Rituximab and CHOP Chemotherapy Plus GM-CSF for Previously Untreated Diffuse Large B-Cell Lymphoma in the Elderly: A Wisconsin Oncology Network Study

被引:19
作者
Chang, Julie E. [2 ]
Seo, Songwong [3 ]
Kim, Kyungmann M. [3 ]
Werndli, Jae E. [4 ]
Bottner, Wayne A. [5 ]
Rodrigues, Gilberto A. [6 ]
Sanchez, Federico A. [6 ]
Saphner, Thomas J. [7 ]
Longo, Walter L. [2 ]
Kahl, Brad S. [1 ,2 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Inst Med Res 4059, Dept Med, Madison, WI 53705 USA
[2] UW Carbone Canc Ctr, Madison, WI USA
[3] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI 53706 USA
[4] Univ Wisconsin Hosp & Clin, Madison, WI 53792 USA
[5] Gundersen Lutheran Hlth Syst, La Crosse, WI USA
[6] ProHlth Care Reg Canc Ctr, Waukesha, WI USA
[7] St Vincent Reg Canc Ctr, Green Bay, WI USA
关键词
DLBCL; Granulocyte-macrophage colony-stimulating factor; Sargramostim; Toxicity; NON-HODGKINS-LYMPHOMA; INTERMEDIATE-GRADE; STANDARD REGIMEN; CD20; EXPRESSION; MITOXANTRONE; DOXORUBICIN; TRIAL; OLDER; AGE; THERAPY;
D O I
10.3816/CLML.2010.n.071
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: Human recombinant granulocyte-macrophage colony-stimulating factor (GM-CSF) may potentiate rituximab activity by upregulating CD20 expression and activating effector cells necessary for antibody-dependent cellular cytotoxicity. GM-CSF was combined with standard rituximab + CHOP (cyclophosphamide/doxorubicin/vincristine/Prednisone) chemotherapy (R-CHOP) in the treatment of elderly patients with de novo diffuse large B-cell lymphoma (DLBCL). Patients and Methods: Thirty-eight patients over the age of 60 years with newly diagnosed DLBCL were treated with R-CHOP every 21 days for 6-8 cycles and GM-CSF 250 mu g/m(2) per day on days 3-10. Patients were evaluated for response after cycles 4, 6, and 8. The primary endpoint was the rate of complete response, and secondary endpoints were progression-free survival (PFS), event-free survival, and overall survival (OS). Results: Thirty-eight patients were enrolled, with a median age of 72 years, and 29% of patients having high-risk disease (International Prognostic Index [IPI] score >= 4). A complete or unconfirmed complete response (CR) was achieved in 53% of patients. After a median follow-up of 51.1 months, the 3-year PFS and OS were 78% and 84%. Twenty-one percent of patients discontinued protocol treatment because of chemotherapy-related toxicity and 16% because of GM-CSF toxicity. Dose intensity for planned chemotherapy cycles was 81.1%. Conclusion: These data suggest that survival outcomes may be modestly improved when GM-CSF is combined with R-CHOP in the treatment of elderly DLBCL. GM-CSF had toxicity precluding planned administration in 16% of patients, which may limit usefulness of this agent. Further investigation of GM-CSF in combination with rituximab-containing chemotherapy is warranted.
引用
收藏
页码:379 / 384
页数:6
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