Pêtre Adeline, Quivrin Magali, Briot Nathalie, Boustani Jihane, Martin Etienne, Bessieres Igor, Cochet Alexandre, Créhange Gilles
Department of Radiation Oncology, Centre Léon Bérard, Lyon, France.
Department of Radiation Oncology, Centre Georges François Leclerc, Dijon, France.
Adv Radiat Oncol. 2022 Jul 28;8(1):101040. doi: 10.1016/j.adro.2022.101040. eCollection 2023 Jan-Feb.
The optimal salvage pelvic treatment for nodal recurrences in prostate cancer is not yet clearly defined. We aimed to compare outcomes of salvage involved-field radiation therapy (s-IFRT) and salvage extended-field radiation therapy (s-EFRT) for positron emission tomography/computed tomography-positive nodal-recurrent prostate cancer and to analyze patterns of progressions after salvage nodal radiation therapy.
Patients with F-fluorocholine or Ga prostate-specific membrane antigen ligand positron emission tomography/computed tomography-positive nodal-recurrent prostate cancer and treated with s-IFRT or s-EFRT were retrospectively selected. Time to biochemical failure, time to palliative androgen deprivation therapy (ADT), and distant metastasis-free survival were analyzed.
Between 2009 and 2019, 86 patients were treated with salvage nodal radiation therapy: 38 with s-IFRT and 48 with s-EFRT. After a median follow-up of 41.9 months (5.4-122.1 months), 47 patients presented a further relapse: 31 after s-IFRT and 16 after s-EFRT, with only 1 in-field relapse. The median time to palliative ADT was 24.8 months (95% confidence interval [CI], 13.3-93.5 months) in the s-IFRT group and not yet reached (95% CI, 40.3 months to not yet reached) in the s-EFRT group ( = .010). The 3-year biochemical failure-free rate was 70.2% (95% CI, 51.5%-82.9%) with s-IFRT and 73.9% (95% CI, 55.4%-85.7%) with s-EFRT ( = .657). The 3-year distant metastasis-free survival was 74.1% (95% CI, 56.0%-85.7%) with s-IFRT and 82.0% (95% CI, 63.0%-91.8%) with s-EFRT ( = .338).
s-EFRT and s-IFRT for positron emission tomography-positive nodal-recurrent prostate cancer provide excellent local control. Time to palliative ADT was longer following s-EFRT than following s-IFRT.
前列腺癌淋巴结复发的最佳挽救性盆腔治疗方案尚未明确界定。我们旨在比较挽救性累及野放射治疗(s-IFRT)和挽救性扩大野放射治疗(s-EFRT)用于正电子发射断层扫描/计算机断层扫描阳性的淋巴结复发前列腺癌的疗效,并分析挽救性淋巴结放射治疗后的进展模式。
回顾性选取接受F-氟胆碱或镓前列腺特异性膜抗原配体正电子发射断层扫描/计算机断层扫描阳性的淋巴结复发前列腺癌且接受s-IFRT或s-EFRT治疗的患者。分析生化复发时间、姑息性雄激素剥夺治疗(ADT)时间和无远处转移生存期。
2009年至2019年期间,86例患者接受了挽救性淋巴结放射治疗:38例接受s-IFRT,48例接受s-EFRT。中位随访41.9个月(5.4 - 122.1个月)后,47例患者出现进一步复发:s-IFRT组31例,s-EFRT组16例,仅1例为野内复发。s-IFRT组姑息性ADT的中位时间为24.8个月(95%置信区间[CI],13.3 - 93.5个月),s-EFRT组尚未达到(95% CI,40.3个月至未达到)(P = 0.010)。s-IFRT组3年无生化复发生存率为70.2%(95% CI,51.5% - 82.9%),s-EFRT组为73.9%(95% CI,55.4% - 85.7%)(P = 0.657)。s-IFRT组3年无远处转移生存期为74.1%(95% CI,56.0% - 85.7%),s-EFRT组为82.0%(95% CI,63.0% - 91.8%)(P = 0.338)。
对于正电子发射断层扫描阳性的淋巴结复发前列腺癌,s-EFRT和s-IFRT可提供良好的局部控制。s-EFRT后的姑息性ADT时间比s-IFRT后的更长。