Identification of patients with prostate cancer who benefit from immediate postoperative radiotherapy: EORTC 22911

Autor: Van der Kwast TH, Bolla M, Van Poppel H, Van Cangh P, Vekemans K, Da Pozzo L, Bosset JF, Kurth KH, Schröder FH, Collette L, and EORTC 22911
Přispěvatelé: Van der Kwast, T, Bolla, M, Van Poppel, H, Van Cangh, P, Vekemans, K, Da Pozzo, L, Bosset, J, Kurth, K, Schröder, F, Collette, L, and EORTC, 2, 06 Operations Centre and intensive care, Département de cancérologie et radiothérapie, CHU Grenoble, Carcinogénèse épithéliale : facteurs prédictifs et pronostiques - UFC ( CEF2P / CARCINO ), Centre Hospitalier Régional Universitaire [Besançon] ( CHRU Besançon ) -Université Bourgogne Franche-Comté ( UBFC ) -Université de Franche-Comté ( UFC ), Carcinogénèse épithéliale : facteurs prédictifs et pronostiques - UFC (EA 3181) (CEF2P / CARCINO), Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), Pathology, Urology
Rok vydání: 2007
Předmět:
Oncology
Male
Cancer Research
MESH: Combined Modality Therapy
medicine.medical_treatment
030232 urology & nephrology
MESH : Aged
law.invention
[ SDV.CAN ] Life Sciences [q-bio]/Cancer
MESH: Proportional Hazards Models
Prostate cancer
0302 clinical medicine
Randomized controlled trial
law
MESH: Risk Factors
Risk Factors
Medicine
Stage (cooking)
MESH : Prostate-Specific Antigen
MESH: Treatment Outcome
MESH: Aged
MESH: Middle Aged
Prostatectomy
Hazard ratio
Middle Aged
MESH : Risk Factors
Combined Modality Therapy
3. Good health
MESH: Prostate-Specific Antigen
Europe
Treatment Outcome
030220 oncology & carcinogenesis
Disease Progression
MESH : Disease-Free Survival
MESH: Disease Progression
Positive Surgical Margin
MESH : Prostatic Neoplasms
medicine.medical_specialty
MESH : Prostatectomy
MESH : Male
MESH : Europe
[SDV.CAN]Life Sciences [q-bio]/Cancer
MESH : Treatment Outcome
Disease-Free Survival
03 medical and health sciences
MESH: Prostatectomy
SDG 3 - Good Health and Well-being
Internal medicine
Humans
MESH : Middle Aged
Aged
Proportional Hazards Models
MESH: Humans
business.industry
MESH : Humans
Cancer
Prostatic Neoplasms
MESH : Disease Progression
Prostate-Specific Antigen
medicine.disease
MESH : Proportional Hazards Models
MESH: Male
Surgery
Radiation therapy
MESH: Prostatic Neoplasms
MESH: Disease-Free Survival
MESH: Europe
business
MESH : Combined Modality Therapy
adjuvant radiotherapy
prostate cancer
survival
outcomes
Zdroj: Journal of clinical oncology, 25(27), 4178-4186. American Society of Clinical Oncology
Journal of Clinical Oncology
Journal of Clinical Oncology, American Society of Clinical Oncology, 2007, 25 (27), pp.4178-4186. 〈10.1200/JCO.2006.10.4067〉
Journal of Clinical Oncology, American Society of Clinical Oncology, 2007, 25 (27), pp.4178-4186. ⟨10.1200/JCO.2006.10.4067⟩
Journal of Clinical Oncology, 25(27), 4178-4186. American Society of Clinical Oncology
ISSN: 1527-7755
0732-183X
DOI: 10.1200/JCO.2006.10.4067〉
Popis: Purpose The randomized controlled European Organisation for Research and Treatment of Cancer (EORTC) trial 22911 studied the effect of radiotherapy after prostatectomy in patients with adverse risk factors. Review pathology data of specimens from participants in this trial were analyzed to identify which factors predict increased benefit from adjuvant radiotherapy. Patients and Methods After prostatectomy, 1,005 patients with stage pT3 and/or positive surgical margins were randomly assigned to a wait-and-see (n = 503) and an adjuvant radiotherapy (60 Gy conventional irradiation) arm (n = 502). Pathologic review data were available for 552 patients from 11 participating centers. The interaction between the review pathology characteristics and treatment benefit was assessed by log-rank test for heterogeneity (P < .05). Results Margin status assessed by review pathology was the strongest predictor of prolonged biochemical disease-free survival with immediate postoperative radiotherapy (heterogeneity, P < .01): by year 5, immediate postoperative irradiation could prevent 291 events/1,000 patients with positive margins versus 88 events/1,000 patients with negative margins. The hazard ratio for immediate irradiation was 0.38 (95% CI, 0.26 to 0.54) and 0.88 (95% CI, 0.53 to 1.46) in the groups with positive and negative margins, respectively. We could not identify a significant impact of the positive margin localization. Conclusion Provided careful pathology of the prostatectomy is performed, our results suggest that immediate postoperative radiotherapy might not be recommended for prostate cancer patients with negative surgical margins. These findings require validation on an independent data set.
Databáze: OpenAIRE