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1.
Support Care Cancer ; 32(1): 37, 2023 Dec 19.
Artigo em Inglês | MEDLINE | ID: mdl-38110581

RESUMO

PURPOSE: Review the literature to update the MASCC guidelines from 2016 for controlling nausea and vomiting with systemic cancer treatment of low and minimal emetic potential. METHODS: A working group performed a systematic literature review using Medline, Embase, and Scopus databases between June 2015 and January 2023 of the management of antiemetic prophylaxis for anticancer therapy of low or minimal emetic potential. A consensus committee reviewed recommendations and required a consensus of 67% or greater and a change in outcome of at least 10%. RESULTS: Of 293 papers identified, 15 had information about managing systemic cancer treatment regimens of low or minimal emetic potential and/or compliance with previous management recommendations. No new evidence was reported that would change the current MASCC recommendations. No antiemetic prophylaxis is recommended for minimal emetic potential therapy, and single agents recommended for low emetic potential chemotherapy for acute emesis, but no prophylaxis is recommended for delayed emesis. Commonly, rescue medication includes antiemetics prescribed for the next higher level of emesis. CONCLUSION: There is insufficient data to change the current guidelines. Future studies should seek to more accurately determine the risk of emesis with LEC beyond the emetogenicity of the chemotherapy to include patient-related risk assessment.


Assuntos
Antieméticos , Antineoplásicos , Humanos , Antieméticos/uso terapêutico , Antineoplásicos/efeitos adversos , Consenso , Eméticos , Náusea/induzido quimicamente , Náusea/prevenção & controle , Náusea/tratamento farmacológico , Vômito/induzido quimicamente , Vômito/tratamento farmacológico , Vômito/prevenção & controle , Revisões Sistemáticas como Assunto , Guias de Prática Clínica como Assunto
2.
Support Care Cancer ; 26(10): 3441-3446, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29679139

RESUMO

PURPOSE: To assess the emetogenic potential of different chemotherapy (CT) regimens in daily clinical practice in an outpatient setting. To optimize antiemetic prophylaxis if necessary METHODS: Prospective and retrospective review of the emetogenic potential of CT regimens used in adult patients in an outpatient setting RESULTS: We assess the chemotherapy-induced nausea and vomiting (CINV) of 50 different CT regimens used on 157 different patients in an outpatient setting. We found that the CT usually classified as highly emetogenic, including cisplatin and anthracycline-cyclophosphamide combination, had the higher incidence of CINV (37.5 and 54.4% respectively). The antineoplastic drugs usually considered to be moderately emetogenic had, as expected, lower rates of emesis with the exception of irinotecan, which presented a pattern of nausea and/or vomiting (NV) similar to the highly emetogenic CT with a global incidence of 48.5%. The appearance of emetic symptoms had impact on quality of life in 70% of the patients, with nausea being the main emetic symptom. CONCLUSION: Antiemetic prophylaxis for highly emetogenic CT could be improve. Irinotecan CT regimens have a high emetogenic potential more than moderate and require more intensive antiemetic prophylaxis too.


Assuntos
Antineoplásicos/efeitos adversos , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Camptotecina/análogos & derivados , Neoplasias/tratamento farmacológico , Neoplasias/epidemiologia , Vômito/induzido quimicamente , Vômito/epidemiologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Antraciclinas/efeitos adversos , Antieméticos/uso terapêutico , Antineoplásicos/administração & dosagem , Camptotecina/administração & dosagem , Camptotecina/efeitos adversos , Cisplatino/efeitos adversos , Ciclofosfamida/efeitos adversos , Eméticos/administração & dosagem , Eméticos/efeitos adversos , Feminino , Humanos , Quimioterapia de Indução/efeitos adversos , Irinotecano , Masculino , Pessoa de Meia-Idade , Náusea/induzido quimicamente , Náusea/epidemiologia , Náusea/patologia , Pacientes Ambulatoriais , Qualidade de Vida , Estudos Retrospectivos , Índice de Gravidade de Doença , Vômito/patologia
3.
J Cancer Res Ther ; 18(4): 1183-1185, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36149184

RESUMO

The incidence of autoimmune thyroid disorders is higher among women with breast cancer (BC) than in other solid malignancies, while it has not a prognostic impact. Trastuzumab (T) is a humanized monoclonal antibody approved for human epidermal growth factor receptor 2 (HER2)-positive BC in the neoadjuvant, adjuvant, and metastatic scenarios. Since 2014, subcutaneous (SC) T has been employed with the same efficacy as the intravenous formulation together with an easier way of administration. To date, autoimmune thyroiditis has been linked rarely to the use of intravenous T, and no cases have been related to the SC presentation. We report two cases of HER2-positive early BC patients who developed hypothyroidism during maintenance therapy with SC T that required levothyroxine supplementation. SC T includes recombinant human hyaluronidase to facilitate tissue penetration of the drug. This enzyme may alter the thyroid gland stroma and facilitate the development of thyroid disorders. Thyroid function tests are recommended in patients on SC T.


Assuntos
Antineoplásicos Imunológicos , Neoplasias da Mama , Glândula Tireoide , Trastuzumab , Antineoplásicos Imunológicos/efeitos adversos , Antineoplásicos Imunológicos/uso terapêutico , Neoplasias da Mama/tratamento farmacológico , Neoplasias da Mama/patologia , Feminino , Humanos , Hialuronoglucosaminidase/uso terapêutico , Injeções Subcutâneas , Receptor ErbB-2/metabolismo , Glândula Tireoide/patologia , Tiroxina/uso terapêutico , Trastuzumab/efeitos adversos , Trastuzumab/uso terapêutico
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