Increasing chemotherapy dose density and intensity: Phase I trials in non-small cell lung cancer and non-Hodgkin's lymphoma

被引:19
作者
Blayney, DW
McGuire, BW
Cruickshank, SE
Johnson, DH
机构
[1] Wilshire Oncol Med Grp Inc, Pasadena, CA USA
[2] Amgen Inc, Dept Med Affairs, Thousand Oaks, CA 91320 USA
[3] Vanderbilt Ingram Canc Ctr, Nashville, TN USA
关键词
chemotherapy; neutropenia; non-small cell lung carcinoma; non-Hodgkin's lymphoma; drug dose-response relationships; filgrastim;
D O I
10.1634/theoncologist.10-2-138
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Dose densification and dose escalation of cytotoxic chemotherapy may be important in improving the cure rates of chemotherapy-responsive cancers. We conducted two phase I studies, in non-small cell lung cancer (NSCLC) and in lymphoma, to explore the possibility of intensifying chemotherapy by compressing the delivery of and escalating the dose of standard combination chemotherapy. One study used etoposide and cisplatin chemotherapy in patients with unresectable stage III or IV NSCLC, intensifying chemotherapy by reducing the cycle length. The second study used cyclophosphamide, doxorubicin, vincristine, and prednisone, CHOP chemotherapy, in the treatment of stage II-IV intermediate or immunoblastic high-grade lymphoma, intensifying chemotherapy first by reducing the cycle length and then by escalating the dosages of cyclophosphamide and doxorubicin. Filgrastim support was used during dose intensification. Fifty-five patients with NSCLC and 49 with non-Hodgkin's lymphoma (NHL) were enrolled and treated in successive cohorts. At standard dosages and intervals of chemotherapy, filgrastim support resulted in incidences of grade 3 and 4 neutropenia that were between 62% and 77% lower than those in the no-filgrastim control; the mean duration of neutropenia was, likewise, more than 80% lower. Absolute neutrophil counts were greater than or equal to2 x 10(9)/1 at day 14 in virtually 100% of patients receiving filgrastim. In the NSCLC trial, etoposide and cisplatin were intensified by >50%, and in the lymphoma trial, cyclophosphamide was intensified by 270% and doxorubicin was intensified by 87%. Chemotherapy reductions or delays for neutropenia were rare in the groups receiving filgrastim; but at higher chemotherapy intensities, dose-limiting thrombocytopenia was encountered. We conclude that the delivery of myelo-suppressive chemotherapy in both a dose-intense and a dose-dense manner is feasible with filgrastim support.
引用
收藏
页码:138 / 149
页数:12
相关论文
共 28 条
[1]
Dose-intense chemotherapy every 2 weeks with dose-intense cyclophosphamide, doxorubicin, vincristine, and prednisone may improve survival in intermediate- and high-grade lymphoma: A phase II study of the Southwest Oncology Group (SWOG 9349) [J].
Blayney, DW ;
LeBlanc, ML ;
Grogan, T ;
Gaynor, ER ;
Chapman, RA ;
Spiridonidis, CH ;
Taylor, SA ;
Bearman, SI ;
Miller, TP ;
Fisher, RI .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (13) :2466-2473
[2]
BLAYNEY DW, 1993, P 5 INT C MAL LYMPH
[3]
BLAYNEY DW, 1992, P AN M AM SOC CLIN, V11, P320
[4]
High-dose therapy in diffuse large cell lymphoma:: results and prognostic factors in 452 patients from the GEL-TAMO Spanish Cooperative Group [J].
Caballero, MD ;
Pérez-Simón, JA ;
Iriondo, A ;
Lahuerta, JJ ;
Sierra, J ;
Marín, J ;
Gandarillas, M ;
Arranz, R ;
Zuazu, J ;
Rubio, V ;
de Sevilla, AF ;
Carreras, E ;
García-Conde, J ;
García-Laraña, J ;
Grande, C ;
Sureda, A ;
Vidal, MJ ;
Rifón, J ;
Pérez-Equiza, C ;
Varela, R ;
Moraleda, JM ;
Ruíz, JCG ;
Albó, C ;
Cabrera, R ;
San Miguel, JF ;
Conde, E .
ANNALS OF ONCOLOGY, 2003, 14 (01) :140-151
[5]
Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: First report of intergroup trial C9741/cancer and leukemia group B trial 9741 [J].
Citron, ML ;
Berry, DA ;
Cirrincione, C ;
Hudis, C ;
Winer, EP ;
Gradishar, WJ ;
Davidson, NE ;
Martino, S ;
Livingston, R ;
Ingle, JN ;
Perez, EA ;
Carpenter, J ;
Hurd, D ;
Holland, JF ;
Smith, BL ;
Sartor, CI ;
Leung, EH ;
Abrams, J ;
Schilsky, RL ;
Muss, HB ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) :1431-1439
[6]
REDUCTION BY GRANULOCYTE COLONY-STIMULATING FACTOR OF FEVER AND NEUTROPENIA INDUCED BY CHEMOTHERAPY IN PATIENTS WITH SMALL-CELL LUNG-CANCER [J].
CRAWFORD, J ;
OZER, H ;
STOLLER, R ;
JOHNSON, D ;
LYMAN, G ;
TABBARA, I ;
KRIS, M ;
GROUS, J ;
PICOZZI, V ;
RAUSCH, G ;
SMITH, R ;
GRADISHAR, W ;
YAHANDA, A ;
VINCENT, M ;
STEWART, M ;
GLASPY, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (03) :164-170
[7]
DONNELLY S, 2003, P AN M AM SOC CLIN, V22, P182
[8]
EPELBAUM R, 1990, CANCER-AM CANCER SOC, V66, P1124, DOI 10.1002/1097-0142(19900915)66:6<1124::AID-CNCR2820660608>3.0.CO
[9]
2-T
[10]
COMPARISON OF A STANDARD REGIMEN (CHOP) WITH 3 INTENSIVE CHEMOTHERAPY REGIMENS FOR ADVANCED NON-HODGKINS-LYMPHOMA [J].
FISHER, RI ;
GAYNOR, ER ;
DAHLBERG, S ;
OKEN, MM ;
GROGAN, TM ;
MIZE, EM ;
GLICK, JH ;
COLTMAN, CA ;
MILLER, TP .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (14) :1002-1006