Clinical

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A multicenter prospective study on the efficacy and safety of denosumab in gastrointestinal cancer patients receiving short-term periodic steroid premedication of chemotherapy-induced nausea and vomiting (ESPRESSO-02/HGCSG1602)


ABSTRACT: Interventions: The dose of denosumab (Prolia) is 60mg administered as a single subcutaneous injection within a week before the induction of chemotherapy. All participants should receive adequate calcium and vitamin D supplementation. Primary outcome(s): To investigate the efficacy of denosumab for preventing a bone mineral density reduction 16 weeks after induction of chemotherapy. Study Design: Single arm Non-randomized

DISEASE(S): Gastrointestinal Cancer: Colorectal Cancer, Non-colorectal Cancer (gastroesophageal, Pancreatic, And Biliary Cancer)

PROVIDER: 2639108 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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