Real-World Outcomes of Trilaciclib Among Patients with Extensive-Stage Small Cell Lung Cancer Receiving Chemotherapy

被引:2
作者
Goldschmidt, Jerome [1 ]
Hart, Lowell [2 ]
Scott, Jeffrey [3 ]
Boykin, Kristen [2 ]
Bailey, Ray [2 ]
Heritage, Trevor [2 ]
Lopez-Gonzalez, Lorena [4 ]
Zhou, Zheng-Yi [5 ]
Edwards, Marie Louise [5 ]
Monnette, Alisha [6 ]
Ogbonnaya, Augustina [7 ]
Deyoung, Kathryn [7 ]
Venkatasetty, Divea [6 ]
Shi, Ping [6 ]
Aton, Lindsay [3 ]
Huang, Huan [4 ]
Conkling, Paul. R. R. [6 ]
Gordan, Lucio [2 ]
机构
[1] Blue Ridge Canc Ctr US Oncol Res, Blacksburg, VA USA
[2] Florida Canc Specialists & Res Inst, Ft Myers, FL USA
[3] Integra Connect, W Palm Beach, FL USA
[4] G1 Therapeut Inc, Res Triangle Pk, NC USA
[5] Anal Grp Inc, 111 Huntington Ave, 14th Floor, Boston, MA 02199 USA
[6] Ontada, The Woodlands, TX USA
[7] Xcenda, Carrollton, TX USA
关键词
Extensive-stage small cell lung cancer; Chemotherapy-induced myelosuppression; Cytopenia; Real world; Supportive care; Trilaciclib; INDUCED MYELOSUPPRESSION; DOSE INTENSITY; IMPACT; 1ST-LINE;
D O I
10.1007/s12325-023-02601-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
IntroductionTrilaciclib was recently approved in the USA for reducing chemotherapy-induced myelosuppression (CIM) among adults with extensive-stage small cell lung cancer (ES-SCLC) when administered prior to chemotherapy. There is limited understanding of real-world outcomes of trilaciclib.MethodsA comprehensive literature review was conducted using a keyword search in the MEDLINE, Embase, and conference abstracts. Additional studies were identified through communications with the authors of relevant studies. Published and unpublished real-world studies of trilaciclib- and comparable non-trilaciclib-treated patients with ES-SCLC were included. Evidence on myelosuppressive hematologic adverse events (HAEs), cytopenia-related healthcare utilization, and other reported outcomes (e.g., hospitalizations, dose reduction, and treatment delay) were synthesized. If feasible, outcomes were compared qualitatively between the trilaciclib and historical reference groups, and between first-line trilaciclib initiators and the overall trilaciclib population. Weighted averages were estimated for selected outcomes using sample size as the weight.ResultsThe literature search identified five unique studies based on eight records-two included trilaciclib only, two non-trilaciclib only, and one both. In trilaciclib cohorts, the weighted average prevalence of grade & GE; 3 myelosuppressive HAEs in & GE; 1 lineage, & GE; 2 lineages, and all three lineages was 40.5%, 14.5%, and 7.5%, respectively. All rates were numerically lower compared to the historical non-trilaciclib cohorts (58.8%, 28.0%, 13.0% respectively). Cytopenia-related healthcare utilization was also lower in the trilaciclib cohorts. In general, first-line trilaciclib initiators had numerically lower myelosuppressive HAEs and cytopenia-related healthcare utilization than the overall trilaciclib patients.ConclusionsThe existing evidence suggests that trilaciclib may reduce single and multilineage grade & GE; 3 myelosuppressive HAEs and cytopenia-related healthcare utilization among patients with ES-SCLC in the real world. It is a promising new treatment for CIM prevention in ES-SCLC and may bring greater benefits to first-line trilaciclib initiators. Future studies are recommended to further evaluate the real-world effectiveness of trilaciclib.
引用
收藏
页码:4189 / 4215
页数:27
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