Pubfacts - Scientific Publication Data
  • Categories
  • |
  • Journals
  • |
  • Authors
  • Login
  • Categories
  • Journals

Search Our Scientific Publications & Authors

Publications
  • Publications
  • Authors
find publications by category +
Translate page:

Active surveillance for prostate cancer: an Australian experience.

Authors:
Joseph J Ischia Chia Y Pang Yeng K Tay Christopher F D Li Wai Suen Hau C Aw Mark Frydenberg

BJU Int 2012 Apr;109 Suppl 3:40-3

Department of Urology, Southern Health, Melbourne, Victoria, Australia.

Objective: To assess the patient and cancer characteristics as well as outcomes of a large cohort of Australian men who chose active surveillance (AS) as initial management of their low-risk prostate cancer.

Patients And Methods: Men treated by one surgeon who had chosen AS as the primary management for prostate cancer were identified from the records. The patient and cancer data recorded included: patient age, prostate-specific antigen (PSA) concentration at diagnosis, mode of prostate cancer detection. For prostate cancer diagnosed at prostate biopsy, data were collected for the number of cores taken as well as positive core number, cancer burden, and Gleason grade. Survival analysis was used to determine the duration of AS.

Results: In all, 154 men with low-risk prostate cancer with a median (range) age 63.0 (36-81) years and a mean (range) PSA concentration of 6.5 (0.3-22) ng/mL underwent AS. The median (range) duration of AS was 1.9 (0.1-16.6) years. AS was ceased in 29 patients (19%) after a mean (range) of 2.4 (0.2-7.9) years. Of these, 26 were upstaged, one chose curative treatment despite stable disease, and two died from disease not related to prostate cancer. Actuarial analysis on the probability of still being on AS after 5 years was 61.9% (95% confidence interval [CI] 46.2-74.2%) and after 10 years was 45.0% (95% CI 21.3-66.2%). While the period of follow-up is short, there were no biochemical recurrences in men who underwent curative treatment and no deaths from prostate cancer.

Conclusion: AS is an acceptable mode of initial treatment in Australian men with low-risk prostate cancer.

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1464-410X.2012.11045.xDOI Listing
April 2012

Publication Analysis

Top Keywords

prostate cancer
28
low-risk prostate
12
prostate
10
cancer
10
australian men
8
men low-risk
8
patient cancer
8
psa concentration
8
curative treatment
8
active surveillance
8
median range
8
men
5
years
5
survival analysis
4
gleason grade
4
[ci] 462-742%
4
analysis determine
4
grade survival
4
interval [ci]
4
range
4

Similar Publications

Discovery of A031 as effective proteolysis targeting chimera (PROTAC) androgen receptor (AR) degrader for the treatment of prostate cancer.

Authors:
Linrong Chen Liuquan Han Shujun Mao Ping Xu Xinxin Xu Ruibo Zhao Zhihua Wu Kai Zhong Guangliang Yu Xiaolei Wang

Eur J Med Chem 2021 Feb 23;216:113307. Epub 2021 Feb 23.

State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, 222 S. Tianshui Rd, Lanzhou, 730000, PR China. Electronic address:

Androgen receptor (AR) is an effective therapeutic target for the treatment of prostate cancer. We report herein the design, synthesis, and biological evaluation of highly effective proteolysis targeting chimeras (PROTAC) androgen receptor (AR) degraders, such as compound A031. It could induce the degradation of AR protein in VCaP cell lines in a time-dependent manner, achieving the IC 50 value of less than 0. Read More

View Article and Full-Text PDF
February 2021
Similar Publications

Fragility index of trials supporting approval of anti-cancer drugs in common solid tumours.

Authors:
Alexandra Desnoyers Brooke E Wilson Michelle B Nadler Eitan Amir

Cancer Treat Rev 2021 Feb 16;94:102167. Epub 2021 Feb 16.

Division of Medical Oncology & Hematology, Department of Medicine, Princess Margaret Cancer Centre and the University of Toronto, 610 University Avenue, Toronto, Ontario M5G 2M9, Canada. Electronic address:

Background: The Fragility Indexquantifies the reliability of positive trials by estimating the number of events, which would change statistically significant results to non-significant results.

Methods: We identified randomized trials supporting drug approvals by the US FDA between 2009 and 2019 in lung, breast, prostate, and colon cancers and in melanoma. We reconstructed survival tablesand calculated the number of events, which would result in a non-significant result for the primary endpoint. Read More

View Article and Full-Text PDF
February 2021
Similar Publications

Synthesis and Cytotoxic Evaluation of Novel Hybrid Estrane Heterocycles as Chemotherapeutic Anti-Cancer Agents.

Authors:
Doaa S Nada Dina S Elkady Ghada H Elsayed Adel A-H Abdel-Rahman Gamal A Elmegeed

Steroids 2021 Feb 27:108813. Epub 2021 Feb 27.

Hormones Department, National Research Centre, 12622 Dokki, Giza, Egypt.

New synthesized hybrid steroidal heterocyclic compounds have received a lot of attention in view of their biological activities as anticancer agents. In this study, a novel class of hybrid estrane heterocyclic compounds were synthesized and evaluated by analytical and spectral data which proved the validity of these derivatives. The cytotoxicity of synthesized compounds 2a, 2b, 2c, 3b, 8, 10a, 10b, 13, 14, 16a and 19 against three human cell lines: breast cancer cells (MCF-7), prostate cancer cells (PC3), and liver cancer cells (HepG2) has been tested using MTT assay. Read More

View Article and Full-Text PDF
February 2021
Similar Publications
© 2021 PubFacts.
  • About PubFacts
  • Privacy Policy
  • Sitemap