Int J Radiat Oncol Biol Phys 2022 Aug 13. Epub 2022 Aug 13.
Department of Radiation Oncology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA. Electronic address:
Objectives: The successes of local therapy for oligometastatic cancers cannot be extrapolated to oligoprogressive disease (OPD) because they are distinct clinical entities. Given the limited prospective data on OPD to date, summative analyses are urgently needed.
Methods: Inclusion criteria for this PRISMA-guided systematic review were as follows. First, only prospective data were included. Second, progression had to have occurred on active/ongoing systemic therapy. Third, the number of progressing areas of disease had to be explicitly listed and ≤5 in number. Fourth, all progressing sites had to undergo local therapy (radiotherapy/surgery/non-radiation ablative procedures).
Results: Eight trials met criteria (summing 290 patients), the vast majority of which utilized stereotactic radiotherapy as the local modality (most commonly, 19-20 Gy in 1 fraction, 27-33 Gy in 3 fractions, or 35-50 Gy in 5 fractions). A study on NSCLC demonstrated that stereotactic radiotherapy improved progression-free survival (PFS) and overall survival compared to historical values with systemic therapy alone. Two additional studies on EGFR-mutated NSCLC also showed acceptable PFS with local therapy, particularly in patients who oligoprogressed on osimertinib. The only randomized trial analyzed herein showed that local therapy improved PFS for NSCLC but not breast cancer. Two trials in castration-resistant prostate cancer illustrated that a substantial proportion of patients did not require any changes in hormonal therapy and/or delayed the need to change systemic therapies. Lastly, two trials of renal cell carcinoma showed high (90-100%) local control and median PFS of 9 months, and potentially a prolonged time to change systemic therapy. Lastly, from all patients in all trials, local therapy was tolerated well, with only 7 instances of grade 3+ toxicities.
Conclusions: Based on the limited data, local therapy for OPD is safe and yields encouraging short-term preliminary outcomes, but trials with larger sample sizes and longer follow-up are required for more robust conclusions.