Yan Xu1, Shuhui Deng2, Xuehan Mao2, Gang An2, Zengjun Li2, Yafei Wang3, Mariateresa Fulciniti4, Matthew Ho4, Jianhong Lin4, Weiwei Sui2, Wei Liu2, Dehui Zou2, Shuhua Yi2, Wenyang Huang2, Hong Liu2, Rui Lv2, Jian Li2, Tingyu Wang2, Chenxing Du2, Nikhil C Munshi5, Lugui Qiu6. 1. State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academic Medical Science and Peking Union Medical College, Tianjin, China; Department of Medical Oncology, Jerome Lipper Center for Multiple Myeloma Research, Lebow Institute for Myeloma Therapeutics, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA. 2. State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academic Medical Science and Peking Union Medical College, Tianjin, China. 3. Department of Hematology, Cancer Institute and Hospital, Tianjin Medical University, Tianjin, China. 4. Department of Medical Oncology, Jerome Lipper Center for Multiple Myeloma Research, Lebow Institute for Myeloma Therapeutics, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA. 5. Department of Medical Oncology, Jerome Lipper Center for Multiple Myeloma Research, Lebow Institute for Myeloma Therapeutics, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA. Electronic address: Nikhil_Munshi@dfci.harvard.edu. 6. State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academic Medical Science and Peking Union Medical College, Tianjin, China. Electronic address: qiulg@ihcams.ac.cn.
Abstract
BACKGROUND: Peripheral neuropathy (PN) is an important toxicity that limits the use of bortezomib (Btz). Attempts to reduce PN have included its subcutaneous (SC) administration. PATIENTS AND METHODS: We retrospectively analyzed 307 patients with newly diagnosed multiple myeloma from a single Chinese center, receiving Btz-based regimens administered either via SC injection (SC group, n = 167) or intravenous (IV) infusion (IV group, n = 140). The efficacy and safety of Btz administration via SC and IV were then compared. RESULTS: Most baseline characteristics were similar between these 2 groups. A lower frequency of adverse events, especially grade ≥ 3 PN (P = .002), was observed in the SC group compared with the IV group. The estimated median Btz dosage when PN developed was higher (20.8 mg/m2 vs. 15.6 mg/m2), and fewer patients reduced or discontinued Btz owing to adverse events in the SC group compared with the IV group. The overall response rate (≥ partial response [PR]) was comparable (94.8% vs. 96.2%). However, patients in the IV group required fewer cycles to achieve PR, whereas a larger proportion of patients in the IV group achieved ≥ very good PR. After a median follow-up of 23 months (range, 1-84 months), no significant difference in median progression-free survival (not arrived vs. 33.0 ± 2.735 months) and overall survival (not arrived vs. 56.0 months) was noted. CONCLUSION: SC Btz is associated with better tolerance; however, IV administration achieves a faster and deeper response in Chinese patients with newly-diagnosed multiple myeloma.
BACKGROUND:Peripheral neuropathy (PN) is an important toxicity that limits the use of bortezomib (Btz). Attempts to reduce PN have included its subcutaneous (SC) administration. PATIENTS AND METHODS: We retrospectively analyzed 307 patients with newly diagnosed multiple myeloma from a single Chinese center, receiving Btz-based regimens administered either via SC injection (SC group, n = 167) or intravenous (IV) infusion (IV group, n = 140). The efficacy and safety of Btz administration via SC and IV were then compared. RESULTS: Most baseline characteristics were similar between these 2 groups. A lower frequency of adverse events, especially grade ≥ 3 PN (P = .002), was observed in the SC group compared with the IV group. The estimated median Btz dosage when PN developed was higher (20.8 mg/m2 vs. 15.6 mg/m2), and fewer patients reduced or discontinued Btz owing to adverse events in the SC group compared with the IV group. The overall response rate (≥ partial response [PR]) was comparable (94.8% vs. 96.2%). However, patients in the IV group required fewer cycles to achieve PR, whereas a larger proportion of patients in the IV group achieved ≥ very good PR. After a median follow-up of 23 months (range, 1-84 months), no significant difference in median progression-free survival (not arrived vs. 33.0 ± 2.735 months) and overall survival (not arrived vs. 56.0 months) was noted. CONCLUSION:SC Btz is associated with better tolerance; however, IV administration achieves a faster and deeper response in Chinese patients with newly-diagnosed multiple myeloma.
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