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Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer
The relationship between clinical response to DNA‐damaging drugs and p53 and p21 status in patients with locally advanced transitional cell carcinoma (TCC) of the bladder was assessed. The response to intraarterial chemotherapy (IAC) comprising 100 mg/m(2) of cisplatin (CDDP) and 40 mg/m(2) of pirar...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926463/ https://www.ncbi.nlm.nih.gov/pubmed/10804290 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00961.x |
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author | Koga, Fumitaka Kitahara, Satoshi Arai, Kyoko Honda, Mikihiko Sumi, Shuhei Yoshida, Ken‐ichiro |
author_facet | Koga, Fumitaka Kitahara, Satoshi Arai, Kyoko Honda, Mikihiko Sumi, Shuhei Yoshida, Ken‐ichiro |
author_sort | Koga, Fumitaka |
collection | PubMed |
description | The relationship between clinical response to DNA‐damaging drugs and p53 and p21 status in patients with locally advanced transitional cell carcinoma (TCC) of the bladder was assessed. The response to intraarterial chemotherapy (IAC) comprising 100 mg/m(2) of cisplatin (CDDP) and 40 mg/m(2) of pirarubicin (THP) and the prognosis were assessed in 23 patients (the mean follow‐up period was 19 months). The p53 gene status of tumors was analyzed at exons 5–8 using polymerase chain reaction‐single strand conformation polymorphism analysis in 19 patients, and paraffinembedded tumor sections were immunostained for p(53) and p(21) in 23 patients. The overall objective response rate (incidence of good responders) was 70%. The negative p53 group (n=17) showed a significantly higher objective response rate than the positive p53 group (n=6) (82% vs. 33%; P=0.045). The p53 gene status or p21 staining status was not significantly associated with responsiveness. When the p53 and p21 immunostaining results were combined, good responders were more accurately predicted than by p53 staining status alone; the negative p53/positive p21 group (n=12) showed an objective response rate of 92%, which was significantly higher than that of the positive p53 and/or negative p21 group (45%, n=11) (P=0.027). Cause‐specific survival of the negative p53 group was significantly superior to that of the positive p53 group (P=0.015). Negative p53/positive p21 immunostaining is a possible predictor of favorable chemotherapeutic response in patients with TCC of the bladder. |
format | Online Article Text |
id | pubmed-5926463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59264632018-05-11 Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer Koga, Fumitaka Kitahara, Satoshi Arai, Kyoko Honda, Mikihiko Sumi, Shuhei Yoshida, Ken‐ichiro Jpn J Cancer Res Article The relationship between clinical response to DNA‐damaging drugs and p53 and p21 status in patients with locally advanced transitional cell carcinoma (TCC) of the bladder was assessed. The response to intraarterial chemotherapy (IAC) comprising 100 mg/m(2) of cisplatin (CDDP) and 40 mg/m(2) of pirarubicin (THP) and the prognosis were assessed in 23 patients (the mean follow‐up period was 19 months). The p53 gene status of tumors was analyzed at exons 5–8 using polymerase chain reaction‐single strand conformation polymorphism analysis in 19 patients, and paraffinembedded tumor sections were immunostained for p(53) and p(21) in 23 patients. The overall objective response rate (incidence of good responders) was 70%. The negative p53 group (n=17) showed a significantly higher objective response rate than the positive p53 group (n=6) (82% vs. 33%; P=0.045). The p53 gene status or p21 staining status was not significantly associated with responsiveness. When the p53 and p21 immunostaining results were combined, good responders were more accurately predicted than by p53 staining status alone; the negative p53/positive p21 group (n=12) showed an objective response rate of 92%, which was significantly higher than that of the positive p53 and/or negative p21 group (45%, n=11) (P=0.027). Cause‐specific survival of the negative p53 group was significantly superior to that of the positive p53 group (P=0.015). Negative p53/positive p21 immunostaining is a possible predictor of favorable chemotherapeutic response in patients with TCC of the bladder. Blackwell Publishing Ltd 2000-04 /pmc/articles/PMC5926463/ /pubmed/10804290 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00961.x Text en |
spellingShingle | Article Koga, Fumitaka Kitahara, Satoshi Arai, Kyoko Honda, Mikihiko Sumi, Shuhei Yoshida, Ken‐ichiro Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer |
title | Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer |
title_full | Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer |
title_fullStr | Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer |
title_full_unstemmed | Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer |
title_short | Negative p53/Positive p21 Immunostaining Is a Predictor of Favorable Response to Chemotherapy in Patients with Locally Advanced Bladder Cancer |
title_sort | negative p53/positive p21 immunostaining is a predictor of favorable response to chemotherapy in patients with locally advanced bladder cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926463/ https://www.ncbi.nlm.nih.gov/pubmed/10804290 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00961.x |
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