A comparison of multimodal therapy and surgery for esophageal adenocarcinoma

被引:1530
作者
Walsh, TN
Noonan, N
Hollywood, D
Kelly, A
Keeling, N
Hennessy, TPJ
机构
[1] ST JAMES HOSP,DEPT SURG,DUBLIN 8,IRELAND
[2] ST JAMES HOSP,DEPT GASTROENTEROL,DUBLIN 8,IRELAND
[3] ST LUKES HOSP,DEPT RADIOTHERAPY,DUBLIN,IRELAND
[4] TRINITY COLL DUBLIN,DEPT COMMUNITY HLTH,DUBLIN,IRELAND
[5] TRINITY COLL DUBLIN,DEPT STAT,DUBLIN,IRELAND
关键词
D O I
10.1056/NEJM199608153350702
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Uncontrolled studies suggest that a combination of chemotherapy and radiotherapy improves the survival of patients with esophageal adenocarcinoma. We conducted a prospective, randomized trial comparing surgery alone with combined chemotherapy, radiotherapy, and surgery. Methods Patients assigned to multimodal therapy received two courses of chemotherapy in weeks 1 and 6 (fluorouracil, 15 mg per kilogram of body weight daily for five days, and cisplatin, 75 mg per square meter of body-surface area on day 7) and a course of radiotherapy (40 Gy, administered in 15 fractions over a three-week period, beginning concurrently with the first course of chemotherapy), followed by surgery. The patients assigned to surgery had no preoperative therapy. Results Of the 58 patients assigned to multimodal therapy and the 55 assigned to surgery, 10 and 1, respectively, were withdrawn for protocol violations. At the time of surgery, 23 of 55 patients (42 percent) treated with preoperative multimodal therapy who could be evaluated had positive nodes or metastases, as compared with 45 of the 55 patients (82 percent) who underwent surgery alone (P<0.001). Thirteen of the 52 patients (25 percent) who underwent surgery after multimodal therapy had complete responses, as determined pathologically. The median survival of patients assigned to multimodal therapy was 16 months, as compared with 11 months for those assigned to surgery alone (P=0.01). At one, two, and three years, 52, 37, and 32 percent, respectively, of patients assigned to multimodal therapy were alive, as compared with 44, 26, and 6 percent of those assigned to surgery, with the survival advantage favoring multimodal therapy reaching significance at three years (P=0.01). Conclusions Multimodal treatment is superior to surgery alone for patients with resectable adenocarcinoma of the esophagus. (C) 1996, Massachusetts Medical Society.
引用
收藏
页码:462 / 467
页数:6
相关论文
共 35 条
  • [1] ADENOCARCINOMA OF THE ESOPHAGUS AND GASTROESOPHAGEAL JUNCTION - CLINICAL AND PATHOLOGICAL ASSESSMENT OF RESPONSE TO INDUCTION CHEMOTHERAPY
    ADELSTEIN, DJ
    RICE, TW
    BOYCE, GA
    SIVAK, MV
    VANKIRK, MA
    KIRBY, TJ
    VANSTOLK, RU
    BUKOWSKI, RM
    [J]. AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1994, 17 (01): : 14 - 18
  • [2] INTENSIVE PREOPERATIVE CHEMOTHERAPY WITH COLONY-STIMULATING FACTOR FOR RESECTABLE ADENOCARCINOMA OF THE ESOPHAGUS OR GASTROESOPHAGEAL JUNCTION
    AJANI, JA
    ROTH, JA
    RYAN, MB
    PUTNAM, JB
    PAZDUR, R
    LEVIN, B
    GUTTERMAN, JU
    MCMURTREY, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (01) : 22 - 28
  • [3] EVALUATION OF PREOPERATIVE AND POSTOPERATIVE CHEMOTHERAPY FOR RESECTABLE ADENOCARCINOMA OF THE ESOPHAGUS OR GASTROESOPHAGEAL JUNCTION
    AJANI, JA
    ROTH, JA
    RYAN, B
    MCMURTREY, M
    RICH, TA
    JACKSON, DE
    ABBRUZZESE, JL
    LEVIN, B
    DECARO, L
    MOUNTAIN, C
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (07) : 1231 - 1238
  • [4] ANDERSON LL, 1982, CANCER, V50, P1587, DOI 10.1002/1097-0142(19821015)50:8<1587::AID-CNCR2820500820>3.0.CO
  • [5] 2-S
  • [6] BEAHRS OH, 1988, MANUAL STAGING CANC, P63
  • [7] RISING INCIDENCE OF ADENOCARCINOMA OF THE ESOPHAGUS AND GASTRIC CARDIA
    BLOT, WJ
    DEVESA, SS
    KNELLER, RW
    FRAUMENI, JF
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (10): : 1287 - 1289
  • [8] AUTOPSY FINDINGS IN CARCINOMA OF THE ESOPHAGUS
    BOSCH, A
    FRIAS, Z
    CALDWELL, WL
    JAESCHKE, WH
    [J]. ACTA RADIOLOGICA ONCOLOGY, 1979, 18 (02): : 103 - 112
  • [9] CAREY RW, 1991, CANCER, V68, P489, DOI 10.1002/1097-0142(19910801)68:3<489::AID-CNCR2820680307>3.0.CO
  • [10] 2-M