EKSPRESI P-GLYCOPROTEIN, NUCLEAR FACTOR KAPPA B, DAN PROPORSI SEL PUNCA KANKER ALDH1-POSITIF SEBAGAI PREDIKTOR KEMORESISTENSI
Introduction Locally advanced breast cancer is still a health problem, either in developed or developing countries. The role of neoadjuvant chemotherapy has been well known, but there was still nonoptimal response due to chemoresistance mechanism. Range of mechanisms involved in chemoresistance incl...
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Main Authors: | , |
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Format: | Theses and Dissertations NonPeerReviewed |
Published: |
[Yogyakarta] : Universitas Gadjah Mada
2013
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Subjects: | |
Online Access: | https://repository.ugm.ac.id/122724/ http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=62828 |
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Institution: | Universitas Gadjah Mada |
Summary: | Introduction
Locally advanced breast cancer is still a health problem, either in developed or
developing countries. The role of neoadjuvant chemotherapy has been well
known, but there was still nonoptimal response due to chemoresistance
mechanism. Range of mechanisms involved in chemoresistance included
overexpression of ATP binding cassette (ABC) transporter, apoptosis
dysregulation, and possibly the excessive number of cancer stem cells.
Chemoresistance process might involve more than one mechanism mentioned.
Objective
This study aimed to reveal the effect of P-glycoprotein, NF-κB, and ALDH1
expression simultaneously towards pathological response after administration of
neoadjuvant chemotherapy FAC regiment, towards recurrence and survival, as
well as if it correlates with other predictive/ prognostic factors.
Material and methods
This was a kohort study. Advanced local stage invasive ductal breast cancer
patients were administered with neoadjuvant chemotherapy regiment FAC
(Fluorouracil 500 mg/m2-Doxorubicin 50 mg/m2-Cyclophosphamide 500 mg/m2
on the first day of each three-week cycle) in 2008-2011. From incisional biopsy
paraffin blocks, the histological grade, nuclear grade, lymphovascular invasion,
expression of estrogen, progesterone, HER-2/neu, and KI-67 receptors were
examined. Then further immunohistochemical examination for P-glycoprotein,
NF-κB, and cancer stem cells ALDH1-positive intratumoral expressions were
conducted. From mastectomy paraffin blocks, the pathologic response was also
examined. Furthermore, they were followed until the outcome emerged, that is the
recurrence and mortality rate until December 2012. Research description was
presented in tables and graphics. Chi square method was used for bivariate
analysis, and Kaplan-Meier (log rank test) method was used for survival analysis
with a significance level of p <0.05. Binary Logistic Regression was used for multivariat analysis for pathological response, whereas for the recurrence and
survival outcome, Proportional Hazards (Cox) Regression was used.
Results
It was suggested that from 131 locally advanced invasive ductal breast carcinoma
patients, mainly in the premenopausal age / <50 years (55%), mostly came with
primary status cT4 (55%), and the lymph nodes status cN1 (56.5%). Molecular
subtypes of triple-negative was the most widely found (38.2%). After neoadjuvant
chemotherapy regiment FAC, 87% of patients achieved clinical partial response
(cPR) and whilst 88.5% achieved objective response (complete and partial
response). Pathological complete response was achieved in 14.5% and major
pathological response in 28.2 %. Only as much as 40.5% patients received
adjuvant radiotherapy, and 43.5% received hormonal therapy. The most common
recurrence location was local recurrence (25.9%), followed by lung (24.2%), and
contralateral (13.8%).
Variables significantly associated with pathological response was the
expression of NF-κB (p = 0.02), while PGP and ALDH1 expression also have
effect but it was insignificant (p = 0.15 and p = 0, 17). Other variables that
significantly influence pathological response after neoadjuvant chemotherapy was
lymphovascular invasion (p = 0.047) and Ki67 expression (p = 0,03). From the
multivariate analysis, it was found that strong predictive factors of poor
pathological response (no response and minor response) is positive Ki67
expression (RR 2.12 |
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