Kaminski Mark S, Tuck Melissa, Estes Judith, Kolstad Arne, Ross Charles W, Zasadny Kenneth, Regan Denise, Kison Paul, Fisher Susan, Kroll Stewart, Wahl Richard L
Department of Internal Medicine, Division of Hematology and Oncology, University of Michigan Medical Center, Ann Arbor, MI 48109-0936, USA.
N Engl J Med. 2005 Feb 3;352(5):441-9. doi: 10.1056/NEJMoa041511.
Advanced-stage follicular B-cell lymphoma is considered incurable. Anti-CD20 radioimmunotherapy is effective in patients who have had a relapse after chemotherapy or who have refractory follicular lymphoma, but it has not been tested in previously untreated patients.
Seventy-six patients with stage III or IV follicular lymphoma received as initial therapy a single course of treatment with 131I-tositumomab therapy (registered as Tositumomab and Iodine I 131 Tositumomab [the Bexxar therapeutic regimen]). This consisted of a dosimetric dose of tositumomab and 131I-labeled tositumomab followed one week later by a therapeutic dose, delivering 75 cGy of radiation to the total body.
Ninety-five percent of the patients had any response, and 75 percent had a complete response. The use of polymerase chain reaction (PCR) to detect rearrangement of the BCL2 gene showed molecular responses in 80 percent of assessable patients who had a clinical complete response. After a median follow-up of 5.1 years, the actuarial 5-year progression-free survival for all patients was 59 percent, with a median progression-free survival of 6.1 years. The annualized rate of relapse progressively decreased over time: 25 percent, 13 percent, and 12 percent during the first, second, and third years, respectively, and 4.4 percent per year after three years. Of 57 patients who had a complete response, 40 remained in remission for 4.3 to 7.7 years. Hematologic toxicity was moderate, with no patient requiring transfusions or hematopoietic growth factors. No cases of myelodysplastic syndrome have been observed.
A single one-week course of 131I-tositumomab therapy as initial treatment can induce prolonged clinical and molecular remissions in patients with advanced follicular lymphoma.
晚期滤泡性B细胞淋巴瘤被认为无法治愈。抗CD20放射免疫疗法对化疗后复发或难治性滤泡性淋巴瘤患者有效,但尚未在未经治疗的患者中进行测试。
76例III期或IV期滤泡性淋巴瘤患者接受了131I-托西莫单抗治疗(注册为托西莫单抗和碘I 131托西莫单抗[Bexxar治疗方案])作为初始治疗的单一疗程。这包括一次剂量测定剂量的托西莫单抗和131I标记的托西莫单抗,一周后给予治疗剂量,全身照射75 cGy。
95%的患者有任何反应,75%的患者完全缓解。使用聚合酶链反应(PCR)检测BCL2基因重排显示,在临床完全缓解的可评估患者中,80%有分子反应。中位随访5.1年后,所有患者的5年无进展生存率为59%,中位无进展生存期为6.1年。复发年化率随时间逐渐下降:第一年、第二年和第三年分别为25%、13%和12%,三年后每年为4.4%。在57例完全缓解的患者中,40例缓解持续4.3至7.7年。血液学毒性为中度,无患者需要输血或造血生长因子。未观察到骨髓增生异常综合征病例。
作为初始治疗,单一疗程的一周131I-托西莫单抗治疗可诱导晚期滤泡性淋巴瘤患者长期的临床和分子缓解。