Comparison of Skeletal Complications and Treatment Patterns Associated With Early vs. Delayed Zoledronic Acid Therapy in Multiple Myeloma

被引:2
作者
Wu, Eric Q. [1 ]
Bensimon, Arielle G. [1 ]
Marynchenko, Maryna [1 ]
Namjoshi, Madhav [2 ]
Guo, Amy [2 ]
Yu, Andrew P. [1 ]
Ericson, Solveig G. [2 ]
Raje, Noopur [3 ]
机构
[1] Anal Grp Inc, Boston, MA 02199 USA
[2] Novartis Pharmaceut, Hlth Econ & Outcomes Res, E Hanover, NJ USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
Medical chart review; Skeletal-related events; Treatment discontinuation; PLACEBO-CONTROLLED TRIAL; LONG-TERM EFFICACY; DOUBLE-BLIND; BREAST-CANCER; PHASE-III; POSTMENOPAUSAL WOMEN; RANDOMIZED-TRIAL; SOLID TUMORS; FOLLOW-UP; PAMIDRONATE;
D O I
10.1016/j.clml.2011.04.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study retrospectively compared the risks of skeletal-related events (SREs) and zoledronic acid (ZOL) treatment discontinuation associated with early vs. delayed ZOL therapy for patients with symptomatic multiple myeloma (MM). Patients and Methods: Data were collected from a physician-administered medical chart review among US patients with a confirmed diagnosis of symptomatic MM treated after 01/01/2002. Early and delayed ZOL therapy were defined, respectively, as initiating ZOL <= 60 days (N = 126) vs. <= 60 days (N = 186) after the first symptomatic MM diagnosis. Kaplan-Meier analysis with a log-rank test was performed to compare the risk of SREs between the cohorts. Cox proportional hazard modeling compared the risk of SREs associated with early vs. delayed ZOL treatment, controlling for demographic factors, stage of MM, bone health status, and presence of major comorbidities at diagnosis. Time to ZOL discontinuation was evaluated using the Kaplan-Meier method, following patients from the date of ZOL initiation. Results: Time to the first SRE was significantly longer for patients who received early treatment with ZOL (P = .005). At 2 years after diagnosis, the SRE-free rate was 74.6% vs. 56.5% in the early vs. delayed treatment group, respectively. Early ZOL therapy was associated with a significantly lower risk of any SRE (hazard rate [HR] = .625 vs. delayed ZOL therapy; P = .029). At 2 years from ZOL therapy initiation, rates of ZOL discontinuation were 9.6% vs. 16.4% among patients with early vs. delayed therapy, respectively (P < .05). Conclusion: Early treatment with ZOL was associated with significantly reduced risks of SREs and with better treatment persistence compared with delayed treatment.
引用
收藏
页码:326 / 335
页数:10
相关论文
共 28 条
  • [1] [Anonymous], 2010, Cancer Facts Figures 2010
  • [2] [Anonymous], National Comprehensive Cancer Network Compendium
  • [3] Efficacy of pamidronate in reducing skeletal events in patients with advanced multiple myeloma
    Berenson, JR
    Lichtenstein, A
    Porter, L
    Dimopoulos, MA
    Bordoni, R
    George, S
    Lipton, A
    Keller, A
    Ballester, O
    Kovacs, MJ
    Blacklock, HA
    Bell, R
    Simeone, J
    Reitsma, DJ
    Heffernan, M
    Seaman, J
    Knight, RD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (08) : 488 - 493
  • [4] Long-term pamidronate treatment of advanced multiple myeloma patients reduces skeletal events
    Berenson, JR
    Lichtenstein, A
    Porter, L
    Dimopoulos, MA
    Bordoni, R
    George, S
    Lipton, A
    Keller, A
    Ballester, O
    Kovacs, M
    Blacklock, H
    Bell, R
    Simeone, JF
    Reitsma, DJ
    Heffernan, M
    Seaman, J
    Knight, RD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) : 593 - 602
  • [5] Zoledronic Acid Effectively Prevents Aromatase Inhibitor-Associated Bone Loss in Postmenopausal Women with Early Breast Cancer Receiving Adjuvant Letrozole: Z-FAST Study 36-Month Follow-up Results
    Brufsky, Adam M.
    Bosserman, Linda D.
    Caradonna, Richard R.
    Haley, Barbara B.
    Jones, Michael
    Moore, Halle C. F.
    Jin, Lixian
    Warsi, Ghulam M.
    Ericson, Solveig G.
    Perez, Edith A.
    [J]. CLINICAL BREAST CANCER, 2009, 9 (02) : 77 - 85
  • [6] Coleman RE, 1997, CANCER, V80, P1588, DOI 10.1002/(SICI)1097-0142(19971015)80:8+<1588::AID-CNCR9>3.0.CO
  • [7] 2-G
  • [8] Bisphosphonates: Clinical experience
    Coleman, RE
    [J]. ONCOLOGIST, 2004, 9 : 14 - 27
  • [9] Collins Conor D, 2005, Cancer Imaging, V5 Spec No A, pS119, DOI 10.1102/1470-7330.2005.0033
  • [10] Bone disease in multiple myeloma
    Croucher, PI
    Apperley, JF
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (04) : 902 - 910