Induction chemotherapy with cisplatin, epirubicin, and paclitaxel (CEP), followed by concomitant radiotherapy and weekly paclitaxel for the management of locally advanced nasopharyngeal carcinoma - A Hellenic Cooperative Oncology Group Phase II Study

被引:22
作者
Fountzilas, G [1 ]
Tolis, C
Kalogera-Fountzila, A
Karanikiotis, C
Bai, M
Misailidou, D
Samantas, E
Athanassiou, E
Papamichael, D
Tsekeris, P
Catodritis, N
Nicolaou, A
Plataniotis, G
Makatsoris, T
Papakostas, P
Zamboglou, N
Daniilidis, J
机构
[1] Aristotle Univ Thessaloniki, Papageorgiou Hosp, Dept Med Oncol, GR-54006 Thessaloniki, Macedonia, Greece
[2] Aristotle Univ Thessaloniki, AHEPA Hosp, GR-54006 Thessaloniki, Macedonia, Greece
[3] Univ Ioannina, Sch Med, GR-45110 Ioannina, Greece
[4] Agii Anargiri Canc Hosp, Athens, Greece
[5] Bank Cyprus Oncol Ctr, Nicosia, Cyprus
[6] Univ Patras, Sch Med, Rio Hosp, GR-26110 Patras, Greece
[7] Hippokrateion Hosp, Athens, Greece
[8] Klinikum Offenbach, Dept Radiotherapy, Offenbach, Germany
关键词
nasopharyngeal cancer; radiation therapy; chemotherapy; paclitaxel; epirubicin; Epstein-Barr virus;
D O I
10.1007/s00066-005-1355-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Clinical research on the treatment of nasopharyngeal cancer (NPC) has been focused primarily on the reduction of incidence of the development of distant metastases as well as the improvement of locoregional control. Patients and Methods: Untreated patients with stage IIB-IVB nonmetastatic NPC were treated with three cycles of induction chemotherapy (IC) consisting of epirubicin 75 mg/m(2) followed by paclitaxel 175 mg/m(2) as 3-h infusion on day 1 and cisplatin 75 mg/m(2) on day 2 every 3 weeks, followed by concomitant radiation therapy (70 Gy), and chemotherapy (CCRT) with weekly paclitaxel 60 mg/m(2). Results: From November 1999 until April 2003, 47 patients entered the study. Complete response rate post IC therapy was 15%, which was raised to 66% after the completion of CCRT. The most frequent side effect from IC was myelotoxicity (55%), whereas stomatitis and xerostomia were the most pronounced (grade 3, 4) toxicities during CCRT. The presence of Epstein-Barr virus (EBV) was detected either by in situ hybridization in tumor tissue sections or by polymerase chain reaction in the peripheral blood in 37 out of 46 patients tested (80%). All three histological types were associated with the presence of EBV. After a median follow-up of 23.5 months, median time to treatment failure was 17.9 months, whilst median survival has not been reached yet. Conclusion: IC followed by CCRT is feasible and produces durable complete responses in the majority of patients with NPC. The case detection rate of EBV in this study appears to be similar to that reported from endemically infected regions.
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收藏
页码:223 / 230
页数:8
相关论文
共 40 条
  • [1] Chemoradiotherapy versus radiotherapy in patients with advanced nasopharyngeal cancer: Phase III randomized intergroup study 0099
    Al-Sarraf, M
    LeBlanc, M
    Giri, PGS
    Fu, KK
    Cooper, J
    Vuong, T
    Forastiere, AA
    Adams, G
    Sakr, WA
    Schuller, DE
    Ensley, JF
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) : 1310 - 1317
  • [2] *AM JOINT CANC, 1998, AJCC CANC STAG MAN 1
  • [3] Beckmann G, 2003, STRAHLENTHER ONKOL, V179, P283, DOI 10.1007/s00066-003-1086-0
  • [4] Phase II study of neoadjuvant carboplatin and paclitaxel followed by radiotherapy and concurrent cisplatin in patients with locoregionally advanced nasopharyngeal carcinoma: Therapeutic monitoring with plasma Epstein-Barr virus DNA
    Chan, ATC
    Ma, BBY
    Lo, D
    Leung, SF
    Kwan, WH
    Hui, EP
    Mok, TSK
    Kam, M
    Chan, LS
    Chiu, SKW
    Yu, KH
    Cheung, KY
    Lai, K
    Lai, M
    Mo, F
    Yeo, W
    King, A
    Johnson, PJ
    Teo, PML
    Zee, B
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (15) : 3053 - 3060
  • [5] Concurrent chemotherapy-radiotherapy compared with radiotherapy alone in locoregionally advanced nasopharyngeal carcinoma: Progression-free survival analysis of a phase III randomized trial
    Chan, ATC
    Teo, PML
    Ngan, RK
    Leung, TW
    Lau, WH
    Zee, B
    Leung, SF
    Cheung, FY
    Yeo, W
    Yiu, HH
    Yu, KH
    Chiu, KW
    Chan, DT
    Mok, T
    Yuen, KT
    Mo, F
    Lai, M
    Kwan, WH
    Choi, P
    Johnson, PJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (08) : 2038 - 2044
  • [6] A PROSPECTIVE RANDOMIZED STUDY OF CHEMOTHERAPY ADJUNCTIVE TO DEFINITIVE RADIOTHERAPY IN ADVANCED NASOPHARYNGEAL CARCINOMA
    CHAN, ATC
    TEO, PML
    LEUNG, TWT
    LEUNG, SF
    LEE, WY
    YEO, W
    CHOI, PHK
    JOHNSON, PJ
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1995, 33 (03): : 569 - 577
  • [7] TOXICITY CRITERIA OF THE RADIATION-THERAPY ONCOLOGY GROUP (RTOG) AND THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER (EORTC)
    COX, JD
    STETZ, J
    PAJAK, TF
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1995, 31 (05): : 1341 - 1346
  • [8] UCNT: Chemocurable sometimes, but not very often
    Cvitkovic, E
    [J]. ANNALS OF ONCOLOGY, 1997, 8 (08) : 723 - 725
  • [9] FANDI A, 1994, SEMIN ONCOL, V21, P382
  • [10] Forastiere A A, 1994, Ann Oncol, V5 Suppl 6, pS51