1998
DOI: 10.1097/00001813-199806000-00002
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Use of granisetron in patients refractory to previous treatment with antiemetics

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Cited by 90 publications
(124 citation statements)
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“…This was in contrast to the better efficacy of granisetron in the prevention of chemotherapy-induced nausea and vomiting, which was proven in a number of studies like those by Specter JI et al [14] Carmichael et al [15] and De Wit et al [16] So also in our study there was no significant advantage of one 5-HT3 receptor blocker over the other for the prevention of PONV over 24 hours.…”
Section: Discussioncontrasting
confidence: 65%
“…This was in contrast to the better efficacy of granisetron in the prevention of chemotherapy-induced nausea and vomiting, which was proven in a number of studies like those by Specter JI et al [14] Carmichael et al [15] and De Wit et al [16] So also in our study there was no significant advantage of one 5-HT3 receptor blocker over the other for the prevention of PONV over 24 hours.…”
Section: Discussioncontrasting
confidence: 65%
“…2) [17]. However, patients receiving doses of cisplatin in excess of 50 mg/m 2 had lower complete response rates (25.0%-57.1%) than those receiving other cytostatic agents (59.3%-67.9%).…”
Section: Breakthrough Emesis and Treatment Failurementioning
confidence: 97%
“…Cisplatin is one of the most highly emetogenic agents, with doses of 50 mg/m 2 or more inducing nausea and vomiting within 24 hours in more than 90% of patients not administered antiemetic prophylaxis. Even in those patients receiving appropriate prophylaxis during multiple-cycle chemotherapy, the risk of vomiting associated with cisplatin is 20% greater than with non-cisplatin-containing regimens [17]. Agents with moderately high emetogenic potentials include methotrexate, doxorubicin, cyclophosphamide, and carboplatin, while vinblastine and bleomycin are considered to have low emetogenicity as monotherapy products [7].…”
Section: Risk Factors For the Development Of Acute Nausea And Vomitingmentioning
confidence: 99%
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“…Moreover, studies comparing granisetron, 40 and 160 mg kg 71 , show a trend towards increased efficacy at the higher dose Soukop, 1994); 24 h after administration of chemotherapeutic agents, 81% of granisetron, 160 mcg kg 71 , were emesis-free compared with 75% receiving granisetron 40 mg kg 71 . In addition, patients refractory to other 5-HT 3 receptor antagonists have been shown to respond well to granisetron, at doses that are higher than generally used, in subsequent chemotherapy cycles (Carmichael et al, 1998).…”
Section: Sirmentioning
confidence: 99%