HILLMEN, P., T. ROBAK, A. JANSSENS, K.G. BABU, J. KLOCZKO, S. GROSICKI, Michael DOUBEK, P. PANAGIOTIDIS, E. KIMBY, A. SCHUH, A.R. PETTITT, T. BOYD, M. MONTILLO, I.V. GUPTA, O. WRIGHT, I. DIXON, J.L. CAREY, C.N. CHANG, S. LISBY, A. MCKEOWN a F. OFFNER. Chlorambucil plus ofatumumab versus chlorambucil alone in previously untreated patients with chronic lymphocytic leukaemia (COMPLEMENT 1): a randomised, multicentre, open-label phase 3 trial. Lancet. New York: Elsevier Science Inc., roč. 385, č. 9980, s. 1873-1883. ISSN 0140-6736. doi:10.1016/S0140-6736(15)60027-7. 2015.
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Základní údaje
Originální název Chlorambucil plus ofatumumab versus chlorambucil alone in previously untreated patients with chronic lymphocytic leukaemia (COMPLEMENT 1): a randomised, multicentre, open-label phase 3 trial
Autoři HILLMEN, P. (826 Velká Británie a Severní Irsko), T. ROBAK (616 Polsko), A. JANSSENS (56 Belgie), K.G. BABU (356 Indie), J. KLOCZKO (616 Polsko, garant), S. GROSICKI (616 Polsko), Michael DOUBEK (203 Česká republika, domácí), P. PANAGIOTIDIS (300 Řecko), E. KIMBY (752 Švédsko), A. SCHUH (826 Velká Británie a Severní Irsko), A.R. PETTITT (826 Velká Británie a Severní Irsko), T. BOYD (840 Spojené státy), M. MONTILLO (380 Itálie), I.V. GUPTA (840 Spojené státy), O. WRIGHT (826 Velká Británie a Severní Irsko), I. DIXON (826 Velká Británie a Severní Irsko), J.L. CAREY (840 Spojené státy), C.N. CHANG (840 Spojené státy), S. LISBY (208 Dánsko), A. MCKEOWN (826 Velká Británie a Severní Irsko) a F. OFFNER (56 Belgie).
Vydání Lancet, New York, Elsevier Science Inc. 2015, 0140-6736.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30200 3.2 Clinical medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 44.002
Kód RIV RIV/00216224:14110/15:00084660
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/S0140-6736(15)60027-7
UT WoS 000354184500031
Klíčová slova anglicky ILLNESS RATING-SCALE; ELDERLY-PATIENTS; MONOCLONAL-ANTIBODIES; 1ST-LINE TREATMENT; HUMAN CD20;
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 12. 11. 2015 16:44.
Anotace
Background Treatment for patients with chronic lymphocytic leukaemia who are elderly or who have comorbidities is challenging because fludarabine-based chemoimmunotherapies are mostly not suitable. Chlorambucil remains the standard of care in many countries. We aimed to investigate whether the addition of ofatumumab to chlorambucil could lead to better clinical outcomes than does treatment with chlorambucil alone, while also being tolerable for patients who have few treatment options. Methods We carried out a randomised, open-label, phase 3 trial for treatment-naive patients with chronic lymphocytic leukaemia in 109 centres in 16 countries. We included patients who had active disease needing treatment, but in whom fludarabine-based treatment was not possible. We randomly assigned patients (1: 1) to receive oral chlorambucil (10 mg/m(2)) on days 1-7 of a 28 day treatment course or to receive chlorambucil by this schedule plus intravenous ofatumumab (cycle 1: 300 mg on day 1 and 1000 mg on day 8; subsequent cycles: 1000 mg on day 1) for three to 12 cycles. Assignment was done with a randomisation list that was computer generated at GlaxoSmithKline, and was stratified, in a block size of two, by age, disease stage, and performance status. The primary endpoint was progression-free survival in the intention-to-treat population and assessment was done by an independent review committee that was masked to group assignment. The study is registered with ClinicalTrials.gov, number NCT00748189. Findings We enrolled 447 patients, median age 69 years (range 35-92). Between Dec 22, 2008, and May 26, 2011, we randomly assigned 221 patients to chlorambucil plus ofatumumab and 226 patients to chlorambucil alone. Median progression-free survival was 22.4 months (95% CI 19.0-25.2) in the group assigned to chlorambucil plus ofatumumab compared with 13.1 months (10.6-13.8) in the group assigned to chlorambucil only (hazard ratio 0.57, 95% CI 0.45-0.72; p<0.0001). Grade 3 or greater adverse events were more common in the chlorambucil plus ofatumumab group (109 [50%] patients; vs 98 [43%] given chlorambucil alone), with neutropenia being the most common event (56 [26%] vs 32 [14%]). Grade 3 or greater infections had similar frequency in both groups. Grade 3 or greater infusion-related adverse events were reported in 22 (10%) patients given chlorambucil plus ofatumumab. Five (2%) patients died during treatment in each group. Interpretation Addition of ofatumumab to chlorambucil led to clinically important improvements with a manageable side-effect profile in treatment-naive patients with chronic lymphocytic leukaemia who were elderly or had comorbidities. Chlorambucil plus ofatumumab is therefore an important treatment option for these patients who cannot tolerate more intensive therapy.
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