Safety and efficacy of PRaG therapy in elderly cancer patients
This retrospective series examines feasibility in older adults, a group often underrepresented in trials.
THE EVIDENCE / PUBLICATIONS
Original publications, clearly explained. Find the question, the findings and the limitations behind each study. Related research is labeled separately.
This retrospective series examines feasibility in older adults, a group often underrepresented in trials.
A prospective Bengbu cohort examined a stereotactic radiotherapy-based PRaG approach and peripheral immune changes.
The protocol adds recombinant human endostatin to PRaG 2.0 to investigate an anti-angiogenic combination.
This report combines PRaG 5.0 with chemotherapy and subsequent chemoimmunotherapy.
This mechanistic study illustrates that radiation-associated myeloid responses can also suppress antitumor immunity.
This protocol examines an antibody–drug conjugate alongside radioimmunotherapy and cytokine support.
A pooled analysis studied whether circulating immune markers could help identify patients at risk of moderate-to-severe adverse events.
A Guangxi report explored PRaG following progression on previous systemic treatments.
The protocol addresses the underrepresentation of very old adults in immunotherapy trials.
A Wuxi–Shanghai report described a prolonged response after combined local and systemic treatment.
NeoPRAG explores a neoadjuvant strategy intended to improve the possibility of surgical resection.
An observational comparison examined three checkpoint-inhibitor-based strategies in MSS/pMMR metastatic colorectal cancer.
An ASCO abstract reports an updated PRaG 2.0 cohort with IL-2 added to the original triplet.
The report explored RANKL inhibition with PRaG in a patient unable to continue chemotherapy.
An independent multicenter study examined a related four-component radioimmunotherapy strategy.
A Jiangsu case report described irradiated and nonirradiated tumor responses under a four-component regimen.
The publication proposes adding intraperitoneal serplulimab to a PRaG-based regimen.
The protocol examines whether thymalfasin adjusted to immune status can support a PRaG-based regimen.
This case combined RC48, radiotherapy, checkpoint inhibition and cytokines after earlier treatment failed.
A Xi’an report explored the antibody–drug conjugate RC48 alongside PRaG after prior trastuzumab-based treatment.
A Sichuan collaboration explored a PRaG-related approach using interstitial implantation radiotherapy.
This report places PRaG within a complex sequence of surgery and systemic treatments.
An early conference update of PRaG 2.0, which adds sequential IL-2 to the original triplet.
An early conference update of PRaG 2.0, which adds sequential IL-2 to the original triplet.
A case report explored the triplet in a tumor subtype usually resistant to checkpoint-inhibitor monotherapy.
The report explored a related triplet for a rare mesenchymal tumor with limited established treatment options.
The foundational phase II report investigated whether the PRaG triplet could produce responses in previously treated metastatic cancer.
This case explored PRaG after several prior systemic treatments.
A Wuhan case report examined PD-1 inhibition, SBRT and GM-CSF in a rare thyroid cancer.
SWORD independently evaluated a related radiotherapy–immunotherapy–cytokine combination in a multicenter phase II program.
An early report from Suzhou explored the three-component approach after previous treatment had failed.
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