First-line R-CVP versus R-CHOP induction immunochemotherapy for indolent lymphoma with rituximab maintenance. A multicentre, phase III randomized study by the Polish Lymphoma Research Group PLRG4

被引:21
作者
Walewski, Jan [1 ]
Paszkiewicz-Kozik, Ewa [1 ]
Michalski, Wojciech [1 ]
Rymkiewicz, Grzegorz [1 ]
Szpila, Tomasz [2 ]
Butrym, Aleksandra [3 ]
Giza, Agnieszka [4 ]
Zaucha, Jan M. [5 ]
Kalinka-Warzocha, Ewa [6 ]
Wieczorkiewicz, Agata [7 ]
Zimowska-Curylo, Dagmara [3 ]
Knopinska-Posluszny, Wanda [8 ]
Tyczynska, Agata [8 ]
Romejko-Jarosinska, Joanna [1 ]
Dabrowska-Iwanicka, Anna [1 ]
Gruszecka, Beata [9 ]
Jamrozek-Jedlinska, Maria [10 ]
Borawska, Anna [1 ]
Holda, Waldemar [11 ]
Porowska, Agnieszka [12 ]
Romanowicz, Agnieszka [12 ]
Hellmann, Andrzej [5 ]
Stella-Holowiecka, Beata [7 ]
Deptala, Andrzej [12 ,13 ]
Jurczak, Wojciech [1 ]
机构
[1] Maria Sklodowska Curie Inst Oncol Ctr, Warsaw, Poland
[2] Inst Hematol & Transfusiol, Warsaw, Poland
[3] Med Univ Wroclaw, Wroclaw, Poland
[4] Jagiellonian Univ, Coll Med, Krakow, Poland
[5] Med Univ Gdansk, Gdansk, Poland
[6] Polish Mothers Mem Hosp, Res Inst, Lodz, Poland
[7] Silesian Med Univ, Katowice, Poland
[8] Maritime Hosp, Gdynia, Poland
[9] Lower Silesia Cell Transplantat Ctr, Wroclaw, Poland
[10] Municipal Hosp, Poznan, Poland
[11] Subcarpathian Voivodeship Hosp, Krosno, Poland
[12] Cent Clin Hosp MSWiA, Warsaw, Poland
[13] Med Univ Warsaw, Warsaw, Poland
关键词
indolent lymphoma; first-line induction immunochemotherapy; rituximab maintenance; FOLLICULAR LYMPHOMA; PLUS RITUXIMAB; RESPONSE CRITERIA; INITIAL TREATMENT; CYCLOPHOSPHAMIDE; VINCRISTINE; PREDNISONE; IMPROVES; FM;
D O I
10.1111/bjh.16264
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
R-CVP (cyclophosphamide, vincristine, prednisone) and R-CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone + rituximab) are immunochemotherapy regimens frequently used for remission induction of indolent non-Hodgkin lymphomas (iNHLs). Rituximab maintenance (RM) significantly improves progression-free survival (PFS) in patients with complete/partial remission (CR/PR). Here we report the final results of a randomized study comparing R-CVP to R-CHOP both followed by RM. Untreated patients in need of systemic therapy with symptomatic and progressive iNHLs including follicular (FL) and marginal zone lymphoma (MZL), mucosa-associated lymphoid tissue (MALT), small lymphocytic (SLL), and lymphoplasmacytic (LPL) lymphoma were eligible. Patients were randomized to receive R-CVP or R-CHOP for eight cycles or until complete response (CR). All patients with CR/PR (partial response) received RM 375 mg/m(2) q 2 months for 12 cycles. Primary endpoint was event-free survival (EFS). Two-hundred and fifty patients [FL 42%, MZL/MALT 38%, LPL/ Waldenstrom Macroglobulinaemia (WM) 11%, SLL 9%] were enrolled and randomized (R-CHOP: 127, R-CVP: 123). Median age was 56 years (21-85), 44% were male, 90% were in stage III-IV, 43% of FL patients had a Follicular Lymphoma International Prognostic Index (FLIPI) score >= 3, and 33 center dot 4% of all patients had an IPI score >= 3. At the end of induction treatment, the CR/PR rate was 43 center dot 6/50 center dot 9% and 36 center dot 3/60 center dot 8% in the R-CHOP and R-CVP groups (P = 0 center dot 218) respectively. After a median follow-up of 67, 66, and 70 months, five-year EFS was 61% vs. 56% (not significant), progression-free survival (PFS) was 71% vs. 69% (not significant) and overall survival (OS) was 84% vs. 89% in the R-CHOP vs. the R-CVP arm respectively. Grade III/IV adverse events (65 vs. 22) occurred in 40 (33 center dot 1%) and 18 (15 center dot 3%) patients, P = 0 center dot 001; neutropenia in 16 (11 center dot 6%) and 4 (3 center dot 4%) patients, P = 0 center dot 017; infection in 14 (10 center dot 7%) and 3 (2 center dot 5%) patients,; P = 0 center dot 011; and a second neoplasm in three versus seven patients., in the R-CHOP and the R-CVP groups respectively. This multicentre randomized study with >five-year follow-up shows similar outcome in patients with indolent lymphoma in need of systemic therapy treated with R-CVP or R-CHOP immunochemotherapy and rituximab maintenance in both arms. The minor toxicity of the R-CVP regimen makes it a reasonable choice for induction treatment, leaving other active agents like doxorubicin or bendamustin for second-line therapy.
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页码:898 / 906
页数:9
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