A proportion of prostate cancer (PCa) patients develop relapse following curative local treatment. Regional nodal recurrence is an emerging clinical situation since the introduction of new molecular imaging methods in the restaging of recurrent prostate cancer. More specifically, a subgroup of these patients is being diagnosed with a recurrence confined to the regional lymph nodes and limited in number (oligorecurrence) using choline or PSMA PET-CT. As there are no specific treatment recommendations for these type of patients, different treatment approaches are currently used, mostly focusing on local ablative treatments using radiotherapy or surgery. These treatments are coined metastasisdirected therapy (MDT). MDT in combination with or without temporary ADT could delay the subsequent risk of progression, and even cure limited regional nodal recurrences. Consequently, lifelong palliative ADT, with its toxicity and excess in non-cancer mortality might be postponed. The proposed trial randomizes patients with oligorecurrent nodal prostate cancer following primary PCa treatment to either metastasis-directed therapy (MDT) (salvage lymph node dissection, sLND or stereotactic body radiotherapy, SBRT) or MDT plus whole pelvis radiotherapy (WPRT: 45 Gy in 25 fractions).
A proportion of prostate cancer (PCa) patients develop a local, regional (N1) or distant (M1) relapse following curative local treatment. For both local and distant relapses, different treatment recommendations are made in the guidelines (EAU guidelines 2016). However, the entity regional nodal recurrence is not mentioned in the guidelines but is an emerging clinical situation since the introduction of choline and more recently PSMA PET-CT in the restaging of recurrent prostate cancer. More specifically, a subgroup of these patients is being diagnosed with a recurrence confined to the regional lymph nodes and limited in number (oligorecurrence) using choline or PSMA PET-CT. As there are no specific treatment recommendations for these type of patients, different treatment approaches are currently used, mostly focusing on local ablative treatments using radiotherapy or surgery. These treatments are coined metastasisdirected therapy (MDT). MDT in combination with or without temporary ADT could delay the subsequent risk of metastases, and even cure limited regional nodal recurrences. Consequently, lifelong palliative ADT, with its toxicity and excess in non-cancer mortality might be postponed. The proposed trial randomizes patients with oligorecurrent nodal prostate cancer following primary PCa treatment to either metastasis-directed therapy (MDT) (sLND or SBRT) or MDT plus WPRT. In the recurrent PCa setting, 2 recent trials have suggested a progression-free and even survival benefit of adding temporary ADT to local salvage prostate bed radiotherapy. Consequently, this positive effect might also be applicable for regional recurrences. Although the optimal duration of ADT is unknown, a minimal duration of 6 months of ADT seems advisable in this setting and will be mandatory for both arms. This trial will improve our insights in the pattern of recurrence following these treatment modalities with the expectation that WPRT will reduce the number of nodal relapses, improving metastasis-free survival and postponing the need for palliative systemic treatments while maintaining quality-of-life. The current phase II trial will try to establish a golden standard in the treatment of oligorecurrent nodal PCa.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
196
addition of prophylactic whole pelvic radiotherapy to a local metastasis-directed treatment
stereotactic body radiotherapy
metastasis-directed treatment
LHRH-agonist (+ anti-androgen) or antagonist for a duration of 6 months
Epworth Healthcare
Melbourne, Australia
GZA
Antwerp, Belgium
AZ St-Jan Brugge
Bruges, Belgium
AZ St-Lucas
Bruges, Belgium
Institut Jules Bordet
Brussels, Belgium
University Hospital Ghent
Ghent, Belgium
AZ Maria Middelares
Ghent, Belgium
AZ Groeninge
Kortrijk, Belgium
UZ Leuven
Leuven, Belgium
CH Mouscron
Mouscron, Belgium
...and 19 more locations
Metastases-free survival
Metastasis-free survival will be defined as the time between randomization and the appearance of a metastatic recurrence (any M1) as suggested by choline, FACBC or PSMA PET-CT or death due to any cause
Time frame: 2 year
Clinical Progression free survival
Clinical Progression-free survival is defined as time between randomization and the appearance of a new recurrence (any N1 or M1) as suggested by PET-CT, symptoms related to progressive PCa, or death due to any cause
Time frame: 2 year
Biochemical progression-free survival
For patients who had previous RP at initial diagnosis, a biochemical recurrence is defined by any confirmed PSA rise above 0.20 ng/ml with a confirmatory rise at least 2 weeks later. For patients who had previous RT to the prostate at initial diagnosis, a biochemical recurrence is defined as the nadir + 2ng/ml (Phoenix definition). Non-responders are considered to have a biochemical recurrence in case a second measurement at least 2 weeks later confirms a rising PSA
Time frame: 2 year
Toxicity: acute toxicity
Radiotherapy toxicity will be assessed according to NCI CTCAE v4.0.
Time frame: 3 months
Toxicity: late toxicity
Radiotherapy toxicity will be assessed according to NCI CTCAE v4.0.
Time frame: 2 year
Patient reported QOL as per EORTC-QLQ C30
Validated questionnaire assessing different health-related parameters (psychological, physical and social well-being) in cancer patients
Time frame: 2 year
Patient reported QOL as per EORTC-QLQ PR25
Validated questionnaire assessing the health-related QOL of prostate cancer patients
Time frame: 2 year
Prostate cancer-specific survival
Cancer specific survival will be read as the time from trial randomization to the date of death due to prostate cancer
Time frame: 5 year
Overall survival
Overall survival will be read as the time from trial randomization to the date of death from any cause
Time frame: 5 year
Time to start of hormonal treatment
Time to hormonal treatment is defined as the time from trial randomization to start of hormonal treatment
Time frame: 2 year
Time to castration-resistant disease
Time to castration resistant disease is defined as the time from trial randomization until castration resistant status
Time frame: 5 year
economical evaluation
Assessment of quality-adjusted-life-years with the EuroQol classification system (EQ-5D-5L)
Time frame: 2 year
Sensitivity/specificity of PET-CT for the detection of nodal recurrences: limited to patients undergoing surgery
Sensitivity/specificity of PET-CT
Time frame: 3 months
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