Aerosol Therapy for Malignancy Involving the Lungs

被引:34
作者
Rao, R. D. [1 ]
Markovic, S. N. [1 ]
Anderson, P. M. [2 ]
机构
[1] Mayo Clin, Dept Med Oncol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Pediat & Adolescent Med, Div Hematol Oncol, Rochester, MN 55905 USA
关键词
D O I
10.2174/1568009033481895
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The lungs are common sites of involvement by primary and metastatic malignant disease. Patients with malignancies in the lung have limited treatment options and are usually not curable. Numerous investigators have studied the potential of delivering various therapeutic agents directly to the lungs and pulmonary lymphatics by nebulization. Most of the research involves the use of immunomodulatory strategies; a few aerosol studies of chemotherapy and gene therapy have also been conducted. Most of these studies have been conducted in animal models. A few human trials have also been completed. Results suggest that aerosol therapies have the potential to shrink pulmonary metastases of selected histologies, and that survival in selected patients with metastatic renal cell cancer may be prolonged. The approach to therapy of cancer in the lungs holds promise as a means to avoid systemic toxicity and obtain an improved therapeutic effect. Research is currently underway to address issues of local versus systemic toxicity, optimal drug delivery and selection of optimal drugs and schedules including outpatient aerosol therapy. Future issues in design of aerosol cancer treatment include identifying effective combinations of agents, schedules, and use of aerosol therapy at home as adjuvant therapy.
引用
收藏
页码:239 / 250
页数:12
相关论文
共 65 条
[1]   EFFECTS OF ROUTE AND FORMULATION ON CLINICAL PHARMACOKINETICS OF INTERLEUKIN-2 [J].
ANDERSON, PM ;
SORENSON, MA .
CLINICAL PHARMACOKINETICS, 1994, 27 (01) :19-31
[2]  
Anderson PM, 1999, CLIN CANCER RES, V5, P2316
[3]   Delivery systems for immunomodulatory proteins and peptides [J].
Anderson, PM .
BIODRUGS, 1997, 7 (01) :51-65
[4]  
ANDERSON PM, 1990, CANCER RES, V50, P1853
[5]   Emerging applications of recombinant human granulocyte-macrophage colony-stimulating factor [J].
Armitage, JO .
BLOOD, 1998, 92 (12) :4491-4508
[6]  
BAXEVANIS CN, 1995, CANCER, V76, P1253, DOI 10.1002/1097-0142(19951001)76:7<1253::AID-CNCR2820760724>3.0.CO
[7]  
2-F
[8]   EVALUATION OF ROUTES OF ADMINISTRATION OF INTERFERON IN CANCER - A REVIEW AND A PROPOSAL [J].
BOCCI, V .
CANCER DRUG DELIVERY, 1984, 1 (04) :337-351
[9]   Inhaled aerosolization of all-trans-retinoic acid for targeted pulmonary delivery [J].
Brooks, AD ;
Tong, W ;
Benedetti, F ;
Kaneda, Y ;
Miller, V ;
Warrell, RP .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2000, 46 (04) :313-318
[10]   MONOCYTE ACTIVATION FOLLOWING SYSTEMIC ADMINISTRATION OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR [J].
CHACHOUA, A ;
ORATZ, R ;
HOOGMOED, R ;
CARON, D ;
PEACE, D ;
LIEBES, L ;
BLUM, RH ;
VILCEK, J .
JOURNAL OF IMMUNOTHERAPY, 1994, 15 (03) :217-224