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The predictive and prognostic role of phosphatase phosphoinositol-3 (PI3) kinase (PIK3CA) mutation in HER2-positive breast cancer receiving HER2-targeted therapy: a meta-analysis

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Abstract

The association between PIK3CA mutation and resistance to anti-HER2 therapy (AHT) is not precisely defined. This meta-analysis intended to explore the clinical utility of PIK3CA mutation in HER2-positive breast cancer treated with AHT. Literature search identified 19 eligible studies. There were 1720 patients with advanced, 828 with early and 1290 patients treated in the neoadjuvant setting. In metastatic breast cancer, AHT showed no differential objective response benefit between the wild type (WT) and the mutated type (MT) PIK3CA subgroups (odds ratio [OR] = 1.09; 95 % CI 0.60–2.00; P = 0.78). AHT favorable affected progression-free survival (PFS) irrespective of PIK3CA mutation. There was no PFS difference between WT and MT regardless of the offered therapy. In early breast cancer, trastuzumab combined with the same chemotherapy conferred consistent relapse-free survival benefit in WT and MT subgroups (WT: HR = 0.59; 95 % CI 0.44–0.80; P < 0.001 vs. MT: HR = 0.42; 95 % CI 0.24–0.74; P < 0.001). In the neoadjuvant setting, AHT-based therapy produced a 72 % higher pathologic complete response (pCR) rate in WT as compared with that in MT PIK3CA tumors (OR = 1.72; 95 % CI 1.29–2.13; P < 0.001). In that setting, there was no disease-free or overall survival difference based on PIK3CA mutational status. In this meta-analysis, AHT did not achieve differential benefit according to PIK3CA mutation in HER2-positive metastatic or early breast cancer; however, in the neoadjuvant setting, patients harboring WT PIK3CA tumors attained a higher pCR rate.

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References

  1. Slamon DJ, Godolphin W, Jones LA, Holt JA, Wong SG, Keith DE, Levin WJ, Stuart SG, Udove J, Ullrich A et al (1989) Studies of the her-2/neu proto-oncogene in human breast and ovarian cancer. Science 244:707–712

    Article  CAS  PubMed  Google Scholar 

  2. Loi S, Haibe-Kains B, Majjaj S, Lallemand F, Durbecq V, Larsimont D, Gonzalez-Angulo AM, Pusztai L, Symmans WF, Bardelli A, Ellis P, Tutt AN, Gillett CE, Hennessy BT, Mills GB, Phillips WA, Piccart MJ, Speed TP, McArthur GA, Sotiriou C (2010) Pik3ca mutations associated with gene signature of low mtorc1 signaling and better outcomes in estrogen receptor-positive breast cancer. Proc Natl Acad Sci USA 107:10208–10213. doi:10.1073/pnas.0907011107

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Kataoka Y, Mukohara T, Shimada H, Saijo N, Hirai M, Minami H (2010) Association between gain-of-function mutations in pik3ca and resistance to HER2-targeted agents in HER2-amplified breast cancer cell lines. Ann Oncol 21:255–262. doi:10.1093/annonc/mdp304

    Article  CAS  PubMed  Google Scholar 

  4. Cescon DW, Bedard PL (2015) Pik3ca genotype and treatment decisions in human epidermal growth factor receptor 2-positive breast cancer. J Clin Oncol. doi:10.1200/JCO.2014.59.3160

    PubMed  Google Scholar 

  5. Wang Y, Liu Y, Du Y, Yin W, Lu J (2013) The predictive role of phosphatase and tensin homolog (pten) loss, phosphoinositol-3 (pi3) kinase (pik3ca) mutation, and pi3K pathway activation in sensitivity to trastuzumab in HER2-positive breast cancer: a meta-analysis. Curr Med Res Opin 29:633–642. doi:10.1185/03007995.2013.794775

    Article  CAS  PubMed  Google Scholar 

  6. Brugge J, Hung MC, Mills GB (2007) A new mutational aktivation in the pi3k pathway. Cancer Cell 12:104–107. doi:10.1016/j.ccr.2007.07.014

    Article  CAS  PubMed  Google Scholar 

  7. Tierney JF, Stewart LA, Ghersi D, Burdett S, Sydes MR (2007) Practical methods for incorporating summary time-to-event data into meta-analysis. Trials 8:16. doi:10.1186/1745-6215-8-16

    Article  PubMed Central  PubMed  Google Scholar 

  8. Parmar MK, Torri V, Stewart L (1998) Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Stat Med 17:2815–2834

    Article  CAS  PubMed  Google Scholar 

  9. Higgins JP, Thompson SG (2002) Quantifying heterogeneity in a meta-analysis. Stat Med 21:1539–1558. doi:10.1002/sim.1186

    Article  PubMed  Google Scholar 

  10. Higgins JP, Thompson SG, Deeks JJ, Altman DG (2003) Measuring inconsistency in meta-analyses. BMJ 327:557–560. doi:10.1136/bmj.327.7414.557

    Article  PubMed Central  PubMed  Google Scholar 

  11. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315:629–634

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50:1088–1101

    Article  CAS  PubMed  Google Scholar 

  13. Wang L, Zhang Q, Zhang J, Sun S, Guo H, Jia Z, Wang B, Shao Z, Wang Z, Hu X (2011) Pi3 k pathway activation results in low efficacy of both trastuzumab and lapatinib. BMC Cancer 11:248. doi:10.1186/1471-2407-11-248

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  14. Krop IE, LoRusso P, Miller KD, Modi S, Yardley D, Rodriguez G, Guardino E, Lu M, Zheng M, Girish S, Amler L, Winer EP, Rugo HS (2012) A phase II study of trastuzumab emtansine in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer who were previously treated with trastuzumab, lapatinib, an anthracycline, a taxane, and capecitabine. J Clin Oncol 30:3234–3241. doi:10.1200/JCO.2011.40.5902

    Article  CAS  PubMed  Google Scholar 

  15. Baselga J, Verma S, Ro J, Huober J, Guardino E, Fang L, Olsen S, Phillips GL, de Haas S, Pegram M (2013) Abstract lb-63: Relationship between tumor biomarkers (bm) and efficacy in emilia, a phase III study of trastuzumab emtansine (t-dm1) in HER2-positive metastatic breast cancer (mbc). Cancer Research 73:LB-63. doi:10.1158/1538-7445.am2013-lb-63

    Article  Google Scholar 

  16. Baselga J, Cortes J, Im SA, Clark E, Ross G, Kiermaier A, Swain SM (2014) Biomarker analyses in cleopatra: a phase III, placebo-controlled study of pertuzumab in human epidermal growth factor receptor 2-positive, first-line metastatic breast cancer. J Clin Oncol 32:3753–3761. doi:10.1200/JCO.2013.54.5384

    Article  CAS  PubMed  Google Scholar 

  17. Kim S-B, Wildiers H, Krop IE, Leung ACF, Trudeau C, Yu R, de Haas S, Gonzalez-Martin A (2014) Relationship between tumor biomarkers (bm) and efficacy in th3resa, a phase 3 study of trastuzumab emtansine (t-dm1) versus treatment of physician’s choice (tpc) in HER2-positive advanced breast cancer (bc) previously treated with trastuzumab and lapatinib. ASCO Meet Abstr 32:605

    Google Scholar 

  18. Miller KD, Dieras V, Harbeck N, Andre F, Mahtani RL, Gianni L, Albain KS, Crivellari D, Fang L, Michelson G, de Haas SL, Burris HA (2014) Phase IIa trial of trastuzumab emtansine with pertuzumab for patients with human epidermal growth factor receptor 2-positive, locally advanced, or metastatic breast cancer. J Clin Oncol 32:1437–1444. doi:10.1200/JCO.2013.52.6590

    Article  CAS  PubMed  Google Scholar 

  19. Xu B, Guan Z, Shen Z, Tong Z, Jiang Z, Yang J, DeSilvio M, Russo M, Leigh M, Ellis C (2014) Association of phosphatase and tensin homolog low and phosphatidylinositol 3-kinase catalytic subunit alpha gene mutations on outcome in human epidermal growth factor receptor 2-positive metastatic breast cancer patients treated with first-line lapatinib plus paclitaxel or paclitaxel alone. Breast Cancer Res 16:405. doi:10.1186/s13058-014-0405-y

    Article  PubMed Central  PubMed  Google Scholar 

  20. Tural D, Serdengecti S, Demirelli F, Ozturk T, Ilvan S, Turna H, Ozguroglu M, Buyukunal E (2014) Clinical significance of p95her2 overexpression, pten loss and pi3k expression in p185 HER2-positive metastatic breast cancer patients treated with trastuzumab-based therapies. Br J Cancer 110:1968–1976. doi:10.1038/bjc.2014.72

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Gianni L, Bianchini G, Kiermaier A, Bianchi G, Im Y-H, Pienkowski T, Roman L, Liu M-C, Tseng L-M, Ratnayake J, Szado T, Ross G, Valagussa P (2011) S5-1: neoadjuvant pertuzumab (p) and trastuzumab (h): Biomarker analyses of a 4-arm randomized phase II study (neosphere) in patients (pts) with her2− positive breast cancer (bc). Cancer Res 71:S5-1. doi:10.1158/0008-5472.sabcs11-s5-1

    Article  Google Scholar 

  22. Dave B, Migliaccio I, Gutierrez MC, Wu M-F, Chamness GC, Wong H, Narasanna A, Chakrabarty A, Hilsenbeck SG, Huang J, Rimawi M, Schiff R, Arteaga C, Osborne CK, Chang JC (2011) Loss of phosphatase and tensin homolog or phosphoinositol-3 kinase activation and response to trastuzumab or lapatinib in human epidermal growth factor receptor 2—overexpressing locally advanced breast cancers. J Clin Oncol 29:166–173. doi:10.1200/jco.2009.27.7814

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. Jinno H, Sato T, Hayashida T, Takahashi M, Hirose S, Kitagawa Y (2012) Abstract p3-06-22: mechanisms behind trastuzumab resistance as neoadjuvant therapy in HER2-positive operable breast cancer. Cancer Res 72:P3-06-22. doi:10.1158/0008-5472.sabcs12-p3-06-22

    Article  Google Scholar 

  24. Guarneri V, Dieci MV, Carbognin L, Maiorana A, Bettelli S, Tortora G, Conte PF, Bria E (2014) 254o activity of neoadjuvant lapatinib (l) plus trastuzumab (t) for early breast cancer (ebc) according to pik3ca mutations: pathological complete response (pcr) rate in the cherlob study and pooled analysis of randomized trials. Ann Oncol 25:iv85. doi:10.1093/annonc/mdu327.2

    Google Scholar 

  25. Loibl S, von Minckwitz G, Schneeweiss A, Paepke S, Lehmann A, Rezai M, Zahm DM, Sinn P, Khandan F, Eidtmann H, Dohnal K, Heinrichs C, Huober J, Pfitzner B, Fasching PA, Andre F, Lindner JL, Sotiriou C, Dykgers A, Guo S, Gade S, Nekljudova V, Loi S, Untch M, Denkert C (2014) Pik3ca mutations are associated with lower rates of pathologic complete response to anti-human epidermal growth factor receptor 2 (her2) therapy in primary HER2-overexpressing breast cancer. J Clin Oncol 32:3212–3220. doi:10.1200/jco.2014.55.7876

    Article  CAS  PubMed  Google Scholar 

  26. Schneeweiss A, Chia S, Hegg R, Tausch C, Deb R, Ratnayake J, McNally V, Ross G, Kiermaier A, Cortes J (2014) Evaluating the predictive value of biomarkers for efficacy outcomes in response to pertuzumab- and trastuzumab-based therapy: an exploratory analysis of the tryphaena study. Breast Cancer Res 16:R73. doi:10.1186/bcr3690

    Article  PubMed Central  PubMed  Google Scholar 

  27. Majewski IJ, Nuciforo P, Mittempergher L, Bosma AJ, Eidtmann H, Holmes E, Sotiriou C, Fumagalli D, Jimenez J, Aura C, Prudkin L, Diaz-Delgado MC, de la Pena L, Loi S, Ellis C, Schultz N, de Azambuja E, Harbeck N, Piccart-Gebhart M, Bernards R, Baselga J (2015) Pik3ca mutations are associated with decreased benefit to neoadjuvant human epidermal growth factor receptor 2-targeted therapies in breast cancer. J Clin Oncol. doi:10.1200/JCO.2014.55.2158

    PubMed  Google Scholar 

  28. Cizkova M, Dujaric ME, Lehmann-Che J, Scott V, Tembo O, Asselain B, Pierga JY, Marty M, de Cremoux P, Spyratos F, Bieche I (2013) Outcome impact of pik3ca mutations in HER2-positive breast cancer patients treated with trastuzumab. Br J Cancer 108:1807–1809. doi:10.1038/bjc.2013.164

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  29. Loi S, Michiels S, Lambrechts D, Fumagalli D, Claes B, Kellokumpu-Lehtinen PL, Bono P, Kataja V, Piccart MJ, Joensuu H, Sotiriou C (2013) Somatic mutation profiling and associations with prognosis and trastuzumab benefit in early breast cancer. J Natl Cancer Inst 105:960–967. doi:10.1093/jnci/djt121

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  30. Pogue-Geile KL, Song N, Jeong JH, Gavin PG, Kim SR, Blackmon NL, Finnigan M, Rastogi P, Fehrenbacher L, Mamounas EP, Swain SM, Wickerham DL, Geyer CE Jr, Costantino JP, Wolmark N, Paik S (2015) Intrinsic subtypes, pik3ca mutation, and the degree of benefit from adjuvant trastuzumab in the nsabp b-31 trial. J Clin Oncol. doi:10.1200/JCO.2014.56.2439

    Google Scholar 

  31. Barbareschi M, Cuorvo LV, Girlando S, Bragantini E, Eccher C, Leonardi E, Ferro A, Caldara A, Triolo R, Cantaloni C, Decarli N, Galligioni E, Dalla Palma P (2012) pi3kca mutations and/or pten loss in HER2-positive breast carcinomas treated with trastuzumab are not related to resistance to anti-her2 therapy. Virchows Arch 461:129–139. doi:10.1007/s00428-012-1267-2

    Article  CAS  PubMed  Google Scholar 

  32. Rastogi P, Anderson SJ, Bear HD, Geyer CE, Kahlenberg MS, Robidoux A, Margolese RG, Hoehn JL, Vogel VG, Dakhil SR, Tamkus D, King KM, Pajon ER, Wright MJ, Robert J, Paik S, Mamounas EP, Wolmark N (2008) Preoperative chemotherapy: updates of national surgical adjuvant breast and bowel project protocols b-18 and b-27. J Clin Oncol 26:778–785. doi:10.1200/JCO.2007.15.0235

    Article  PubMed  Google Scholar 

  33. Cortazar P, Zhang L, Untch M, Mehta K, Costantino JP, Wolmark N, Bonnefoi H, Cameron D, Gianni L, Valagussa P, Swain SM, Prowell T, Loibl S, Wickerham DL, Bogaerts J, Baselga J, Perou C, Blumenthal G, Blohmer J, Mamounas EP, Bergh J, Semiglazov V, Justice R, Eidtmann H, Paik S, Piccart M, Sridhara R, Fasching PA, Slaets L, Tang S, Gerber B, Geyer CE Jr, Pazdur R, Ditsch N, Rastogi P, Eiermann W, von Minckwitz G (2014) Pathological complete response and long-term clinical benefit in breast cancer: the ctneobc pooled analysis. Lancet 384:164–172. doi:10.1016/S0140-6736(13)62422-8

    Article  PubMed  Google Scholar 

  34. Nagata Y, Lan KH, Zhou X, Tan M, Esteva FJ, Sahin AA, Klos KS, Li P, Monia BP, Nguyen NT, Hortobagyi GN, Hung MC, Yu D (2004) Pten activation contributes to tumor inhibition by trastuzumab, and loss of pten predicts trastuzumab resistance in patients. Cancer Cell 6:117–127. doi:10.1016/j.ccr.2004.06.022

    Article  CAS  PubMed  Google Scholar 

  35. Esteva FJ, Guo H, Zhang S, Santa-Maria C, Stone S, Lanchbury JS, Sahin AA, Hortobagyi GN, Yu D (2010) Pten, pik3ca, p-akt, and p-p70s6k status: association with trastuzumab response and survival in patients with HER2-positive metastatic breast cancer. Am J Pathol 177:1647–1656. doi:10.2353/ajpath.2010.090885

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  36. Berns K, Horlings HM, Hennessy BT, Madiredjo M, Hijmans EM, Beelen K, Linn SC, Gonzalez-Angulo AM, Stemke-Hale K, Hauptmann M, Beijersbergen RL, Mills GB, van de Vijver MJ, Bernards R (2007) A functional genetic approach identifies the pi3k pathway as a major determinant of trastuzumab resistance in breast cancer. Cancer Cell 12:395–402. doi:10.1016/j.ccr.2007.08.030

    Article  CAS  PubMed  Google Scholar 

  37. Saal LH, Holm K, Maurer M, Memeo L, Su T, Wang X, Yu JS, Malmstrom PO, Mansukhani M, Enoksson J, Hibshoosh H, Borg A, Parsons R (2005) Pik3ca mutations correlate with hormone receptors, node metastasis, and erbb2, and are mutually exclusive with pten loss in human breast carcinoma. Cancer Res 65:2554–2559. doi:10.1158/0008-5472-CAN-04-3913

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Ezzeldin M. Ibrahim.

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The meta-analysis complies with the current laws of Saudi Arabia.

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Ibrahim, E.M., Kazkaz, G.A., Al-Mansour, M.M. et al. The predictive and prognostic role of phosphatase phosphoinositol-3 (PI3) kinase (PIK3CA) mutation in HER2-positive breast cancer receiving HER2-targeted therapy: a meta-analysis. Breast Cancer Res Treat 152, 463–476 (2015). https://doi.org/10.1007/s10549-015-3480-6

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