Human tissue Kallikreins: Blood levels and response to radiotherapy in intermediate risk prostate cancer. Issue 3 (September 2017)
- Record Type:
- Journal Article
- Title:
- Human tissue Kallikreins: Blood levels and response to radiotherapy in intermediate risk prostate cancer. Issue 3 (September 2017)
- Main Title:
- Human tissue Kallikreins: Blood levels and response to radiotherapy in intermediate risk prostate cancer
- Authors:
- Nasser, Nicola J.
Thoms, John
Soosaipillai, Antoninus
Pintilie, Melania
Wang, Ri
Diamandis, Eleftherios P.
Bristow, Robert G. - Abstract:
- Abstract: Objectives: Kallikreins are serine proteases over expressed in many malignancies. In this study, we measure changes in serum kallikrein (KLKs) levels during intensity-modulated radiotherapy (IMRT) in prostate cancer patients, and find potential correlations between serum kallikrein level and normal tissues toxicity during radiation. Methods: Forty-nine patients with prostate cancer were recruited as follows: group 1, definitive standard fractionation IMRT (78 Gy in 39 fractions, n = 15); group 2, definitive hypofractionated IMRT (60 Gy in 20 fractions, n = 15); and group 3, IMRT postprostatectomy (66 Gy in 33 fractions, n = 19). Patients treated with definitive radiation therapy were intermediate risk. Blood samples were collected at baseline and quarterly during IMRT and at each follow-up visit. Acute toxicity was graded weekly during radiotherapy using CTC-AE v4.0 criteria. Multiplexed immunoassays were used to quantify total, free, and intact Prostate Specific Antigen (PSA), as well as Kallikreins 2, 4, 6, and 11. Results: The serum kallikreins, PSA (total, free and intact), KLK2, 6, and 11 change significantly after definitive radiotherapy. KLK2 and intact PSA decrease as fast as two weeks after initiation of radiation, while the first significant decrease in total and free PSA is noted only at the completion of radiation. KLK6 and KLK11 surge temporarily during radiation therapy and decrease below baseline levels at 8 weeks and 12 months, respectively afterAbstract: Objectives: Kallikreins are serine proteases over expressed in many malignancies. In this study, we measure changes in serum kallikrein (KLKs) levels during intensity-modulated radiotherapy (IMRT) in prostate cancer patients, and find potential correlations between serum kallikrein level and normal tissues toxicity during radiation. Methods: Forty-nine patients with prostate cancer were recruited as follows: group 1, definitive standard fractionation IMRT (78 Gy in 39 fractions, n = 15); group 2, definitive hypofractionated IMRT (60 Gy in 20 fractions, n = 15); and group 3, IMRT postprostatectomy (66 Gy in 33 fractions, n = 19). Patients treated with definitive radiation therapy were intermediate risk. Blood samples were collected at baseline and quarterly during IMRT and at each follow-up visit. Acute toxicity was graded weekly during radiotherapy using CTC-AE v4.0 criteria. Multiplexed immunoassays were used to quantify total, free, and intact Prostate Specific Antigen (PSA), as well as Kallikreins 2, 4, 6, and 11. Results: The serum kallikreins, PSA (total, free and intact), KLK2, 6, and 11 change significantly after definitive radiotherapy. KLK2 and intact PSA decrease as fast as two weeks after initiation of radiation, while the first significant decrease in total and free PSA is noted only at the completion of radiation. KLK6 and KLK11 surge temporarily during radiation therapy and decrease below baseline levels at 8 weeks and 12 months, respectively after completion of radiation. KLK4 levels did not change with radiation. There was no correlation between GU or GI toxicities and serum kallikreins. Conclusions: PSA, KLK2, 6, and 11, change significantly after definitive prostate radiotherapy, though KLK2 and PSA decrease by the end of the radiation course while KLK6 and KLK11 decrease significantly starting at 2 and 12 months, respectively, after radiation. There was no correlation between GU or GI toxicities and serum kallikreins. … (more)
- Is Part Of:
- Radiotherapy and oncology. Volume 124:Issue 3(2017:Sep.)
- Journal:
- Radiotherapy and oncology
- Issue:
- Volume 124:Issue 3(2017:Sep.)
- Issue Display:
- Volume 124, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 124
- Issue:
- 3
- Issue Sort Value:
- 2017-0124-0003-0000
- Page Start:
- 427
- Page End:
- 432
- Publication Date:
- 2017-09
- Subjects:
- Prostate -- Biomarker -- Kallikreins -- Radiation -- Toxicity
Oncology -- Periodicals
Radiotherapy -- Periodicals
Tumors -- Periodicals
Medical Oncology -- Periodicals
Neoplasms -- radiotherapy -- Periodicals
Radiotherapy -- Periodicals
Radiothérapie -- Périodiques
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Electronic journals
616.9940642 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01678140 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01678140 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01678140 ↗
http://www.estro.org/ ↗
http://www.elsevier.com/journals ↗
http://www.journals.elsevier.com/radiotherapy-and-oncology/ ↗ - DOI:
- 10.1016/j.radonc.2017.03.023 ↗
- Languages:
- English
- ISSNs:
- 0167-8140
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7240.790000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4702.xml