Literature DB >> 2804976

Relationship between tumor size and curability of prostatic cancer by combined chemo-hormonal therapy in rats.

J T Isaacs1.   

Abstract

Nearly all men with metastatic prostatic cancer respond to androgen ablation, demonstrating that at least a portion of their cancer cells are androgen responsive. Unfortunately, however, individual prostatic cancers contain clones of androgen-independent, in addition to androgen-responsive, cancer cells. Due to this tumor cell heterogeneity, essentially all patients treated with androgen ablation alone eventually relapse to a state unresponsive to further antiandrogen therapy; cures are rarely produced. To produce cures, additional nonhormonal therapy targeted at the androgen-independent prostatic cancer cells within the patient should be combined with androgen ablation targeted at the androgen-dependent cancer cells. The validity of such combined chemo-hormonal therapy was tested using, as the experimental model, two members of the Dunning system of serially transplantable rat prostatic cancers. Specifically the slow growing, well differentiated H and the fast growing, poorly differentiated G Dunning sublines were used, since these cover the clinical extremes observed for human prostatic cancers. The chemotherapeutic agent used in combination with surgical androgen ablation (i.e., castration) in these studies was Cytoxan. These studies demonstrate that for both the H and G cancer-bearing rats, the mean survival following combined chemo-hormonal therapy was increased above that found for castrate or Cytoxan when either was used as monotherapy. In addition, an inverse relationship between tumor size at the time of initiation of therapy and the ability of the combined chemo-hormonal therapy to cure animal bearing either the H or G sublines was demonstrated. Such combined chemo-hormonal therapy could only cure a proportion (i.e., 30-40%) of H or G tumor-bearing animals if initiated when the tumor was less than or equal to 0.2 cm3 in size. In contrast, if the tumor was 1-2 cm3 in starting size when the chemo-hormonal therapy was initiated, no animal was cured. Neither of the monotherapies (i.e., castrates or Cytoxan alone) could cure any animals regardless of the starting size.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2804976

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  10 in total

Review 1.  The long and winding road for the development of tasquinimod as an oral second-generation quinoline-3-carboxamide antiangiogenic drug for the treatment of prostate cancer.

Authors:  John T Isaacs
Journal:  Expert Opin Investig Drugs       Date:  2010-10       Impact factor: 6.206

2.  Biochemical (Prostate-Specific Antigen) Relapse: An Oncologist's Perspective.

Authors:  Mary-Ellen Taplin
Journal:  Rev Urol       Date:  2003

3.  Biochemical (Prostate-Specific Antigen) Relapse: An Oncologist's Perspective.

Authors:  Mary-Ellen Taplin
Journal:  Rev Urol       Date:  2003

Review 4.  Intermittent androgen deprivation.

Authors:  N A Dawson
Journal:  Curr Oncol Rep       Date:  2000-09       Impact factor: 5.075

5.  Long-term control or possible cure? Treatment of stage D2 prostate cancer under chemotherapy using cisplatin and estramustine phosphate followed by maximal androgen blockade.

Authors:  Shinji Urakami; Hiroaki Shiina; Masahiro Sumura; Satoshi Honda; Koji Wake; Takeo Hiraoka; Shogo Inoue; Noriyoshi Ishikawa; Mikio Igawa
Journal:  Int Urol Nephrol       Date:  2008       Impact factor: 2.370

6.  The current state of preclinical prostate cancer animal models.

Authors:  Kenneth J Pienta; Cory Abate-Shen; David B Agus; Ricardo M Attar; Leland W K Chung; Norman M Greenberg; William C Hahn; John T Isaacs; Nora M Navone; Donna M Peehl; Jonathon W Simons; David B Solit; Howard R Soule; Terry A VanDyke; Michael J Weber; Lily Wu; Robert L Vessella
Journal:  Prostate       Date:  2008-05-01       Impact factor: 4.104

7.  Systemic chemotherapy combined with local adoptive immunotherapy cures rats bearing 9L gliosarcoma.

Authors:  C A Kruse; D H Mitchell; B K Kleinschmidt-DeMasters; D Bellgrau; J M Eule; J R Parra; Q Kong; K O Lillehei
Journal:  J Neurooncol       Date:  1993-02       Impact factor: 4.130

8.  Inhibition of growth of experimental prostate cancer with sustained delivery systems (microcapsules and microgranules) of the luteinizing hormone-releasing hormone antagonist SB-75.

Authors:  E Korkut; L Bokser; A M Comaru-Schally; K Groot; A V Schally
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-01       Impact factor: 11.205

9.  Ultra-early versus early salvage androgen deprivation therapy for post-prostatectomy biochemical recurrence in pT2-4N0M0 prostate cancer.

Authors:  Satoru Taguchi; Hiroshi Fukuhara; Takeshi Azuma; Motofumi Suzuki; Tetsuya Fujimura; Tohru Nakagawa; Akira Ishikawa; Haruki Kume; Yasuhiko Igawa; Yukio Homma
Journal:  BMC Urol       Date:  2014-10-16       Impact factor: 2.264

10.  Identification of microRNAs and mRNAs associated with multidrug resistance of human laryngeal cancer Hep-2 cells.

Authors:  Wanzhong Yin; Ping Wang; Xin Wang; Wenzhi Song; Xiangyan Cui; Hong Yu; Wei Zhu
Journal:  Braz J Med Biol Res       Date:  2013-06-12       Impact factor: 2.590

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.