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1.
Gan To Kagaku Ryoho ; 47(6): 917-922, 2020 Jun.
Artigo em Japonês | MEDLINE | ID: mdl-32541168

RESUMO

We evaluated the incidence of proteinuria after receiving ramucirumab for the patients with advanced colorectal cancer using claim database. Among 1,706 evaluable patients, incidence proportion of proteinuria was 21.8% and incidence rate (/100 person-years)was 75.3. In patients with history of proteinuria or previous bevacizumab use, incidence rate was high and many patients tend to occur proteinuria in the early stage after initiating ramucirumab prescription. Appropriate management by periodical monitoring from the early stage after initiating ramucirumab prescription is important.


Assuntos
Anticorpos Monoclonais Humanizados/efeitos adversos , Neoplasias Colorretais , Proteinúria/epidemiologia , Protocolos de Quimioterapia Combinada Antineoplásica , Estudos de Coortes , Humanos , Incidência , Japão , Proteinúria/induzido quimicamente , Ramucirumab
2.
Gan To Kagaku Ryoho ; 38(13): 2607-16, 2011 Dec.
Artigo em Japonês | MEDLINE | ID: mdl-22189227

RESUMO

To elucidate the detailed profiles of major adverse events associated with gemcitabine hydrochloride, such as myelosuppression and interstitial pneumonitis (IP), we reanalyzed the results from Japanese clinical studies conducted by Eli Lilly Japan K. K. in patients with various types of cancer. Myelosuppression was clearly apparent after starting therapy at 2-3 weeks in the 28- day course monotherapy group, and at 2 weeks in the 21-day course combination therapy group with paclitaxel, cisplatin, or docetaxel. Increases in the number of courses did not necessarily lead to worsening of myelosuppression. IP possibly related to gemcitabine was seen in 6 out of 5 23 monotherapy patients and 5 out of 233 combination therapy patients. Five of these 11 patients were diagnosed in the first course; however, another patient was diagnosed with IP in Course 6. Two of these patients died of IP, one of whom had a past history of interstitial lung disease. These results indicate that ample attention should be paid to myelosuppression 2-3 weeks after the start of therapy, and to IP during the entire course of therapy.


Assuntos
Antimetabólitos Antineoplásicos/efeitos adversos , Desoxicitidina/análogos & derivados , Antimetabólitos Antineoplásicos/uso terapêutico , Proliferação de Células/efeitos dos fármacos , Ensaios Clínicos como Assunto , Desoxicitidina/efeitos adversos , Desoxicitidina/uso terapêutico , Humanos , Japão , Doenças Pulmonares Intersticiais/induzido quimicamente , Células Mieloides/efeitos dos fármacos , Neoplasias/tratamento farmacológico , Gencitabina
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