Ofatumumab maintenance prolongs progression-free survival in relapsed chronic lymphocytic leukemia: final analysis of the PROLONG study
Jazyk angličtina Země Spojené státy americké Médium electronic
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
PubMed
31801940
PubMed Central
PMC6893027
DOI
10.1038/s41408-019-0260-2
PII: 10.1038/s41408-019-0260-2
Knihovny.cz E-zdroje
- MeSH
- chronická lymfatická leukemie diagnóza farmakoterapie mortalita MeSH
- dospělí MeSH
- humanizované monoklonální protilátky aplikace a dávkování škodlivé účinky terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- opakovaná terapie MeSH
- protinádorové látky imunologicky aktivní aplikace a dávkování škodlivé účinky terapeutické užití MeSH
- recidiva MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- udržovací chemoterapie MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- humanizované monoklonální protilátky MeSH
- ofatumumab MeSH Prohlížeč
- protinádorové látky imunologicky aktivní MeSH
We report the final analysis of the PROLONG study on ofatumumab maintenance in relapsed chronic lymphocytic leukemia (CLL). In all, 480 patients with CLL in complete or partial remission after second- or third-line treatment were randomized 1:1 to ofatumumab (300 mg first week, followed by 1000 mg every 8 weeks for up to 2 years) or observation. Median follow-up duration was 40.9 months. Median progression-free survival was 34.2 and 16.9 months for ofatumumab and observation arms, respectively, (hazard ratio, 0.55 [95% confidence interval, 0.43-0.70]; P < 0.0001). Median time to next treatment for ofatumumab and observation arms, respectively, was 37.4 and 27.6 months (0.72 [0.57-0.91]; P = 0.0044). Overall survival was similar in both arms; median was not reached (0.99 [0.72-1.37]). Grade ≥ 3 adverse events occurred in 62% and 51% of patients in ofatumumab and observation arms, respectively, the most common being neutropenia (23% and 10%), pneumonia (13% and 12%) and febrile neutropenia (6% and 4%). Up to 60 days after the last treatment, four deaths were reported in the ofatumumab arm versus six in the observation arm, none considered related to ofatumumab. Ofatumumab maintenance significantly prolonged progression-free survival in patients with relapsed CLL and was well tolerated.
Academisch Medisch Centrum and HOVON Amsterdam The Netherlands
Albert Schweitzer Ziekenhuis Dordrecht and HOVON Dordrecht The Netherlands
Azienda Ospedaliero Universitaria Pisana Pisa Italy
Department of Hematology and Cancer Prevention Silesian Medical University Katowice Poland
Novartis Oncology East Hanover NJ USA
Novartis Pharma AG Basel Switzerland
Rigshospitalet Koebenhavn Copenhagen Denmark
Universitair Ziekenhuis Gent Gent Belgium
University Hospital and Faculty of Medicine Hradec Kralove Czech Republic
Zobrazit více v PubMed
van Oers MH, et al. Ofatumumab maintenance versus observation in relapsed chronic lymphocytic leukemia (PROLONG): an open-label, multicenter, randomized phase 3 study. Lancet Oncol. 2015;16:1370–1379. doi: 10.1016/S1470-2045(15)00143-6. PubMed DOI
Hallek M, et al. International Workshop on Chronic Lymphocytic Leukemia. Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia: a report from the International Workshop on Chronic Lymphocytic Leukemia updating the National Cancer Institute-Working Group 1996 guidelines. Blood. 2008;111:5446–5456. doi: 10.1182/blood-2007-06-093906. PubMed DOI PMC
Greil R, et al. Rituximab maintenance versus observation alone in patients with chronic lymphocytic leukemia who respond to first-line or second-line rituximab-containing chemoimmunotherapy: final results of the AGMT CLL-8a Mabtenance randomized trial. Lancet Haematol. 2016;3:e317–e329. doi: 10.1016/S2352-3026(16)30045-X. PubMed DOI
Vidal L, et al. Rituximab maintenance for the treatment of patients with follicular lymphoma: an updated systematic review and meta-analysis of randomized trials. J. Natl. Cancer Inst. 2011;103:1799–1806. doi: 10.1093/jnci/djr418. PubMed DOI
Huang BT, Zeng QC, Zhao WH, Li BS, Chen RL. How to determine post-FCR therapy for cytogenetic risk-tailored elderly patients with chronic lymphocytic leukemia, maintenance rituximab or observation. Med. Oncol. 2014;31:104. doi: 10.1007/s12032-014-0104-7. PubMed DOI
Chanan-Khan AA, et al. Lenalidomide maintenance therapy in previously treated chronic lymphocytic leukemia (CONTINUUM): a randomized, double-blind, placebo-controlled, phase 3 trial. Lancet Haematol. 2017;4:e534–e543. doi: 10.1016/S2352-3026(17)30168-0. PubMed DOI
Fink AM, et al. Lenalidomide maintenance after first-line therapy for high-risk chronic lymphocytic leukemia (CLLM1): final results from a randomized, double-blind, phase 3 study. Lancet Haematol. 2017;4:e475–e486. doi: 10.1016/S2352-3026(17)30171-0. PubMed DOI
Dartigeas C, et al. Rituximab maintenance versus observation following abbreviated induction with chemoimmunotherapy in elderly patients with previously untreated chronic lymphocytic leukaemia (CLL 2007 SA): an open-label, randomized phase 3 study. Lancet Haematol. 2018;5:e82–e94. doi: 10.1016/S2352-3026(17)30235-1. PubMed DOI
Byrd JC, et al. Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia. N. Engl. J. Med. 2013;369:32–42. doi: 10.1056/NEJMoa1215637. PubMed DOI PMC
Burger JA, et al. Ibrutinib as initial therapy for patients with chronic lymphocytic leukemia. N. Engl. J. Med. 2015;373:2425–2437. doi: 10.1056/NEJMoa1509388. PubMed DOI PMC
Furman RR, et al. Idelalisib and rituximab in relapsed chronic lymphocytic leukemia. N. Engl. J. Med. 2014;370:997–1007. doi: 10.1056/NEJMoa1315226. PubMed DOI PMC
Roberts AW, et al. Targeting BCL2 with venetoclax in relapsed chronic lymphocytic leukemia. N. Engl. J. Med. 2016;374:311–322. doi: 10.1056/NEJMoa1513257. PubMed DOI PMC
Stilgenbauer S, et al. Venetoclax in relapsed or refractory chronic lymphocytic leukemia with 17p deletion: a multicenter, open-label, phase 2 study. Lancet Oncol. 2016;17:768–778. doi: 10.1016/S1470-2045(16)30019-5. PubMed DOI
Komarova NL, Burger JA, Wodarz D. Evolution of ibrutinib resistance in chronic lymphocytic leukemia (CLL) Proc. Natl Acad. Sci. USA. 2014;111:13906–13911. doi: 10.1073/pnas.1409362111. PubMed DOI PMC
Woyach JA, et al. Resistance mechanisms for the Bruton’s tyrosine kinase inhibitor ibrutinib. N. Engl. J. Med. 2014;370:2286–2294. doi: 10.1056/NEJMoa1400029. PubMed DOI PMC
Chang BY, et al. Use of tumor genomic profiling to reveal mechanisms of resistance to the BTK inhibitor ibrutinib in chronic lymphocytic leukemia (CLL) J. Clin. Oncol. 2013;31(Suppl. 15):7014.