Review Article - Journal of Molecular Oncology Research (2018) Volume 2, Issue 1
Applying precision medicine approach to metastatic castration-resistant prostate cancer: urgent education need on genomic oncology
University of Arizona Cancer Center at Dignity Health St. Joseph’s, Phoenix, AZ, USA
- *Corresponding Author:
- Jue Wang
University of Arizona Cancer Center
Dignity Health St. Joseph’s, Phoenix AZ, USA
E-mail: [email protected] health.org
Accepted date: 04 December, 2017
Citation: Wang J. Applying precision medicine approach to metastatic castration-resistant prostate cancer: urgent education need on genomic oncology. J Mol Oncol Res. 2018;2(1):6-10.
Metastatic castration-resistant prostate cancer (mCRPC) remains a therapeutic challenge. As a result of advances in genomic sequencing technology, “next-generation sequencing” (NGS) is increasingly incorporated into clinical trials and routine oncology clinical practice. Molecular profiling of mCRPC can be a valuable way of defining molecular alterations that might contribute to optimal treatments while reduce risk of adverse effects. To effectively apply cutting edge research to daily patient care, oncologists must grasp the fundamentals of genomic oncology, molecular testing and interpretation. There is an urgent need for health professional education to allow implementation of these novel precision medicine tools.
Metastatic castration-resistant prostate cancer (mCRPC), Personalized medicine, Next-generation sequencing, Genomic oncology, Professional education, Cancer genomics, DNA damage response (DDR), Homologous recombination (HR), BRCA1, BRCA2, Poly(ADP-ribose) polymerases (PARP), PARP inhibitors, Cell-free DNA (cfDNA).
Prostate cancer is the most commonly diagnosed cancer in men and the second leading cause of cancer-related deaths in the United States . Androgen-deprivation therapy (ADT) has been the standard first line therapy for metastatic prostate cancer for last six decades. While ADT initially shows clinical benefit for the majority of patients, prostate cancer inevitably progresses to metastatic castration-resistant prostate cancer (mCRPC) . In the last six years, five novel treatments have been approved by U.S. Food and Drug Administration (FDA). These novel treatments have distinct mechanisms of action: novel microtubule-targeted agent (cabazitaxel); first-of-type immunotherapy (sipuleucel-T); steroidal CYP17A1 inhibitor (abiraterone); androgen receptor (AR) blockade (enzalutamide); and alpha particle-emitting radiopharmaceutical agent (radium-223) [3,4]. While therapeutic options for these patients have significantly improved, mCRPC remains a lethal disease.
Prostate cancer is now recognized as a genetic disorder resulting from the accumulation of various genetic alterations . In a study of Whole-exome gene analysis of a cohort of 150 patients with mCRPC, aberrations of AR, ETS genes, TP53, and PTEN were identified in 40%–60% of cases, with TP53 and AR alterations enriched in mCRPC compared to primary prostate cancer [6-8]. Aberrations of BRCA2, BRCA1, and ATM were observed at much higher frequencies (19.3% overall) compared to those in primary prostate cancers. Clinically actionable alterations were identified in 89% individuals with aberrations in AR, 8% with actionable pathogenic germline alterations, 65% in other cancer-related genes [9,10].
The current progress on mCRPC genomic analysis can be summarized into two aspects: the identification of clinically actionable targets; and novel mutations in mCRPC genomes. Incorporation of practice NGS technology into clinical trials and routine clinical will hopefully advance our understanding of aggressive biological behavior of mCRPC, which will in turn lead to personalized therapy for mCRPC [9-11]. The National Comprehensive Cancer Network (NCCN) clinical practice guidelines for metastatic disease now include a reference to molecular profiling as a permissible consideration for treatment decision making. The reduced cost and faster turn-around-times, clinical applications for genomic testing likely continue to increase.
Genomic DNA is constantly exposed to various genotoxic insults from both internal and external environments that can lead to different types of distinct DNA damage. Unrepaired DNA damage can impact the integrity of the genome, creating genomic instability and leading to accumulation of further genomic aberrations that support cancer cell growth, proliferation and survival [8,9].
DNA damage response (DDR) are important mechanism to maintain genomic integrity [12,13]. The single-strand breaks (SSBs) are repaired primarily through the base excision repair (BER) pathway. SSBs may accumulate because of damaged repair pathways, resulting in the formation of a double-strand break (DSB). One of the major pathways of DSB repair is homologous recombination (HR).
In advanced prostate cancer, the enrichment of genomic instability could be attributed to impaired ability of DNA repair . BRCA2 alteration was identified in 12.7% of cases of mCRPC and the most frequent gene mutation . Overall DNA repair gene aberrations were found in 22.7% of patients, with ATM and BRCA1 alterations occurring in 19.3% of patients. In addition, 3.4% of patients have CDK12, FANCA, RAD51B and RAD51C mutations . These findings of distinct molecular subtype of mCRPC have important implications for developing novel therapy.
Poly-(ADPribose) Polymerase and DNA Repair
Poly-(ADP-ribose) polymerases (PARP) are DNA damage repair enzymes activated by DNA single-(SSB) or double strand breaks (DSB) [17-20]. In the situation of PARP inhibition, cells switch over to homologous recombination (HR) for DNA repair. BRCA1- and BRCA2-mutated cells, which are HR deficient, are hypersensitive to PARP inhibition through the mechanism of synthetic lethality . Similarly, HR deficient cancer cells also show increased sensitivity to PARP inhibitor.
Clinical Trials Investigating PARP Inhibitors in mCRPC
Several PARP inhibitors have entered in early clinical trials. In a multi-center, Phase I clinical trial with PARP inhibitor olaparib (Lynparza), sixty patients with various refractory caners were enrolled. Antitumor activity was observed in patients of BRCA mutation carriers, who had ovarian, breast, or prostate cancer. Among the three patients with mCRPC recruited, only one had a BRCA2 mutation . This patient had a partial prostate-specific antigen (PSA) response and a complete radiographic response of bone metastases.
In a Phase I dose-escalation study of Niraparib (MK-4827) in BRCA mutation carriers and patients with sporadic cancer, 30% of 21 mCRPC patients had a decrease of circulating tumor cells (CTC) counts and one patient had partial PSA response . In addition, stable disease (SD) was reported in 43% of patients.
In a Phase II clinical trial of olaparib in BRCA1/2-associated cancers, 50% response rates (RR), 25% SD were reported in eight previously heavily treated mCRPC patients with germline BRCA1/2 mutations. Median progression-free survival and the Overall Survival (OS) were 7.2 and 18.4 months, respectively, with 50% of patients were still alive at 12 months .
In the TOPARP-A phase II trial reported in The New England Journal of Medicine by investigators from the Institute of Cancer Research (ICR) and The Royal Marsden Hospital in London, olaparib produced an impressive high RR in patients with previously heavily treated mCRPC with tumors exhibiting defects in DNA-repair genes . Overall, sixteen of 49 evaluable patients had a RR of 33%. Median OS was 10.1 months. In 16 of 49 (33%) evaluable patients, DNA-repair genes defects (BRCA1/2, ATM, Fanconi's anemia genes, and CHEK2) were identified by Next-generation sequencing. 88% of those patients with identifiable DNA-repair defects had a response to olaparib. Based on the impressive results of this trial, the FDA has granted Breakthrough Therapy designation to olaparib for patients with BRCA1/2 or ATM gene mutated mCRPC, who had taxane-based chemotherapy and at least one androgen signaling pathway inhibitor . Larger clinical trials exploring the interaction between PARP inhibitors and DNA-repair defects in patients with mCRPC are currently ongoing (Table 1).
|Olaparib with or without cediranib [II]||NCT02893917|
|Rucaparib versus Abiraterone acetate or Enzalutamide or Docetaxel [III]||NCT02975934|
|Olaparib versus Enzalutamide or Abiraterone Acetate [III]||NCT02987543|
Table 1: Ongoing Clinical Trials (Phase I/II/III) with PARP-1 inhibitors for metastatic castration-resistant prostate cancer.
Challenges of Precision Therapy
Successful precision therapy is tailored based on examining the genomic alterations in tumor tissues. However, tissue biopsy is very challenging because bone metastases are predominant in patients with advanced prostate cancer. Biopsies are invasive, morbid, and are subject to sampling bias, biopsy of single site metastatic lesion may not represent the overall tumor genetic changes. mCRPC is a progressive disease with accumulations of gene alterations during disease progression. Serial biopsies are required in order to identify genes might contribute to disease recurrence and resistance to therapy. Further, accurate next-generation sequencing in metastatic bone lesions-derived DNA is technically challenging.
There has been an increasing interest in developing liquid biopsies test such as cell-free DNA (cfDNA) as a predictive biomarker for monitoring therapeutic response, and detecting recurrence. cfDNA is a blood-based test is an appealing alternative as it is non-invasive and poses minimal risk to patients. It is easy to perform, can be repeated at the time of recurrence. cfDNA is derived from all tumor sites, therefore it may represent a more complete repertoire of tumor genome variations [26-29]. It has been shown that tumor genomic abnormalities are well reflected in cfDNA during cancer progression [30-33].
Urgent Education Need on Genomic Oncology
The advances in genomics and expansion of molecular testing likely pave the way for precision cancer medicine for prostate patients in the near future. With more cancer-specific genetic information available, patients can be directed toward to appropriate therapies or clinical trials. There is clearly increasing availability of molecular profiling tests in recent years (Table 2). Commercial laboratories have begun to market such genomic tests to oncologists. Patients express willingness to get those tests . However, genomic oncology has not typically been part of the training for oncology fellowship.
|FoundationOne||Foundation Medicine||Tissue, blood||Next Generation Sequencing||236 genes|
|Caris Molecular Intelligence®||CarisLife Sciences||Tissue||IHC, FISH, Next Generation Sequencing||40 genes|
|Paradigm Cancer Diagnostic (PCDx) test||Paradigm||Tissue||IHC, Next Generation Sequencing||131 genes|
|Guardant360||Guardant Health||Blood||Next Generation Sequencing||54 genes|
Table 2: Examples of current available molecular tests from commercial laboratories.
Even for physicians with substantial expertise in genitourinary oncology, NGS based tests are new term to them, which provide so much information and so many possible uses for it, in some cases, not actionable at all. A recent study showed there is no consensus on how physicians to use molecular assays for personalized cancer care and suggest an urgent need for health professional education to allow implementation and optimal use of these novel personalized medicine tools . In the future, evidence-based genomic tests may help guide the optimal utilization of these tests.
University of Arizona Cancer Center (UACC) Experience
We have applied next generation sequencing using both tumor tissue and cfDNA in patients with mCRPC. As part of a multi-disciplinary molecular tumor board at UACC, specialists meet together to discuss patient cases and findings from molecular profiling tests. The genomic testing is appropriate for a given patient of pursuing these tests are usually made at our Molecular Tumor Board for those refractory patients who have run out of standards options. Recently, we and others reported the results from a multi-institutional study showed that DNA-based liquid biopsy has great potential to examine molecular alterations in advanced prostate cancer .
Based on the molecular profiling findings of DNA repair defects, several heavily pretreated, refractory mCRPC patients were found eligible and treated with olaparib. One patient with BRCA 2 deletion who had partial response lasting eight months. Another patient with TMPRSS2-ERG fusion and PTEN loss had complete pathological response (Table 3). Olaparib monotherapy at the dose of 400 mg bid was generally well tolerated in our patients, with the majority of adverse events being of mild to moderate severity. Further studies are ongoing to examine the utility of cfDNA as a predict biomarker for treatment response and clinical outcomes. There are numerous challenges that need to be surpassed before delivering on the promise of personalized cancer therapy. These include tumor heterogeneity, the requirement of tissue sample for Next-generation sequencing, potential morbidity of biopsies, technical limitations of current available molecular tests, costs, and reimbursement hurdles.
|Patient ID||Age||ECOG||Gleason||Gene alterations||Source||Treatment||Best response|
|2||62||0||5+4||BRCA2||tumor tissue||DOCETAXEL||PSA CR|
|3||63||1||5+4||BRCA2, TMPRSS2-ERG gene fusion, and TP53||tumor tissue and cfDNA||Olaparib||PR|
|5||67||1||5+4||PTEN, RB, TMPRSS2-ERG gene fusion, and TP53||tumor tissue||Olaparib||PCR|
Table 3: Summary of University of Arizona Cancer Center (UACC) experience on the application of next generation sequencing in the management of patients with metastatic castration-resistant prostate cancer. ECOG: Eastern Cooperation Oncology Group; RB: retinoblastoma gene; BRCA1: breast cancer 1; BRCA2: breast cancer 2; cfDNA: Cell-free DNA; PSA: Prostate-specific antigen (PSA); CR: Complete remission; PR: Partial response; SD: stable disease; PCR: Pathological complete remission; CR: Complete remission.
Since genomics-guided therapy will be integrated into treatment paradigm of mCRPC (Table 4), there is a critical need for education in genomics among oncology professionals. In order to take full advantage of valid and clinically useful genomic tests, oncologists must become knowledgeable about indications and interpretation, limitations of current available tests. In addition, they need aware that the survival benefits of genomic guided therapy largely have not been proved and the perceived benefit may be overestimated . Continued critical evaluation of emerging NGS and other new technologies, their clinical utility, interpretation, and indications for the use of such tests are necessary to ensure the optimal integration into appropriate patient care. At UACC genitourinary oncology division, we are developing case based approach on genomic medicine education for our oncology providers, resident physicians, oncology trainees, and community oncologists.
Precision medicine shows great promise in the management of mCRPC, but it is still in the very early stages. Advancement in mCRPC precision medicine is dependent on continuous research in prostate cancer genomics and enrolling patients into clinical trials. Given the rapid integration of genomics into genitourinary oncology, health care providers for prostate cancer should be educated in genomic medicine.
- Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin. 2016;66(1):7-30.
- Attard G, Sarker D, Reid A, et al. Improving the outcome of patients with castration-resistant prostate cancer through rational drug development. Br J Cancer. 2006;95(7):767-74.
- Tannock IF, de Wit R, Berry WR, et al. Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer. N Engl J Med. 2004;351:1502-12.
- de Bono JS, Oudard S, Ozguroglu M, et al. Prednisone plus cabazitaxel or mitoxantrone for metastatic castration-resistant prostate cancer progressing after docetaxel treatment: a randomised open-label trial. Lancet. 2010;376:1147-54.
- de Bono JS, Logothetis CJ, Molina A, et al. Abiraterone and increased survival in metastatic prostate cancer. N Engl J Med. 2011;364:1995-2005.
- Kantoff PW, Higano CS, Shore ND, et al. Sipuleucel-T immunotherapy for castration-resistant prostate cancer. N Engl J Med. 2010;363:411-22.
- Fizazi K, Carducci M, Smith M, et al. Denosumab versus zoledronic acid for treatment of bone metastases in men with castration-resistant prostate cancer: a randomised, double-blind study. Lancet. 2011;377:813-22.
- Taylor BS, Schultz N, Hieronymus H, et al. Integrative genomic profiling of human prostate cancer. Cancer Cell. 2010;18:11–22.
- Grasso CS, Wu YM, Robinson DR, et al. The mutational landscape of lethal castration- resistant prostate cancer. Nature. 2012;487:239–43.
- Beltran H, Yelensky R, Frampton GM, et al. Targeted next-generation sequencing of advanced prostate cancer identifies potential therapeutic targets and disease heterogeneity. Eur Urol. 2013;63(5):920-6.
- Robinson D, Van Allen EM, Wu YM, et al. Integrative clinical genomics of advanced prostate cancer. Cell. 2015;161(5):1215-28.
- Fan R, Kumaravel TS, Jalali F, et al. Defective DNA strand break repair after DNA damage in prostate cancer cells: implications for genetic instability and prostate cancer progression. Cancer Res. 2004;64:8526–33.
- Dietlein F, Reinhardt HC. Molecular Pathways: exploiting tumor specific molecular defects in DNA repair pathways for precision cancer therapy. Clin Cancer Res. 2014;20(23):5882-87.
- Krajewska M, Fehrmann R, de Vries EG, et al. Regulators of homologous recombination repair as novel targets for cancer treatment. Front Genet. 2015;6:96.
- Consortium TB. Cancer risks in BRCA2 mutation carriers. J Natl Cancer Inst. 1999;91:1310–16.
- Castro E, Goh C, Olmos D et al. Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer. J Clin Oncol. 2013;31(14):1748–57.
- Dhawan M, Ryan CJ, Ashworth A. DNA repair deficiency is common in advanced prostate cancer: new therapeutic opportunities. Oncologist. 2016;21(8):940-45.
- Durkacz BW, Omidiji O, Gray DA, et al. (ADP-ribose)n participates in DNA excision repair. Nature. 1980;283:593–610.
- Menissier-de Murcia J, Molinete M, Gradwohl G, et al. Zinc-binding domain of poly (ADP-ribose) polymerase participates in the recognition of single strand breaks on DNA. J Mol Biol. 1989;210(1): 229-33.
- McCabe, Turner NC, Lord CJ, et al. Deficiency in the repair of DNA damage by homologous recombination and sensitivity to poly (ADP-ribose) polymerase inhibition. Cancer Res. 2006;66(16):8109–15.
- Farmer H, McCabe N, Lord CJ, et al. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature. 2005;434(7035):917–21.
- Fong PC, Boss DS, Yap TA, et al. Inhibition of poly (ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med. 2009;361(2):123-34.
- Sandhu SK, Schelman WR, Wilding G, et al. The poly(ADP-ribose) polymerase inhibitor niraparib (MK4827) in BRCA mutation carriers and patients with sporadic cancer: a phase 1 dose-escalation trial. Lancet Oncol. 2013;14(9):882-92.
- Kaufman B, Shapira-Frommer R, Schmutzler RK, et al. Olaparib monotherapy in patients with advanced cancer and a germline BRCA1/2 mutation. J Clin Oncol. 2015;33(3), 244–50.
- Mateo J, Carreira S, Sandhu S, et al. DNA-Repair Defects and Olaparib in Metastatic Prostate Cancer. N Engl J Med. 2015;373(18):1697-708.
- Crowley E, Di Nicolantonio F, Loupakis F, et al. Liquid biopsy: monitoring cancer-genetics in the blood. Nat Rev Clin Oncol. 2013;10:472–84.
- Heitzer E, Ulz P, Geigl JB. Circulating tumor DNA as a liquid biopsy for cancer. Clin Chem. 2015;61:112–23.
- Diaz LA Jr, Bardelli A. Liquid biopsies: genotyping circulating tumor DNA. J Clin Oncol. 2014;32:579–86.
- Leary RJ, Sausen M, Kinde I, et al. Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing. Sci Transl Med. 2012;4(162):ra154.
- Heitzer E, Ulz P, Belic J, et al. Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing. Genome Med.2012;4(162):154.
- Murtaza M, Dawson SJ, Tsui DW. Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA. Nature. 2013;497:108–12.
- Chan KC, Jiang P, Zheng YW, et al. Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing. Clin Chem. 2013;59:211–24.
- Gray SW, Hicks-Courant K, Lathan CS, et al. Attitudes of patients with cancer about personalized medicine and somatic genetic testing. J Oncol Pract. 2012;8:329–35.
- Gray SW, Hicks-Courant K, Cronin A, et al. Physicians attitudes about multiplex tumor genomic testing. J Clin Oncol. 2014;32(13):1317-23.
- Sonpavde G, Nagy RJ, Agarwal N, et al. Profiling of circulating tumor (ct)-DNA for potentially actionable targets in prostate cancer (PCa). J Clin Oncol. 2016 .
- Tannock IF, Hickman JA. Limits to Personalized Cancer Medicine. N Engl J Med. 2016;375(13):1289-94.