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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 臨床醫學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/99592
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dc.contributor.advisor盧彥伸zh_TW
dc.contributor.advisorYen-Shen Luen
dc.contributor.author賴育柔zh_TW
dc.contributor.authorYu-Jou Laien
dc.date.accessioned2025-09-16T16:13:04Z-
dc.date.available2025-09-17-
dc.date.copyright2025-09-16-
dc.date.issued2025-
dc.date.submitted2025-06-23-
dc.identifier.citation1. Bray F, Laversanne M, Sung H, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229-63. doi:10.3322/caac.21834.
2. National Cancer Institute. SEER cancer stat facts: breast cancer subtypes. Surveillance, Epidemiology, and End Results Program. Accessed March 20, 2025. https://seer.cancer.gov/statfacts/html/breast-subtypes.html
3. Wolff AC, Somerfield MR, Dowsett M, et al. Human epidermal growth factor receptor 2 testing in breast cancer: ASCO-College of American Pathologists guideline update. J Clin Oncol. 2023;41(22):3867-72. doi:10.1200/JCO.23.00707.
4. Giordano SH, Franzoi MAB, Temin S, et al. Systemic therapy for advanced human epidermal growth factor receptor 2-positive breast cancer: ASCO guideline update. J Clin Oncol. 2022;40(23):2612-2635. doi:10.1200/JCO.22.00519
5. Modi S, Jacot W, Yamashita T, et al. Trastuzumab deruxtecan in previously treated HER2-low advanced breast cancer. N Engl J Med. 2022;387(1):9-20. doi:10.1056/NEJMoa2203690
6. Bardia A, Hu X, Dent R, et al. Trastuzumab deruxtecan after endocrine therapy in metastatic breast cancer. N Engl J Med. 2024;391(12):1127-39. doi:10.1056/NEJMoa2407117.
7. Gradishar WJ, Moran MS, Abraham J, et al. Breast cancer, version 3.2024, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2024;22(5):331-357. doi:10.6004/jnccn.2024.0035
8. Bardia A, Hurvitz SA, Tolaney SM, et al. Sacituzumab govitecan in metastatic triple-negative breast cancer. N Engl J Med. 2021;384(16):1529-41. doi:10.1056/NEJMoa2028485.
9. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. PLoS Med. 2021;18(3):e1003583. doi:10.1371/journal.pmed.1003583.
10. Sterne JAC, Savović J, Page MJ, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366:l4898. doi:10.1136/bmj.l4898
11. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177-88. doi:10.1016/0197-2456(86)90046-2.
12. Cochran WG. The combination of estimates from different experiments. Biometrics. 1954;10(1):101-29. doi:10.2307/3001599.
13. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557-60. doi:10.1136/bmj.327.7414.557.
14. Rugo HS, Bardia A, Marmé F, et al. Sacituzumab govitecan in hormone receptor-positive/human epidermal growth factor receptor 2-negative metastatic breast cancer. J Clin Oncol. 2022;40(29):3365-76. doi:10.1200/JCO.22.01002.
15. Bardia A, Jhaveri K, Im S, et al. Datopotamab deruxtecan versus chemotherapy in previously treated inoperable/metastatic hormone receptor-positive human epidermal growth factor receptor 2-negative breast cancer: primary results from TROPION-Breast01. J Clin Oncol. Published online 2024. doi:10.1200/JCO.24.00920
16. Xu B, Wang S, Yan M, et al. Sacituzumab govitecan in HR+HER2− metastatic breast cancer: the randomized phase 3 EVER-132-002 trial. Nat Med. 2024;30(12):3709-16. doi:10.1038/s41591-024-03269-z.
17. Schettini F, Nucera S, Pascual T, Martínez-Sáez O, Sánchez-Bayona R, Conte B, et al. Efficacy and safety of antibody-drug conjugates in pretreated HER2-low metastatic breast cancer: a systematic review and network meta-analysis. Cancer Treat Rev. 2025;132:102865. doi:10.1016/j.ctrv
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/99592-
dc.description.abstract背景:抗體藥物複合體(ADC)在第二型人類表皮生長因子受體(HER2)非過度表現的轉移性乳腺癌中,顯示出較化療更優的療效。然而,不同患者亞組的療效差異及最佳ADC選擇仍待釐清。

方法:本研究依據系統性回顧與統合分析首選報告項目(PRISMA)指引,系統檢索PubMed、Embase、Cochrane Library及ClinicalTrials.gov,納入截至2025年05月17日已完整出版的文獻,並輔以會議摘要進行亞組分析。主要療效指標包括ADC相較於化療的總反應率(ORR)勝算比(OR)、無進展生存期(PFS)及總生存期(OS)的風險比(HR)。

結果:共納入六項隨機分派臨床試驗(N=3,558),涵蓋三種核准上市之ADC。整體而言,所有ADC在ORR、PFS及OS三項療效指標均顯著優於化療。賀爾蒙受體陰性患者的ORR勝算比高於賀爾蒙受體陽性患者。在賀爾蒙受體陽性患者中,HER2低表達(HER2-low,定義為免疫組織化學染色[IHC] 1+至2+)疾病使用ADC的ORR(OR 3.40 vs. 2.12)及PFS(HR 0.56 vs. 0.65)療效優於HER2零表達(HER2-zero,IHC 0)疾病。反之,在賀爾蒙受體陰性患者中,ADC於HER2-zero疾病的療效較HER2-low更顯著(ORR OR 12.42 vs. 5.15;PFS HR 0.38 vs. 0.45)。無論賀爾蒙受體狀態,OS在不同HER2表現水平間無顯著差異。HER2-ADC與Trop2-ADC在各亞組的PFS及OS效益相近,但在賀爾蒙受體陽性患者的ORR中,HER2-ADC表現更佳(OR 3.83 vs. 1.70)。對於賀爾蒙受體陰性/HER2-zero患者,僅Trop2-ADC數據顯示顯著療效(ORR OR 12.42,PFS HR 0.38,OS HR 0.50)。

結論:ADC的療效因賀爾蒙受體狀態及HER2表現水平而異,ORR的差異尤為顯著。在賀爾蒙受體陽性患者中,HER2-ADC的ORR勝算比優於Trop2-ADC,顯示其潛在的優先應用價值。
zh_TW
dc.description.abstractBackground: Antibody-drug conjugates (ADCs) have shown superior efficacy over chemotherapy in HER2 non-overexpressing metastatic breast cancer. However, efficacy across different patient subgroups and the optimal ADC choice remains undefined.

Methods: Literature search in PubMed, Embase, Cochrane Library, and ClinicalTrials.gov was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guideline, and full paper publications up to 17 May, 2025 were enrolled. Additional conference abstracts were collected for subgroup analyses. Primary outcomes were odds ratio (OR) for overall response rate (ORR), hazard ratio (HR) for progression-free survival (PFS) and overall survival (OS) when ADCs were compared to chemotherapies.

Results: Six randomized trials (N=3,558) which consisted of three approved ADCs were enrolled; all showed superior efficacy of ADCs over chemotherapy. In general, higher OR for ORR was observed in hormone receptor-negative (HR-neg) patients than in hormone receptor-positive (HR-pos) patients. Among HR-pos patients, ADC efficacy in ORR (OR 3.40 vs. 2.12) and PFS (HR 0.56 vs. 0.65) was more prominent in HER2-low (immunohistochemical staining [IHC] 1+ to 2+) disease than in HER2-zero (IHC 0) disease. Conversely, among HR-neg patients, ADCs were preferentially better in HER2-zero disease (ORR OR 12.42 vs. 5.15 and PFS HR 0.38 vs. 0.45). Regardless of hormone receptor status, OS benefits remained consistent across HER2 expression levels. HER2-ADC and Trop2-ADCs provided similar benefit in PFS and OS. While HER2-ADC appeared to have superior ORR than Trop-2-ADCs in HR-pos patients (OR 3.83 vs. 1.70); for HR-neg/HER2-zero patients, available data were limited to Trop2-ADC only, with outstanding results (ORR OR 12.4, PFS HR 0.38 and OS HR 0.5).

Conclusions: Differential benefits of ADCs in ORR and PFS were observed across different patient subgroups defined by hormone receptor status and HER2 expression level. In HR-pos patients, HER2 ADC had superior odds in ORR than Trop2 ADCs.
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dc.description.tableofcontentsACKNOWLEDGMENTS i
中文摘要 ii
ABSTRACT iii
CONTENTS v
LIST OF FIGURES vii
LIST OF TABLES Viii
1. Introduction 1
2. Methods 4
2.1 Data Retrieval Strategies 4
2.2 Population, Intervention, Comparison, and Outcomes 4
2.3 Inclusion Criteria 4
2.4 Data Extraction 5
2.5 Statistical Analysis 5
3. RESULTS 7
3.1 Characteristics of the Included Studies 7
3.2 Risk of Bias of the Included Studies 7
3.3 ADCs vs Chemotherapy 8
3.4 Subgroup Analysis by Hormone Receptor Status: HR-positive and HR-negative 8
3.5 Subgroup Analysis by HER2 Expression: HER2-Low and HER2-Zero 9
3.6 Subgroup Analysis by ADC type: Trop2-ADC and HER2-ADC 10
4. Discussion 11
5. Conclusion 14
FIGURES 15
TABLES 20
REFERENCE 28
APPENDIX 31
CONTENTS 32
LIST OF FIGURES 36
LIST OF TABLES 37
1. PROTOCOL SUMMARY 38
1.1 Protocol Synopsis 38
1.2 Trial Schema 45
1.3 Schedule of Activities 45
2. INTRODUCTION 52
2.1 Study Rationale 52
2.1.1 Study Background 52
2.1.2 HER2 Expression and Subtype Classification 52
2.1.3 Current Treatment Landscape and Limitations 53
2.1.4 Meta-Analysis Insights and Evidence Gaps 53
2.1.5 Study Design and Justification 54
2.2 Background on Study Interventions 55
2.2.1 Trastuzumab Deruxtecan 55
2.2.2 Sacituzumab Govitecan 56
3. OBJECTIVES AND ENDPOINTS 59
4. HYPOTHESES 60
4.1 Hypotheses for Cohort 1: HR-positive Patients 60
4.2 Hypotheses for Cohort 2: HR-negative Patients 60
5. STUDY DESIGN 61
5.1 Overall Design 61
5.2 Study Duration 61
5.3 Study Treatments 62
5.4 Treatment Discontinuation 62
5.5 Study Withdrawal 62
5.6 Safety and Survival Follow-up 63
6. POPULATION 64
6.1 Inclusion Criteria 64
6.2 Exclusion Criteria 65
7. STUDY INTERVENTIONS 67
7.1 Study Treatments 67
7.2 Treatment Groups 67
7.3 Method of Treatment Allocation 67
7.4 Description and Handling of Trastuzumab Deruxtecan 68
7.4.1 Formulation 68
7.4.2 Packaging and Labeling 68
7.4.3 Storage and Handling 68
7.4.4 Premedication and Prophylaxis 69
7.4.5 Dosage and Administration 69
7.4.6 Dose Modification and Treatment Delays 69
7.4.7 Dose Reductions and Discontinuation 70
7.5 Description and Handling of Sacituzumab Govitecan 78
7.5.1 Formulation 78
7.5.2 Packaging and Labeling 78
7.5.3 Storage and Handling 79
7.5.4 Premedication and Prophylaxis 79
7.5.5 Dosage and Administration 79
7.5.6 Dose Modification and Treatment Delays 80
7.5.7 Dose Reductions and Discontinuation 80
7.5.8 Treatment Delays 82
7.6 Concomitant Medications and Treatments 83
7.7 Prohibited Medications and Treatments of Trastuzumab Deruxtecan 83
7.8 Prohibited Medications and Treatments of Sacituzumab Govitecan 84
8. STUDY PROCEDURES 86
8.1 Informed Consent 86
8.2 Screening 86
8.3 Screen Failures 86
8.4 Study Procedures 87
8.4.1 Physical Examinations 87
8.4.2 Vital Signs 87
8.4.3 Electrocardiograms 87
8.4.4 Echocardiograms/Multiple Gated Acquisition Scans 88
8.4.5 Ophthalmologic Assessments 88
8.4.6 Clinical Safety Laboratory Assessments 89
8.4.7 ECOG Performance Status 90
8.4.8 Efficacy Assessments 90
9. ADVERSE EVENTS AND TOXICITY MANAGEMENT 92
9.1 Adverse Events 92
9.2 Serious Adverse Events 93
10. STATISTICS 95
10.1 Sample size calculation 95
10.2 Definition of variables 96
10.3 General Statistical Consideration 96
11. ETHICAL ASPECTS 99
11.1 Local Regulations 99
11.2 Informed Consent 99
11.3 Institutional Review Board/ Ethics Committee 100
11.4 Disposition of Subject Samples 100
12. CONDITIONS FOR MODIFYING THE PROTOCOL 101
13. CONDITIONS FOR TERMINATING THE STUDY 102
14. STUDY DOCUMENTATION, AND RECORD KEEPING 103
14.1 Investigator’s Files and Retention of Documents 103
14.2 Source Documents and Background Data 104
14.3 Audits and Inspections 104
14.4 Case Report Forms 104
REFERENCE 106
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dc.language.isoen-
dc.subject抗體藥物複合體zh_TW
dc.subject轉移性乳腺癌zh_TW
dc.subjectHER2低表達zh_TW
dc.subject賀爾蒙受體zh_TW
dc.subject總反應率zh_TW
dc.subject無進展生存期zh_TW
dc.subject總生存期zh_TW
dc.subjectmetastatic breast canceren
dc.subjectoverall survivalen
dc.subjectprogression-free survivalen
dc.subjectoverall response rateen
dc.subjecthormone receptoren
dc.subjectHER2-lowen
dc.subjectAntibody-drug conjugateen
dc.title抗體藥物複合體用於第二型人類表皮生長因子受體非過度表現之轉移性乳癌:系統性回顧及統合分析與臨床試驗計畫書zh_TW
dc.titleAntibody-drug Conjugates in HER2 Non-overexpressing Metastatic Breast Cancer: A Systematic Review, Meta-Analysis and Clinical Trial Protocolen
dc.typeThesis-
dc.date.schoolyear113-2-
dc.description.degree碩士-
dc.contributor.oralexamcommittee邵文逸;林季宏zh_TW
dc.contributor.oralexamcommitteeWen-Yi Shau;Ching-Hung Linen
dc.subject.keyword抗體藥物複合體,轉移性乳腺癌,HER2低表達,賀爾蒙受體,總反應率,無進展生存期,總生存期,zh_TW
dc.subject.keywordAntibody-drug conjugate,metastatic breast cancer,HER2-low,hormone receptor,overall response rate,progression-free survival,overall survival,en
dc.relation.page107-
dc.identifier.doi10.6342/NTU202500994-
dc.rights.note同意授權(限校園內公開)-
dc.date.accepted2025-06-24-
dc.contributor.author-college醫學院-
dc.contributor.author-dept臨床醫學研究所-
dc.date.embargo-lift2025-09-17-
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