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CHOP-GR疗法用于晚期滤泡性淋巴瘤的II期研究。

Phase II study of CHOP-GR therapy for advanced-stage follicular lymphoma.

作者信息

Tomita Naoto, Kodama Fumio, Oshima Rika, Hashimoto Chizuko, Koharazawa Hideyuki, Takemura Sachiya, Yamazaki Etsuko, Fujimaki Katsumichi, Sakai Rika, Fujita Hiroyuki, Fujisawa Shin, Kanamori Heiwa, Motomura Shigeki, Ishigatsubo Yoshiaki

机构信息

Department of Hematology, Yokohama City University Medical Center, Yokohama, Japan.

出版信息

Leuk Lymphoma. 2006 Jun;47(6):1041-7. doi: 10.1080/10428190500472784.

Abstract

Recently, the cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP) regimen plus rituximab (R-CHOP) have been used widely to treat patients with follicular lymphoma. We investigated a fixed scheme of combination chemotherapy protocol including CHOP, granulocyte colony stimulating factor (G-CSF) and rituximab (CHOP-GR) for patients with advanced-stage grade 1 or grade 2 follicular lymphoma in a phase II clinical trial, assessing enhancement of antibody-dependent cellular cytotoxicity of rituximab by G-CSF. Twenty-one untreated patients received two courses of CHOP chemotherapy followed by four courses of CHOP-GR, including G-CSF (s.c.) on days 11 - 14 and rituximab on day 15. Overall response rate was 76% (16 of 21 patients). Two patients, one with no response and subsequent allogeneic hematopoietic stem cell transplantation and one with progressive disease, died of lymphoma. One patient refused to continue therapy, whereas two were rediagnosed and no longer met histologic criteria; these three patients were classified as nonresponders. After a median observation time of 23 months, the 19 histologically assessable patients showed a 2-year progression-free survival rate of 82%, whereas 2-year overall survival was 95%. Fifteen patients (79%) continued in remission during this median follow-up period. Of seven patients with initial bulky mass, five responded to therapy. The most frequent adverse events were leukocytopenia (100%) and neutropenia (100%), followed in turn by alopetia (94%) and nausea/vomiting (79%). Of 11 patients examined for bcl-2 translocation in peripheral blood or marrow by polymerase chain reaction (PCR), four were positive, whereas three of the four had complete remissions and converted to PCR negativity after therapy. According to short-term observation, CHOP-GR is a safe and effective therapy for patients with advanced-stage follicular lymphoma.

摘要

最近,环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)方案联合利妥昔单抗(R-CHOP)已被广泛用于治疗滤泡性淋巴瘤患者。在一项II期临床试验中,我们研究了一种固定的联合化疗方案,包括CHOP、粒细胞集落刺激因子(G-CSF)和利妥昔单抗(CHOP-GR),用于治疗晚期1级或2级滤泡性淋巴瘤患者,评估G-CSF对利妥昔单抗抗体依赖性细胞毒性的增强作用。21例未经治疗的患者接受了两个疗程的CHOP化疗,随后接受四个疗程的CHOP-GR,包括第11 - 14天皮下注射G-CSF和第15天注射利妥昔单抗。总缓解率为76%(21例患者中的16例)。两名患者,一名无反应并随后接受异基因造血干细胞移植,另一名疾病进展,死于淋巴瘤。一名患者拒绝继续治疗,而两名患者被重新诊断且不再符合组织学标准;这三名患者被归类为无反应者。经过23个月的中位观察时间,19例可进行组织学评估的患者2年无进展生存率为82%,而2年总生存率为95%。在这个中位随访期内,15例患者(79%)持续缓解。7例初始有大包块的患者中,5例对治疗有反应。最常见的不良事件是白细胞减少(100%)和中性粒细胞减少(100%),其次依次是脱发(94%)和恶心/呕吐(79%)。通过聚合酶链反应(PCR)检测外周血或骨髓中bcl-2易位的11例患者中,4例呈阳性,而这4例中的3例完全缓解并在治疗后转为PCR阴性。根据短期观察,CHOP-GR是治疗晚期滤泡性淋巴瘤患者的一种安全有效的疗法。

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