Abstract Background and Hypothesis Defective hepatic alanine-glyoxylate aminotransferase (AGT) leads to oxalate overproduction in primary hyperoxaluria type 1 (PH1). Nedosiran and lumasiran are RNA interference (RNAi) agents inhibiting oxalate production. In PH1 patients with kidney failure isolated kidney transplantation (iKTx) might be possible with RNAi medication. Methods We report on 17 PH1 patients on hemodialysis, who received lumasiran (8 patients, 1-68 years, 6 females), lumasiran post nedosiran (2 patients, both 6.5 years, male), double RNAi (dRNAi) (4 patients, 37 years, 3 infants, all male) and nedosiran (4 patients, 11-58 years, 2 female). Plasma oxalate (Pox) pre-HD was measured and systemic oxalate grading (SOG) was evaluated mainly by bone MRI and speckle echocardiography before start and repeatedly during treatment. Results In 4 patients iKTx was performed, being successful or with recurrence in 2 patients each. In others, development of Pox values under RNAi treatment and thus SOG increment and clinical deterioration were profound arguments for transplant decisions. Based on that iKTx is now planned in 5 and liver/kidney Tx in 4 patients (one liver already transplanted). Three patients have died. Conclusion Pox should not be the sole parameter to decide on Tx procedure. In patients with minor oxalate deposition, no SOG deterioration and sensitivity to vitamin B6 or under efficacious RNAi treatment, iKTx can be considered. Severe (and deteriorating) systemic oxalosis, high Pox during RNAi treatment and maximum dialysis, makes us reconsider combined or sequential LKTx rather than iKTx. Patients with severe systemic oxalosis at time of diagnosis still have a high mortality rate.
Martín-Higueras et al. (Fri,) studied this question.