Pathologic Complete Response Achieved in Early- Stage HER2-Positive Breast Cancer After Neoadjuvant Therapy With Trastuzumab and Chemotherapy vs. Trastuzumab, Chemotherapy, and Pertuzumab: A Systematic Review and Meta- Analysis of Clinical Trials

被引:3
作者
Fazal, Faizan [1 ]
Bashir, Muhammad Nauman [2 ]
Adil, Maham Leeza [2 ]
Tanveer, Usama [2 ]
Ahmed, Mansoor [3 ]
Chaudhry, Taha Zahid [2 ]
Ijaz, Ali Ahmad [2 ]
Haider, Muhammad [4 ]
机构
[1] Rawalpindi Med Univ, Dept Med, Rawalpindi, Pakistan
[2] Holy Family Hosp, Dept Med, Rawalpindi, Pakistan
[3] Holy Family Hosp, Dept Surg, Rawalpindi, Pakistan
[4] Holy Family Hosp, Dept Orthoped, Rawalpindi, Pakistan
关键词
her2; randomized clinical trial; pathologic complete response (pcr); her2+ breast cancer; docetaxel-trastuzumab-pertuzumab therapy; systemic chemotherapy; neoadjuvant systemic therapy; SAFETY; EFFICACY; RECEPTOR; MULTICENTER;
D O I
10.7759/cureus.39780
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients diagnosed with human epidermal growth factor receptor 2 (HER2)-positive breast cancer require treatment upfront because of the aggressive nature of this type of cancer. Patients with early-stage HER2-positive breast cancer are usually treated with neoadjuvant therapy. This neoadjuvant therapy comprises targeted therapy and chemotherapy. Targeted therapy is given with trastuzumab. Pertuzumab is either administered or not with trastuzumab as a targeted therapy. This systematic review and meta-analysis aim to find out and compare the benefit achieved in terms of pathologic complete response (pCR) by adding pertuzumab to the neoadjuvant treatment regimen for early-stage HER2-positive breast cancer patients. Various databases were searched to find out relevant clinical trials. After going through PubMed, Embase, and Cochrane, three clinical trials were shortlisted for this systematic review and meta-analysis. These three clinical trials were double-armed. Pertuzumab was present in one arm while being absent in one arm to assess the benefit of adding pertuzumab in terms of pCR achieved. Data were analyzed using RevMan Web (Cochrane, London, UK). The odds ratio and 95% confidence interval were calculated for the outcome. The Mantel-Haenszel method and random effect model were used for analysis. The risk of bias in studies was evaluated using the Cochrane risk of bias tool for randomized controlled trials (ROB2). The summary statistics showed that the incidence of pCR was more in the experimental group (having pertuzumab) as compared to the control group (without pertuzumab) with an odds ratio of 2.10 (95% CI: 1.56-2.83) with I2 = 0%. In three double-arm trials, there were 840 participants, 445 in the experimental group and 395 in the control group. A total of 203 (45%) patients out of 445 in the experimental group achieved pCR, whereas 127 (32%) patients out of 395 in the control group achieved pCR. Through the results of this study, it can be concluded that the rate of pCR achieved was higher in that arm in which pertuzumab was present compared to the study arm in which only trastuzumab was given as targeted therapy. Thus, it can be suggested that pertuzumab be added to the neoadjuvant regimen for early-stage HER2-positive breast cancer patients. This would result in achieving a better pCR. And by improving pCR rates, the survival outcomes of patients can be significantly improved.
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页数:10
相关论文
共 25 条
[1]   Response Rate and Safety of a Neoadjuvant Pertuzumab, Atezolizumab, Docetaxel, and Trastuzumab Regimen for Patients With ERBB2-Positive Stage II/III Breast Cancer The Neo-PATH Phase 2 Nonrandomized Clinical Trial [J].
Ahn, Hee Kyung ;
Sim, Sung Hoon ;
Suh, Koung Jin ;
Kim, Min Hwan ;
Jeong, Jae Ho ;
Kim, Ji-Yeon ;
Lee, Dae-Won ;
Ahn, Jin-Hee ;
Chae, Heejung ;
Lee, Kyung-Hun ;
Kim, Jee Hyun ;
Lee, Keun Seok ;
Sohn, Joo Hyuk ;
Choi, Yoon-La ;
Im, Seock-Ah ;
Jung, Kyung Hae ;
Park, Yeon Hee .
JAMA ONCOLOGY, 2022, 8 (09) :1271-1277
[2]   Awareness and current knowledge of breast cancer [J].
Akram, Muhammad ;
Iqbal, Mehwish ;
Daniyal, Muhammad ;
Khan, Asmat Ullah .
BIOLOGICAL RESEARCH, 2017, 50
[3]   Estrogen receptor breast cancer phenotypes in the surveillance, epidemiology, and end results database [J].
Anderson, WF ;
Chatterjee, N ;
Ershler, WB ;
Brawley, OW .
BREAST CANCER RESEARCH AND TREATMENT, 2002, 76 (01) :27-36
[4]  
Arora Shalabh, 2021, Cancer Treat Res Commun, V29, P100483, DOI 10.1016/j.ctarc.2021.100483
[5]   Treatment of HER2-positive breast cancer: current status and future perspectives [J].
Arteaga, Carlos L. ;
Sliwkowski, Mark X. ;
Osborne, C. Kent ;
Perez, Edith A. ;
Puglisi, Fabio ;
Gianni, Luca .
NATURE REVIEWS CLINICAL ONCOLOGY, 2012, 9 (01) :16-32
[6]  
Arzanova E, 2022, EPIDEMIOLOGY BREAST, DOI [10.36255/exon-publications-breast-cancer-epidemiology, DOI 10.36255/EXON-PUBLICATIONS-BREAST-CANCER-EPIDEMIOLOGY]
[7]   Pertuzumab/Trastuzumab/CT Versus Trastuzumab/CT Therapy for HER2+Breast Cancer: Results from the Prospective Neoadjuvant Breast Registry Symphony Trial (NBRST) [J].
Beitsch, Peter ;
Whitworth, Pat ;
Baron, Paul ;
Rotkis, Michael C. ;
Mislowsky, Angela M. ;
Richards, Paul D. ;
Murray, Mary K. ;
Pellicane, James V. ;
Dul, Carrie L. ;
Nash, Charles H. ;
Stork-Sloots, Lisette ;
de Snoo, Femke ;
Untch, Sarah ;
Lee, Laura A. .
ANNALS OF SURGICAL ONCOLOGY, 2017, 24 (09) :2539-2546
[8]  
Bergh J, 2021, LANCET ONCOL, V22, P1139, DOI 10.1016/S1470-2045(21)00288-6
[9]   HER-2, TOP2A and chromosome 17 alterations in breast cancer [J].
Beser, Ash Rehber ;
Tuzlali, Sitki ;
Guzey, Deniz ;
Guler, Semra Dolek ;
Hacihanefioglu, Seniha ;
Dalay, Nejat .
PATHOLOGY & ONCOLOGY RESEARCH, 2007, 13 (03) :180-185
[10]  
Bilici A, 2022, J CLIN ONCOL, V40