Singh Suvir, Joshi Kaveri, Sharma Rintu, Singh Jagdeep, Jain Kunal, Garg Nitish, Maini Nandita, Bansal Ekta
Department of Clinical Haematology and Stem Cell Transplantation, Dayanand Medical College and Hospital, Ludhiana, Punjab 141001 India.
Department of Medical Oncology, Dayanand Medical College and Hospital, Ludhiana, Punjab 141001 India.
Indian J Hematol Blood Transfus. 2025 Apr;41(2):340-348. doi: 10.1007/s12288-024-01858-z. Epub 2024 Sep 5.
Myeloma patients with high involved free light chains (iFLC) at diagnosis may exhibit a worse clinical course, independent of established prognostic factors. This study aimed to evaluate clinical and renal outcomes in Indian patients with baseline iFLC exceeding 1000 mg/L. All MM patients diagnosed between January 2021 and July 2023 with iFLC > 1000 mg/L were included with the primary and secondary objectives to describe overall survival (OS) and renal outcomes, respectively. Thirty-eight patients (M: F = 26:12) with a median age of 63 years were included. Renal impairment (eGFR < 40 ml/min) was present in 24 (63%) patients with a median eGFR of 9 (6-15.25). At diagnosis, median involved free light chain (iFLC) was 5262 mg/L (kappa: 1996 mg/L, lambda: 36 mg/dL). VCD was most frequent initial therapy (55%), followed by VRD (21%); 76% patients received Bortezomib. Ten patients (26%) required dialysis at presentation. At first reassessment after a median of 91 days, median eGFR was 36 ml/min/1.73m2. Of twenty assessable patients, one patient (15%) had partial renal response, and three (15%) each had complete and minimal response, respectively. After a median follow up of 38 months, median OS was 76 months (1- and 3-year survival: 78% and 54%). Dialysis independence was achieved in 60% of patients. There was no correlation between final serum creatinine and baseline value of iFLC. This study describes the first Indian data on patients with myeloma and high initial iFLC (> 1000 mg/L). Compared to published data, we observed a higher frequency of renal impairment, dialysis requirement, and shorter OS. Our data suggests a potential role between high iFLC and clinial outcomes, warranting further evaluation as its role as an independent risk factor.
诊断时伴有高受累游离轻链(iFLC)的骨髓瘤患者可能会呈现出更差的临床病程,这与既定的预后因素无关。本研究旨在评估基线iFLC超过1000mg/L的印度患者的临床和肾脏结局。纳入了2021年1月至2023年7月期间诊断为iFLC>1000mg/L的所有骨髓瘤患者,主要和次要目标分别是描述总生存期(OS)和肾脏结局。纳入了38例患者(男:女=26:12),中位年龄为63岁。24例(63%)患者存在肾功能损害(估算肾小球滤过率[eGFR]<40ml/min),中位eGFR为9(6-15.25)。诊断时,中位受累游离轻链(iFLC)为5262mg/L(κ链:1996mg/L,λ链:36mg/dL)。VCD是最常用的初始治疗方案(55%),其次是VRD(21%);76%的患者接受硼替佐米治疗。10例(26%)患者在就诊时需要透析。在中位91天的首次重新评估时,中位eGFR为36ml/min/1.73m²。在20例可评估的患者中,1例患者(15%)有部分肾脏反应,3例患者(各占15%)分别有完全反应和最小反应。在中位随访38个月后,中位OS为76个月(1年和3年生存率分别为78%和54%)。60%的患者实现了无需透析。最终血清肌酐与iFLC的基线值之间无相关性。本研究描述了印度首例关于骨髓瘤和高初始iFLC(>1000mg/L)患者的数据。与已发表的数据相比,我们观察到肾功能损害、透析需求的频率更高,且OS更短。我们的数据表明高iFLC与临床结局之间可能存在关联,有必要进一步评估其作为独立危险因素的作用。