Cargando…

Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia

BACKGROUND: Methotrexate (MTX) and actinomycin D (ActD) have been used as first-line chemotherapy agents in the treatment of low-risk gestational trophoblastic neoplasia (GTN). Although low-risk GTN is considered a curable disease, its reported primary remission rates of 49 to 93% reflect the diffic...

Descripción completa

Detalles Bibliográficos
Autores principales: Sheikhhasani, Shahrzad, Abdolrazaghnejad, Aghdas, Mousavi, Azam Sadat, Akhavan, Setareh, Zamani, Narges, Feizabad, Elham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878912/
https://www.ncbi.nlm.nih.gov/pubmed/36741497
http://dx.doi.org/10.22088/cjim.14.1.47
_version_ 1784878590274306048
author Sheikhhasani, Shahrzad
Abdolrazaghnejad, Aghdas
Mousavi, Azam Sadat
Akhavan, Setareh
Zamani, Narges
Feizabad, Elham
author_facet Sheikhhasani, Shahrzad
Abdolrazaghnejad, Aghdas
Mousavi, Azam Sadat
Akhavan, Setareh
Zamani, Narges
Feizabad, Elham
author_sort Sheikhhasani, Shahrzad
collection PubMed
description BACKGROUND: Methotrexate (MTX) and actinomycin D (ActD) have been used as first-line chemotherapy agents in the treatment of low-risk gestational trophoblastic neoplasia (GTN). Although low-risk GTN is considered a curable disease, its reported primary remission rates of 49 to 93% reflect the difficulties of treatment and different factors influencing it. Hence, this study aimed to determine the remission rates and related factors of single-agent chemotherapy resistance in low-risk GTN patients. METHODS: This retrospective study included patients with diagnosed low-risk GTN who received either MTX once a week (IM, 30mg/m2) or ActD once every two weeks (pulsed IV, 1.25mg/m2). Then, the patients were followed-up until complete remission or single-agent treatment failure to assess resistance rate and related factors. RESULTS: Eighty-four patients were included in the study (18 patients were receiving MTX and 66 patients were receiving ActD). 85.7% of all participants achieved complete remission after first-line chemotherapy (72.2% in MTX vs 89.4% in ActD). There was a significant association for higher tumor size (P=0.046), the occurrence of metastasis (P=0.019), and pretreatment β-HCG levels (P=0.005) with resistance to treatment. CONCLUSION: This study demonstrated higher tumor size, the occurrence of metastasis, and pretreatment β-HCG levels have been associated with increased resistance to first-line chemotherapy agents.
format Online
Article
Text
id pubmed-9878912
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Babol University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-98789122023-02-03 Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia Sheikhhasani, Shahrzad Abdolrazaghnejad, Aghdas Mousavi, Azam Sadat Akhavan, Setareh Zamani, Narges Feizabad, Elham Caspian J Intern Med Original Article BACKGROUND: Methotrexate (MTX) and actinomycin D (ActD) have been used as first-line chemotherapy agents in the treatment of low-risk gestational trophoblastic neoplasia (GTN). Although low-risk GTN is considered a curable disease, its reported primary remission rates of 49 to 93% reflect the difficulties of treatment and different factors influencing it. Hence, this study aimed to determine the remission rates and related factors of single-agent chemotherapy resistance in low-risk GTN patients. METHODS: This retrospective study included patients with diagnosed low-risk GTN who received either MTX once a week (IM, 30mg/m2) or ActD once every two weeks (pulsed IV, 1.25mg/m2). Then, the patients were followed-up until complete remission or single-agent treatment failure to assess resistance rate and related factors. RESULTS: Eighty-four patients were included in the study (18 patients were receiving MTX and 66 patients were receiving ActD). 85.7% of all participants achieved complete remission after first-line chemotherapy (72.2% in MTX vs 89.4% in ActD). There was a significant association for higher tumor size (P=0.046), the occurrence of metastasis (P=0.019), and pretreatment β-HCG levels (P=0.005) with resistance to treatment. CONCLUSION: This study demonstrated higher tumor size, the occurrence of metastasis, and pretreatment β-HCG levels have been associated with increased resistance to first-line chemotherapy agents. Babol University of Medical Sciences 2023 /pmc/articles/PMC9878912/ /pubmed/36741497 http://dx.doi.org/10.22088/cjim.14.1.47 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sheikhhasani, Shahrzad
Abdolrazaghnejad, Aghdas
Mousavi, Azam Sadat
Akhavan, Setareh
Zamani, Narges
Feizabad, Elham
Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
title Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
title_full Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
title_fullStr Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
title_full_unstemmed Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
title_short Resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
title_sort resistance to single-agent chemotherapy in low-risk gestational trophoblastic neoplasia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878912/
https://www.ncbi.nlm.nih.gov/pubmed/36741497
http://dx.doi.org/10.22088/cjim.14.1.47
work_keys_str_mv AT sheikhhasanishahrzad resistancetosingleagentchemotherapyinlowriskgestationaltrophoblasticneoplasia
AT abdolrazaghnejadaghdas resistancetosingleagentchemotherapyinlowriskgestationaltrophoblasticneoplasia
AT mousaviazamsadat resistancetosingleagentchemotherapyinlowriskgestationaltrophoblasticneoplasia
AT akhavansetareh resistancetosingleagentchemotherapyinlowriskgestationaltrophoblasticneoplasia
AT zamaninarges resistancetosingleagentchemotherapyinlowriskgestationaltrophoblasticneoplasia
AT feizabadelham resistancetosingleagentchemotherapyinlowriskgestationaltrophoblasticneoplasia