Neoadjuvant chemotherapy and radical surgery versus exclusive radiotherapy in locally advanced squamous cell cervical cancer: Results from the Italian Multicenter Randomized study

被引:311
作者
Benedetti-Panici, P
Greggi, S
Colombo, A
Amoroso, M
Smaniotto, D
Giannarelli, D
Amunni, G
Raspagliesi, F
Zola, P
Mangioni, C
Landoni, F
机构
[1] Catholic Univ, Rome, Italy
[2] Ist Regina Elena, I-00161 Rome, Italy
[3] Univ Milan, Osped San Gerardo, I-20122 Milan, Italy
[4] Univ Florence, I-50121 Florence, Italy
[5] Natl Canc Inst, Naples, Italy
[6] Univ Turin, Turin, Italy
关键词
D O I
10.1200/JCO.20.1.179
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Neoadjuvant chemotherapy (NACT) and radical surgery (RS) have emerged as a possible alternative to conventional radiation therapy (RT) in locally advanced cervical carcinoma. In 1990, a phase III trial was undertaken to verify such a hypothesis in terms of survival and treatment-related morbidity. Patients and Methods: Patients with squamous cell, International Federation of Gynecology and Obstetrics stage IB2 to III cervical cancer were eligible for the study. They received cisplatin-based NACT followed by RS (type III to V radical hysterectomy plus systematic pelvic lymphadenectomy) (arm A) or external-beam RT (45 to 50 Gy) followed by brachyradiotherapy (20 to 30 Gy) (arm B). Results: Of 441 patients randomly assigned to NACT+RS or RT, eligibility was confirmed in 210 and 199 patients, respectively. Treatment was administered according to protocol in 76% of arm A patients and 72% of arm B patients. Adjuvant treatment was delivered in 48 operated patients (29%). There was no evidence for any significant excess of severe morbidity in one of the two arms. The 5-year overall survival (OS) and progression-free survival (PFS) rates were 58.9% and 55.4% for arm A and 44.5% and 41.3% for arm B (P = .007 and P = .02), respectively. Subgroup survival analysis shows OS and PFS rates of 64.7% and 59.7% (stage IB2-IIB, NACT+RS), 46.4% and 46.7% (stage IB2-IIB, RT) (P = .005 and P = .02), 41.6% and 41.9% (stage III, NCAT+RS), 36.7% and 36.4% (stage III, RT) (P = .36 and P = .29), respectively. Treatment had a significant impact on OS and PFS. Conclusion: Although significant only for the stage 1132 to 1113 group, a survival benefit seems to be associated with the NACT+RS compared with conventional RT. (C) 2001 by American Society of Clinical Oncology.
引用
收藏
页码:179 / 188
页数:10
相关论文
共 46 条
  • [32] PIVER MS, 1974, OBSTET GYNECOL, V44, P265
  • [33] Concurrent cisplatin-based radiotherapy and chemotherapy for locally advanced cervical cancer
    Rose, PG
    Bundy, BN
    Watkins, EB
    Thigpen, JT
    Deppe, G
    Maiman, MA
    Clarke-Pearson, DL
    Insalaco, S
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (15) : 1144 - 1153
  • [34] Sananes C, 1998, EUR J GYNAECOL ONCOL, V19, P368
  • [35] RESULTS OF A PROSPECTIVE RANDOMIZED TRIAL WITH NEOADJUVANT CHEMOTHERAPY IN STAGE-IB, BULKY, SQUAMOUS CARCINOMA OF THE CERVIX
    SARDI, J
    SANANES, C
    GIAROLI, A
    BAYO, J
    RUEDA, NG
    VIGHI, S
    GUARDADO, N
    PANICERES, G
    SNAIDAS, L
    VICO, C
    DIPAOLA, G
    [J]. GYNECOLOGIC ONCOLOGY, 1993, 49 (02) : 156 - 165
  • [36] NEOADJUVANT CHEMOTHERAPY IN LOCALLY ADVANCED-CARCINOMA OF THE CERVIX UTERI
    SARDI, J
    SANANES, C
    GIAROLI, A
    MAYA, G
    DIPAOLA, G
    [J]. GYNECOLOGIC ONCOLOGY, 1990, 38 (03) : 486 - 493
  • [37] Randomized trial with neoadjuvant chemotherapy in stage IIIB squamous carcinoma cervix uteri: An unexpected therapeutic management
    Sardi, J
    Giaroli, A
    Sananes, C
    Rueda, NG
    Vighi, S
    Ferreira, M
    Bastardas, M
    Paniceres, G
    diPaola, G
    [J]. INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 1996, 6 (02) : 85 - 93
  • [38] Long-term follow-up of the first randomized trial using neoadjuvant chemotherapy in stage Ib squamous carcinoma of the cervix: The final results
    Sardi, JE
    Giaroli, A
    Sananes, C
    Ferreira, M
    Soderini, A
    Bermudez, A
    Snaidas, L
    Vighi, S
    Rueda, NG
    diPaola, G
    [J]. GYNECOLOGIC ONCOLOGY, 1997, 67 (01) : 61 - 69
  • [39] Sardi JE, 1998, INT J GYNECOL CANCER, V8, P441
  • [40] SOUHAMI L, 1992, INT J ONCOL, V1, P289