2017
Association between quality of response and outcomes in patients with newly diagnosed mantle cell lymphoma receiving VR-CAP versus R-CHOP in the phase 3 LYM-3002 study
VERHOEF, G.; T. ROBAK; H.Q. HUANG; H. PYLYPENKO; N. SIRITANARATKUL et. al.Základní údaje
Originální název
Association between quality of response and outcomes in patients with newly diagnosed mantle cell lymphoma receiving VR-CAP versus R-CHOP in the phase 3 LYM-3002 study
Autoři
VERHOEF, G.; T. ROBAK; H.Q. HUANG; H. PYLYPENKO; N. SIRITANARATKUL; J. PEREIRA; J. DRACH; Jiří MAYER; R. OKAMOTO; L.X. PEI; B. ROONEY; A. CAKANA; H. van de VELDE a F. CAVALLI
Vydání
Haematologica, PAVIA, FERRATA STORTI FOUNDATION, 2017, 0390-6078
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Itálie
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 9.090
Kód RIV
RIV/00216224:14110/17:00098741
Organizační jednotka
Lékařská fakulta
UT WoS
000402490900026
EID Scopus
2-s2.0-85018971634
Klíčová slova anglicky
3 LYM-3002
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 20. 3. 2018 18:52, Soňa Böhmová
Anotace
V originále
In the phase 3 LYM-3002 study comparing intravenous VR-CAP with R-CHOP in patients with newly-diagnosed, measurable stage II-IV mantle cell lymphoma, not considered or ineligible for transplant, the median progression-free survival was significantly improved with VR-CAP (24.7 versus 14.4 months with R-CHOP; P<0.001). This post-hoc analysis evaluated the association between the improved outcomes and quality of responses achieved with VR-CAP versus R-CHOP in LYM-3002. Patients were randomized to six to eight 21-day cycles of VR-CAP or R-CHOP. Outcomes included progression-free survival, duration of response (both assessed by an independent review committee), and time to next anti-lymphoma treatment, evaluated by response (complete response/unconfirmed complete response and partial response), MIPI risk status, and maximum reduction of lymph-node measurements expressed as the sum of the product of the diameters. Within each response category, the median progression-free survival was longer for patients given VR-CAP than for those given R-CHOP (complete response/unconfirmed complete response: 40.9 versus 19.8 months; partial response: 17.1 versus 11.7 months, respectively); similarly, the median time to next anti-lymphoma treatment was longer among the patients given VR-CAP than among those treated with R-CHOP (complete response/unconfirmed complete response: not evaluable versus 26.6 months; partial response: 35.3 versus 24.3 months). Within the complete/unconfirmed complete and partial response categories, improvements in progression-free survival, duration of response and time to next anti-lymphoma treatment were more pronounced in patients with low- and intermediate-risk MIPI treated with VR-CAP than with R-CHOP. In each response category, more VR-CAP than R-CHOP patients had a sum of the product of the diameters nadir of 0 during serial radiological assessments. Results of this post-hoc analysis suggest a greater duration and quality of response in patients treated with VR-CAP in comparison with those treated with R-CHOP, with the improvements being more evident in patients with low-and intermediate-risk MIPI. LYM-3002 ClinicalTrials.gov: NCT00722137.