Skip to main content
Top
Published in: International Journal of Clinical Oncology 2/2019

01-02-2019 | Breast Cancer | Review Article

Clinical target sequencing for precision medicine of breast cancer

Authors: Junko Tsuchida, Jami Rothman, Kerry-Ann McDonald, Masayuki Nagahashi, Kazuaki Takabe, Toshifumi Wakai

Published in: International Journal of Clinical Oncology | Issue 2/2019

Login to get access

Abstract

Precision medicine can be defined as the customization of medical treatment based on the individual genetic profile, which enables one to identify patients who respond to therapies while sparing side effects for those who do not. Breast cancer patients have been treated based on subtyping, which is considered a prototype of precision medicine. Furthermore, the development of multigene panel testing has resulted in a paradigm shift in the treatment of breast cancer. The knowledge generated from the Human Genome Project, and subsequently The Cancer Genome Atlas, has provided the concept of precision medicine, in which cancer patients can be sub-classified based on actionable driver mutations that can be selectively targeted by molecular targeted drugs and treated by appropriate molecular targeted therapies. Development of next-generation sequencing has both dramatically advanced genomic sequencing technology and revealed actionable driver mutations for individual cancer patients when applied to a clinical setting. Clinical target sequencing by next-generation sequencing enables one to formulate treatment strategies, not only by selecting a subgroup of patients who are expected to experience more effectiveness of each drug, but also by revealing patients with drug resistance based on their actionable driver mutations.
Literature
2.
go back to reference Early Breast Cancer Trialists’ Collaborative Group (EBCTCG) (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717CrossRef Early Breast Cancer Trialists’ Collaborative Group (EBCTCG) (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717CrossRef
3.
go back to reference Katsnelson A (2013) Momentum grows to make ‘personalized’ medicine more ‘precise’. Nat Med 19:249CrossRefPubMed Katsnelson A (2013) Momentum grows to make ‘personalized’ medicine more ‘precise’. Nat Med 19:249CrossRefPubMed
8.
go back to reference Mata DA, Katchi FM, Ramasamy R (2017) Precision medicine and men’s health. Am J Mens Health 11:1124–1129CrossRefPubMed Mata DA, Katchi FM, Ramasamy R (2017) Precision medicine and men’s health. Am J Mens Health 11:1124–1129CrossRefPubMed
9.
go back to reference Jain KK (2005) Personalised medicine for cancer: from drug development into clinical practice. Expert Opin Pharmacother 6:1463–1476CrossRefPubMed Jain KK (2005) Personalised medicine for cancer: from drug development into clinical practice. Expert Opin Pharmacother 6:1463–1476CrossRefPubMed
12.
go back to reference Perou CM, Sorlie T, Eisen MB et al (2000) Molecular portraits of human breast tumours. Nature 406:747–752CrossRefPubMed Perou CM, Sorlie T, Eisen MB et al (2000) Molecular portraits of human breast tumours. Nature 406:747–752CrossRefPubMed
13.
go back to reference Perou CM, Jeffrey SS, van de Rijn M et al (1999) Distinctive gene expression patterns in human mammary epithelial cells and breast cancers. Proc Natl Acad Sci USA 96:9212–9217CrossRefPubMedPubMedCentral Perou CM, Jeffrey SS, van de Rijn M et al (1999) Distinctive gene expression patterns in human mammary epithelial cells and breast cancers. Proc Natl Acad Sci USA 96:9212–9217CrossRefPubMedPubMedCentral
14.
go back to reference Bonadonna G, Brusamolino E, Valagussa P et al (1976) Combination chemotherapy as an adjuvant treatment in operable breast cancer. N Engl J Med 294:405–410CrossRefPubMed Bonadonna G, Brusamolino E, Valagussa P et al (1976) Combination chemotherapy as an adjuvant treatment in operable breast cancer. N Engl J Med 294:405–410CrossRefPubMed
15.
go back to reference Bonadonna G, Moliterni A, Zambetti M et al (2005) 30 years’ follow up of randomised studies of adjuvant CMF in operable breast cancer: cohort study. BMJ 330:217CrossRefPubMedPubMedCentral Bonadonna G, Moliterni A, Zambetti M et al (2005) 30 years’ follow up of randomised studies of adjuvant CMF in operable breast cancer: cohort study. BMJ 330:217CrossRefPubMedPubMedCentral
16.
go back to reference Goldhirsch A, Wood WC, Coates AS et al (2011) Strategies for subtypes–dealing with the diversity of breast cancer: highlights of the St. Gallen International Expert Consensus on the primary therapy of early breast cancer 2011. Ann Oncol 22:1736–1747CrossRefPubMedPubMedCentral Goldhirsch A, Wood WC, Coates AS et al (2011) Strategies for subtypes–dealing with the diversity of breast cancer: highlights of the St. Gallen International Expert Consensus on the primary therapy of early breast cancer 2011. Ann Oncol 22:1736–1747CrossRefPubMedPubMedCentral
17.
go back to reference Prat A, Fan C, Fernandez A et al (2015) Response and survival of breast cancer intrinsic subtypes following multi-agent neoadjuvant chemotherapy. BMC Med 13:303CrossRefPubMedPubMedCentral Prat A, Fan C, Fernandez A et al (2015) Response and survival of breast cancer intrinsic subtypes following multi-agent neoadjuvant chemotherapy. BMC Med 13:303CrossRefPubMedPubMedCentral
18.
go back to reference Chia SK, Bramwell VH, Tu D et al (2012) A 50-gene intrinsic subtype classifier for prognosis and prediction of benefit from adjuvant tamoxifen. Clin Cancer Res 18:4465–4472CrossRefPubMedPubMedCentral Chia SK, Bramwell VH, Tu D et al (2012) A 50-gene intrinsic subtype classifier for prognosis and prediction of benefit from adjuvant tamoxifen. Clin Cancer Res 18:4465–4472CrossRefPubMedPubMedCentral
19.
go back to reference Cheang MC, Voduc KD, Tu D et al (2012) Responsiveness of intrinsic subtypes to adjuvant anthracycline substitution in the NCIC.CTG MA.5 randomized trial. Clin Cancer Res 18:2402–2412CrossRefPubMedPubMedCentral Cheang MC, Voduc KD, Tu D et al (2012) Responsiveness of intrinsic subtypes to adjuvant anthracycline substitution in the NCIC.CTG MA.5 randomized trial. Clin Cancer Res 18:2402–2412CrossRefPubMedPubMedCentral
20.
go back to reference Prat A, Galvan P, Jimenez B et al (2016) Prediction of response to neoadjuvant chemotherapy using core needle biopsy samples with the prosigna assay. Clin Cancer Res 22:560–566CrossRefPubMed Prat A, Galvan P, Jimenez B et al (2016) Prediction of response to neoadjuvant chemotherapy using core needle biopsy samples with the prosigna assay. Clin Cancer Res 22:560–566CrossRefPubMed
21.
22.
go back to reference Myers MB (2016) Targeted therapies with companion diagnostics in the management of breast cancer: current perspectives. Pharmgenomics Pers Med 9:7–16PubMedPubMedCentral Myers MB (2016) Targeted therapies with companion diagnostics in the management of breast cancer: current perspectives. Pharmgenomics Pers Med 9:7–16PubMedPubMedCentral
23.
go back to reference Cronin M, Sangli C, Liu ML et al (2007) Analytical validation of the Oncotype DX genomic diagnostic test for recurrence prognosis and therapeutic response prediction in node-negative, estrogen receptor-positive breast cancer. Clin Chem 53:1084–1091CrossRefPubMed Cronin M, Sangli C, Liu ML et al (2007) Analytical validation of the Oncotype DX genomic diagnostic test for recurrence prognosis and therapeutic response prediction in node-negative, estrogen receptor-positive breast cancer. Clin Chem 53:1084–1091CrossRefPubMed
24.
go back to reference Paik S (2007) Development and clinical utility of a 21-gene recurrence score prognostic assay in patients with early breast cancer treated with tamoxifen. Oncologist 12:631–635CrossRefPubMed Paik S (2007) Development and clinical utility of a 21-gene recurrence score prognostic assay in patients with early breast cancer treated with tamoxifen. Oncologist 12:631–635CrossRefPubMed
25.
go back to reference Paik S, Shak S, Tang G et al (2004) A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer. N Engl J Med 351:2817–2826CrossRefPubMed Paik S, Shak S, Tang G et al (2004) A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer. N Engl J Med 351:2817–2826CrossRefPubMed
26.
go back to reference Paik S, Tang G, Shak S et al (2006) Gene expression and benefit of chemotherapy in women with node-negative, estrogen receptor-positive breast cancer. J Clin Oncol 24:3726–3734CrossRefPubMed Paik S, Tang G, Shak S et al (2006) Gene expression and benefit of chemotherapy in women with node-negative, estrogen receptor-positive breast cancer. J Clin Oncol 24:3726–3734CrossRefPubMed
27.
go back to reference Harris L, Fritsche H, Mennel R et al (2007) American Society of Clinical Oncology 2007 update of recommendations for the use of tumor markers in breast cancer. J Clin Oncol 25:5287–5312CrossRefPubMed Harris L, Fritsche H, Mennel R et al (2007) American Society of Clinical Oncology 2007 update of recommendations for the use of tumor markers in breast cancer. J Clin Oncol 25:5287–5312CrossRefPubMed
28.
go back to reference van ‘t Veer LJ, Dai H, van de Vijver MJ et al (2002) Gene expression profiling predicts clinical outcome of breast cancer. Nature 415:530–536CrossRefPubMed van ‘t Veer LJ, Dai H, van de Vijver MJ et al (2002) Gene expression profiling predicts clinical outcome of breast cancer. Nature 415:530–536CrossRefPubMed
29.
go back to reference van de Vijver MJ, He YD, van’t Veer LJ et al (2002) A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med 347:1999–2009CrossRefPubMed van de Vijver MJ, He YD, van’t Veer LJ et al (2002) A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med 347:1999–2009CrossRefPubMed
30.
31.
go back to reference Cancer Genome Atlas Network (2012) Comprehensive molecular portraits of human breast tumours. Nature 490:61–70CrossRef Cancer Genome Atlas Network (2012) Comprehensive molecular portraits of human breast tumours. Nature 490:61–70CrossRef
32.
go back to reference Dowsett M, Sestak I, Lopez-Knowles E et al (2013) Comparison of PAM50 risk of recurrence score with oncotype DX and IHC4 for predicting risk of distant recurrence after endocrine therapy. J Clin Oncol 31:2783–2790CrossRefPubMed Dowsett M, Sestak I, Lopez-Knowles E et al (2013) Comparison of PAM50 risk of recurrence score with oncotype DX and IHC4 for predicting risk of distant recurrence after endocrine therapy. J Clin Oncol 31:2783–2790CrossRefPubMed
33.
go back to reference Beahrs OH, Carr DT, Rubin P et al (1977) AJCC cancer staging manual, 1st edn. American Joint Committee, Illinois Beahrs OH, Carr DT, Rubin P et al (1977) AJCC cancer staging manual, 1st edn. American Joint Committee, Illinois
34.
go back to reference Beahrs OH, Myers MH (1983) AJCC cancer staging manual, 2nd edn. J B Lippincott Company, Philadelphia Beahrs OH, Myers MH (1983) AJCC cancer staging manual, 2nd edn. J B Lippincott Company, Philadelphia
35.
go back to reference Beahrs OH, Henson DE, Hutter RVP et al (1988) AJCC cancer staging manual, 3rd edn. J B Lippincott Company, Philadelphia Beahrs OH, Henson DE, Hutter RVP et al (1988) AJCC cancer staging manual, 3rd edn. J B Lippincott Company, Philadelphia
36.
go back to reference Beahrs OH, Henson DE, Hutter RVP et al (1992) AJCC cancer staging manual, 4th edn. J B Lippincott Company, Philadelphia Beahrs OH, Henson DE, Hutter RVP et al (1992) AJCC cancer staging manual, 4th edn. J B Lippincott Company, Philadelphia
37.
go back to reference Fleming ID, Cooper JS, Henson DE et al (1997) AJCC cancer staging manual, 5th edn. Lippincott - Raven, Philadelphia Fleming ID, Cooper JS, Henson DE et al (1997) AJCC cancer staging manual, 5th edn. Lippincott - Raven, Philadelphia
38.
go back to reference Greene FL, Page DL, Fleming ID et al (2002) AJCC cancer staging manual, 6th edn. Springer, New York et alCrossRef Greene FL, Page DL, Fleming ID et al (2002) AJCC cancer staging manual, 6th edn. Springer, New York et alCrossRef
39.
go back to reference Edge SB, Byrd DR, Compton CC et al (2009) AJCC cancer staging manual, 7th edn. Springer, New York Edge SB, Byrd DR, Compton CC et al (2009) AJCC cancer staging manual, 7th edn. Springer, New York
40.
go back to reference Amin MB, Edge SB, Greene FL et al (2016) AJCC cancer staging manual, 8th edn. Springer, New York Amin MB, Edge SB, Greene FL et al (2016) AJCC cancer staging manual, 8th edn. Springer, New York
41.
go back to reference Cardoso F, van’t Veer LJ, Bogaerts J et al (2016) 70-gene signature as an aid to treatment decisions in early-stage breast cancer. N Engl J Med 375:717–729CrossRefPubMed Cardoso F, van’t Veer LJ, Bogaerts J et al (2016) 70-gene signature as an aid to treatment decisions in early-stage breast cancer. N Engl J Med 375:717–729CrossRefPubMed
42.
go back to reference Su Y, Subedee A, Bloushtain-Qimron N et al (2015) Somatic cell fusions reveal extensive heterogeneity in basal-like breast cancer. Cell Rep 11:1549–1563CrossRefPubMed Su Y, Subedee A, Bloushtain-Qimron N et al (2015) Somatic cell fusions reveal extensive heterogeneity in basal-like breast cancer. Cell Rep 11:1549–1563CrossRefPubMed
43.
go back to reference Lehmann BD, Bauer JA, Chen X et al (2011) Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. J Clin Invest 121:2750–2767CrossRefPubMedPubMedCentral Lehmann BD, Bauer JA, Chen X et al (2011) Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. J Clin Invest 121:2750–2767CrossRefPubMedPubMedCentral
44.
go back to reference Marotti JD, de Abreu FB, Wells WA et al (2017) Triple-negative breast cancer: next-generation sequencing for target identification. Am J Pathol 187:2133–2138CrossRefPubMed Marotti JD, de Abreu FB, Wells WA et al (2017) Triple-negative breast cancer: next-generation sequencing for target identification. Am J Pathol 187:2133–2138CrossRefPubMed
45.
go back to reference Collins FS, Green ED, Guttmacher AE et al (2003) A vision for the future of genomics research. Nature 422:835–847CrossRefPubMed Collins FS, Green ED, Guttmacher AE et al (2003) A vision for the future of genomics research. Nature 422:835–847CrossRefPubMed
48.
go back to reference Shendure J, Porreca GJ, Reppas NB et al (2005) Accurate multiplex polony sequencing of an evolved bacterial genome. Science 309:1728–1732CrossRefPubMed Shendure J, Porreca GJ, Reppas NB et al (2005) Accurate multiplex polony sequencing of an evolved bacterial genome. Science 309:1728–1732CrossRefPubMed
49.
50.
go back to reference Ramanathan R, Olex AL, Dozmorov M et al (2017) Angiopoietin pathway gene expression associated with poor breast cancer survival. Breast Cancer Res Treat 162:191–198CrossRefPubMedPubMedCentral Ramanathan R, Olex AL, Dozmorov M et al (2017) Angiopoietin pathway gene expression associated with poor breast cancer survival. Breast Cancer Res Treat 162:191–198CrossRefPubMedPubMedCentral
51.
go back to reference Kawaguchi T, Yan L, Qi Q et al (2017) Overexpression of suppressive microRNAs, miR-30a and miR-200c are associated with improved survival of breast cancer patients. Sci Rep 7:15945CrossRefPubMedPubMedCentral Kawaguchi T, Yan L, Qi Q et al (2017) Overexpression of suppressive microRNAs, miR-30a and miR-200c are associated with improved survival of breast cancer patients. Sci Rep 7:15945CrossRefPubMedPubMedCentral
52.
go back to reference Young J, Kawaguchi T, Yan L et al (2017) Tamoxifen sensitivity-related microRNA-342 is a useful biomarker for breast cancer survival. Oncotarget 8:99978–99989PubMedPubMedCentral Young J, Kawaguchi T, Yan L et al (2017) Tamoxifen sensitivity-related microRNA-342 is a useful biomarker for breast cancer survival. Oncotarget 8:99978–99989PubMedPubMedCentral
53.
go back to reference Kim SY, Kawaguchi T, Yan L et al (2017) Clinical relevance of microRNA expressions in breast cancer validated using the Cancer Genome Atlas (TCGA). Ann Surg Oncol 10:2943–2949CrossRef Kim SY, Kawaguchi T, Yan L et al (2017) Clinical relevance of microRNA expressions in breast cancer validated using the Cancer Genome Atlas (TCGA). Ann Surg Oncol 10:2943–2949CrossRef
56.
go back to reference Arnedos M, Vicier C, Loi S et al (2015) Precision medicine for metastatic breast cancer–limitations and solutions. Nat Rev Clin Oncol 12:693–704CrossRefPubMed Arnedos M, Vicier C, Loi S et al (2015) Precision medicine for metastatic breast cancer–limitations and solutions. Nat Rev Clin Oncol 12:693–704CrossRefPubMed
57.
go back to reference Kummar S, Williams PM, Lih CJ et al (2015) Application of molecular profiling in clinical trials for advanced metastatic cancers. J Natl Cancer Inst 107 Kummar S, Williams PM, Lih CJ et al (2015) Application of molecular profiling in clinical trials for advanced metastatic cancers. J Natl Cancer Inst 107
58.
go back to reference Renfro LA, Sargent DJ (2016) Statistical controversies in clinical research: basket trials, umbrella trials, and other master protocols: a review and examples. Ann Oncol 28:34–43PubMedCentral Renfro LA, Sargent DJ (2016) Statistical controversies in clinical research: basket trials, umbrella trials, and other master protocols: a review and examples. Ann Oncol 28:34–43PubMedCentral
60.
go back to reference Willyard C (2013) ‘Basket studies’ will hold intricate data for cancer drug approvals. Nat Med 19:655CrossRefPubMed Willyard C (2013) ‘Basket studies’ will hold intricate data for cancer drug approvals. Nat Med 19:655CrossRefPubMed
61.
go back to reference Schmidt KT, Chau CH, Price DK et al (2016) Precision oncology medicine: the clinical relevance of patient specific biomarkers used to optimize cancer treatment. J Clin Pharmacol 56:1484–1499CrossRefPubMedPubMedCentral Schmidt KT, Chau CH, Price DK et al (2016) Precision oncology medicine: the clinical relevance of patient specific biomarkers used to optimize cancer treatment. J Clin Pharmacol 56:1484–1499CrossRefPubMedPubMedCentral
62.
go back to reference Do K, O’Sullivan Coyne G, Chen AP (2015) An overview of the NCI precision medicine trials-NCI MATCH and MPACT. Chin Clin Oncol 4:31PubMed Do K, O’Sullivan Coyne G, Chen AP (2015) An overview of the NCI precision medicine trials-NCI MATCH and MPACT. Chin Clin Oncol 4:31PubMed
63.
go back to reference Hyman DM, Solit DB, Arcila ME et al (2015) Precision medicine at Memorial Sloan Kettering Cancer Center: clinical next-generation sequencing enabling next-generation targeted therapy trials. Drug Discov Today 20:1422–1428CrossRefPubMedPubMedCentral Hyman DM, Solit DB, Arcila ME et al (2015) Precision medicine at Memorial Sloan Kettering Cancer Center: clinical next-generation sequencing enabling next-generation targeted therapy trials. Drug Discov Today 20:1422–1428CrossRefPubMedPubMedCentral
64.
go back to reference Lih CJ, Harrington RD, Sims DJ et al (2017) Analytical validation of the next-generation sequencing assay for a nationwide signal-finding clinical trial: Molecular Analysis for Therapy Choice clinical trial. J Mol Diagn 19:313–327CrossRefPubMedPubMedCentral Lih CJ, Harrington RD, Sims DJ et al (2017) Analytical validation of the next-generation sequencing assay for a nationwide signal-finding clinical trial: Molecular Analysis for Therapy Choice clinical trial. J Mol Diagn 19:313–327CrossRefPubMedPubMedCentral
65.
go back to reference Mullard A (2015) NCI-MATCH trial pushes cancer umbrella trial paradigm. Nat Rev Drug Discov 14:513–515CrossRefPubMed Mullard A (2015) NCI-MATCH trial pushes cancer umbrella trial paradigm. Nat Rev Drug Discov 14:513–515CrossRefPubMed
66.
68.
go back to reference Lipson D, Capelletti M, Yelensky R et al (2012) Identification of new ALK and RET gene fusions from colorectal and lung cancer biopsies. Nat Med 18:382–384CrossRefPubMedPubMedCentral Lipson D, Capelletti M, Yelensky R et al (2012) Identification of new ALK and RET gene fusions from colorectal and lung cancer biopsies. Nat Med 18:382–384CrossRefPubMedPubMedCentral
69.
go back to reference Redig AJ, Janne PA (2015) Basket trials and the evolution of clinical trial design in an era of genomic medicine. J Clin Oncol 33:975–977CrossRefPubMed Redig AJ, Janne PA (2015) Basket trials and the evolution of clinical trial design in an era of genomic medicine. J Clin Oncol 33:975–977CrossRefPubMed
70.
go back to reference Meric-Bernstam F, Johnson A, Holla V et al (2015) A decision support framework for genomically informed investigational cancer therapy. J Natl Cancer Inst 107 Meric-Bernstam F, Johnson A, Holla V et al (2015) A decision support framework for genomically informed investigational cancer therapy. J Natl Cancer Inst 107
71.
go back to reference Pritchard CC, Salipante SJ, Koehler K et al (2014) Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens. J Mol Diagn 16:56–67CrossRefPubMedPubMedCentral Pritchard CC, Salipante SJ, Koehler K et al (2014) Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens. J Mol Diagn 16:56–67CrossRefPubMedPubMedCentral
72.
go back to reference Frampton GM, Fichtenholtz A, Otto GA et al (2013) Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing. Nat Biotechnol 31:1023–1031CrossRefPubMedPubMedCentral Frampton GM, Fichtenholtz A, Otto GA et al (2013) Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing. Nat Biotechnol 31:1023–1031CrossRefPubMedPubMedCentral
73.
go back to reference Wagle N, Berger MF, Davis MJ et al (2012) High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. Cancer Discov 2:82–93CrossRefPubMed Wagle N, Berger MF, Davis MJ et al (2012) High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. Cancer Discov 2:82–93CrossRefPubMed
74.
go back to reference Nagahashi M, Wakai T, Shimada Y et al (2016) Genomic landscape of colorectal cancer in Japan: clinical implications of comprehensive genomic sequencing for precision medicine. Genome Med 8:136CrossRefPubMedPubMedCentral Nagahashi M, Wakai T, Shimada Y et al (2016) Genomic landscape of colorectal cancer in Japan: clinical implications of comprehensive genomic sequencing for precision medicine. Genome Med 8:136CrossRefPubMedPubMedCentral
75.
go back to reference Shimada Y, Yagi R, Kameyama H et al (2017) Utility of comprehensive genomic sequencing for detecting HER2-positive colorectal cancer. Hum Pathol 66:1–9CrossRefPubMed Shimada Y, Yagi R, Kameyama H et al (2017) Utility of comprehensive genomic sequencing for detecting HER2-positive colorectal cancer. Hum Pathol 66:1–9CrossRefPubMed
76.
go back to reference Shimada Y, Kameyama H, Nagahashi M et al (2017) Comprehensive genomic sequencing detects important genetic differences between right-sided and left-sided colorectal cancer. Oncotarget 8:93567–93579CrossRefPubMedPubMedCentral Shimada Y, Kameyama H, Nagahashi M et al (2017) Comprehensive genomic sequencing detects important genetic differences between right-sided and left-sided colorectal cancer. Oncotarget 8:93567–93579CrossRefPubMedPubMedCentral
77.
78.
go back to reference Douillard JY, Oliner KS, Siena S et al (2013) Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med 369:1023–1034CrossRefPubMed Douillard JY, Oliner KS, Siena S et al (2013) Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med 369:1023–1034CrossRefPubMed
79.
go back to reference Collins DC, Sundar R, Lim JS et al (2017) Towards precision medicine in the clinic: from biomarker discovery to novel therapeutics. Trends Pharmacol Sci 38:25–40CrossRefPubMed Collins DC, Sundar R, Lim JS et al (2017) Towards precision medicine in the clinic: from biomarker discovery to novel therapeutics. Trends Pharmacol Sci 38:25–40CrossRefPubMed
81.
go back to reference Lavaud P, Andre F (2014) Strategies to overcome trastuzumab resistance in HER2-overexpressing breast cancers: focus on new data from clinical trials. BMC Med 12:132CrossRefPubMedPubMedCentral Lavaud P, Andre F (2014) Strategies to overcome trastuzumab resistance in HER2-overexpressing breast cancers: focus on new data from clinical trials. BMC Med 12:132CrossRefPubMedPubMedCentral
82.
go back to reference de Oliveira Taveira M, Nabavi S, Wang Y et al (2017) Genomic characteristics of trastuzumab-resistant Her2-positive metastatic breast cancer. J Cancer Res Clin Oncol 143:1255–1262CrossRefPubMedPubMedCentral de Oliveira Taveira M, Nabavi S, Wang Y et al (2017) Genomic characteristics of trastuzumab-resistant Her2-positive metastatic breast cancer. J Cancer Res Clin Oncol 143:1255–1262CrossRefPubMedPubMedCentral
83.
go back to reference Andre F, Hurvitz S, Fasolo A et al (2016) Molecular alterations and everolimus efficacy in human epidermal growth factor receptor 2-overexpressing metastatic breast cancers: combined exploratory biomarker analysis from BOLERO-1 and BOLERO-3. J Clin Oncol 34:2115–2124CrossRefPubMed Andre F, Hurvitz S, Fasolo A et al (2016) Molecular alterations and everolimus efficacy in human epidermal growth factor receptor 2-overexpressing metastatic breast cancers: combined exploratory biomarker analysis from BOLERO-1 and BOLERO-3. J Clin Oncol 34:2115–2124CrossRefPubMed
84.
go back to reference Goel S, Wang Q, Watt AC et al (2016) Overcoming therapeutic resistance in HER2-positive breast cancers with CDK4/6 inhibitors. Cancer Cell 29:255–269CrossRefPubMedPubMedCentral Goel S, Wang Q, Watt AC et al (2016) Overcoming therapeutic resistance in HER2-positive breast cancers with CDK4/6 inhibitors. Cancer Cell 29:255–269CrossRefPubMedPubMedCentral
85.
go back to reference Malumbres M (2016) CDK4/6 Inhibitors resTORe therapeutic sensitivity in HER2+ breast cancer. Cancer Cell 29:243–244CrossRefPubMed Malumbres M (2016) CDK4/6 Inhibitors resTORe therapeutic sensitivity in HER2+ breast cancer. Cancer Cell 29:243–244CrossRefPubMed
86.
go back to reference Tan O, Shrestha R, Cunich M et al (2018) Application of next-generation sequencing to improve cancer management: a review of the clinical effectiveness and cost-effectiveness. Clin Genet 93:533–544CrossRefPubMed Tan O, Shrestha R, Cunich M et al (2018) Application of next-generation sequencing to improve cancer management: a review of the clinical effectiveness and cost-effectiveness. Clin Genet 93:533–544CrossRefPubMed
87.
go back to reference Li Y, Bare LA, Bender RA et al (2015) Cost effectiveness of sequencing 34 cancer-associated genes as an aid for treatment selection in patients with metastatic melanoma. Mol Diagn Ther 19:169–177CrossRefPubMedPubMedCentral Li Y, Bare LA, Bender RA et al (2015) Cost effectiveness of sequencing 34 cancer-associated genes as an aid for treatment selection in patients with metastatic melanoma. Mol Diagn Ther 19:169–177CrossRefPubMedPubMedCentral
88.
go back to reference Norum J, Hagen AI, Maehle L et al (2008) Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers: a cost-effectiveness analysis. Eur J Cancer 44:963–971CrossRefPubMed Norum J, Hagen AI, Maehle L et al (2008) Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers: a cost-effectiveness analysis. Eur J Cancer 44:963–971CrossRefPubMed
89.
go back to reference Muller D, Danner M, Rhiem K et al (2018) Cost-effectiveness of different strategies to prevent breast and ovarian cancer in German women with a BRCA 1 or 2 mutation. Eur J Health Econ 19:341–353CrossRefPubMed Muller D, Danner M, Rhiem K et al (2018) Cost-effectiveness of different strategies to prevent breast and ovarian cancer in German women with a BRCA 1 or 2 mutation. Eur J Health Econ 19:341–353CrossRefPubMed
Metadata
Title
Clinical target sequencing for precision medicine of breast cancer
Authors
Junko Tsuchida
Jami Rothman
Kerry-Ann McDonald
Masayuki Nagahashi
Kazuaki Takabe
Toshifumi Wakai
Publication date
01-02-2019
Publisher
Springer Singapore
Published in
International Journal of Clinical Oncology / Issue 2/2019
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-018-1373-5

Other articles of this Issue 2/2019

International Journal of Clinical Oncology 2/2019 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine