Literature DB >> 27646945

Risk of Neutropenia-Related Hospitalization in Patients Who Received Colony-Stimulating Factors With Chemotherapy for Breast Cancer.

Abiy Agiro1, Qinli Ma1, Anupama Kurup Acheson1, Sze-Jung Wu1, Debra A Patt1, John J Barron1, Jennifer L Malin1, Alan Rosenberg1, Richard L Schilsky1, Gary H Lyman1.   

Abstract

Purpose To describe outcomes after granulocyte colony-stimulating factor (G-CSF) prophylaxis in patients with breast cancer who received chemotherapy regimens with low-to-intermediate risk of induction of neutropenia-related hospitalization. Patients and Methods We identified 8,745 patients age ≥ 18 years from a medical and pharmacy claims database for 14 commercial US health plans. This retrospective analysis included patients with breast cancer who began first-cycle chemotherapy from 2008 to 2013 using docetaxel and cyclophosphamide (TC); docetaxel, carboplatin, and trastuzumab (TCH); or doxorubicin and cyclophosphamide (conventional-dose AC) regimens. Primary prophylaxis (PP) was defined as G-CSF administration within 5 days of beginning chemotherapy. Outcome was neutropenia, fever, or infection-related hospitalization within 21 days of initiating chemotherapy. Multivariable regressions and number-needed-to-treat analyses were used. Results A total of 4,815 patients received TC (2,849 PP; 1,966 no PP); 2,292 patients received TCH (1,444 PP; 848 no PP); and 1,638 patients received AC (857 PP; 781 no PP) regimen. PP was associated with reduced risk of neutropenia-related hospitalization for TC (2.0% PP; 7.1% no PP; adjusted odds ratio [AOR], 0.29; 95% CI, 0.22 to 0.39) and TCH (1.3% PP; 7.1% no PP; AOR, 0.19; 95% CI, 0.12 to 0.30), but not AC (4.7% PP; 3.8% no PP; AOR, 1.21; 95% CI, 0.75 to 1.93) regimens. For the TC regimen, 20 patients (95% CI, 16 to 26) would have to be treated for 21 days to avoid one neutropenia-related hospitalization; with the TCH regimen, 18 patients (95% CI, 13 to 25) would have to be treated. Conclusion Primary G-CSF prophylaxis was associated with low-to-modest benefit in lowering neutropenia-related hospitalization in patients with breast cancer who received TC and TCH regimens. Further evaluation is needed to better understand which patients benefit most from G-CSF prophylaxis in this setting.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27646945     DOI: 10.1200/JCO.2016.67.2899

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  5 in total

Review 1.  Mitigating acute chemotherapy-associated adverse events in patients with cancer.

Authors:  Nicole M Kuderer; Aakash Desai; Maryam B Lustberg; Gary H Lyman
Journal:  Nat Rev Clin Oncol       Date:  2022-10-11       Impact factor: 65.011

2.  Evaluation of risk factors associated with carboplatin and nab-paclitaxel treatment suspension in patients with non-small cell lung cancer.

Authors:  Yoshitaka Saito; Yoh Takekuma; Naofumi Shinagawa; Mitsuru Sugawara
Journal:  Support Care Cancer       Date:  2022-01-23       Impact factor: 3.603

3.  Pathway-Based Analysis of Genome-Wide Association Data Identified SNPs in HMMR as Biomarker for Chemotherapy- Induced Neutropenia in Breast Cancer Patients.

Authors:  Behzad Bidadi; Duan Liu; Krishna R Kalari; Matthias Rubner; Alexander Hein; Matthias W Beckmann; Brigitte Rack; Wolfgang Janni; Peter A Fasching; Richard M Weinshilboum; Liewei Wang
Journal:  Front Pharmacol       Date:  2018-03-13       Impact factor: 5.810

4.  Patient factors and their impact on neutropenic events: a systematic review and meta-analysis.

Authors:  Pinkie Chambers; Yogini Jani; Li Wei; Emma Kipps; Martin D Forster; Ian C K Wong
Journal:  Support Care Cancer       Date:  2019-04-16       Impact factor: 3.603

5.  Using claims data to attribute patients with breast, lung, or colorectal cancer to prescribing oncologists.

Authors:  Ezra Fishman; John Barron; Ying Liu; Santosh Gautam; Justin E Bekelman; Amol S Navathe; Michael J Fisch; Ann Nguyen; Gosia Sylwestrzak
Journal:  Pragmat Obs Res       Date:  2019-03-29
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.