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. 2015 Apr 13;6(11):8491–8524. doi: 10.18632/oncotarget.3455

Table 11. Oligometastatic prostate cancer.

1st Author, Year [Ref] Strength of evidence-based on study design / endpoints Prospective (P) / Retrospective (R) Sample size Definition-Oligometa stases Therapy Endpoints Conclusion
James, 2014 [137] 1ii /A P 917 N/A – newly diagnosed M1 LT ADT FFS- 11 mths. 2yr FFS- 29%. MOS- 42 mth. 2yr OS- 72%. Survival disappointing in M1 disease started only on LT ADT, despite active treatments available at first ADT failure. Spend most of their time in CR relapse.
Singh, 2004 [149] 3iii/A R 30 ≤5 met lesions External RT 5- and 10yr OS- 73% and 36% in OM, as compared to 45% and 18% in those with > 5 met lesions Findings suggest early detection and aggressive treatment is worth testing to improve long-term survival
Engel, 2010 [101] 3iii /A R 938 +LNs +/− RP 5yr- and 10yr OS- 84% and 64% with completed RP, and 60% and 28%, with aborted RP. PCa-specific survival at 5- and 10-yrs- 95% and 86%, with completed RP and was 70% and 40%, with aborted RP Abandonment of RP in men with positive LNs may not be appropriate
Tabata, 2012 [148] 3iii/A R 35 <6 bone mets on bone scan, each site less than 50% the size of a vertebral body RT 3yr OS- 77%; 14/16 (87%) of pats who had pain were improved 1 mth after RT; median duration of pain control 12 month RT for bone OM in PCa was effective for long-term pain relief
Schick, 2013 [141] 3iii /A R 50 1–4 mets, synchronous or metachronous Mets- ADT and HDRT 3yr biochemical relapse-free survival (bRFS), clinical failure-free survival, and OS- 54.5, 58.6, and 92% OM may be treated w short ADT and HDRT to the met regions. High dose improves bRFS. May prolong failure-free interval between 2 consecutive ADT courses.
Ponti, 2014 [143] 3iii/A R 16 Distant relapse in a limited number of regions, ≤5 mets SBRT +/− HT Local control, biochemical PFS, OS, toxicity. OS at 29 mths 95% Distant relapse in a limited number of regions, ≤5 mets SBRT safe, effective, minimally invasive in limited LN recurrence in OMPCa
Jereczek-Fossa, 2014 [147] 3iii/A R 69 Single abdominal LN recurrence SBRT 3-yr in-field PFS, PFS, OS- 64%, 11.7%, and 50% SBRT is feasible for single abdominal LN recurrence, offering excellent in-field tumor control.
Cadeddu, 1997 [132] 3iii /B R 38 +LN: pelvic lymph adenopathy PLND +/− RP PCa-specific survival at 5- and 10-yrs- (93% and 56% in the PLND/RP group and 58% and 34% in the PLND group RP, as compared to conservative therapy, may prolong survival
Ahmed, 2013 [145] 3iii/B R 17 ≤5 met lesions SBRT Local control-100% at 6mo; cancer specific survival (CSS)-6- and 12mo-100%; freedom from distant progression (FFDP)- 6- and 12mo- 74%, 40% Excellent LC with SBRT for OM PCa; over 50% patients achieved undetectable PSA after SBRT
Ost, 2014 [142] 3iii /B R 80 Metachronous mets Mets- ADT, AS, or MDT Median PCSS- 6.6 yrs. Longer PSA DT, involvement of nodes or axial skeleton and lower # mets assoc w improved PCSS.
Decaestecker, 2014 [144] 3iii/B R 50 ≤3 metachronous asymptomatic mets SBRT (2 RT schedules used) +/− HT Median PFS- 19mo; median ADT-FS- 25 month; 2-, 5yr PCSS-96%, 90% Repeated SBRT for OM PCa postpones palliative ADT
Berkovic, 2013 [146] 3iii/Di R 24 Biochemical recurrence after curative treatment to primary (RP, RT, or both), then ≤3 synchronous asymptomatic mets SBRT Androgen deprivation therapy-free survival (ADT-FS)- 1-, 2yr-82%, 54%; clinical progression free survival- 1-, 2yr- 72% and 42% Repeated salvage SBRT feasible, well tolerated, and defers palliative ADT with a median 38mo in OMPca
Ost, 2014 [133] 3iii/Diii R 450 Metachronous mets with controlled primary, + underwent MDT for recurrent PCa RT or LND About 50% PFS at 1–3 yrs post-MDT MDT promising approach for OM PCa recurrence but low level of evidence

Abbreviations: M1 = distant metastases; LT ADT = long-term androgen deprivation therapy; FFS = failure-free survival; OS = overall survival; CR = castrate resistance; met = metastasis; RT = radiation therapy; OM = oligometastasis; LNs = lymph nodes; RP = radical prostatectomy; PCa = prostate cancer; HDRT = high dose radiation therapy; ADT = androgen deprivation therapy; SBRT = stereotactic body radiation therapy; HT = hormone therapy; PFS = progression free survival; LN = lymph node; OM PCa = oligometastatic prostate cancer; PLND = positive lymph node dissection; LC = local control; PSA = prostate specific antigen; PCSS = prostate cancer specific survival; AS = active surveillance; MDT = metastasis directed therapy; DT = doubling time; ADT-FS = androgen deprivation free survival; LND = lymph node dissection; PFS = progression free survival