Alimena G, Morra E, Lazzarino M, Liberati A M, Montefusco E, Inverardi D, Bernasconi P, Mancini M, Donti E, Grignani F
Department of Human Biopathology, University La Sapienza, Rome, Italy.
Eur J Haematol Suppl. 1990;52:25-8. doi: 10.1111/j.1600-0609.1990.tb00901.x.
We treated 114 Ph'+ chronic myeloid leukemia (CML) patients, 105 of whom were in chronic phase (CP) and 9 in accelerated phase (AP), with interferon alpha-2b (IFN alpha-2b) at intermittent or daily doses of 2-5 MU/m2. Of 35 previously untreated CP patients, 22 (63%) showed complete hematological response (CHR). This was significantly influenced by initial risk status. In 19 of the 22 CHR patients the median of Ph'+ cells decreased from 100% to 58%. Of 36 patients pretreated for less than 12 months, 19 (53%) achieved CHR. CHR rate was significantly related to IFN dose. Cytogenetic improvement was observed in 15 of the 19 patients, the median of Ph'+ cells dropping from 100% to 76%, with complete suppression of the Ph' chromosome in 1 case. Of the 34 patients pretreated for greater than 12 months, 21 (62%) obtained CHR. Cytogenetic improvement was observed in 10 cases, the median of Ph'+ cells declining from 100% to 66%. 1 of 9 AP patients obtained CHR. After a median follow-up of 32 months for the 63 CHR patients, 49 (78%) are still in disease control: 34 on IFN therapy, 15 after bone marrow transplantation (BMT) (13 autologous and 2 allogeneic). Blastic transformation (BT) occurred in 9 of 63 (14%) CHR patients and in 24 of 51 (47%) patients with less than CHR. IFN alpha-2b has proved to be an effective treatment for CML. Its combination with other treatment modalities represents an interesting and promising approach for future studies.
我们使用干扰素α-2b(IFNα-2b)对114例Ph+慢性髓性白血病(CML)患者进行了治疗,其中105例处于慢性期(CP),9例处于加速期(AP),干扰素α-2b的间歇剂量或每日剂量为2-5 MU/m²。在35例既往未治疗的CP患者中,22例(63%)出现完全血液学缓解(CHR)。这受到初始风险状态的显著影响。在22例CHR患者中的19例中,Ph+细胞的中位数从100%降至58%。在36例预处理时间少于12个月的患者中,19例(53%)实现了CHR。CHR率与IFN剂量显著相关。在19例患者中的15例观察到细胞遗传学改善,Ph+细胞的中位数从100%降至76%,1例患者的Ph'染色体完全被抑制。在34例预处理时间超过12个月的患者中,21例(62%)获得CHR。在10例患者中观察到细胞遗传学改善,Ph+细胞的中位数从100%降至66%。9例AP患者中有1例获得CHR。对63例CHR患者进行了中位32个月的随访后,49例(78%)仍处于疾病控制状态:34例接受IFN治疗,15例在骨髓移植(BMT)后(13例自体移植和2例异体移植)。63例(14%)CHR患者中有9例发生急变(BT),51例CHR以下的患者中有24例(47%)发生急变。IFNα-2b已被证明是治疗CML的有效方法。它与其他治疗方式的联合是未来研究中一种有趣且有前景的方法。