monitored at our clinic for 60 months after surgical removal of the rectal metastasis. The findings from this case should alert oncologists to the potential danger of rectal metastasis from primary colon cancer and the benefits of timely complete resection in terms of improved patient outcomes.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cecal Neoplasms/mortality , Hepatectomy/mortality , Liver Neoplasms/mortality , Neoplasms, Second Primary/mortality , Rectal Neoplasms/mortality , Splenic Neoplasms/mortality , Adenocarcinoma/mortality , Adenocarcinoma/secondary , Adenocarcinoma/therapy , Aged , Cecal Neoplasms/pathology , Cecal Neoplasms/therapy , Combined Modality Therapy , Humans , Liver Neoplasms/secondary , Liver Neoplasms/therapy , Male , Neoplasms, Second Primary/secondary , Neoplasms, Second Primary/therapy , Prognosis , Rectal Neoplasms/secondary , Rectal Neoplasms/therapy , Splenic Neoplasms/secondary , Splenic Neoplasms/therapy , Survival Rate , Tomography, X-Ray Computed
20.
Leuk Lymphoma ; 55(8): 1854-60, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24206091

ABSTRACT

Splenectomy is considered as one of the first-line treatments for symptomatic patients with splenic marginal zone lymphoma (SMZL). Between 1997 and 2012, 100 hepatitis C virus-negative patients with SMZL were treated by splenectomy as first-line treatment. At 6 months, all patients but three recovered from all cytopenias. The median lymphocyte count at 6 months and 1 year was 11.51 × 10(9)/L and 6.9 × 10(9)/L, respectively. Median progression-free survival (PFS) was 8.25 years. The 5-year and 10-year overall survival (OS) rates were 84% and 67%, respectively. Histological transformation occurred in 11% of patients, and was the only parameter significantly associated with a shorter time to progression (p = 0.0001). Significant prognostic factors for OS were age (p = 0.0356) and histological transformation (p = 0.0312). In this large retrospective cohort, we confirmed that splenectomy as first-line treatment in patients with SMZL corrected cytopenias and lymphocytosis within the first year and was associated with a good PFS.


Subject(s)
Lymphoma, B-Cell, Marginal Zone/surgery , Splenectomy , Splenic Neoplasms/surgery , Adult , Aged , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Female , Follow-Up Studies , Humans , Immunophenotyping , Lymphoma, B-Cell, Marginal Zone/diagnosis , Lymphoma, B-Cell, Marginal Zone/mortality , Lymphoma, B-Cell, Marginal Zone/therapy , Male , Middle Aged , Neoplasm Grading , Neoplasm Staging , Prognosis , Risk Factors , Splenic Neoplasms/diagnosis , Splenic Neoplasms/mortality , Splenic Neoplasms/therapy , Treatment Outcome
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