Hensel Manfred, Villalobos Matthias, Kornacker Martin, Krasniqi Fatime, Ho Anthony D
Department of Internal Medicine V, University of Heidelberg, Im Neuenheimer Feld 410, D-69120 Heidelberg, Germany.
Clin Lymphoma Myeloma. 2005 Sep;6(2):131-5. doi: 10.3816/CLM.2005.n.039.
Pentostatin has demonstrated significant activity as a single agent in patients with low-grade B-cell and T-cell lymphomas and is less myelosuppressive than other purine analogues.
We conducted a phase II trial with the combination regimen of PC-R (pentostatin/cyclophosphamide with or without rituximab) in 14 patients with Waldenstrom's macroglobulinemia (WM) and 3 patients with lymphoplasmacytic lymphoma (LL) without monoclonal serum immunoglobulin M (IgM), followed by a maintenance regimen with rituximab (375 mg/m2 every 3 months) for patients exhibiting a complete response (CR) or a partial response (PR) after 4-6 cycles. Nine patients were untreated, and 8 had been previously treated with 1-3 regimens. The first 9 patients received PC therapy (pentostatin 4 mg/m2 plus cyclophosphamide 600 mg/m2), and 8 patients received the same combination with rituximab 375 mg/m2 on day 1. Cycles were repeated every 3 weeks.
An objective tumor response after PC and PC-R was confirmed in 11 of 17 evaluable patients (64.7%), with 2 CRs (11.7%) and 9 PRs (52.9%). In patients who received rituximab (n = 13) simultaneously or subsequently, the overall response rate was 76.9%. Grade 2/3 nausea and grade 2 vomiting was generally mild based on World Health Organization criteria. Grade 3 hematologic toxicity occurred after 9 of 49 cycles (18.3%), and grade 4 toxicity occurred after 2 cycles (4%). Ten patients were subsequently treated with rituximab every 3 months for 2-9 cycles to date (median, 4 cycles). No patients have had disease relapse to date, and all exhibited stable IgM serum levels. In 3 patients with a PR after completion of chemotherapy, remission has improved further, with normalization of the IgM level in 1 patient and another patient exhibiting a CR.
Our data indicate that PC-R is safe and highly effective in patients with WM. Maintenance therapy with rituximab for WM as a single infusion every 3 months can be administered safely and can improve remission status.
喷司他丁作为单一药物,在低度B细胞和T细胞淋巴瘤患者中已显示出显著活性,且其骨髓抑制作用比其他嘌呤类似物小。
我们对14例华氏巨球蛋白血症(WM)患者和3例无单克隆血清免疫球蛋白M(IgM)的淋巴浆细胞淋巴瘤(LL)患者采用PC-R(喷司他丁/环磷酰胺,联合或不联合利妥昔单抗)联合方案进行了一项II期试验,对于在4-6个周期后出现完全缓解(CR)或部分缓解(PR)的患者,随后采用利妥昔单抗(375mg/m²,每3个月一次)维持治疗。9例患者未接受过治疗,8例患者曾接受过1-3种方案的治疗。前9例患者接受PC治疗(喷司他丁4mg/m²加环磷酰胺600mg/m²),8例患者在第1天接受相同方案联合利妥昔单抗375mg/m²。每3周重复一个周期。
17例可评估患者中有11例(64.7%)在接受PC和PC-R治疗后出现客观肿瘤反应,其中2例CR(11.7%),9例PR(52.9%)。在同时或随后接受利妥昔单抗治疗的患者(n = 13)中,总缓解率为76.9%。根据世界卫生组织标准,2/3级恶心和2级呕吐一般较轻。49个周期中有9个周期(18.3%)出现3级血液学毒性,2个周期(4%)出现4级毒性。10例患者随后每3个月接受利妥昔单抗治疗2-9个周期(中位周期数为4个周期)。迄今为止,没有患者出现疾病复发,所有患者的IgM血清水平均保持稳定。在3例化疗结束后达到PR的患者中,缓解情况进一步改善,1例患者的IgM水平恢复正常,另1例患者达到CR。
我们的数据表明,PC-R方案对WM患者安全且高效。每3个月单剂量输注利妥昔单抗对WM进行维持治疗可安全实施,并可改善缓解状态。