Evidence map›Paper›PMID 39205559›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

High Expression of Vascular Endothelial Growth Factor, Ki-67, and Protein 53 are Risk Factors for Poor Response of Paclitaxel-Carboplatin Neoadjuvant Chemotherapy in Stadium IB3, IIA2, and IIB Cervical Cancer.

I Gde Sastra Winata, Fenyta Christyani

Abstract read
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Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

I Gde Sastra WinataDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Udayana, Prof. Dr. I.G.N.G. Ngoerah, Denpasar, Bali, Indonesia.
Fenyta ChristyaniDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Udayana, Prof. Dr. I.G.N.G. Ngoerah, Denpasar, Bali, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe therapeutic strategy for stage IB3, IIA2, and IIB cervical cancer is still controversial. The modalities are chemoradiation, radical hysterectomy surgery, or administration of neoadjuvant chemotherapy followed by radical hysterectomy. Response to chemotherapy is determined by tumor vascularization or angiogenesis, proliferative activity, and genetic instability of cervical cancer. The marker of tumor cell proliferation is the Ki-67 protein. In cervical cancer, the p53 gene is suppressed by human papillomavirus (HPV). The HPV E6 protein promotes the degradation of p53 thereby inhibiting stabilization and activation of p53. This study aimed to prove that high expression of VEGF, Ki-67, and p53 are risk factors for a poor response to neoadjuvant chemotherapy.

methodsThis was a case-control study that was conducted at the Department of Obstetrics and Gynecology in one tertiary hospital in Denpasar from October 2021 to April 2022. There were 56 samples included in this study, which were divided into two equal groups, namely good response and poor response to neoadjuvant chemotherapy. Data were analyzed using the software SPSS-24 including the Kolmogorov-Smirnov normality test, Chi-square, and multiple regression logistics. Data were presented in tables and described narratively.

resultsIt was found that the risk of a poor response to chemotherapy on the expression of VEGF VEGF, Ki-67, and p53 were 11.5, 15.0, and 8.33 times, respectively. We obtained a formula for calculating chemotherapy response, y = -7.3+ 1.6 VEGF + 1.6 Ki-67 + 1.8 p53. High VEGF, Ki-67, and p53 expressions were scored 1, and low expressions were scored 2. The limit value used is 0.05. The result y < 0.05 means the risk of poor response to chemotherapy and the value of y > 0.05 means good response.

conclusionThis formulation can be used as a parameter to assess the risk of poor response to neoadjuvant chemotherapy in stage IB3, IIA2, and IIB cervical cancer which can be applied in clinical practice in the treatment of cervical cancer.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarboplatinKi-67 AntigenNeoadjuvant TherapyPaclitaxelTumor Suppressor Protein p53Uterine Cervical NeoplasmsVascular Endothelial Growth Factor AAdultBiomarkers, TumorCase-Control StudiesFemaleFollow-Up StudiesHumansMiddle AgedNeoplasm StagingBiomarkers, TumorCarboplatinKi-67 AntigenPaclitaxelTP53 protein, humanTumor Suppressor Protein p53Vascular Endothelial Growth Factor AVEGFA protein, humanKeywords: Cervical cancerKi-67paclitaxel-carboplatinprotein 53Vascular Endothelial Growth Factor

Identifiers

PMID39205559
PMCPMC11495431

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.