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Interferon-α-based Immunotherapy in Metastatic Renal Cell Carcinoma Patients with the Primary Tumor In Situ

Objective We reviewed the outcomes of metastatic renal cell carcinoma patients with the primary tumor in situ who initially underwent interferon-α-based immunotherapy to evaluate the effect of this therapy on metastatic sites as well as primary kidney tumor and survival. Methods Thirty-one patients,...

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Published in:Japanese journal of clinical oncology 2012-02, Vol.42 (2), p.113-119
Main Authors: Shinohara, Nobuo, Abe, Takashige, Sazawa, Ataru, Maruyama, Satoru, Shindo, Junri, Sato, Soshu, Suzuki, Shin, Nonomura, Katsuya
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container_issue 2
container_start_page 113
container_title Japanese journal of clinical oncology
container_volume 42
creator Shinohara, Nobuo
Abe, Takashige
Sazawa, Ataru
Maruyama, Satoru
Shindo, Junri
Sato, Soshu
Suzuki, Shin
Nonomura, Katsuya
description Objective We reviewed the outcomes of metastatic renal cell carcinoma patients with the primary tumor in situ who initially underwent interferon-α-based immunotherapy to evaluate the effect of this therapy on metastatic sites as well as primary kidney tumor and survival. Methods Thirty-one patients, for whom upfront cytoreductive nephrectomy was considered to be inappropriate because of poor performance status and far-advanced disease, were the subject of the present study. Tumor response and reduction in the size of metastatic sites and primary kidney tumor were assessed. Overall survival distributions were estimated using the Kaplan-Meier method with the significance determined using the log-rank test. Results Partial response was observed in 11 patients, yielding an overall response rate of 35%. Seventeen patients had regression or stabilization of metastatic sites, while progression of metastatic sites was observed in the remaining 14 patients. Regarding the maximum response of primary kidney tumor, a reduction in kidney primary tumor size was observed in 42% of the patients and the mean reduction rate in these patients was 18.2% (range: 3-36%). Furthermore, the reduction in the size of metastatic sites was significantly associated with that in the size of primary kidney tumor (R 2= 0.432, P< 0.0001). The median survival for the 31 patients was 17 months. The median survival was 42 months in patients with regression or stabilization of metastatic sites and 7 months in those without (P< 0.001). Conclusions The present study suggests that metastatic sites as well as primary kidney tumor respond to interferon-α-based immunotherapy in metastatic renal cell carcinoma patients with primary tumor in situ.
doi_str_mv 10.1093/jjco/hyr176
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Methods Thirty-one patients, for whom upfront cytoreductive nephrectomy was considered to be inappropriate because of poor performance status and far-advanced disease, were the subject of the present study. Tumor response and reduction in the size of metastatic sites and primary kidney tumor were assessed. Overall survival distributions were estimated using the Kaplan-Meier method with the significance determined using the log-rank test. Results Partial response was observed in 11 patients, yielding an overall response rate of 35%. Seventeen patients had regression or stabilization of metastatic sites, while progression of metastatic sites was observed in the remaining 14 patients. Regarding the maximum response of primary kidney tumor, a reduction in kidney primary tumor size was observed in 42% of the patients and the mean reduction rate in these patients was 18.2% (range: 3-36%). Furthermore, the reduction in the size of metastatic sites was significantly associated with that in the size of primary kidney tumor (R 2= 0.432, P&lt; 0.0001). The median survival for the 31 patients was 17 months. The median survival was 42 months in patients with regression or stabilization of metastatic sites and 7 months in those without (P&lt; 0.001). Conclusions The present study suggests that metastatic sites as well as primary kidney tumor respond to interferon-α-based immunotherapy in metastatic renal cell carcinoma patients with primary tumor in situ.</description><identifier>ISSN: 0368-2811</identifier><identifier>EISSN: 1465-3621</identifier><identifier>DOI: 10.1093/jjco/hyr176</identifier><identifier>PMID: 22131341</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Carcinoma in Situ - drug therapy ; Carcinoma in Situ - immunology ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - immunology ; Carcinoma, Renal Cell - pathology ; Carcinoma, Renal Cell - surgery ; Chemotherapy, Adjuvant ; Cimetidine - administration &amp; dosage ; Dexamethasone - administration &amp; dosage ; Female ; Humans ; Immunotherapy - methods ; Interferon-alpha - immunology ; Interferon-alpha - therapeutic use ; Kaplan-Meier Estimate ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - immunology ; Kidney Neoplasms - pathology ; Kidney Neoplasms - surgery ; Male ; Middle Aged ; Neoadjuvant Therapy - methods ; Nephrectomy ; Thiazines - administration &amp; dosage ; Thiazoles - administration &amp; dosage ; Treatment Outcome</subject><ispartof>Japanese journal of clinical oncology, 2012-02, Vol.42 (2), p.113-119</ispartof><rights>The Author 2011. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22131341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shinohara, Nobuo</creatorcontrib><creatorcontrib>Abe, Takashige</creatorcontrib><creatorcontrib>Sazawa, Ataru</creatorcontrib><creatorcontrib>Maruyama, Satoru</creatorcontrib><creatorcontrib>Shindo, Junri</creatorcontrib><creatorcontrib>Sato, Soshu</creatorcontrib><creatorcontrib>Suzuki, Shin</creatorcontrib><creatorcontrib>Nonomura, Katsuya</creatorcontrib><title>Interferon-α-based Immunotherapy in Metastatic Renal Cell Carcinoma Patients with the Primary Tumor In Situ</title><title>Japanese journal of clinical oncology</title><addtitle>Jpn J Clin Oncol</addtitle><description>Objective We reviewed the outcomes of metastatic renal cell carcinoma patients with the primary tumor in situ who initially underwent interferon-α-based immunotherapy to evaluate the effect of this therapy on metastatic sites as well as primary kidney tumor and survival. Methods Thirty-one patients, for whom upfront cytoreductive nephrectomy was considered to be inappropriate because of poor performance status and far-advanced disease, were the subject of the present study. Tumor response and reduction in the size of metastatic sites and primary kidney tumor were assessed. Overall survival distributions were estimated using the Kaplan-Meier method with the significance determined using the log-rank test. Results Partial response was observed in 11 patients, yielding an overall response rate of 35%. Seventeen patients had regression or stabilization of metastatic sites, while progression of metastatic sites was observed in the remaining 14 patients. Regarding the maximum response of primary kidney tumor, a reduction in kidney primary tumor size was observed in 42% of the patients and the mean reduction rate in these patients was 18.2% (range: 3-36%). Furthermore, the reduction in the size of metastatic sites was significantly associated with that in the size of primary kidney tumor (R 2= 0.432, P&lt; 0.0001). The median survival for the 31 patients was 17 months. The median survival was 42 months in patients with regression or stabilization of metastatic sites and 7 months in those without (P&lt; 0.001). Conclusions The present study suggests that metastatic sites as well as primary kidney tumor respond to interferon-α-based immunotherapy in metastatic renal cell carcinoma patients with primary tumor in situ.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Carcinoma in Situ - drug therapy</subject><subject>Carcinoma in Situ - immunology</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - immunology</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Carcinoma, Renal Cell - surgery</subject><subject>Chemotherapy, Adjuvant</subject><subject>Cimetidine - administration &amp; dosage</subject><subject>Dexamethasone - administration &amp; dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Immunotherapy - methods</subject><subject>Interferon-alpha - immunology</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Kaplan-Meier Estimate</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - immunology</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidney Neoplasms - surgery</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy - methods</subject><subject>Nephrectomy</subject><subject>Thiazines - administration &amp; 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dosage</topic><topic>Thiazoles - administration &amp; dosage</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shinohara, Nobuo</creatorcontrib><creatorcontrib>Abe, Takashige</creatorcontrib><creatorcontrib>Sazawa, Ataru</creatorcontrib><creatorcontrib>Maruyama, Satoru</creatorcontrib><creatorcontrib>Shindo, Junri</creatorcontrib><creatorcontrib>Sato, Soshu</creatorcontrib><creatorcontrib>Suzuki, Shin</creatorcontrib><creatorcontrib>Nonomura, Katsuya</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shinohara, Nobuo</au><au>Abe, Takashige</au><au>Sazawa, Ataru</au><au>Maruyama, Satoru</au><au>Shindo, Junri</au><au>Sato, Soshu</au><au>Suzuki, Shin</au><au>Nonomura, Katsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interferon-α-based Immunotherapy in Metastatic Renal Cell Carcinoma Patients with the Primary Tumor In Situ</atitle><jtitle>Japanese journal of clinical oncology</jtitle><addtitle>Jpn J Clin Oncol</addtitle><date>2012-02</date><risdate>2012</risdate><volume>42</volume><issue>2</issue><spage>113</spage><epage>119</epage><pages>113-119</pages><issn>0368-2811</issn><eissn>1465-3621</eissn><abstract>Objective We reviewed the outcomes of metastatic renal cell carcinoma patients with the primary tumor in situ who initially underwent interferon-α-based immunotherapy to evaluate the effect of this therapy on metastatic sites as well as primary kidney tumor and survival. Methods Thirty-one patients, for whom upfront cytoreductive nephrectomy was considered to be inappropriate because of poor performance status and far-advanced disease, were the subject of the present study. Tumor response and reduction in the size of metastatic sites and primary kidney tumor were assessed. Overall survival distributions were estimated using the Kaplan-Meier method with the significance determined using the log-rank test. Results Partial response was observed in 11 patients, yielding an overall response rate of 35%. Seventeen patients had regression or stabilization of metastatic sites, while progression of metastatic sites was observed in the remaining 14 patients. Regarding the maximum response of primary kidney tumor, a reduction in kidney primary tumor size was observed in 42% of the patients and the mean reduction rate in these patients was 18.2% (range: 3-36%). Furthermore, the reduction in the size of metastatic sites was significantly associated with that in the size of primary kidney tumor (R 2= 0.432, P&lt; 0.0001). The median survival for the 31 patients was 17 months. The median survival was 42 months in patients with regression or stabilization of metastatic sites and 7 months in those without (P&lt; 0.001). Conclusions The present study suggests that metastatic sites as well as primary kidney tumor respond to interferon-α-based immunotherapy in metastatic renal cell carcinoma patients with primary tumor in situ.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>22131341</pmid><doi>10.1093/jjco/hyr176</doi><tpages>7</tpages></addata></record>
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source Oxford Journals Online
subjects Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Carcinoma in Situ - drug therapy
Carcinoma in Situ - immunology
Carcinoma, Renal Cell - drug therapy
Carcinoma, Renal Cell - immunology
Carcinoma, Renal Cell - pathology
Carcinoma, Renal Cell - surgery
Chemotherapy, Adjuvant
Cimetidine - administration & dosage
Dexamethasone - administration & dosage
Female
Humans
Immunotherapy - methods
Interferon-alpha - immunology
Interferon-alpha - therapeutic use
Kaplan-Meier Estimate
Kidney Neoplasms - drug therapy
Kidney Neoplasms - immunology
Kidney Neoplasms - pathology
Kidney Neoplasms - surgery
Male
Middle Aged
Neoadjuvant Therapy - methods
Nephrectomy
Thiazines - administration & dosage
Thiazoles - administration & dosage
Treatment Outcome
title Interferon-α-based Immunotherapy in Metastatic Renal Cell Carcinoma Patients with the Primary Tumor In Situ
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