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1.
Eur J Obstet Gynecol Reprod Biol ; 282: 140-145, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36716537

ABSTRACT

BACKGROUND: After exhausting other therapeutic options, pelvic exenteration is performed in patients who suffer from relapsed gynaecologic tumours, with most of them requiring some sort of urinary diversion. MATERIAL AND METHODS: The main objective of this study was to assess the short- and medium/long-term urinary complications associated with the Bricker ileal conduit versus double-barrelled wet colostomy after performing a pelvic exenteration for gynaecologic malignancies. RESULTS: A total of 61 pelvic exenterations were identified between November 2010 and April 2022; 29 Bricker ileal conduits and 20 double-barrelled wet colostomies were included in the urinary diversion analysis. Regarding the specific short-term urinary complications, no differences were found in the rate of urinary leakage (3 vs 0 %; p = 1), urostomy complications (7 vs 0 %; p = 0.51), acute renal failure (10 vs 20 %; p = 0.24) or urinary infection (0 vs 5 %; p = 0.41). Up to 69 % of patients with Bricker ileal conduits and 65 % of double-barrelled wet colostomies (p = 0.76) presented specific medium/long-term urinary complications. No differences in the rates of pyelonephritis (59 vs 53 %; p = 0.71), urinary fistula (0 vs 12 %; p = 0.13), ureteral stricture (10 vs 6 %; p = 1), conduit failure and reconstruction (7 vs 0 %; p = 0.53), renal failure (38 vs 29 %; p = 0.56) or electrolyte disorders (24 vs 18 %; p = 0.72) were found. CONCLUSIONS: There are no significant differences in the rate of complications between double-barrelled wet colostomy and the Bricker ileal conduit. The long-term complications related to urinary diversion remained high regardless of the type of technique. In this context, the double-barrelled wet colostomy presents advantages such as the single stoma placement and the simplicity of the technique.


Subject(s)
Genital Neoplasms, Female , Pelvic Exenteration , Pyelonephritis , Urinary Diversion , Female , Humans , Genital Neoplasms, Female/surgery , Colostomy/adverse effects , Colostomy/methods , Pelvic Exenteration/adverse effects , Pelvic Exenteration/methods , Urinary Diversion/adverse effects , Urinary Diversion/methods
2.
J Clin Med ; 10(21)2021 Oct 30.
Article in English | MEDLINE | ID: mdl-34768625

ABSTRACT

(1) Background: Intravesical mitomycin-C (MMC) combined with hyperthermia is increasingly used in non-muscle invasive bladder cancer (NMIBC), especially in the context of a relative BCG shortage. We aim to determine real-world data on the long-term treatment outcomes of adjunct hyperthermic intravesical chemotherapy (HIVEC) with MMC and a COMBAT® bladder recirculation system (BRS); (2) Methods: A prospective observational trial was performed on patients with NMIBC treated with HIVEC using BRS in nine academic institutions in Spain between 2012-2020 (HIVEC-E). Treatment effectiveness (recurrence, progression and overall mortality) was evaluated in patients treated with HIVEC MMC 40mg in the adjuvant setting, with baseline data and a clinical follow-up, that comprise the Full Analysis Set (FAS). Safety, according to the number and severity of adverse effects (AEs), was evaluated in the safety (SAF) population, composed by patients with at least one adjunct HIVEC MMC instillation; (3) Results: The FAS population (n = 502) received a median number of 8.78 ± 3.28 (range 1-20) HIVEC MMC instillations. The median follow-up duration was 24.5 ± 16.5 (range 1-81) months. Its distribution, based on EAU risk stratification, was 297 (59.2%) for intermediate and 205 (40.8%) for high-risk. The figures for five-year recurrence-free and progression-free survival were 50.37% (53.3% for intermediate and 47.14% for high-risk) and 89.83% (94.02% for intermediate and 84.23% for high-risk), respectively. A multivariate analysis identified recurrent tumors (HR 1.83), the duration of adjuvant HIVEC therapy <4 months (HR 1.72) and that high-risk group (HR 1.47) were at an increased risk of recurrence. Independent factors of progression were high-risk (HR 3.89), recurrent tumors (HR 3.32) and the induction of HIVEC therapy without maintenance (HR 2.37). The overall survival was determined by patient age at diagnosis (HR 3.36) and the treatment duration (HR 1.82). The SAF population (n = 592) revealed 406 (68.58%) patients without AEs and 186 (31.42%) with at least one AE: 170 (28.72%) of grade 1-2 and 16 (2.7%) of grade 3-4. The most frequent AEs were dysuria (10%), pain (7.1%), urgency (5.7%), skin rash (4.9%), spasms (3.7%) and hematuria (3.6%); (4) Conclusions: HIVEC using BRS is efficacious and well tolerated. A longer treatment duration, its use in naïve patients and the intermediate-risk disease are independent determinants of success. Furthermore, a monthly maintenance of adjunct MMC HIVEC diminishes the progression rate of NMIBC.

3.
Urol Int ; 99(1): 121-123, 2017.
Article in English | MEDLINE | ID: mdl-26159374

ABSTRACT

Malignant triton tumor (MTT) is a variant of the peripheral nerve sheath tumor. It is very uncommon but shows an aggressive course and limited survival. Half of the cases present symptoms related to neurofibromatosis type 1 disease. There is no standardized treatment, but multimodal approach is the best option. We present the case of a primary MTT located in the kidney, in a 43-year-old woman who received neoadjuvant chemotherapy as first-line treatment followed by surgical resection and adjuvant chemotherapy.


Subject(s)
Kidney Neoplasms/pathology , Peripheral Nervous System Neoplasms/pathology , Adult , Biomarkers, Tumor/genetics , Chemotherapy, Adjuvant , Fatal Outcome , Female , Humans , Kidney Neoplasms/diagnostic imaging , Kidney Neoplasms/genetics , Kidney Neoplasms/therapy , Neoadjuvant Therapy , Nephrectomy , Peripheral Nervous System Neoplasms/diagnostic imaging , Peripheral Nervous System Neoplasms/genetics , Peripheral Nervous System Neoplasms/therapy , Time Factors , Tomography, X-Ray Computed , Treatment Outcome
4.
Theor Biol Med Model ; 11 Suppl 1: S3, 2014 May 07.
Article in English | MEDLINE | ID: mdl-25080066

ABSTRACT

BACKGROUND: Superficial bladder cancer has been the subject of numerous studies for many years, but the evolution of the disease still remains not well understood. After the tumor has been surgically removed, it may reappear at a similar level of malignancy or progress to a higher level. The process may be reasonably modeled by means of a Markov process. However, in order to more completely model the evolution of the disease, this approach is insufficient. The semi-Markov framework allows a more realistic approach, but calculations become frequently intractable. In this context, flowgraph models provide an efficient approach to successfully manage the evolution of superficial bladder carcinoma. Our aim is to test this methodology in this particular case. RESULTS: We have built a successful model for a simple but representative case. CONCLUSION: The flowgraph approach is suitable for modeling of superficial bladder cancer.


Subject(s)
Models, Biological , Urinary Bladder/pathology , Disease Progression , Humans , Markov Chains , Neoplasm Recurrence, Local/pathology
5.
Eur Urol ; 51(4): 962-9; discussion 969-70, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17084017

ABSTRACT

OBJECTIVES: Three-dimensional (3D) spheroids are a good model for studying in vitro chemosensitivity because they reproduce unicellular and multicellular mechanisms of drug resistance. We aimed to develop a chemosensitivity test for intravesical drugs and to also verify the effects of verapamil (VPM) and ciprofloxacin (CIPRO). METHODS: Cold cup biopsies from 40 superficial bladder tumours were taken, fragmented, and left in culture. 3D-spheroids were obtained and transferred into a 24 multiwell dish containing (1) wells 1-3: 1 mg/ml epirubicin (EPI); (2) 4-6: 1 mg/ml EPI+0.5 mg/ml VPM; (3) 7-9: 1 mg/ml adriamycin (ADR); (4) 10-12: 1 mg/ml thiotepa (THIO); (5) 13-15: 1 mg/ml mitomycin C (MMC); (6) 16-18: 1mg/ml EPI+0.2 mg/ml CIPRO; (7) 19-21: 0.2 mg/ml CIPRO; (8) 22-24: controls. Sensitivity was calculated by using the trypan blue assay. RESULTS: Evaluability of clinically relevant tests (G1-G2 lesions) was 84% (21 of 25 patients). MMC was the best agent (p<0.001) with mean sensitivity being 50%, followed by THIO (37%), EPI (7%), and ADR (3%). We found no significant difference (p=0.370) between CIPRO and the control, or between EPI+CIPRO and EPI alone (p=0.550). VPM markedly enhanced sensitivity to EPI compared with EPI alone (97% vs. 7%, p<0.001). CONCLUSIONS: Our assay allows determining sensitivity to several drugs in superficial bladder tumours. It might be used in clinical practice to select the best drug for each patient. It also has experimental utility in investigating the effect of new drugs or combinations. VPM reverted resistance to EPI. CIPRO showed no effect on bladder tumour spheroids.


Subject(s)
Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Spheroids, Cellular/drug effects , Urinary Bladder Neoplasms/drug therapy , Ciprofloxacin/pharmacology , Doxorubicin/pharmacology , Doxorubicin/therapeutic use , Drug Resistance, Neoplasm , Drug Screening Assays, Antitumor , Epirubicin/pharmacology , Epirubicin/therapeutic use , Humans , Mitomycin/pharmacology , Mitomycin/therapeutic use , Thiotepa/pharmacology , Thiotepa/therapeutic use , Tumor Cells, Cultured , Urinary Bladder Neoplasms/pathology , Verapamil/pharmacology
6.
Scand J Urol Nephrol ; 37(1): 90-2, 2003.
Article in English | MEDLINE | ID: mdl-12745754

ABSTRACT

Infective endocarditis (IE) presents with several signs and symptoms that are mainly heart-related and the result of bacteremia. We describe the case of a woman with severe renal hemorrhage due to a septic embolic cortical infarction, who was also receiving anticoagulation therapy because of cardiopathy, whose retroperitoneal hematoma was the first manifestation of IE.


Subject(s)
Anticoagulants/adverse effects , Embolism/etiology , Endocarditis, Bacterial/complications , Hemorrhage/etiology , Infarction/etiology , Kidney Diseases/etiology , Mitral Valve Stenosis/complications , Mitral Valve Stenosis/drug therapy , Aged , Embolism/diagnosis , Embolism/therapy , Endocarditis, Bacterial/diagnosis , Endocarditis, Bacterial/therapy , Female , Hemorrhage/diagnosis , Hemorrhage/therapy , Humans , Infarction/diagnosis , Infarction/therapy , Kidney Diseases/diagnosis , Kidney Diseases/therapy , Mitral Valve Stenosis/diagnosis , Syndrome
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