Salvage combined chemotherapy with paclitaxel, ifosfamide and nedaplatin for patients with advanced germ cell tumors

Objectives To investigate the efficacy of combined regimen with paclitaxel, ifosfamide and nedaplatin as salvage chemotherapy in patients with cisplatin‐refractory or multiple relapsed germ cell tumors. Methods A total of 65 patients refractory to cisplatin‐based chemotherapy or with relapse after i...

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Veröffentlicht in:International journal of urology 2015-03, Vol.22 (3), p.288-293
Hauptverfasser: Nakamura, Terukazu, Ueda, Takashi, Oishi, Masakatsu, Nakanishi, Hiroyuki, Fujihara, Atsuko, Naya, Yoshio, Hongo, Fumiya, Kamoi, Kazumi, Okihara, Koji, Miki, Tsuneharu
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container_end_page 293
container_issue 3
container_start_page 288
container_title International journal of urology
container_volume 22
creator Nakamura, Terukazu
Ueda, Takashi
Oishi, Masakatsu
Nakanishi, Hiroyuki
Fujihara, Atsuko
Naya, Yoshio
Hongo, Fumiya
Kamoi, Kazumi
Okihara, Koji
Miki, Tsuneharu
description Objectives To investigate the efficacy of combined regimen with paclitaxel, ifosfamide and nedaplatin as salvage chemotherapy in patients with cisplatin‐refractory or multiple relapsed germ cell tumors. Methods A total of 65 patients refractory to cisplatin‐based chemotherapy or with relapse after induction or salvage chemotherapy received paclitaxel 210 mg/m2 on day 1, ifosfamide 1.2 g/m2 on days 2–6 and nedaplatin 100 mg/m2 on day 2 of a 3‐week cycle. The primary and secondary end‐points were the response rate and overall survival, respectively. Results Paclitaxel, ifosfamide and nedaplatin therapy was carried out as second‐line therapy in 17 patients, third‐line in 31 and fourth‐line or later in 17. Patients were pretreated with a median of six cycles of platinum‐based chemotherapy (range 3–15 cycles). The overall response rate was 62.9%, including one patient with complete response and 38 with partial response. Serum tumor marker levels normalized in 35 (56.5%) patients. Overall survival at a median follow up of 34 months was 59.3%, and median time to progression was 12 months. Multivariate analysis showed that serum tumor marker normalization was the only independent predictor of better progression‐free survival and overall survival. Grade 3/4 of neutropenia, anemia and thrombocytopenia was observed in 96.9%, in 81.5%, and in 90.8% of patients, respectively. Conclusion Paclitaxel, ifosfamide and nedaplatin chemotherapy appears to be effective when used as first or second salvage treatment in advanced relapsed germ cell tumors. Even after fourth‐line therapy, patients with serum tumor marker normalization might have a chance for a cure.
doi_str_mv 10.1111/iju.12665
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Methods A total of 65 patients refractory to cisplatin‐based chemotherapy or with relapse after induction or salvage chemotherapy received paclitaxel 210 mg/m2 on day 1, ifosfamide 1.2 g/m2 on days 2–6 and nedaplatin 100 mg/m2 on day 2 of a 3‐week cycle. The primary and secondary end‐points were the response rate and overall survival, respectively. Results Paclitaxel, ifosfamide and nedaplatin therapy was carried out as second‐line therapy in 17 patients, third‐line in 31 and fourth‐line or later in 17. Patients were pretreated with a median of six cycles of platinum‐based chemotherapy (range 3–15 cycles). The overall response rate was 62.9%, including one patient with complete response and 38 with partial response. Serum tumor marker levels normalized in 35 (56.5%) patients. Overall survival at a median follow up of 34 months was 59.3%, and median time to progression was 12 months. Multivariate analysis showed that serum tumor marker normalization was the only independent predictor of better progression‐free survival and overall survival. Grade 3/4 of neutropenia, anemia and thrombocytopenia was observed in 96.9%, in 81.5%, and in 90.8% of patients, respectively. Conclusion Paclitaxel, ifosfamide and nedaplatin chemotherapy appears to be effective when used as first or second salvage treatment in advanced relapsed germ cell tumors. 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Methods A total of 65 patients refractory to cisplatin‐based chemotherapy or with relapse after induction or salvage chemotherapy received paclitaxel 210 mg/m2 on day 1, ifosfamide 1.2 g/m2 on days 2–6 and nedaplatin 100 mg/m2 on day 2 of a 3‐week cycle. The primary and secondary end‐points were the response rate and overall survival, respectively. Results Paclitaxel, ifosfamide and nedaplatin therapy was carried out as second‐line therapy in 17 patients, third‐line in 31 and fourth‐line or later in 17. Patients were pretreated with a median of six cycles of platinum‐based chemotherapy (range 3–15 cycles). The overall response rate was 62.9%, including one patient with complete response and 38 with partial response. Serum tumor marker levels normalized in 35 (56.5%) patients. Overall survival at a median follow up of 34 months was 59.3%, and median time to progression was 12 months. Multivariate analysis showed that serum tumor marker normalization was the only independent predictor of better progression‐free survival and overall survival. Grade 3/4 of neutropenia, anemia and thrombocytopenia was observed in 96.9%, in 81.5%, and in 90.8% of patients, respectively. Conclusion Paclitaxel, ifosfamide and nedaplatin chemotherapy appears to be effective when used as first or second salvage treatment in advanced relapsed germ cell tumors. Even after fourth‐line therapy, patients with serum tumor marker normalization might have a chance for a cure.</description><subject>Adolescent</subject><subject>Adult</subject><subject>advanced germ cell tumors</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cisplatin - therapeutic use</subject><subject>Disease-Free Survival</subject><subject>Drug Administration Schedule</subject><subject>Drug Resistance, Neoplasm</subject><subject>Humans</subject><subject>ifosfamide</subject><subject>Ifosfamide - administration &amp; dosage</subject><subject>Ifosfamide - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>nedaplatin</subject><subject>Neoplasm Recurrence, Local - drug therapy</subject><subject>Neoplasms, Germ Cell and Embryonal - drug therapy</subject><subject>Organoplatinum Compounds - administration &amp; dosage</subject><subject>Organoplatinum Compounds - therapeutic use</subject><subject>paclitaxel</subject><subject>Paclitaxel - administration &amp; 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Ueda, Takashi ; Oishi, Masakatsu ; Nakanishi, Hiroyuki ; Fujihara, Atsuko ; Naya, Yoshio ; Hongo, Fumiya ; Kamoi, Kazumi ; Okihara, Koji ; Miki, Tsuneharu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3875-92e7ff416f657ce9bf0e2ece9311605e76a9447dad55a51d95bdc982dc0277233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>advanced germ cell tumors</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Cisplatin - therapeutic use</topic><topic>Disease-Free Survival</topic><topic>Drug Administration Schedule</topic><topic>Drug Resistance, Neoplasm</topic><topic>Humans</topic><topic>ifosfamide</topic><topic>Ifosfamide - administration &amp; dosage</topic><topic>Ifosfamide - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>nedaplatin</topic><topic>Neoplasm Recurrence, Local - drug therapy</topic><topic>Neoplasms, Germ Cell and Embryonal - drug therapy</topic><topic>Organoplatinum Compounds - administration &amp; dosage</topic><topic>Organoplatinum Compounds - therapeutic use</topic><topic>paclitaxel</topic><topic>Paclitaxel - administration &amp; dosage</topic><topic>Paclitaxel - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Salvage Therapy - methods</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakamura, Terukazu</creatorcontrib><creatorcontrib>Ueda, Takashi</creatorcontrib><creatorcontrib>Oishi, Masakatsu</creatorcontrib><creatorcontrib>Nakanishi, Hiroyuki</creatorcontrib><creatorcontrib>Fujihara, Atsuko</creatorcontrib><creatorcontrib>Naya, Yoshio</creatorcontrib><creatorcontrib>Hongo, Fumiya</creatorcontrib><creatorcontrib>Kamoi, Kazumi</creatorcontrib><creatorcontrib>Okihara, Koji</creatorcontrib><creatorcontrib>Miki, Tsuneharu</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakamura, Terukazu</au><au>Ueda, Takashi</au><au>Oishi, Masakatsu</au><au>Nakanishi, Hiroyuki</au><au>Fujihara, Atsuko</au><au>Naya, Yoshio</au><au>Hongo, Fumiya</au><au>Kamoi, Kazumi</au><au>Okihara, Koji</au><au>Miki, Tsuneharu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salvage combined chemotherapy with paclitaxel, ifosfamide and nedaplatin for patients with advanced germ cell tumors</atitle><jtitle>International journal of urology</jtitle><addtitle>Int J Urol</addtitle><date>2015-03</date><risdate>2015</risdate><volume>22</volume><issue>3</issue><spage>288</spage><epage>293</epage><pages>288-293</pages><issn>0919-8172</issn><eissn>1442-2042</eissn><abstract>Objectives To investigate the efficacy of combined regimen with paclitaxel, ifosfamide and nedaplatin as salvage chemotherapy in patients with cisplatin‐refractory or multiple relapsed germ cell tumors. Methods A total of 65 patients refractory to cisplatin‐based chemotherapy or with relapse after induction or salvage chemotherapy received paclitaxel 210 mg/m2 on day 1, ifosfamide 1.2 g/m2 on days 2–6 and nedaplatin 100 mg/m2 on day 2 of a 3‐week cycle. The primary and secondary end‐points were the response rate and overall survival, respectively. Results Paclitaxel, ifosfamide and nedaplatin therapy was carried out as second‐line therapy in 17 patients, third‐line in 31 and fourth‐line or later in 17. Patients were pretreated with a median of six cycles of platinum‐based chemotherapy (range 3–15 cycles). The overall response rate was 62.9%, including one patient with complete response and 38 with partial response. Serum tumor marker levels normalized in 35 (56.5%) patients. Overall survival at a median follow up of 34 months was 59.3%, and median time to progression was 12 months. Multivariate analysis showed that serum tumor marker normalization was the only independent predictor of better progression‐free survival and overall survival. Grade 3/4 of neutropenia, anemia and thrombocytopenia was observed in 96.9%, in 81.5%, and in 90.8% of patients, respectively. Conclusion Paclitaxel, ifosfamide and nedaplatin chemotherapy appears to be effective when used as first or second salvage treatment in advanced relapsed germ cell tumors. Even after fourth‐line therapy, patients with serum tumor marker normalization might have a chance for a cure.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>25393104</pmid><doi>10.1111/iju.12665</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
Adult
advanced germ cell tumors
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Cisplatin - therapeutic use
Disease-Free Survival
Drug Administration Schedule
Drug Resistance, Neoplasm
Humans
ifosfamide
Ifosfamide - administration & dosage
Ifosfamide - therapeutic use
Male
Middle Aged
Multivariate Analysis
nedaplatin
Neoplasm Recurrence, Local - drug therapy
Neoplasms, Germ Cell and Embryonal - drug therapy
Organoplatinum Compounds - administration & dosage
Organoplatinum Compounds - therapeutic use
paclitaxel
Paclitaxel - administration & dosage
Paclitaxel - therapeutic use
Retrospective Studies
Salvage Therapy - methods
Treatment Outcome
Young Adult
title Salvage combined chemotherapy with paclitaxel, ifosfamide and nedaplatin for patients with advanced germ cell tumors
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