The oxysilicate apatite host CaLa(SiO)O has been explored for immobilization of radioactive nuclides. Divalent ion, trivalent rare earth ion, and combined ionic substitutions in the silicate oxyapatite were carried out to optimize the simulated wasteform composition. The phases were characterized by powder X-ray diffraction, FT-IR, TGA, SEM-EDS, and HT-XRD techniques. The results revealed the effect of ionic substitutions on the structure and thermal expansion behavior. The investigation resulted in the formulation of simulated wasteforms such as LaCePrNdSmGdY(SiO)O (WF-1) and CaSrPbLaCePrNdSmGdY(SiO)O (WF-2). In comparison to the average axial thermal expansion coefficients of the hexagonal unit cell of the parent CaLa(SiO)O measured in the temperature range 298-1073 K (α' = 9.74 × 10 K and α' = 10.10 × 10 K), rare earth ion substitution decreases the thermal expansion coefficients, as in the case of LaCePrNdSmGdY(SiO)O (α' = 8.67 × 10 K and α' = 7.94 × 10 K). However, the phase CaSrPbLaCePrNdSmGdY(SiO)O shows an increase in the values of thermal expansion coefficients: α' = 11.74 × 10 K and α' = 11.70 × 10 K.