The impact of chemotherapy dose intensity and supportive care on the risk of febrile neutropenia in patients with early stage breast cancer: a prospective cohort study
© Culakova et al. 2015
Received: 16 July 2015
Accepted: 17 July 2015
Published: 6 August 2015
Febrile neutropenia (FN) is a major dose-limiting toxicity of cancer chemotherapy resulting in considerable morbidity, mortality, and cost. This study evaluated the time course of neutropenic events and patterns of supportive care interventions in patients receiving chemotherapy for early-stage breast cancer treated in oncology community practices.
A prospective cohort study of adult cancer patients initiating a new chemotherapy regimen was conducted at 115 US sites. Toxicity associated with chemotherapy including neutropenic and infectious complications was recorded over four cycles. Clinical interventions were recorded including reductions in chemotherapy dose intensity and use of supportive care measures.
A total of 1,202 patients with stage I–III breast cancer were evaluated. The majority of neutropenic (116 of 196) and infection events (179 of 325) occurred in the initial cycle. A decrease in occurrence of FN and infection was observed in the subsequent cycles, along with an increase in utilization of colony stimulating factors (CSFs), antibiotics and reductions in chemotherapy dose intensity. The overall risk of FN in all patients was 16.3%. In patients who started treatment at or near full dose intensity, the FN risk reached 21.0% without primary CSF prophylaxis and it was 9.0% with prophylaxis. There was no significant difference in FN rates by menopausal or hormone receptors status.
The risk of neutropenic complications is greatest in the initial cycle when most patients receive full-dose chemotherapy. A decrease in neutropenic events during subsequent cycles is associated with reduced dose intensity or increased use of supportive care measures. However, the cumulative risk of FN remains high in patients with early-stage breast cancer receiving full dose chemotherapy without prophylactic measures.
Among women, breast cancer is the most prevalent cancer type with over a quarter of a million newly diagnosed patients annually and accounting for approximately 40,000 deaths each year in the US, only exceeded by lung cancer in terms of cancer-related mortality (American Cancer Society 2015; Gradishar et al. 2015). Largely attributable to advancements in diagnostic techniques and preventive care, the disease is often detected early before the development of evident distant metastases (Onitilo et al. 2013). Early-stage breast cancer (ESBC) is considered a curable malignancy. However, it is a heterogeneous disease with prognosis and also treatment decisions depending on the clinical parameters, molecular type, as well as patient’s functional status (Goldhirsch et al. 2013; Perou and Borresen-Dale 2011).
An important part of the treatment decision in ESBC is whether chemotherapy will be beneficial and if so, the choice of chemotherapy regimen (Theriault et al. 2013; Bonadonna et al. 2005; Aebi et al. 2014). All regimens before being implemented into the routine clinic practice were developed in a series of clinical trials. Deviations from the established schedule either by implementing drug dose reductions or treatment delays, resulting in reduced relative dose intensity (RDI), may compromise treatment outcome (Bonadonna et al. 1995; Budman et al. 1998; Lyman 2009). When delivered RDI falls below a certain threshold the patient may get little or no clinical benefit of treatment while still facing multiple burdens from myelotoxic treatment (Bonadonna et al. 1995).
Chemotherapy-related toxicities often cause modifications or interruption of treatment (Lyman et al. 2003, 2013a). Among the toxicities, chemotherapy-induced neutropenia, especially febrile neutropenia (FN), is considered to be a major adverse event frequently requiring hospitalization (Weycker et al. 2014; Kreys et al. 2014). It has not only negative effects on treatment schedule but is often connected with considerable morbidity, high risk of infection-related early mortality, and an increased treatment cost (Hendricks et al. 2011; Klastersky and Paesmans 2011; Kuderer et al. 2006; Lee et al. 2015; Pathak et al. 2015). Patients have the highest risk of neutropenic events at the beginning of treatment, with 50–75% of initial events happening in the first cycle of chemotherapy (Crawford et al. 2008; Vogel et al. 2005; Timmer-Bonte and Tjan-Heijnen 2006; Gomez et al. 1998). Moreover, patients who have experienced an initial neutropenic event are at increased risk for additional neutropenic events. Neutropenic or infectious events often generate a response from treating clinicians in the management of the subsequent cycles with implementing one or more of the following options: (1) addition of prophylactic use of colony stimulating factors (CSFs); (2) prophylactic use of antibiotics; (3) reduction of chemotherapy dose; (4) delay in the initiation of the next treatment cycle; (5) interruption and/or cessation of the planned regimen. Execution of any of these measures may decrease the risk of neutropenic complications observed in the subsequent cycles (Timmer-Bonte and Tjan-Heijnen 2006). However, in a curative setting such as ESBC, a decrease in chemotherapy dose intensity may result in compromised survival rates (Bonadonna et al. 1995; Budman et al. 1998).
Patterns of utilization of supportive measures implemented in efforts to reduce neutropenic events during the course of chemotherapy within routine community clinical practice are largely unknown. The general population receiving chemotherapy includes patients with comorbidities, frail or elderly, and may differ from patients with cancer treated in randomized control trials (RCTs) who are often healthier and highly preselected (Murthy et al. 2004). The main aim of this study was to assess timing of neutropenic events in relation to clinical interventions such as modification of chemotherapy dose or schedule or addition of supportive care in patients receiving chemotherapy treatment in oncology practice within a community setting. The data from a prospective observational registry study were utilized (Crawford et al. 2008) and the report evaluating all patients with solid tumors or lymphoma was published earlier (Culakova et al. 2014). This analysis is focused on patients with stage I–III breast cancer.
A prospective observational, multi-center cohort registry study comprised of adult ambulatory patients with solid tumors or lymphoma receiving chemotherapy was conducted between 2002 and 2006. The primary goals of the study were to address questions about the frequency and severity of treatment-related complications and the use of supportive care in cancer patients treated in community-based practices. There was no treatment intervention mandated by the study and choice of the chemotherapy regimen and adjunctive supportive care was at the discretion of the treating oncologist. Patient eligibility was generally not restrictive in order to enroll typical patients cared for in community oncology practices, including those who would not be eligible for most clinical trials because of advanced age or preexisting comorbidities. The study protocol was approved by the University of Rochester Research Subjects’ Review Board (Rochester, NY, USA). Data analyses, interpretation, and reporting were performed at the Study Coordinating Center independent of the funding agency.
Participating patients had to be at least 18 years old with a diagnosis of ESBC starting a new myelosuppressive chemotherapy regimen and anticipated to receive at least four cycles. There was no upper age limit for participation and no restrictions based on the comorbid conditions or performance status. The patients had to be willing to return for scheduled nadir visits and to sign informed consent. In order to lessen the chance of selection bias, sites were required to enroll consecutive eligible patients and maintain a log of all patients who were offered participation in the study. Lactating females, patients treated with continuous chemotherapy, with active infection, receiving concurrent cytotoxic therapy for non-cancer condition, or participating in a double blind clinical trial were excluded. The analysis presented here is based on patients with available toxicity data for at least the first cycle of chemotherapy.
Demographic information, patient and disease characteristics, comorbid conditions, performance status and data concerning the planned chemotherapy treatment were gathered at baseline prior to chemotherapy initiation. Laboratory data, chemotherapy information, and concomitant medications were collected at the start of each cycle for the first four cycles of chemotherapy. Treatment modifications including dose reductions and delays as well as supportive care interventions such as use of antibiotics and CSFs were captured for each cycle. Additionally, laboratory data were collected at the time of expected lowest neutrophil counts (nadir), and during midcycle visits. Adverse events and chemotherapy-associated toxicities, including fever and infection, were most often recorded at the start of the subsequent cycle of chemotherapy. Therefore, some data related to adverse events and toxicities for cycle 4 may be incomplete. Infection was determined based on the report of the treating physician. Similarly, fever was defined as reported by a clinician or the record of a temperature >38.1°C.
Based on type of drugs, dosing and schedule recorded at the baseline, chemotherapy regimens were matched with recognized standard regimens recommended for treatment of ESBC by American Society of Clinical Oncology or National Comprehensive Cancer Network guidelines in order to determine RDI. The planned, current cycle and overall actual RDI were calculated based on the doses and schedule planned at the initiation, cycle related, and given over the course of four cycles, respectively (Culakova et al. 2014).
Definition of outcomes
Outcomes of interest for this analysis included occurrence of FN, occurrence of severe or febrile neutropenia (SN/FN), reductions in RDI, utilization of CSF and/or antibiotics as primary prophylaxis or overall. SN was defined as absolute neutrophil count (ANC) <500/mm3 and FN as ANC <1,000/mm3 with reported fever or infection in the same chemotherapy cycle. Primary CSF prophylaxis was defined as CSF use planned at the beginning of the first cycle or prior to a neutropenic event within the first cycle. For subsequent cycles, patients were considered to be treated prophylactically with CSF if it was reported before or at the baseline of the cycle.
The goal of this prospective cohort study was to describe the frequency and time course of treatment-related complications and patterns of clinical management including supportive care and was, therefore, primarily descriptive in nature. Clinically relevant variables were summarized using standard descriptive statistics utilizing proportions for categorical variables, and measures of central tendency and variability summarized as mean, median, and/or standard error (SE) for continuous variables. Neutropenic events were assessed as proportions of patients with an event and were measured by cycle as well as cumulatively across cycles. Similarly, proportions of patients receiving supportive care were reported. To evaluate the timing of neutropenic events and clinical interventions aimed at preventing them, hazard rates were estimated using actuarial methods. Statistical analysis was conducted using SAS version 9.3 (SAS Institute Inc.; Cary, NC, USA).
Descriptive characteristics of the entire cohort and stratified by hormonal status
ER+ or PR+
ER− and PR−
Baseline body surface area
Body mass indexa
30 to <35 kg/m2
ECOG performance status
CHF or MI
History of anemia
Number of comorbidities
Standard AC or EC
Dose dense AC or EC
CAF or CEF
TAC or TEC
AT or ET
Neutropenic and infectious events
Relative dose intensity
Patients with reduced relative dose intensity (RDI) (percent of patients with reductions are presented)
Planned RDI <85% of standard (%)
Overall actual RDI <85% (%)
RDI <85% for 1+ cycle (%)
Planned RDI <90% of standard (%)
Overall actual RDI <90% (%)
RDI <90% for 1+ cycle (%)
All (n = 1,176)a
<50 years (n = 443)
50–64 years (n = 537)
≥65 years (n = 196)
Pre-menopausal (n = 479)
Post-menopausal (n = 690)
ECOG performance status
0 (n = 917)
1 (n = 235)
2–4 (n = 24)
No (n = 1,085)
Yes (n = 91)
Baseline body surface area
≤2 m2 (n = 908)
>2 m2 (n = 268)
Body mass indexa
<30 kg/m2 (n = 750)
30 to <35 kg/m2 (n = 220)
≥35 kg/m2 (n = 203)
ER+ or PR+ (n = 753)
ER− and PR− (n = 378)
Supportive care measures
First cycle and subsequent cycles
Toxicities and treatment completion
In this prospective cohort study of ESBC patients receiving conventional chemotherapy in a community practice setting, the risk of the initial neutropenic complications was greatest during the first cycle of chemotherapy. This is consistent with reports from other studies (Vogel et al. 2005; Haim et al. 2005; Chan et al. 2011; Martin et al. 2006). It is in line with earlier reports utilizing data from this prospective study, and it applies across tumors types (Crawford et al. 2008; Culakova et al. 2014).
At the initiation of treatment, most patients received the full dose of chemotherapy, often with no primary prophylaxis with CSFs or antibiotics. The decrease in neutropenic events during subsequent cycles was likely the result of clinical interventions such as reductions in chemotherapy dose intensity and/or the additional use of supportive care measures prompted by neutropenic events in cycle 1. A recent trial by Aarts et al. tested the hypothesis that in order to decrease treatment cost, the use of granulocyte colony-stimulating factor (G-CSF) may be limited to the initial cycles (Aarts et al. 2013). Breast cancer patients with estimated FN risk above 20% were randomized to G-CSF prophylaxis with pegfilgrastim given only in cycle 1 and 2 (experimental arm) versus pegfilgrastim in all cycles. In contrast to the expected results, in the experimental arm, FN rates climbed after G-CSF was discontinued to the maximum of 24% in the third cycle, and reached overall risk of 36%, compared to 10% rates in the standard arm with continued prophylaxis.
Hematologic toxicities as well as chemotherapy dose intensity are often underreported in the published reports of clinical trials (Lyman 2009; Dale et al. 2003; Truong et al. 2015). A recent systematic review by Younis et al. (2012) studied FN rates outside of RCTs for two commonly used regimens: (1) docetaxel 75 mg/m2, cyclophosphamide 600 mg/m2 every 21 days for four cycles (TC) and (2) 5-fluorouracil 500 mg/m2, epirubicin 100 mg/m2, and cyclophosphamide 500 mg/m2 on day 1 every 21 days for three cycles followed by docetaxel 100 mg/m2 day 1 every 21 days for three cycles (FEC-D). The average FN rate was 17% (range 7–33%) for 13 studies with TC regimen reaching 29% when prophylactic G-CSF was not given, compared to 5% reported in the trial (Younis et al. 2012; Jones et al. 2006). Similarly, for nine retrospective studies of FEC-D treatment, the FN rate was 24% (18–35%) reaching 31% without G-CSF prophylaxis compared to 11.2% reported in the PACS-01 trial (Younis et al. 2012; Roche et al. 2006). In the study reported here, 16% of patients developed FN over four cycles. While one-fourth of patients received prophylactic CSFs initially, clinical events resulted in the use of CSFs in nearly two-thirds of patients over the period of observation. In patients initiating treatment with full dose chemotherapy and without G-CSF support, the rate of FN exceeded 20% and approximately one-half received G-CSF after cycle 1. Of note, there were no meaningful differences in G-CSF use or in FN events based on menopausal or hormone receptor status in this group.
The safety and efficacy of primary prophylaxis with G-CSF in patients with solid tumors including breast cancer receiving chemotherapy was established in RCTs (Vogel et al. 2005; Timmer-Bonte et al. 2005; Lyman et al. 2015a). A meta-analysis of RCTs of chemotherapy with or without prophylactic G-CSF confirmed significant reductions in FN, early mortality, and infection-related mortality (Kuderer et al. 2007). In addition, a systematic review of RCTs in patients with breast cancer demonstrated significant reductions in FN, early mortality, risk of hospitalization, and use of intravenous antibiotics (Renner et al. 2012). Another meta-analysis reported improved overall survival with more intense breast cancer regimens supported by G-CSF (Lyman et al. 2013b). While routine prophylactic CSFs are recommended in patients at 20% or greater risk of FN, the use of prophylactic antibiotics is discouraged due to concerns over rising rates of antimicrobial resistance (Aapro et al. 2011; Crawford et al. 2013; Smith et al. 2006). Current guidelines oppose antimicrobial prophylaxis unless prolonged severe neutropenia is expected (Flowers et al. 2013). In the study reported here, 4% of patients received prophylactic antibiotics in the absence of fever or infection in cycle 1 increasing to 17% over the four cycles observed.
Although neutropenia commonly results from cytotoxic chemotherapy and lowering chemotherapy dose intensity may reduce the risk of FN, reductions in chemotherapy dose intensity may compromise long term outcome and shorten overall survival. RCTs as well as observational studies have demonstrated the importance of maintaining chemotherapy dose intensity in the curative setting of ESBC (Bonadonna et al. 1995; Budman et al. 1998; Chirivella et al. 2009; Perez-Fidalgo et al. 2014). In the study reported here, one-fifth of patients received overall RDI below 85% while 13% started the treatment with planned RDI <85%. Of note, reduced RDI was more common for older patients, patients with poor performance status, and obese patients. Planned dose reductions were twice as common with BSA >2 m2 compared to those with BSA ≤2 m2. Guidelines on appropriate chemotherapy dosing of obese adult patients with cancer recommend dosing based on calculations using actual body weight for most cytotoxic agents (Griggs et al. 2012). Routine dose reductions, such as capping of the doses at 2 m2, are discouraged. Most published data indicate no increase in treatment-related toxicities in obese patients with cancer receiving full dosing estimated by using actual weight (Griggs et al. 2012; Carroll et al. 2012). In addition, clinicians are encouraged to use the same rules when responding to the toxicities in non-obese and obese patients (Griggs et al. 2012).
It is important to note limitations to the current study. The population of this prospective observational study received chemotherapy between 2002 and 2006, and may not be representative of chemotherapy regimens and supportive care introduced subsequent to that period. Importantly, toxicity data including fever, infection, and FN for cycle 4 are likely underreported with nearly 20% of patients completing all four cycles missing toxicity data for the last cycle. Also, patients who discontinued chemotherapy prematurely have incomplete data and represent a potentially more vulnerable group with higher risk of adverse events. Additionally, only data during the first four cycles were captured and long term follow-up is not available. Nevertheless, this prospective cohort is the largest prospective study of cancer patients capturing detailed chemotherapy treatment and its complications in the community setting in US oncology practices.
In summary, while the risk of neutropenic complications is greatest in the initial cycle, the cumulative risk of neutropenic events remains high in patients receiving full dose chemotherapy without prophylactic measures. The apparent reduction in the risk of neutropenic complications in subsequent cycles appears to be associated with efforts to reduce risk through chemotherapy dose reductions and treatment delays or the secondary use of prophylactic measures including CSFs, antibiotics or both. While other patient-, disease-, and treatment-related factors may also influence toxicity patterns, they likely played less of a role in the observed events. Moreover, most ESBC patients are treated with a curative intent and delivery of full-dose chemotherapy is important to sustain favorable long term outcome. Nevertheless, the influence of patient and provider decisions, as well as institutional and payer policies on the observed rates of treatment-related toxicities require additional research (Lyman et al. 2015b). Further, the potential impact of educational efforts, practice guidelines or pathways as well as direct and out of pocket healthcare costs on treatment and supportive care strategies as well as clinical and economic outcomes require further investigation.
All authors contributed to the design and implementation of this study. Drs. Culakova, Poniewierski and Lyman conducted the data analysis presented. All authors contributed to the review of study results, manuscript preparation, and final review. All authors read and approved the final manuscript.
Dr. Lyman is PI on a research Grant to the Fred Hutchinson Cancer Research Center from Amgen. Dr. Crawford has served as a consultant to Celgene, Hospira, Amgen, Merck and Novartis. Dr. Dale is PI on a research grant to the University of Washington from Amgen and has also served as a consultant to Amgen.
Compliance with ethical guidelines
Competing interests Eva Culakova, Marek Poniewierski and Debra Wolff report no competing interests.
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- Aapro MS, Bohlius J, Cameron DA, Dal Lago L, Donnelly JP, Kearney N et al (2011) 2010 Update of EORTC guidelines for the use of granulocyte-colony stimulating factor to reduce the incidence of chemotherapy-induced febrile neutropenia in adult patients with lymphoproliferative disorders and solid tumours. Eur J Cancer 47(1):8–32. doi:10.1016/j.ejca.2010.10.013 View ArticleGoogle Scholar
- Aarts MJ, Peters FP, Mandigers CM, Dercksen MW, Stouthard JM, Nortier HJ et al (2013) Primary granulocyte colony-stimulating factor prophylaxis during the first two cycles only or throughout all chemotherapy cycles in patients with breast cancer at risk for febrile neutropenia. J Clin Oncol 31(34):4290–4296. doi:10.1200/JCO.2012.44.6229 View ArticleGoogle Scholar
- Aebi S, Gelber S, Anderson SJ, Lang I, Robidoux A, Martin M et al (2014) Chemotherapy for isolated locoregional recurrence of breast cancer (CALOR): a randomised trial. Lancet Oncol 15(2):156–163. doi:10.1016/S1470-2045(13)70589-8 View ArticleGoogle Scholar
- American Cancer Society. http://www.cancer.org/acs/groups/content/@research/documents/webcontent/acspc-042151.pdf. Accessed 11 June 2015
- Bonadonna G, Valagussa P, Moliterni A, Zambetti M, Brambilla C (1995) Adjuvant cyclophosphamide, methotrexate, and fluorouracil in node-positive breast cancer: the results of 20 years of follow-up. N Engl J Med 332(14):901–906. doi:10.1056/NEJM199504063321401 View ArticleGoogle Scholar
- Bonadonna G, Moliterni A, Zambetti M, Daidone MG, Pilotti S, Gianni L et al (2005) 30 years’ follow up of randomised studies of adjuvant CMF in operable breast cancer: cohort study. BMJ 330(7485):217. doi:10.1136/bmj.38314.622095.8F View ArticleGoogle Scholar
- Budman DR, Berry DA, Cirrincione CT, Henderson IC, Wood WC, Weiss RB et al (1998) Dose and dose intensity as determinants of outcome in the adjuvant treatment of breast cancer. The Cancer and Leukemia Group B. J Natl Cancer Inst 90(16):1205–1211View ArticleGoogle Scholar
- Carroll J, Protani M, Walpole E, Martin JH (2012) Effect of obesity on toxicity in women treated with adjuvant chemotherapy for early-stage breast cancer: a systematic review. Breast Cancer Res Treat 136(2):323–330. doi:10.1007/s10549-012-2213-3 View ArticleGoogle Scholar
- Chan A, Fu WH, Shih V, Coyuco JC, Tan SH, Ng R (2011) Impact of colony-stimulating factors to reduce febrile neutropenic events in breast cancer patients receiving docetaxel plus cyclophosphamide chemotherapy. Support Care Cancer 19(4):497–504. doi:10.1007/s00520-010-0843-8 View ArticleGoogle Scholar
- Chirivella I, Bermejo B, Insa A, Perez-Fidalgo A, Magro A, Rosello S et al (2009) Optimal delivery of anthracycline-based chemotherapy in the adjuvant setting improves outcome of breast cancer patients. Breast Cancer Res Treat 114(3):479–484. doi:10.1007/s10549-008-0018-1 View ArticleGoogle Scholar
- Crawford J, Dale DC, Kuderer NM, Culakova E, Poniewierski MS, Wolff D et al (2008) Risk and timing of neutropenic events in adult cancer patients receiving chemotherapy: the results of a prospective nationwide study of oncology practice. J Natl Compr Canc Netw 6(2):109–118Google Scholar
- Crawford J, Armitage J, Balducci L, Becker PS, Blayney DW, Cataland SR et al (2013) Myeloid growth factors. J Natl Compr Canc Netw 11(10):1266–1290Google Scholar
- Culakova E, Thota R, Poniewierski MS, Kuderer NM, Wogu AF, Dale DC et al (2014) Patterns of chemotherapy-associated toxicity and supportive care in US oncology practice: a nationwide prospective cohort study. Cancer Med 3(2):434–444. doi:10.1002/cam4.200 View ArticleGoogle Scholar
- Dale DC, McCarter GC, Crawford J, Lyman GH (2003) Myelotoxicity and dose intensity of chemotherapy: reporting practices from randomized clinical trials. J Natl Compr Canc Netw 1(3):440–454Google Scholar
- Flowers CR, Seidenfeld J, Bow EJ, Karten C, Gleason C, Hawley DK et al (2013) Antimicrobial prophylaxis and outpatient management of fever and neutropenia in adults treated for malignancy: American Society of Clinical Oncology clinical practice guideline. J Clin Oncol 31(6):794–810. doi:10.1200/JCO.2012.45.8661 View ArticleGoogle Scholar
- Goldhirsch A, Winer EP, Coates AS, Gelber RD, Piccart-Gebhart M, Thurlimann B et al (2013) Personalizing the treatment of women with early breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2013. Ann Oncol. doi:10.1093/annonc/mdt303 Google Scholar
- Gomez H, Hidalgo M, Casanova L, Colomer R, Pen DL, Otero J et al (1998) Risk factors for treatment-related death in elderly patients with aggressive non-Hodgkin’s lymphoma: results of a multivariate analysis. J Clin Oncol 16(6):2065–2069Google Scholar
- Gradishar WJ, Anderson BO, Balassanian R, Blair SL, Burstein HJ, Cyr A et al (2015) Breast cancer version 2.2015. J Natl Compr Canc Netw 13(4):448–475Google Scholar
- Griggs JJ, Mangu PB, Anderson H, Balaban EP, Dignam JJ, Hryniuk WM et al (2012) Appropriate chemotherapy dosing for obese adult patients with cancer: American Society of Clinical Oncology clinical practice guideline. J Clin Oncol 30(13):1553–1561. doi:10.1200/JCO.2011.39.9436 View ArticleGoogle Scholar
- Haim N, Shulman K, Goldberg H, Tsalic M (2005) The safety of full-dose chemotherapy with secondary prophylactic granulocyte colony stimulating factor (G-CSF) following a prior cycle with febrile neutropenia. Med Oncol 22(3):229–232. doi:10.1385/MO:22:3:229 View ArticleGoogle Scholar
- Hendricks AM, Loggers ET, Talcott JA (2011) Costs of home versus inpatient treatment for fever and neutropenia: analysis of a multicenter randomized trial. J Clin Oncol 29(30):3984–3989. doi:10.1200/JCO.2011.35.1247 View ArticleGoogle Scholar
- Jones SE, Savin MA, Holmes FA, O’Shaughnessy JA, Blum JL, Vukelja S et al (2006) Phase III trial comparing doxorubicin plus cyclophosphamide with docetaxel plus cyclophosphamide as adjuvant therapy for operable breast cancer. J Clin Oncol 24(34):5381–5387. doi:10.1200/JCO.2006.06.5391 View ArticleGoogle Scholar
- Klastersky JA, Paesmans M (2011) Treatment of febrile neutropenia is expensive: prevention is the answer. Onkologie 34(5):226–228. doi:10.1159/000327818 View ArticleGoogle Scholar
- Kreys ED, Kim TY, Delgado A, Koeller JM (2014) Impact of cancer supportive care pathways compliance on emergency department visits and hospitalizations. J Oncol Pract 10(3):168–173. doi:10.1200/JOP.2014.001376 View ArticleGoogle Scholar
- Kuderer NM, Dale DC, Crawford J, Cosler LE, Lyman GH (2006) Mortality, morbidity, and cost associated with febrile neutropenia in adult cancer patients. Cancer 106(10):2258–2266. doi:10.1002/cncr.21847 View ArticleGoogle Scholar
- Kuderer NM, Dale DC, Crawford J, Lyman GH (2007) Impact of primary prophylaxis with granulocyte colony-stimulating factor on febrile neutropenia and mortality in adult cancer patients receiving chemotherapy: a systematic review. J Clin Oncol 25(21):3158–3167. doi:10.1200/JCO.2006.08.8823 View ArticleGoogle Scholar
- Lee EK, Wong WW, Trudeau ME, Chan KK (2015) Cost-effectiveness of prophylactic granulocyte colony-stimulating factor for febrile neutropenia in breast cancer patients receiving FEC-D. Breast Cancer Res Treat 150(1):169–180. doi:10.1007/s10549-015-3309-3 View ArticleGoogle Scholar
- Lyman GH (2009) Impact of chemotherapy dose intensity on cancer patient outcomes. J Natl Compr Canc Netw 7(1):99–108Google Scholar
- Lyman GH, Dale DC, Crawford J (2003) Incidence and predictors of low dose-intensity in adjuvant breast cancer chemotherapy: a nationwide study of community practices. J Clin Oncol 21(24):4524–4531. doi:10.1200/JCO.2003.05.002 View ArticleGoogle Scholar
- Lyman GH, Dale DC, Tomita D, Whittaker S, Crawford J (2013a) A retrospective evaluation of chemotherapy dose intensity and supportive care for early-stage breast cancer in a curative setting. Breast Cancer Res Treat 139(3):863–872. doi:10.1007/s10549-013-2582-2 View ArticleGoogle Scholar
- Lyman GH, Dale DC, Culakova E, Poniewierski MS, Wolff DA, Kuderer NM et al (2013b) The impact of the granulocyte colony-stimulating factor on chemotherapy dose intensity and cancer survival: a systematic review and meta-analysis of randomized controlled trials. Ann Oncol 24(10):2475–2484. doi:10.1093/annonc/mdt226 View ArticleGoogle Scholar
- Lyman GH, Reiner M, Morrow PK, Crawford J (2015a) The effect of filgrastim or pegfilgrastim on survival outcomes of patients with cancer receiving myelosuppressive chemotherapy. Ann Oncol. doi:10.1093/annonc/mdv174 Google Scholar
- Lyman GH, Dale DC, Legg JC, Abella E, Morrow PK, Whittaker S et al (2015b) Assessing patients’ risk of febrile neutropenia: is there a correlation between physician-assessed risk and model-predicted risk? Cancer Med. doi:10.1002/cam4.454 Google Scholar
- Martin M, Lluch A, Segui MA, Ruiz A, Ramos M, Adrover E et al (2006) Toxicity and health-related quality of life in breast cancer patients receiving adjuvant docetaxel, doxorubicin, cyclophosphamide (TAC) or 5-fluorouracil, doxorubicin and cyclophosphamide (FAC): impact of adding primary prophylactic granulocyte-colony stimulating factor to the TAC regimen. Ann Oncol 17(8):1205–1212. doi:10.1093/annonc/mdl135 View ArticleGoogle Scholar
- Murthy VH, Krumholz HM, Gross CP (2004) Participation in cancer clinical trials: race-, sex-, and age-based disparities. JAMA 291(22):2720–2726. doi:10.1001/jama.291.22.2720 View ArticleGoogle Scholar
- Onitilo AA, Engel JM, Liang H, Stankowski RV, Miskowiak DA, Broton M et al (2013) Mammography utilization: patient characteristics and breast cancer stage at diagnosis. AJR Am J Roentgenol. doi:10.2214/AJR.13.10733 Google Scholar
- Pathak R, Giri S, Aryal MR, Karmacharya P, Bhatt VR, Martin MG (2015) Mortality, length of stay, and health care costs of febrile neutropenia-related hospitalizations among patients with breast cancer in the United States. Support Care Cancer 23(3):615–617. doi:10.1007/s00520-014-2553-0 View ArticleGoogle Scholar
- Perez-Fidalgo JA, Bermejo B, Chirivella I, Martinez MT, Gonzalez I, Cejalvo JM et al (2014) Retrospective analysis of the use of G-CSF and its impact on dose response for anthracycline plus taxane-based schedules in early breast cancer. Clin Transl Oncol. doi:10.1007/s12094-013-1153-7 Google Scholar
- Perou CM, Børresen-Dale AL (2011) Systems biology and genomics of breast cancer. Cold Spring Harb Perspect Biol 3(2). doi:10.1101/cshperspect.a003293
- Renner P, Milazzo S, Liu JP, Zwahlen M, Birkmann J, Horneber M (2012) Primary prophylactic colony-stimulating factors for the prevention of chemotherapy-induced febrile neutropenia in breast cancer patients. Cochrane Database Syst Rev 10:CD007913. doi:10.1002/14651858.CD007913.pub2 Google Scholar
- Roche H, Fumoleau P, Spielmann M, Canon JL, Delozier T, Serin D et al (2006) Sequential adjuvant epirubicin-based and docetaxel chemotherapy for node-positive breast cancer patients: the FNCLCC PACS 01 Trial. J Clin Oncol 24(36):5664–5671. doi:10.1200/JCO.2006.07.3916 View ArticleGoogle Scholar
- Smith TJ, Khatcheressian J, Lyman GH, Ozer H, Armitage JO, Balducci L et al (2006) 2006 update of recommendations for the use of white blood cell growth factors: an evidence-based clinical practice guideline. J Clin Oncol 24(19):3187–3205. doi:10.1200/JCO.2006.06.4451 View ArticleGoogle Scholar
- Theriault RL, Carlson RW, Allred C, Anderson BO, Burstein HJ, Edge SB et al (2013) Breast cancer, version 3.2013: featured updates to the NCCN guidelines. J Natl Compr Canc Netw 11(7):753–760 (quiz 761) Google Scholar
- Timmer-Bonte JN, Tjan-Heijnen VC (2006) Febrile neutropenia: highlighting the role of prophylactic antibiotics and granulocyte colony-stimulating factor during standard dose chemotherapy for solid tumors. Anticancer Drugs 17(8):881–889. doi:10.1097/01.cad.0000224455.46824.b5 View ArticleGoogle Scholar
- Timmer-Bonte JN, de Boo TM, Smit HJ, Biesma B, Wilschut FA, Cheragwandi SA et al (2005) Prevention of chemotherapy-induced febrile neutropenia by prophylactic antibiotics plus or minus granulocyte colony-stimulating factor in small-cell lung cancer: a Dutch Randomized Phase III Study. J Clin Oncol 23(31):7974–7984. doi:10.1200/JCO.2004.00.7955 View ArticleGoogle Scholar
- Truong J, Lee E, Trudeau ME, Chan KK (2015) Interpreting the febrile neutropenia rates from randomized controlled trials for consideration of primary prophylaxis in the real world: a systematic review and meta-analysis. ASCO Meeting Abstracts 33(15_suppl):9626Google Scholar
- Vogel CL, Wojtukiewicz MZ, Carroll RR, Tjulandin SA, Barajas-Figueroa LJ, Wiens BL et al (2005) First and subsequent cycle use of pegfilgrastim prevents febrile neutropenia in patients with breast cancer: a multicenter, double-blind, placebo-controlled phase III study. J Clin Oncol 23(6):1178–1184. doi:10.1200/JCO.2005.09.102 View ArticleGoogle Scholar
- Weycker D, Li X, Edelsberg J, Barron R, Kartashov A, Xu H et al (2014) Risk of febrile neutropenia in patients receiving emerging chemotherapy regimens. Support Care Cancer 22(12):3275–3285. doi:10.1007/s00520-014-2362-5 View ArticleGoogle Scholar
- Younis T, Rayson D, Thompson K (2012) Primary G-CSF prophylaxis for adjuvant TC or FEC-D chemotherapy outside of clinical trial settings: a systematic review and meta-analysis. Support Care Cancer 20(10):2523–2530. doi:10.1007/s00520-011-1375-6 View ArticleGoogle Scholar