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The Clinical Problem of Prostate Cancer

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Progress in Anti-Cancer Chemotherapy

Part of the book series: Progress in Anti-Cancer Chemotherapy ((ANTI-CANCER,volume 4))

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Abstract

Prostate cancer is the most common non-cutaneous malignancy and the second leading cause of cancer death in men. It is estimated that in 1999, 179,300 new cases of prostate cancer will be diagnosed and 37,000 men will die of the disease in the United States alone. One in every six men born in the United States will develop clinically significant prostate cancer in their lifetime [1]. These sobering and staggering statistics speak to the enormous clinical problem that prostate cancer represents in our society, not to mention the tremendous financial cost for diagnosis and treatment that is brought to bear on our already overburdened health care system. In recent years, there has been a decline in the mortality rate from prostate cancer, which some experts argue reflects the success of early detection programs combined with effective local therapy [1, 2]. The sobering truth remains that a patient’s potential for cure lies more in the underlying biologic virulence of their prostatic neoplasm, rather than in early intervention. The observation that fewer men are dying of metastatic prostate cancer is clearly not the result of a significant advance in treatment efficacy, as there hasn’t been one. Instead, this decline in the mortality from prostate cancer more reflects a stage migration, where the cancer is found at an earlier stage and is thus perhaps more amenable to local therapy with surgery or radiotherapy. There remains no effective systemic therapy for prostate cancer that reliably provides a cure when the cancer has progressed beyond the confines of the prostate gland. The biology of prostate cancer is heterogeneous and unpredictable, which contributes to the paucity of effective therapies for aggressive disease. As we enter a new millennium, the standard of care for the treatment of metastatic prostate cancer remains hormone ablation therapy, which was initially described as an effective palliative treatment at the beginning of this century [3]. In the intervening years, we have remained relatively in the dark about the complex biological processes that result in prostate carcinogenesis and progression. This ignorance has directly hampered the development of novel therapeutic approaches. However, with increased funding for basic science research, increased public awareness of the problem, and an increased commitment from the academic, public, and private sector, it is believed that this disease can ultimately be conquered.

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References

  1. Landis SH, Murray T, Bolden S, Wingo PA (1999) Cancer Statistics, 1999. CA Cancer J Clin 49:8–31

    Article  PubMed  CAS  Google Scholar 

  2. Hankey BF, Feuer EJ, Clegg LX, et al (1999) Cancer Surveillance Series: Interpreting trends in prostate cancer- Part I. Evidence of the effects of screening in recent prostate cancer incidence, mortality, and survival rates. JNCI 91:1017–1024

    Article  PubMed  CAS  Google Scholar 

  3. Huggins C, Hodges C (1972) Studies on prostatic cancer. I. The effect of castration, of estrogen and androgen injection on serum phosphatases in metastatic carcinoma of the prostate. CA Cancer J Clin 22(4):232–40

    Article  PubMed  CAS  Google Scholar 

  4. D’Amico AV, Whittington R, Malkowicz SB et al (1998) Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer. JAMA 280:969–974

    Article  PubMed  Google Scholar 

  5. Catalona WJ, Smith DS (1998) Cancer recurrence and survival rates after anatomic radical retropubic prostatectomy for prostate cancer: Intermediate term results. J Urol 160: 2428–2434

    Article  PubMed  CAS  Google Scholar 

  6. Obek C, Louis P, Civantos F, Soloway MS (1999) Comparison of digital rectal examination and biopsy results with the radical prostatectomy specimen. J Urol 161(2):494–8; discussion 498–9

    Google Scholar 

  7. Mills SE, Fowler JE Jr. (1986) Gleason histologic grading of prostatic carcinoma. Correlations between biopsy and prostatectomy specimens. Cancer 57(2):346–9

    CAS  Google Scholar 

  8. Catalona WJ, Ramos CG, Carvalhal GF (1999) Contemporary results of anatomic radical prostatectomy. CA Cancer J Clin. 49: 282–296

    Article  PubMed  CAS  Google Scholar 

  9. Pettaway CA, Pathak S, Greene G, Ramirez E, Wilson MR, Killion JJ, Fidler IJ (1996) Selection of highly metastatic variants of different human prostatic carcinomas using orthotopic implantation in nude mice. Clin Cancer Res (9): 1627–36

    Google Scholar 

  10. Curtis Pettaway, personal communication

    Google Scholar 

  11. Kim J, Logothetis CJ (1999) Serologic tumor markers, clinical biology, and therapy of prostatic carcinoma. Urol Clin North Am 26(2):281–90

    Article  PubMed  CAS  Google Scholar 

  12. Melnyk O, Zimmerman M, Kim KJ, Shuman M (1999) Neutralizing anti-vascular endothelial growth factor antibody inhibits further growth of established prostate cancer and metastases in a pre-clinical model. J Urol 161(3):960–3

    Article  PubMed  CAS  Google Scholar 

  13. Theodorescu D, Broder SR, Boyd JC, Mills SE, Frierson HF Jr. (1997) p53, bcl-2 and retinoblastoma proteins as long-term prognostic markers in localized carcinoma of the prostate. J Urol 158(1): 131–7

    Article  PubMed  CAS  Google Scholar 

  14. Gleave M, Tolcher A, Miyake H, Nelson C, Brown B, Beraldi E, Goldie J (1999) Progression to androgen independence is delayed by adjuvant treatment with antisense Bcl-2 oligo-deoxynucleotides after castration in the LNCaP prostate tumor model. Clin Cancer Res 5(10):2891–8

    PubMed  CAS  Google Scholar 

  15. Dorai T, Perlman H, Walsh K, Shabsigh A, Goluboff ET, Olsson CA, Buttyan R (1999) A recombinant defective adenoviral agent expressing anti-bcl-2 ribozyme promotes apoptosis of bcl-2-expressing human prostate cancer cells. Int J Cancer 82(6):846–52

    Article  PubMed  CAS  Google Scholar 

  16. Moul JW (1999) Angiogenesis, p53, bcl-2 and Ki-67 in the progression of prostate cancer after radical prostatectomy. Eur Urol 35(5–6):399–407

    Article  PubMed  CAS  Google Scholar 

  17. Wood CG, Fenton R, Troncoso P, Pettaway CA, von Eschenbach AC, Liebert M, Wilusz J, Chung LWK (1997) G-Rich Sequence Factor 1 (GRSF-1): A novel marker of prostate cancer progression. J Urol 157(4):343

    Google Scholar 

  18. Chen ME, Troncoso P, Tang K, Babaian RJ, Johnston D (1999) Comparison of prostate biopsy schemes by computer simulation. Urology 1999 53(5):951–60

    Article  PubMed  CAS  Google Scholar 

  19. Millon R, Jacqmin D, Muller D, Guillot J, Eber M, Abecassis J (1999) Detection of prostate-specific antigen- or prostate-specific membrane antigen-positive circulating cells in prostatic cancer patients: clinical implications. Eur Urol 36(4):278–85

    Article  PubMed  CAS  Google Scholar 

  20. Sanz G, Robles JE, Gimenez M, Arocena J, Sanchez D, Rodriguez-Rubio F, Rosell D, Richter JA, Berian JM (1999) Positron emission tomography with 18fluorine-labelled deoxyglucose: utility in localized and advanced prostate cancer. BJU Int 84(9): 1028–1031

    Article  PubMed  CAS  Google Scholar 

  21. Texter JH Jr, Neal CE (1998) The role of monoclonal antibody in the management of prostate adenocarcinoma. J Urol 160(6 Pt 2):2393–5

    PubMed  Google Scholar 

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© 2000 Springer-Verlag France

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Wood, C.G., von Eschenbach, A.C. (2000). The Clinical Problem of Prostate Cancer. In: Khayat, D., Hortobagyi, G.N. (eds) Progress in Anti-Cancer Chemotherapy. Progress in Anti-Cancer Chemotherapy, vol 4. Springer, Paris. https://doi.org/10.1007/978-2-8178-0920-5_14

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  • DOI: https://doi.org/10.1007/978-2-8178-0920-5_14

  • Publisher Name: Springer, Paris

  • Print ISBN: 978-2-287-59692-6

  • Online ISBN: 978-2-8178-0920-5

  • eBook Packages: Springer Book Archive

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