Biotechnology Research Unit, Aprigliano, Cosenza, Italy.
Department of Hematology and Bone Marrow Transplant Unit, Augusta Victoria Hospital, Jerusalem, Israel.
Eur J Haematol. 2021 Jun;106(6):831-835. doi: 10.1111/ejh.13614. Epub 2021 Apr 7.
To validate the predictive value on time to first treatment (TTFT) of AIPS-E and IPS-E evaluated in an independent cohort of newly diagnosed and non-referred Binet stage A CLL patients enrolled in the O-CLL1-GISL protocol (clinicaltrial.gov identifier: NCT00917540).
A cohort of 292 newly diagnosed Binet A CLL cases has been enrolled in the study. Patients from several Italian Institutions were prospectively enrolled within 12 months of diagnosis into the O-CLL1-GISL protocol.
The majority of patients were male (62%); median age was 60.4 years, 102 cases (34.9%) showed unmutated IGHV genes, 8 cases (2.8) the presence of del(11q)/del(17p), 142 cases (48.6%) the presence of palpable lymph nodes and 146 cases (50%) and ALC > 15 × 10 /l. After a median follow-up of 7.2 years, 130 patients underwent treatment. According to the AIPS-E, 96 patients were classified as low-risk, 128 as intermediate-risk, and 68 as high-risk. These groups showed significant differences in terms of TTFT. The C-statistic was 0.71 (P < .0001) for predicting TTFT. According to IPS-E, 77 patients were classified as low-risk, 135 as intermediate-risk, and 80 as high-risk. These groups showed significant differences in terms of TTFT. The C-statistic was 0.705 (P < .0001) for predicting TTFT.
Our data confirm an accurate prognostic utility of both AIPS-E and IPS-E at the individual patient level. These data may be useful for a precise stratification of early-stage patients.
验证在非推荐的 Binet 期 A CLL 患者中,评估 AIPS-E 和 IPS-E 的预测价值,这些患者是在 O-CLL1-GISL 方案(clinicaltrial.gov 标识符:NCT00917540)中招募的新诊断和未转诊的 Binet 期 A 病例队列中进行评估的。
本研究纳入了 292 例新诊断的 Binet A CLL 病例。来自意大利多个机构的患者在诊断后 12 个月内前瞻性地入组到 O-CLL1-GISL 方案中。
大多数患者为男性(62%);中位年龄为 60.4 岁,102 例(34.9%)IGHV 基因未突变,8 例(2.8%)存在 del(11q)/del(17p),142 例(48.6%)存在可触及的淋巴结,146 例(50%)和 ALC>15×10 /l。中位随访 7.2 年后,130 例患者接受了治疗。根据 AIPS-E,96 例患者被归类为低危,128 例为中危,68 例为高危。这些组在 TTFT 方面有显著差异。预测 TTFT 的 C 统计量为 0.71(P<.0001)。根据 IPS-E,77 例患者被归类为低危,135 例为中危,80 例为高危。这些组在 TTFT 方面有显著差异。预测 TTFT 的 C 统计量为 0.705(P<.0001)。
我们的数据证实了 AIPS-E 和 IPS-E 在个体患者水平上具有准确的预后效用。这些数据可能对早期患者的精确分层有用。