Belhadj K, Delfau-Larue M-H, Elgnaoui T, Beaujean F, Beaumont J-L, Pautas C, Gaillard I, Kirova Y, Allain A, Gaulard P, Farcet J-P, Reyes F, Haioun C
CHU Henri Mondor, Service d'Hématologie Clinique, Creteil, France.
Ann Oncol. 2004 Mar;15(3):504-10. doi: 10.1093/annonc/mdh090.
Rituximab induces clinical response in advanced B-cell lymphoma and is efficient in removing circulating B-cell from peripheral blood. We therefore postulated that rituximab might be a useful in vivo purging agent before high-dose therapy in this setting.
Fourteen patients with relapsed follicular, marginal zone and mantle cell lymphomas (11, two and one cases, respectively) and a PCR-detectable molecular marker were treated first with rituximab, then a mobilization chemotherapeutic regimen, followed by high-dose therapy with peripheral blood stem cell transplantation. PCR analyses were performed in peripheral blood before rituximab and during follow-up, and in harvest.
Harvests were free of PCR-detectable molecular marker in nine of the 11 studied cases (82%). After high-dose therapy, clinical complete remission was obtained in 13 (93%) patients and molecular remission in 11 (79%). With a median follow-up of 3 years, the 14 transplanted patients were alive, 11 of them remaining in clinical complete remission and eight in molecular remission at last follow-up.
Rituximab treatment followed by high dose therapy appears to be effective in achieving complete clinical and molecular response. In vivo harvest purging is predictive of prolonged clinical and molecular remission.
利妥昔单抗可诱导晚期B细胞淋巴瘤产生临床反应,且能有效清除外周血中的循环B细胞。因此,我们推测在这种情况下,利妥昔单抗可能是高剂量治疗前一种有用的体内净化剂。
14例复发的滤泡性、边缘区和套细胞淋巴瘤患者(分别为11例、2例和1例),且具有PCR可检测的分子标志物,首先接受利妥昔单抗治疗,然后进行动员化疗方案,随后进行外周血干细胞移植的高剂量治疗。在使用利妥昔单抗前、随访期间以及采集时对外周血进行PCR分析。
在11例研究病例中的9例(82%)采集物中未检测到PCR可检测的分子标志物。高剂量治疗后,13例(93%)患者获得临床完全缓解,11例(79%)患者获得分子缓解。中位随访3年时,14例接受移植的患者均存活,其中11例在最后一次随访时仍处于临床完全缓解状态,8例处于分子缓解状态。
利妥昔单抗治疗后进行高剂量治疗似乎能有效实现完全的临床和分子反应。体内采集净化可预测临床和分子缓解期的延长。