Patrick Craig Walsh
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Patrick Craig Walsh has a total of 125 co-authors. Here are the top co-authors by number of shared publications:
- William B. Isaacs
Department of Urology, The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine , Baltimore, MD
7 shared publications - Bao-Li Chang
Center for Human Genomics, Wake Forest University School of Medicine, Winston‐Salem, North Carolina
6 shared publications - Deborah A. Meyers
Center for Human Genomics, Wake Forest University School of Medicine, Winston‐Salem, North Carolina
6 shared publications - Jianfeng Xu
Center for Cancer Genomics, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA
6 shared publications - Eugene R. Bleecker
Department of Medicine, University of Arizona, Tucson, Arizona, USA
4 shared publications - Gregory A. Hawkins
Center for Genomics and Personalized Medicine Research, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157, USA
4 shared publications
Latest Publications
- 13 August 2025
- Published by Springer Nature
- p. 329-332
Humanism in Surgery
- 5 January 2022
- Published by Elsevier in Urologic Oncology: Seminars and Original Investigations
- Vol. 40 (2) , 15-17
2021 Joseph A. Smith, Jr. Mentorship lecture: Discovery
- 5 January 2022
- Published by Elsevier in Urologic Oncology: Seminars and Original Investigations
- Vol. 40 (2) , 15-17
2021 Joseph A. Smith, Jr. Mentorship lecture: Discovery
- 1 November 2019
- Published by Elsevier in European Urology
- Vol. 76 (5) , 704
Re: Association of Treatment with 5α-Reductase inhibitors with Time to Diagnosis and Mortality in Prostate Cancer
- 1 November 2019
- Published by Elsevier in European Urology
- Vol. 76 (5) , 704
Re: Association of Treatment with 5α-Reductase inhibitors with Time to Diagnosis and Mortality in Prostate Cancer
- 30 October 2018
- Published by Oxford University Press (OUP) in JNCI: Journal of the National Cancer Institute
- Vol. 111 (7) , 747
RE: Risk of Prostate Cancer in Men Treated With 5α-Reductase Inhibitors—A Large Population-Based Prospective Study
- 30 October 2018
- Published by Oxford University Press (OUP) in JNCI: Journal of the National Cancer Institute
- Vol. 111 (7) , 747
RE: Risk of Prostate Cancer in Men Treated With 5α-Reductase Inhibitors—A Large Population-Based Prospective Study
- 1 November 2017
- Published by Elsevier in European Urology
- Vol. 72 (5) , 657-659
The Search for the Missing Heritability of Prostate Cancer
- 1 November 2017
- Published by Elsevier in European Urology
- Vol. 72 (5) , 657-659
The Search for the Missing Heritability of Prostate Cancer
- 1 October 2017
- Published by Elsevier in European Urology
- Vol. 72 (4) , 482
If You Want to Make an Important Discovery, Listen to Your Patients
- 1 October 2017
- Published by Elsevier in European Urology
- Vol. 72 (4) , 482
If You Want to Make an Important Discovery, Listen to Your Patients
- Open Access
- 15 June 2017
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 376 (24) , 2401-2402
Prostate Cancer Screening
The dramatic decline in observed prostate cancer mortality after the introduction of prostate-specific antigen (PSA) screening provides compelling evidence in support of testing. Pinsky et al. (March 30 issue)1 state that from the late 1980s to the present, the prostate cancer mortality rate fell 45%. This underestimates what really happened. Because PSA testing did not become widespread until 1990, prostate cancer mortality rates continued to rise past the late 1980s. Recently, the American Cancer Society reported that the prostate cancer mortality rate fell 51% from 1993 to 2014.2 Furthermore, Pinsky et al. suggest that this finding is equivocal because of “likely confounding by increasingly effective systemic therapies.” It has been shown that there was no improvement in overall or cause-specific survival among men with metastatic disease who presented between 1988 and 2009.3 What systemic therapies administered between 1993 and 2014 were responsible for the observed decline in mortality?
- 15 June 2017
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 376 (24) , 2401-2402
Open AccessProstate Cancer Screening
The dramatic decline in observed prostate cancer mortality after the introduction of prostate-specific antigen (PSA) screening provides compelling evidence in support of testing. Pinsky et al. (March 30 issue)1 state that from the late 1980s to the present, the prostate cancer mortality rate fell 45%. This underestimates what really happened. Because PSA testing did not become widespread until 1990, prostate cancer mortality rates continued to rise past the late 1980s. Recently, the American Cancer Society reported that the prostate cancer mortality rate fell 51% from 1993 to 2014.2 Furthermore, Pinsky et al. suggest that this finding is equivocal because of “likely confounding by increasingly effective systemic therapies.” It has been shown that there was no improvement in overall or cause-specific survival among men with metastatic disease who presented between 1988 and 2009.3 What systemic therapies administered between 1993 and 2014 were responsible for the observed decline in mortality?
- 20 May 2017
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 35 (15_suppl) , 5020
Stereotactic ablative radiation therapy for the treatment of oligometastatic prostate cancer.
5020 Background: The importance of local treatment in oligometastatic prostate cancer (OPC) is unknown. Stereotactic ablative radiotherapy (SABR) is highly focused, high-dose radiation that is well suited for treatment of oligometastases. Here we report on the safety and preliminary clinical outcomes of SABR in a modern cohort of OPC men. Methods: Eighty four men who satisfied criteria of OPC diagnosed on imaging underwent consolidative SABR were then followed prospectively on our IRB approved registry by our GU multidisciplinary team. We collected demographic, clinical, toxicity and efficacy information. We examined the first 66 men in this preliminary report to allow for a minimum of 4.5 months follow-up. SABR was delivered in 1-5 fractions of 5-18 Gy. Kaplan-Meier method was used to assess local progression-free survival (LPFS), biochemical progression-free survival (bPFS; PSA nadir+2), distant progression free survival (DPFS), ADT-free survival (ADT-FS) and time-to-next intervention (TTNI). Results: Of the 66 OPC patients analyzed, 25 (38%) men presented as synchronous OPC and the remaining 41 had recurrent OPC. Median and mean follow-up was 61 and 66 weeks, respectively. Patient and disease factors as listed in the Table. Crude Grade 1 and 2 acute toxicities were 36% and 11%, respectively, with no Grade > 2 toxicity. SABR was delivered to 134 metastases: 89 bone (66%), 40 nodal (30%) and 5 (4%) visceral metastases. Overall LPFS at 1-year was 92%. The bPFS and DPFS at 1-year were 69% and 69%, respectively. Median TTNI was not reached yet. Of the 18 men with hormone sensitive prostate cancer who had their ADT deferred, 11/18 (56%) remain free of disease following SABR (1-year ADT-FS was 78%) and in 17 castration resistant men, 11 had > 50% PSA declines with 1-year TTNI of 30% with a median of 45 weeks. Conclusions: Consolidative SABRfor OPCis feasible and well tolerated. The preliminary clinical outcomes in our series is limited by heterogeneity and size but our data suggests that this approach is worthy of further prospective study. [Table: see text]
- 20 May 2017
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 35 (15_suppl) , 5020
Stereotactic ablative radiation therapy for the treatment of oligometastatic prostate cancer.
5020 Background: The importance of local treatment in oligometastatic prostate cancer (OPC) is unknown. Stereotactic ablative radiotherapy (SABR) is highly focused, high-dose radiation that is well suited for treatment of oligometastases. Here we report on the safety and preliminary clinical outcomes of SABR in a modern cohort of OPC men. Methods: Eighty four men who satisfied criteria of OPC diagnosed on imaging underwent consolidative SABR were then followed prospectively on our IRB approved registry by our GU multidisciplinary team. We collected demographic, clinical, toxicity and efficacy information. We examined the first 66 men in this preliminary report to allow for a minimum of 4.5 months follow-up. SABR was delivered in 1-5 fractions of 5-18 Gy. Kaplan-Meier method was used to assess local progression-free survival (LPFS), biochemical progression-free survival (bPFS; PSA nadir+2), distant progression free survival (DPFS), ADT-free survival (ADT-FS) and time-to-next intervention (TTNI). Results: Of the 66 OPC patients analyzed, 25 (38%) men presented as synchronous OPC and the remaining 41 had recurrent OPC. Median and mean follow-up was 61 and 66 weeks, respectively. Patient and disease factors as listed in the Table. Crude Grade 1 and 2 acute toxicities were 36% and 11%, respectively, with no Grade > 2 toxicity. SABR was delivered to 134 metastases: 89 bone (66%), 40 nodal (30%) and 5 (4%) visceral metastases. Overall LPFS at 1-year was 92%. The bPFS and DPFS at 1-year were 69% and 69%, respectively. Median TTNI was not reached yet. Of the 18 men with hormone sensitive prostate cancer who had their ADT deferred, 11/18 (56%) remain free of disease following SABR (1-year ADT-FS was 78%) and in 17 castration resistant men, 11 had > 50% PSA declines with 1-year TTNI of 30% with a median of 45 weeks. Conclusions: Consolidative SABRfor OPCis feasible and well tolerated. The preliminary clinical outcomes in our series is limited by heterogeneity and size but our data suggests that this approach is worthy of further prospective study. [Table: see text]
- 1 February 2016
- Published by Elsevier in European Urology
- Vol. 69 (2) , 191-192
Immediate Adjuvant Radiation Therapy Following Radical Prostatectomy Should Not Be Advised for Men with Extraprostatic Extension Who Have Negative Surgical Margins
- 1 February 2016
- Published by Elsevier in European Urology
- Vol. 69 (2) , 191-192
Immediate Adjuvant Radiation Therapy Following Radical Prostatectomy Should Not Be Advised for Men with Extraprostatic Extension Who Have Negative Surgical Margins
- 14 November 2013
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 369 (20) , 1967-1968
Survival in the Prostate Cancer Prevention Trial
- 14 November 2013
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 369 (20) , 1967-1968
Survival in the Prostate Cancer Prevention Trial