dc.contributor.author |
Kellokumpu-Lehtinen, Pirkko-Liisa |
|
dc.contributor.author |
Marttila, Timo |
|
dc.contributor.author |
Jekunen, Antti |
|
dc.contributor.author |
Hervonen, Petteri |
|
dc.contributor.author |
Klintrup, Katariina |
|
dc.contributor.author |
Kataja, Vesa |
|
dc.contributor.author |
Utriainen, Tapio |
|
dc.contributor.author |
Luukkaa, Marjaana |
|
dc.contributor.author |
Leskinen, Markku |
|
dc.contributor.author |
Pulkkanen, Kalevi |
|
dc.contributor.author |
Kautio, Anna-Liisa |
|
dc.contributor.author |
Huttunen, Teppo |
|
dc.date.accessioned |
2021-04-30T21:53:29Z |
|
dc.date.available |
2021-12-18T03:46:02Z |
|
dc.date.issued |
2020-12 |
|
dc.identifier.citation |
Kellokumpu-Lehtinen , P-L , Marttila , T , Jekunen , A , Hervonen , P , Klintrup , K , Kataja , V , Utriainen , T , Luukkaa , M , Leskinen , M , Pulkkanen , K , Kautio , A-L & Huttunen , T 2020 , ' Biweekly Cabazitaxel Is a Safe Treatment Option for Metastatic Castration-resistant Prostate Cancer (mCRPC) Patients After Docetaxel - A Final Analysis of the Prosty II Trial ' , Anticancer Research , vol. 40 , no. 12 , pp. 6915-6921 . https://doi.org/10.21873/anticanres.14715 |
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dc.identifier.other |
PURE: 160101843 |
|
dc.identifier.other |
PURE UUID: 5b83ea6e-7f36-47bf-a926-d96c77c1a054 |
|
dc.identifier.other |
WOS: 000599522300034 |
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dc.identifier.uri |
http://hdl.handle.net/10138/329571 |
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dc.description.abstract |
Background/Aim: Our phase III trial showed that biweekly docetaxel (D) is better tolerated than triweekly D in metastatic castration-resistant prostate cancer (mCRPC). The safety of biweekly cabazitaxel (CBZ) post-docetaxel was studied in mCRPC. Patients and Methods: Altogether, 60 patients received CBZ 16 mg/m2 i.v. on day 1 and day 14 of a 4-week cycle. The mean serum PSA levels were 305 ng/ml, and the mean age 67 years. The primary endpoint was safety according to CTCAEv4.0. Results: A total of 255 4-week cycles of CBZ were administered. The most common grade 3/4 adverse events were neutropenia (16.7%), pain (13.3%), fatigue (10.0%), anemia (5.0%) and non-neutropenic infection (10.0%). PSA responses occurred in 10 patients (16.7%). Clinical benefit rate was 38.3% and median survival 10 months. Conclusion: Biweekly CBZ is a well-tolerated treatment resulting in meaningful benefits for heavily pretreated mCRPC patients. |
en |
dc.format.extent |
7 |
|
dc.language.iso |
eng |
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dc.relation.ispartof |
Anticancer Research |
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dc.rights.uri |
info:eu-repo/semantics/openAccess |
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dc.subject |
mCRPC |
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dc.subject |
cabazitaxel |
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dc.subject |
postdocetaxel |
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dc.subject |
biweekly dosing |
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dc.subject |
MITOXANTRONE PLUS PREDNISONE |
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dc.subject |
INCREASED SURVIVAL |
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dc.subject |
PHASE-III |
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dc.subject |
THERAPY |
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dc.subject |
RECOMMENDATIONS |
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dc.subject |
ENZALUTAMIDE |
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dc.subject |
ABIRATERONE |
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dc.subject |
MANAGEMENT |
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dc.subject |
3122 Cancers |
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dc.title |
Biweekly Cabazitaxel Is a Safe Treatment Option for Metastatic Castration-resistant Prostate Cancer (mCRPC) Patients After Docetaxel - A Final Analysis of the Prosty II Trial |
en |
dc.type |
Article |
|
dc.contributor.organization |
HUS Comprehensive Cancer Center |
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dc.contributor.organization |
Department of Oncology |
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dc.description.reviewstatus |
Peer reviewed |
|
dc.relation.doi |
https://doi.org/10.21873/anticanres.14715 |
|
dc.relation.issn |
0250-7005 |
|
dc.rights.accesslevel |
openAccess |
|
dc.type.version |
publishedVersion |
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