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Covariates adjustment
———————

In order to maintain the same statistical unit for analysis, hypertension, hyperlipidemia, ischemic heart disease, number of G-CSF transfusions, duration of hospital stay, and body mass index (BMI) were adjusted as covariates. The reference group included patients without comorbidity. Multivariate linear regression analysis was performed to adjust covariates.

Sensitivity analysis
——————–

All of the subgroup analyses were planned a priori and were as rigorous as possible. To determine the robustness of the main findings, we performed several sensitivity analyses to further examine the consistent effects in each subgroup.

Specifically, we tested the following sensitivity analyses to evaluate the robustness of our analysis: 1) We also performed separate models stratified by different transfusion regimens; 2) We further adjusted for number of G-CSF transfusions, which represents cumulative transfusion amount; 3) We further adjusted for total dose of G-CSF; 4) Finally, we also stratified the data by age (\< 75 years vs ≥ 75 years) and type of cancer (squamous vs non-squamous).

Secondary outcomes
——————

There were limited data regarding major adverse events (including death, infection, and hemorrhage) during hospitalization. Therefore, we conducted descriptive analyses of those secondary outcomes to evaluate the safety of G-CSF.

Statistical analyses
——————–

Continuous variables were reported as the median (inter-quartile range) and the minimum-maximum, and discrete variables were reported as the absolute number (percentage). The differences between subgroups were calculated by *χ*^2^ test for categorical variables and Mann-Whitney test for continuous variables. Univariate and multivariate regression analyses were performed to estimate the association between PRS and outcomes of interest, adjusting for covariates.

To account for the cluster effect in the allocation process, we used generalized estimating equations (GEE

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