| Literature DB >> 30039440 |
Masaharu Tamaki1, Hideki Nakasone1, Ayumi Gomyo1, Jin Hayakawa1, Yu Akahoshi1, Naonori Harada1, Machiko Kusuda1, Yuko Ishihara1, Koji Kawamura1, Aki Tanihara1, Miki Sato1, Kiriko Terasako-Saito1, Kazuaki Kameda1, Hidenori Wada1, Misato Kikuchi1, Shun-Ichi Kimura1, Shinichi Kako1, Yoshinobu Kanda2.
Abstract
High-dose melphalan followed by autologous hematopoietic stem cell transplantation (ASCT) is a standard treatment for younger myeloma patients. However, the correlation between its toxicity and renal impairment is not clear. We analyzed this relationship, focusing on estimated glomerular filtration rate (eGFR) as an index of renal function. We evaluated 78 multiple myeloma patients who underwent ASCT following high-dose melphalan at our center. Patients were divided into a higher eGFR group (eGFR ≥ 60) and a lower eGFR group (eGFR < 60). Multivariate analyses revealed that lower eGFR was independently associated with alkaline phosphatase elevation (OR 10.2, P = 0.038), mucositis (OR 10.5, P = 0.032), grade 2-4 co-elevation of both aspartate aminotransferase and alanine aminotransferase (OR 21.3, P = 0.016), delay of reticulocyte engraftment (HR 0.524, P = 0.034), and delay of platelet engraftment (HR 0.535, P = 0.0016). However, lower eGFR was not correlated with overall survival or time-to-next treatment. In summary, renal dysfunction secondary to administration of high-dose melphalan was associated with increased hepatic and mucosal toxicity and delay of hematological recovery, but did not affect survival outcomes.Entities:
Keywords: Autologous transplantation; Estimated GFR; Melphalan; Multiple myeloma
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Year: 2018 PMID: 30039440 DOI: 10.1007/s12185-018-2507-2
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490