Prognostic Factors Differ by Tumor Stage for Small Cell Lung Cancer A Pooled Analysis of North Central Cancer Treatment Group Trials

被引:111
作者
Foster, Nathan R. [1 ]
Mandrekar, Sumithra J. [1 ]
Schild, Steven E. [2 ]
Nelson, Garth D. [1 ]
Rowland, Kendrith M., Jr. [3 ]
Deming, Richard L. [4 ]
Kozelsky, Timothy F. [2 ]
Marks, Randolph S. [5 ]
Jett, James R. [5 ]
Adjei, Alex A. [6 ]
机构
[1] Mayo Clin & Mayo Fdn, Div Biomed Stat & Informat, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Radiat Oncol, Rochester, MN 55905 USA
[3] Carle Canc Ctr, Dept Med Oncol, Urbana, IL USA
[4] Therapeut Radiol Associates, Dept Radiat Oncol, Des Moines, IA USA
[5] Mayo Clin & Mayo Fdn, Dept Med Oncol, Rochester, MN 55905 USA
[6] Roswell Pk Canc Inst, Dept Med Oncol, Buffalo, NY 14263 USA
关键词
multivariate modeling; small cell lung cancer; pooled analysis; prognostic factors; PROPHYLACTIC CRANIAL IRRADIATION; COMBINED-MODALITY TREATMENT; THORACIC RADIATION-THERAPY; PHASE-II; ALTERNATING CHEMOTHERAPY; DATA-BASE; G-CSF; CISPLATIN; ETOPOSIDE; SURVIVAL;
D O I
10.1002/cncr.24314
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: An analysis of 14 small cell lung cancer (SCLC) trials was performed to improve the current understanding of potential prognostic factors for overall survival (OS) and progression-free survival (PFS) in groups of patients with limited-stage disease SCLC (LD-SCLC) and extensive-stage disease SCLC (ED-SCLC) separately. METHODS: Data on 688 patients with LID-SCLC and 910 patients with ED-SCLC were included. Clinical and laboratory factors were tested for their prognostic significance using Cox regression models that were stratified by protocol. Recursive partitioning and amalgamation (RPA) analyses were used to identify prognostic subgroups. RESULTS: Poorer performance status (PS) led to worse OS and PFS in the ED-SCLC group but not in the LD-SCLC group. The prognostic impact of PS was strong for men but weak for women in the ED-SCLC group (interaction P value <.012 for OS and PFS). Other negative prognostic factors included increased age and men for the LD-SCLC group and increased age, men, increased number of metastatic sites at baseline, and increased creatinine levels for the ED-SCLC group. In patients with the ED-SCLC, RPA analyses identified 5 subgroups with different prognosis based on baseline PS, creatinine levels, sex, and the number of metastatic sites. CONCLUSIONS: The current pooled analysis identified baseline creatinine levels and the number of metastatic sites as important prognostic factors in patients with ED-SCLC in addition to the well established factors of sex, age, and PS. There was a significant interaction between sex and PS within the ED-SCLC group, suggesting that PS is highly prognostic in men but has no significant impact in women. Within the LD-SCLC group, only age and sex were identified as important prognostic factors. RPA analyses confirmed many of these findings. Cancer 2009;115:2721-31. (C) 2009 American Cancer Society.
引用
收藏
页码:2721 / 2731
页数:11
相关论文
共 37 条
[1]   DETERMINANTS OF IMPROVED OUTCOME IN SMALL-CELL LUNG-CANCER - AN ANALYSIS OF THE 2,580-PATIENT SOUTHWEST ONCOLOGY GROUP DATA-BASE [J].
ALBAIN, KS ;
CROWLEY, JJ ;
LEBLANC, M ;
LIVINGSTON, RB .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (09) :1563-1574
[2]   Prophylactic cranial irradiation for patients with small-cell lung cancer in complete remission [J].
Aupérin, A ;
Arriagada, R ;
Pignon, JP ;
Le Péchoux, C ;
Gregor, A ;
Stephens, RJ ;
Kristjansen, PEG ;
Johnson, BE ;
Ueoka, H ;
Wagner, H ;
Aisner, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (07) :476-484
[3]   Phase III comparison of twice-daily split-course irradiation versus once-daily irradiation for patients with limited stage small-cell lung carcinoma [J].
Bonner, JA ;
Sloan, JA ;
Shanahan, TG ;
Brooks, BJ ;
Marks, RS ;
Krook, JE ;
Gerstner, JB ;
Maksymiuk, A ;
Levitt, R ;
Mailliard, JA ;
Tazelaar, HD ;
Hillman, S ;
Jett, JR .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2681-2691
[4]   PRETREATMENT PROGNOSTIC FACTORS AND SCORING SYSTEM IN 407 SMALL-CELL LUNG-CANCER PATIENTS [J].
CERNY, T ;
BLAIR, V ;
ANDERSON, H ;
BRAMWELL, V ;
THATCHER, N .
INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (02) :146-149
[5]  
COX DR, 1972, J R STAT SOC B, V34, P187
[6]  
Fry WA, 1996, CANCER, V77, P1947, DOI 10.1002/(SICI)1097-0142(19960501)77:9<1947::AID-CNCR27>3.0.CO
[7]  
2-Z
[8]   Infusion cisplatin chemotherapy and hyperfractionated thoracic radiotherapy for small-cell lung cancer [J].
Frytak, S ;
Shaw, EG ;
Jett, JR ;
Richardson, RL ;
Foote, RL ;
Creagan, ET ;
Eagan, RT ;
Su, JQ .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1996, 19 (02) :193-198
[9]   Phase I North Central Cancer Treatment Group trial-N9923 of escalating doses of twice-daily thoracic radiation therapy with amifostine and with alternating chemotherapy in limited stage small-cell lung cancer [J].
Garces, Yolanda I. ;
Okuno, Scott H. ;
Schild, Steven E. ;
Mandrekar, Sumithra J. ;
Bot, Brian M. ;
Martens, John M. ;
Wender, Donald B. ;
Soori, Gamini S. ;
Moore, Dennis F., Jr. ;
Kozelsky, Timothy F. ;
Jett, James R. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 67 (04) :995-1001
[10]  
GRAMBSCH PM, 1994, BIOMETRIKA, V81, P515