Department of Pathology & Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, US.
Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, US.
Am J Clin Pathol. 2024 Nov 4;162(5):464-470. doi: 10.1093/ajcp/aqae061.
To determine whether the information provided by short tandem repeat (STR) testing and bone marrow (BM) biopsy specimens following hematopoietic stem cell transplant (HSCT) provides redundant information, leading to test overutilization, without additional clinical benefit.
Cases with synchronous STR and flow cytometric immunophenotyping (FCI) testing, as part of the BM evaluation, were assessed for STR/FCI concordance.
Of 1199 cases (410 patients), we found the overall concordance between STR and FCI was 93%, with most cases (1063) classified as STR-/FCI-. Of all discordant cases, 75 (6%) were STR+/FCI-, with only 5 (6.7%) cases best explained as identification of disease relapse. Eight cases were STR-/FCI+, representing relapsed/residual disease. Analysis of cases 1 year or more from transplant (54% of all cases) indicated only 9 (1.5%) were STR+/FCI-, and none uniquely identified relapse.
These data suggest that STR analysis performed 1 year or more post-HSCT does not identify unknown cases of relapse. Furthermore, while STR testing is critical for identifying graft failure/rejection within the first year posttransplant, FCI appears superior to STR at detecting late relapses with low-level disease. Therefore, STR testing from patients 1 year or more post-HSCT may be unnecessary, as BM biopsy evaluation is sufficient to identify disease relapse.
确定造血干细胞移植(HSCT)后短串联重复(STR)检测和骨髓(BM)活检标本提供的信息是否存在冗余,导致过度检测而无额外临床获益。
评估同步 STR 和流式细胞免疫表型(FCI)检测的病例,作为 BM 评估的一部分,以评估 STR/FCI 一致性。
在 1199 例(410 例患者)中,我们发现 STR 和 FCI 之间的总体一致性为 93%,大多数病例(1063 例)被归类为 STR-/FCI-。所有不一致的病例中,有 75 例(6%)为 STR+/FCI-,其中仅 5 例(6.7%)可最好地解释为疾病复发的识别。8 例为 STR-/FCI+,代表复发/残留疾病。对移植后 1 年或以上的病例(所有病例的 54%)进行分析表明,仅 9 例(1.5%)为 STR+/FCI-,且无一例可唯一识别复发。
这些数据表明,HSCT 后 1 年或以上进行 STR 分析不会发现未知的复发病例。此外,虽然 STR 检测对于识别移植后 1 年内的移植物失败/排斥至关重要,但 FCI 在检测低水平疾病的晚期复发方面优于 STR。因此,HSCT 后 1 年或以上的患者进行 STR 检测可能是不必要的,因为 BM 活检评估足以识别疾病复发。