2017
DOI: 10.3892/ol.2017.5576
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Gemcitabine-associated thrombotic microangiopathy in a patient with lung cancer: A case report

Abstract: Gemcitabine is frequently used for the treatment of a number of different cancer types. Gemcitabine-related thrombotic microangiopathy (TMA) has rarely been described, but it is a life-threatening complication. The incidence of the complication varies between 0.015 and 1.4%. The present study reports the case of a 63-year-old Caucasian male who was treated with 3 cycles of carboplatin plus gemcitabine, followed by 7 cycles of gemcitabine only, and developed clinical symptoms that, together with laboratory find… Show more

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Cited by 8 publications
(6 citation statements)
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“…The majority of cases are idiopathic, but several etiologies have been recognized, including drugs, and cytotoxic chemotherapies, such as gemcitabine, carboplatin, cisplatin, bleomycin, and a vinca alkaloid [3][4][5][6][7][8]. TMA induced by the use of an icos agonist in combination with a PD-1 inhibitor has not been described [9], and was not the cause of TMA in this case, as confirmed by autopsy findings.…”
supporting
confidence: 52%
“…The majority of cases are idiopathic, but several etiologies have been recognized, including drugs, and cytotoxic chemotherapies, such as gemcitabine, carboplatin, cisplatin, bleomycin, and a vinca alkaloid [3][4][5][6][7][8]. TMA induced by the use of an icos agonist in combination with a PD-1 inhibitor has not been described [9], and was not the cause of TMA in this case, as confirmed by autopsy findings.…”
supporting
confidence: 52%
“…32 Drug-induced TMA has also been reported after treatment with a number of chemotherapeutic agents, including gemcitabine and the already mentioned cisplatin. 33 The exact incidence of drug-induced TMA is difficult to estimate because cases are underreported and the clinical presentation is sometimes confused with other causes. The mechanism by which the chemotherapeutic agent induces TMA can either be non-dose-dependent (immune-related) or more frequently dose-related (toxic).…”
Section: Immune Checkpoint Inhibitorsmentioning
confidence: 99%
“…A disintegrin and metalloproteinase with a thrombospondin type 1 motif 13 (ADAMTS13) is demonstrated to be significant in the pathophysiology of TTP when either antibodies against ADAMTS13 are present (acquired TTP) or when antibodies against ADAMTS13 are lacking (inherited TTP). A severe deficiency of ADAMTS‐1 activity, with clinical symptoms of acute thrombocytopenia and evidence of microangiopathic hemolytic anemia, constitutes a diagnosis of TTP [ 9 ]. HUS is not associated with a deficiency in ADAMTS13 activity [ 9 ].…”
Section: Discussionmentioning
confidence: 99%