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1.
Actas Urol Esp (Engl Ed) ; 48(4): 262-272, 2024 May.
Article in English, Spanish | MEDLINE | ID: mdl-38575068

ABSTRACT

Radical cystectomy is the current treatment of choice for patients with BCG-unresponsive non-muscle invasive bladder tumor (NMIBC). However, the high comorbidity of this surgery and its effects on the quality of life of patients require the investigation and implementation of bladder-sparing treatment options. These must be evaluated individually by the uro-oncology committee based on the characteristics of the BCG failure, type of tumor, patient preferences and treatment options available in each center. Based on FDA-required oncologic outcomes (6-month complete response rate for CIS: 50%; duration of response in responders for CIS and papillary: 30% at 12 months and 25% at 18 months), there is not currently a strong preference for one treatment over another, although the intravesical route seems to offer less toxicity. This work summarizes the evidence on the management of BCG-unresponsive NMIBC based on current scientific evidence and provides consensus recommendations on the most appropriate treatment.


Subject(s)
Adjuvants, Immunologic , BCG Vaccine , Neoplasm Invasiveness , Urinary Bladder Neoplasms , Urinary Bladder Neoplasms/pathology , Urinary Bladder Neoplasms/drug therapy , Urinary Bladder Neoplasms/therapy , Humans , BCG Vaccine/therapeutic use , BCG Vaccine/administration & dosage , Adjuvants, Immunologic/therapeutic use , Cystectomy/methods , Treatment Failure , Administration, Intravesical , Consensus
2.
Ann Oncol ; 27(4): 706-11, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26658889

ABSTRACT

BACKGROUND: Patients with metastatic renal carcinoma (mRCC) treated with first-line pazopanib were not included in the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) prognostic model. SPAZO (NCT02282579) was a nation-wide retrospective observational study designed to assess the effectiveness and validate the IMDC prognostic model in patients treated with first-line pazopanib in clinical practice. PATIENTS AND METHODS: Data of 278 patients, treated with first-line pazopanib for mRCC in 34 centres in Spain, were locally recorded and externally validated. Mean age was 66 years, there were 68.3% male, 93.5% clear-cell type, 74.8% nephrectomized, and 81.3% had ECOG 0-1. Metastatic sites were: lung 70.9%, lymph node 43.9%, bone 26.3%, soft tissue/skin 20.1%, liver 15.1%, CNS 7.2%, adrenal gland 6.5%, pleura/peritoneum 5.8%, pancreas 5%, and kidney 2.2%. After median follow-up of 23 months, 76.4% had discontinued pazopanib (57.2% due to progression), 47.9% had received second-line targeted therapy, and 48.9% had died. RESULTS: According to IMDC prognostic model, 19.4% had favourable risk (FR), 57.2% intermediate risk (IR), and 23.4% poor risk (PR). No unexpected toxicities were recorded. Response rate was 30.3% (FR: 44%, IR: 30% PR: 17.3%). Median progression-free survival (whole population) was 11 months (32 in FR, 11 in IR, 4 in PR). Median and 2-year overall survival (whole population) were 22 months and 48.1%, respectively (FR: not reached and 81.6%, IR: 22 and 48.7%, PR: 7 and 18.8%). These estimations and their 95% confidence intervals are fully consistent with the outcomes predicted by the IMDC prognostic model. CONCLUSION: Our results validate the IMDC model for first-line pazopanib in mRCC and confirm the effectiveness and safety of this treatment.


Subject(s)
Carcinoma, Renal Cell/drug therapy , Molecular Targeted Therapy , Prognosis , Pyrimidines/administration & dosage , Sulfonamides/administration & dosage , Adult , Aged , Carcinoma, Renal Cell/pathology , Databases, Factual , Disease-Free Survival , Female , Humans , Indazoles , Kaplan-Meier Estimate , Male , Middle Aged , Pyrimidines/adverse effects , Retrospective Studies , Risk Factors , Spain , Sulfonamides/adverse effects
3.
Adv Ther ; 28 Suppl 6: 39-49, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21922394

ABSTRACT

This section considers the treatment options for perimenopausal women with breast cancer. The perimenopause period begins in the so-called stage 2 of menopausal transition (early menopausal transition, where the length of the cycles changes by 7 days or more) and ends after 12 months of amenorrhea. It is characterized by an early increase in follicle-stimulating hormone and is associated with the presence of anovulatory cycles, irregular periods, and loss of menstrual cycles. The recommended treatment is tamoxifen (TAM) with or without ovarian ablation for 2 or 3 years followed by a re-evaluation. TAM should be maintained if the patient is premenopausal and aromatase inhibitors (AI) are recommended once the menopausal status is confirmed. Ovarian suppression is an acceptable adjuvant therapy in those patients with hormone-sensitive tumors. AI should only be used in postmenopausal women or in combination with chemical castration in premenopausal women. This supplement paper includes the key points of roundtable presentations and discussions of hormonal therapy in breast cancer.


Subject(s)
Antineoplastic Agents, Hormonal/administration & dosage , Aromatase Inhibitors/administration & dosage , Breast Neoplasms/drug therapy , Breast Neoplasms/mortality , Perimenopause/drug effects , Adult , Age Factors , Antineoplastic Agents, Hormonal/adverse effects , Aromatase Inhibitors/adverse effects , Breast Neoplasms/pathology , Breast Neoplasms/surgery , Chemotherapy, Adjuvant , Disease-Free Survival , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Humans , Mastectomy/methods , Middle Aged , Neoplasm Invasiveness/pathology , Neoplasm Staging , Patient Selection , Perimenopause/physiology , Prognosis , Randomized Controlled Trials as Topic , Risk Assessment , Survival Analysis , Tamoxifen/administration & dosage , Tamoxifen/adverse effects , Treatment Outcome
4.
Clin. transl. oncol. (Print) ; 11(11): 770-772, nov. 2009. ilus
Article in English | IBECS | ID: ibc-123710

ABSTRACT

Desmoplastic small round cell tumor is a very rare neoplasm, that usually appears in children and young adolescents. There is no standard therapy, and responses to chemotherapy are infrequent. Surgery is still the main treatment for this disease. We report the case of a 39 year-old man and briefly summarize the evidence about this tumor (AU)


No disponible


Subject(s)
Male , Adult , Humans , Peritoneal Neoplasms/diagnosis , Peritoneal Neoplasms/drug therapy , Sarcoma, Ewing/diagnosis , Disease Progression , Sarcoma, Ewing/drug therapy , Sarcoma, Small Cell/complications , Sarcoma, Small Cell/diagnosis , Sarcoma, Small Cell/drug therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Fatal Outcome , Lymph Nodes/pathology , Neoplasm Metastasis , Peritoneal Neoplasms/pathology , Peritoneum/pathology , Prognosis , Sarcoma, Ewing/pathology , Sarcoma, Small Cell/pathology , Treatment Outcome
5.
Clin Transl Oncol ; 11(1): 60-2, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19155206

ABSTRACT

Glucagonoma is an uncommon disease, a neuroendocrine tumour that develops from glucagon-producing pancreatic cells. They are usually slow-growing, but generally advanced at diagnosis, and metastatic disease is virtually incurable. Liver is the most common site of metastatic disease. We present the case of a 48-year-old man with a glucagonoma being diagnosed from a pulmonary mass. This case had no liver affection in the whole evolution of the disease, and showed a particularly aggressive course, with very little response to all therapies administered, and a survival from diagnosis of just 16 months.


Subject(s)
Glucagonoma/secondary , Lung Neoplasms/secondary , Pancreatic Neoplasms/pathology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Diagnosis, Differential , Fatal Outcome , Glucagonoma/physiopathology , Glucagonoma/therapy , Humans , Lung Neoplasms/therapy , Male , Middle Aged , Pancreatic Neoplasms/physiopathology , Pancreatic Neoplasms/therapy , Tomography, X-Ray Computed
6.
Clin. transl. oncol. (Print) ; 11(1): 60-62, ene. 2009. ilus
Article in English | IBECS | ID: ibc-123577

ABSTRACT

Glucagonoma is an uncommon disease, a neuroendocrine tumour that develops from glucagon-producing pancreatic cells. They are usually slow-growing, but generally advanced at diagnosis, and metastatic disease is virtually incurable. Liver is the most common site of metastatic disease. We present the case of a 48-year-old man with a glucagonoma being diagnosed from a pulmonary mass. This case had no liver affection in the whole evolution of the disease, and showed a particularly aggressive course, with very little response to all therapies administered, and a survival from diagnosis of just 16 months (AU)


No disponible


Subject(s)
Humans , Male , Middle Aged , Glucagonoma/secondary , Lung Neoplasms/secondary , Pancreatic Neoplasms/pathology , Fatal Outcome , Glucagonoma/physiopathology , Glucagonoma/therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Diagnosis, Differential , Lung Neoplasms/therapy , Pancreatic Neoplasms/physiopathology , Pancreatic Neoplasms/therapy , Tomography Scanners, X-Ray Computed
7.
Clin. transl. oncol. (Print) ; 8(10): 729-734, oct. 2006.
Article in English | IBECS | ID: ibc-125320

ABSTRACT

The hematopoietic growth factors (HGFs) are a family of glycoproteins which plays a major role in the proliferation, differentiation, and survival of primitive hematopoietic stem and progenitor cells, and in the functions of some mature cells. More than 20 different molecules of HGF have been identified. Among them, granulocyte colony-stimulating factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF) have been demostrated to be effective in reducing the incidence of febrile neutropenia when administered inmediately after chemotherapy and as supportive therapy in patients undergoing bone marrow transplantation. Chemotherapy used for treatment of cancer often causes neutropenia, which may be profound, requiring hospitalization, and leading to potentially fatal infection. The uses of the recombinant human hematopoietic colony-stimulating factors G-CSF and GM-CSF for treatment and prophylaxis of chemotherapy-induced febrile neutropenia will be reviewed here (AU)


Subject(s)
Humans , Aged , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/adverse effects , Bone Marrow Transplantation , Granulocyte Colony-Stimulating Factor/administration & dosage , Granulocyte Colony-Stimulating Factor/adverse effects , Granulocyte Colony-Stimulating Factor/therapeutic use , Granulocyte-Macrophage Colony-Stimulating Factor/administration & dosage , Granulocyte-Macrophage Colony-Stimulating Factor/adverse effects , Granulocyte-Macrophage Colony-Stimulating Factor/therapeutic use , Fever/chemically induced , Fever/prevention & control , Acute Disease , Data Interpretation, Statistical , Injections, Subcutaneous , Leukemia, Myeloid/drug therapy , Neutropenia/chemically induced , Neutropenia/prevention & control , Controlled Clinical Trials as Topic , Time Factors , Risk Factors , Neoplasms/drug therapy , Neoplasms/radiotherapy , Meta-Analysis as Topic
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