File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1111/bju.14677
- Scopus: eid_2-s2.0-85062970946
- Find via
Supplementary
-
Citations:
- Scopus: 0
- Appears in Collections:
Conference Paper: The clinical outcome of prostate ductal adenocarcinoma: a multicentre matched cohort comparative study
Title | The clinical outcome of prostate ductal adenocarcinoma: a multicentre matched cohort comparative study |
---|---|
Authors | |
Issue Date | 2019 |
Publisher | Wiley-Blackwell Publishing Ltd. The Journal's web site is located at http://www.bjui.org/ |
Citation | The 23rd Hong Kong Urological Assoication Annual Scientific Meeting, Hong Kong, 4 November 2018. In BJU International, v. 123 n. S1, p. 8-9 How to Cite? |
Abstract | Objective:
Prostate Ductal Adenocarcinoma(PDA) is a rare variant of prostate cancer(PCa). There are conflicting reports regarding its oncological outcome and prognosis. To date, there is no consensus on what is the optimal treatment.
Patients and Methods:
All patients diagnosed with PDA in three institutions from London(UK), Hong Kong and Kingston(Jamaica) during 2005–2015 were included. Treatment included radical surgery, radical radiotherapy or hormone manipulation. Patients who were diagnosed with >=Gleason8 prostate acinar adenocarcinoma(PAA) served as control groups.
Results:
Of 9812 patients diagnosed with PCa, 157 (1.8%) had PDA; 958 had PAA. PSA at presentation was lower for PDA. 346 (247‐PAA,99‐PDA) had radical prostatectomy; 314 (295‐PAA,19‐PDA) had radical radiotherapy; 449 (416‐PAA,33‐PDA) had hormone treatment.
In surgery group, positive margin were 51%(PDA) vs 54%(PAA), p = 0.13. 57%(PDA) vs 46%(PAA) developed biochemical recurrence. 14%(PDA) vs 5.3%(PAA), p = 0.08 developed distant metastasis and 4.5%(PDA) vs 5.3%(PAA) have died. In radiotherapy group,16%(PDA) vs 22%(PAA) had biochemical recurrence, 16%(PDA) vs 9%(PAA), p = 0.01 developed distant metastasis, 17%(PDA) vs 18%(PAA), p = 0.76 have died. In hormone group, 71%(PDA) vs 47%(PAA) developed metastasis at 32 months; 71%(PDA) vs 45%(PAA) have died. Mean follow‐up for all groups is 71 months.
Conclusion:
PDA patients had higher risk of metastasis compared to the acinar group regardless of treatment offered. Early adjuvant treatment may be required in prostate ductal cancer. |
Description | Oral Presentation |
Persistent Identifier | http://hdl.handle.net/10722/266484 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.337 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yuen, SKK | - |
dc.contributor.author | Lam, PW | - |
dc.contributor.author | Elhage, O | - |
dc.contributor.author | Morrison, B | - |
dc.contributor.author | Tsu, HLJ | - |
dc.contributor.author | Kiberu, Y | - |
dc.contributor.author | Khan, N | - |
dc.contributor.author | Suleman, MT | - |
dc.contributor.author | Persad, R | - |
dc.contributor.author | Chandra, A | - |
dc.contributor.author | Dasgupta, P | - |
dc.date.accessioned | 2019-01-18T08:20:34Z | - |
dc.date.available | 2019-01-18T08:20:34Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | The 23rd Hong Kong Urological Assoication Annual Scientific Meeting, Hong Kong, 4 November 2018. In BJU International, v. 123 n. S1, p. 8-9 | - |
dc.identifier.issn | 1464-4096 | - |
dc.identifier.uri | http://hdl.handle.net/10722/266484 | - |
dc.description | Oral Presentation | - |
dc.description.abstract | Objective: Prostate Ductal Adenocarcinoma(PDA) is a rare variant of prostate cancer(PCa). There are conflicting reports regarding its oncological outcome and prognosis. To date, there is no consensus on what is the optimal treatment. Patients and Methods: All patients diagnosed with PDA in three institutions from London(UK), Hong Kong and Kingston(Jamaica) during 2005–2015 were included. Treatment included radical surgery, radical radiotherapy or hormone manipulation. Patients who were diagnosed with >=Gleason8 prostate acinar adenocarcinoma(PAA) served as control groups. Results: Of 9812 patients diagnosed with PCa, 157 (1.8%) had PDA; 958 had PAA. PSA at presentation was lower for PDA. 346 (247‐PAA,99‐PDA) had radical prostatectomy; 314 (295‐PAA,19‐PDA) had radical radiotherapy; 449 (416‐PAA,33‐PDA) had hormone treatment. In surgery group, positive margin were 51%(PDA) vs 54%(PAA), p = 0.13. 57%(PDA) vs 46%(PAA) developed biochemical recurrence. 14%(PDA) vs 5.3%(PAA), p = 0.08 developed distant metastasis and 4.5%(PDA) vs 5.3%(PAA) have died. In radiotherapy group,16%(PDA) vs 22%(PAA) had biochemical recurrence, 16%(PDA) vs 9%(PAA), p = 0.01 developed distant metastasis, 17%(PDA) vs 18%(PAA), p = 0.76 have died. In hormone group, 71%(PDA) vs 47%(PAA) developed metastasis at 32 months; 71%(PDA) vs 45%(PAA) have died. Mean follow‐up for all groups is 71 months. Conclusion: PDA patients had higher risk of metastasis compared to the acinar group regardless of treatment offered. Early adjuvant treatment may be required in prostate ductal cancer. | - |
dc.language | eng | - |
dc.publisher | Wiley-Blackwell Publishing Ltd. The Journal's web site is located at http://www.bjui.org/ | - |
dc.relation.ispartof | BJU International | - |
dc.rights | Preprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Postprint This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.title | The clinical outcome of prostate ductal adenocarcinoma: a multicentre matched cohort comparative study | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Lam, PW: lamwayne@hku.hk | - |
dc.identifier.email | Tsu, HLJ: jamestsu@hku.hk | - |
dc.identifier.authority | Lam, PW=rp02305 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1111/bju.14677 | - |
dc.identifier.scopus | eid_2-s2.0-85062970946 | - |
dc.identifier.hkuros | 296741 | - |
dc.identifier.volume | 123 | - |
dc.identifier.issue | S1 | - |
dc.identifier.spage | 8 | - |
dc.identifier.epage | 9 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1464-4096 | - |