The burdens of cancer therapy - Clinical and economic outcomes of chemotherapy-induced mucositis

被引:442
作者
Elting, LS
Cooksley, C
Chambers, M
Cantor, SB
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, U196,Sect Hlth Res, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Head & Neck Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Gen Internal Med Ambulatory Treatment & Emer, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Pallat Care & Rehabil Med, Sect Med Support Care, Houston, TX 77030 USA
关键词
mucositis; chemotherapy toxicity; infection; bleeding; outcomes;
D O I
10.1002/cncr.11671
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Mucositis is a common but poorly studied problem among patients with solid tumors. The authors examined the clinical and economic outcomes of oral and gastrointestinal (GI) mucositis among patients receiving myelosuppressive chemotherapy. METHODS. A retrospective, random sample of 599 patients who developed chemotherapy-induced myelosuppression was followed for development of oral or GI mucositis and for development of subsequent episodes of bleeding or infection. Multilevel regression models of the risk of bleeding and infection were fit with chemotherapy cycles nested within patients. RESULTS. Mucositis developed during 37% of 1236 cycles of chemotherapy. Episodes of bleeding were significantly more common during cycles with GI mucositis than during cycles without GI mucositis (13% vs. 8%; P = 0.04). Episodes of infection were significantly more common during cycles with mucositis (especially GI mucositis) than during cycles without mucositis (73% vs. 36%; P < 0.0001). The mean durations of hospitalization were 4 days, 6 days, and 12 days during cycles with no mucositis, oral mucositis, and GI mucositis, respectively. After accounting for the depth and duration of myelosuppression and for other predictive factors, GI mucositis was associated with both bleeding (odds ratio [OR], 2.0; P = 0.01) and infection (OR, 2.24; P < 0.0001), whereas oral mucositis was associated with infection only (OR, 2.4; P < 0.0001). CONCLUSIONS. Mucositis was clinically and economically significant among patients with solid tumors who were receiving myelosuppressive chemotherapy. New preventive and therapeutic agents are needed. Cancer 2003;98:1531-9. (C) 2003 American Cancer Society.
引用
收藏
页码:1531 / 1539
页数:9
相关论文
共 26 条
[1]  
BEAM TR, 1992, CLIN INFECT DIS S1, V15, P5
[2]  
Bellm LA, 2000, SUPPORT CARE CANCER, V8, P33
[3]  
Cancer Therapy Evaluation Program, 1999, COMM TOX CRIT VERS 2
[4]   Stratification in clinical trials of febrile neutropenia [J].
Elting, LS .
SUPPORTIVE CARE IN CANCER, 1998, 6 (05) :457-461
[5]   The bleeding risk index - A clinical prediction rule to guide the prophylactic use of platelet transfusions in patients with lymphoma or solid tumors [J].
Elting, LS ;
Martin, CG ;
Kurtin, DJ ;
Cantor, SB ;
Rubenstein, EB ;
Rodriguez, S ;
Kanesan, K ;
Vadhan-Raj, S ;
Benjamin, RS .
CANCER, 2002, 94 (12) :3252-3262
[6]   Incidence, cost, and outcomes of bleeding and chemotherapy dose modification among solid tumor patients with chemotherapy-induced thrombocytopenia [J].
Elting, LS ;
Rubenstein, EB ;
Martin, CG ;
Kurtin, D ;
Rodriguez, S ;
Laiho, E ;
Kanesan, K ;
Cantor, SB ;
Benjamin, RS .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (04) :1137-1146
[7]  
Epstein JB, 1999, ORAL SURG ORAL MED O, V88, P273
[8]  
Epstein JB, 1999, HEAD NECK-J SCI SPEC, V21, P1
[9]   Criteria for response in patients in clinical trials of empiric antibiotic regimens for febrile neutropenia. Is there agreement? [J].
Feld, R .
SUPPORTIVE CARE IN CANCER, 1998, 6 (05) :444-448
[10]  
Harrell FE, 1996, STAT MED, V15, P361, DOI 10.1002/(SICI)1097-0258(19960229)15:4<361::AID-SIM168>3.0.CO