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Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study

BACKGROUND: Based primarily on studies concerning early-stage tumours (treated surgically), and locally advanced disease (treated with chemoradiation), the prognosis for women with adenocarcinoma (AC) or adenosquamous (AS) carcinoma has been reported to be poorer than those with squamous cell carcin...

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Autores principales: Seamon, Leigh G, Java, James J, Monk, Bradley J, Penson, Richard T, Brown, Jubilee, Mannel, Robert S, Oaknin, Anna, Leitao, Mario M, Eisenhauer, Eric L, Long, Harry J, Liao, Shu Y, Tewari, Krishnansu S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785748/
https://www.ncbi.nlm.nih.gov/pubmed/29182608
http://dx.doi.org/10.1038/bjc.2017.400
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author Seamon, Leigh G
Java, James J
Monk, Bradley J
Penson, Richard T
Brown, Jubilee
Mannel, Robert S
Oaknin, Anna
Leitao, Mario M
Eisenhauer, Eric L
Long, Harry J
Liao, Shu Y
Tewari, Krishnansu S
author_facet Seamon, Leigh G
Java, James J
Monk, Bradley J
Penson, Richard T
Brown, Jubilee
Mannel, Robert S
Oaknin, Anna
Leitao, Mario M
Eisenhauer, Eric L
Long, Harry J
Liao, Shu Y
Tewari, Krishnansu S
author_sort Seamon, Leigh G
collection PubMed
description BACKGROUND: Based primarily on studies concerning early-stage tumours (treated surgically), and locally advanced disease (treated with chemoradiation), the prognosis for women with adenocarcinoma (AC) or adenosquamous (AS) carcinoma has been reported to be poorer than those with squamous cell carcinoma (SCCA) of the cervix. It is unclear whether differences in prognosis also persist in the setting of recurrent or metastatic disease treated using chemotherapy doublets with or without bevacizumab. METHODS: Cases were pooled from three Gynaecologic Oncology Group randomised phase III trials of chemotherapy doublets. Pearson’s test was used to evaluate response rate (RR) of AC/AS vs SCCA, Kaplan–Meier method to estimate progression-free survival (PFS) and overall survival (OS), and Cox proportional hazards model to estimate the impact of histology on PFS and OS. RESULTS: Of 781 evaluable patients, 77% (N=599) had SCCA and 23% (N=182) AC/AS. There were no significant differences in RRs between histologic subgroups. The adjusted hazard ratio (HR) for death for SCCA vs AC/AS was 1.13 (95% CI 0.93, 1.38 P=0.23). When comparing SC/AS (N=661, 85%) to AC alone (N=120, 15%), the adjusted HR for death was 1.23 (95% CI 0.97, 1.57, P=0.09). CONCLUSIONS: AC/AS and SCCA have similar survival in recurrent or metastatic cervical carcinoma when treated with chemotherapy doublets.
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spelling pubmed-57857482019-01-01 Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study Seamon, Leigh G Java, James J Monk, Bradley J Penson, Richard T Brown, Jubilee Mannel, Robert S Oaknin, Anna Leitao, Mario M Eisenhauer, Eric L Long, Harry J Liao, Shu Y Tewari, Krishnansu S Br J Cancer Clinical Study BACKGROUND: Based primarily on studies concerning early-stage tumours (treated surgically), and locally advanced disease (treated with chemoradiation), the prognosis for women with adenocarcinoma (AC) or adenosquamous (AS) carcinoma has been reported to be poorer than those with squamous cell carcinoma (SCCA) of the cervix. It is unclear whether differences in prognosis also persist in the setting of recurrent or metastatic disease treated using chemotherapy doublets with or without bevacizumab. METHODS: Cases were pooled from three Gynaecologic Oncology Group randomised phase III trials of chemotherapy doublets. Pearson’s test was used to evaluate response rate (RR) of AC/AS vs SCCA, Kaplan–Meier method to estimate progression-free survival (PFS) and overall survival (OS), and Cox proportional hazards model to estimate the impact of histology on PFS and OS. RESULTS: Of 781 evaluable patients, 77% (N=599) had SCCA and 23% (N=182) AC/AS. There were no significant differences in RRs between histologic subgroups. The adjusted hazard ratio (HR) for death for SCCA vs AC/AS was 1.13 (95% CI 0.93, 1.38 P=0.23). When comparing SC/AS (N=661, 85%) to AC alone (N=120, 15%), the adjusted HR for death was 1.23 (95% CI 0.97, 1.57, P=0.09). CONCLUSIONS: AC/AS and SCCA have similar survival in recurrent or metastatic cervical carcinoma when treated with chemotherapy doublets. Nature Publishing Group 2018-01 2017-11-28 /pmc/articles/PMC5785748/ /pubmed/29182608 http://dx.doi.org/10.1038/bjc.2017.400 Text en Copyright © 2018 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Seamon, Leigh G
Java, James J
Monk, Bradley J
Penson, Richard T
Brown, Jubilee
Mannel, Robert S
Oaknin, Anna
Leitao, Mario M
Eisenhauer, Eric L
Long, Harry J
Liao, Shu Y
Tewari, Krishnansu S
Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study
title Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study
title_full Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study
title_fullStr Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study
title_full_unstemmed Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study
title_short Impact of tumour histology on survival in advanced cervical carcinoma: an NRG Oncology/Gynaecologic Oncology Group Study
title_sort impact of tumour histology on survival in advanced cervical carcinoma: an nrg oncology/gynaecologic oncology group study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785748/
https://www.ncbi.nlm.nih.gov/pubmed/29182608
http://dx.doi.org/10.1038/bjc.2017.400
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