High-dose interleukin-2 in patients with metastatic melanoma whose disease progressed after biochemotherapy

被引:1
作者
Buzaid, Antonio Carlos
Schmerling, Rafael Aron [1 ]
Vieira Guedes, Rodrigo Antonio [3 ]
de Freitas, Daniela [2 ]
William, William Nassib, Jr. [4 ]
机构
[1] Hosp Sao Jose, Ctr Oncol, BR-01321001 Sao Paulo, Brazil
[2] Hosp Sirio Libanes, Sao Paulo, Brazil
[3] Clin AMO, Salvador, BA, Brazil
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
drug therapy; interleukin-2; melanoma; neoplasms; THERAPY; CHEMOTHERAPY; TRIAL; INTERFERON-ALPHA-2B; DACARBAZINE;
D O I
10.1097/CMR.0b013e32834710b5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objective of this study was to report our experience with 38 consecutive patients with metastatic melanoma treated with high-dose (HD) bolus interleukin (IL)-2 after disease progression on or after biochemotherapy as the only earlier treatment for metastatic disease. We conducted a retrospective review of all patients with metastatic melanoma treated with HD IL-2 at the Oncology Center of Hospital Sirio-Libanes between October 2000 and December 2009. The treatment consisted of IL-2, of 600 000U/kg every 8 h for up to 14 doses, followed by 1-week rest and readmission for the second cycle. Responders received up to four additional cycles. Median follow-up was 9 months. The overall response rate was 23.6%, and we found no correlation between earlier response to biochemotherapy and response to HD IL-2. The median survival was 9.5 months for all patients and 36.1 months for the responders. The most frequent grade 3 or 4 adverse events were hypotension, diarrhea, and respiratory distress, and one patient died from septic shock. We concluded that HD IL-2 has clinically meaningful antitumor activity in patients with metastatic melanoma whose disease has progressed after biochemotherapy. This is a treatment alternative in patients with no central nervous system involvement and who are fit enough to tolerate it, regardless of the initial response to biochemotherapy. Melanoma Res 21:370-375 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:370 / 375
页数:6
相关论文
共 23 条
[1]   Nitric oxide and neopterin levels and clinical response in stage III melanoma patients receiving concurrent biochemotherapy [J].
Anderson, CM ;
Buzaid, AC ;
Sussman, J ;
Lee, JJ ;
Ali-Osman, F ;
Braunschweiger, PG ;
Plager, C ;
Bedikian, A ;
Papadopoulos, N ;
Eton, O ;
Legha, SS ;
Grimm, EA .
MELANOMA RESEARCH, 1998, 8 (02) :149-155
[2]  
[Anonymous], 2000, COCHRANE DB SYST REV
[3]   High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993 [J].
Atkins, MB ;
Lotze, MT ;
Dutcher, JP ;
Fisher, RI ;
Weiss, G ;
Margolin, K ;
Abrams, J ;
Sznol, M ;
Parkinson, D ;
Hawkins, M ;
Paradise, C ;
Kunkel, L ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (07) :2105-2116
[4]  
Atkins MB, 2000, CANCER J SCI AM, V6, pS11
[5]   Phase III Trial Comparing Concurrent Biochemotherapy With Cisplatin, Vinblastine, Dacarbazine, Interleukin-2, and Interferon Alfa-2b With Cisplatin, Vinblastine, and Dacarbazine Alone in Patients With Metastatic Malignant Melanoma (E3695): A Trial Coordinated by the Eastern Cooperative Oncology Group [J].
Atkins, Michael B. ;
Hsu, Jessie ;
Lee, Sandra ;
Cohen, Gary I. ;
Flaherty, Lawrence E. ;
Sosman, Jeffrey A. ;
Sondak, Vernon K. ;
Kirkwood, John M. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (35) :5748-5754
[6]   Multicenter phase III randomized trial of polychemotherapy (CVD regimen) versus the same chemotherapy (CT) plus subcutaneous interleukin-2 and interferon-α2b in metastatic melanoma [J].
Bajetta, E ;
Del Vecchio, M ;
Nova, P ;
Fusi, A ;
Daponte, A ;
Sertoli, MR ;
Queirolo, P ;
Taveggia, P ;
Bernengo, MG ;
Legha, SS ;
Formisano, B ;
Cascinelli, N .
ANNALS OF ONCOLOGY, 2006, 17 (04) :571-577
[7]   Final version of the American Joint Committee on Cancer staging system for cutaneous melanoma [J].
Balch, CM ;
Buzaid, AC ;
Soong, SJ ;
Atkins, MB ;
Cascinelli, N ;
Coit, DG ;
Fleming, ID ;
Gershenwald, JE ;
Houghton, A ;
Kirkwood, JM ;
McMasters, KM ;
Mihm, MF ;
Morton, DL ;
Reintgen, DS ;
Ross, MI ;
Sober, A ;
Thompson, JA ;
Thompson, JF .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3635-3648
[8]   Bcl-2 antisense (oblimersen sodium) plus dacarbazine in patients with advanced melanoma: The oblimersen melanoma study group [J].
Bedikian, Agop Y. ;
Millward, Michael ;
Pehamberger, Hubert ;
Conry, Robert ;
Gore, Martin ;
Trefzer, Uwe ;
Pavlick, Anna C. ;
DeConti, Ronald ;
Hersh, Evan M. ;
Hersey, Peter ;
Kirkwood, John M. ;
Haluska, Frank G. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (29) :4738-4745
[9]   MECHANISM OF THE ANTITUMOR EFFECT OF BIOCHEMOTHERAPY IN MELANOMA - PRELIMINARY-RESULTS [J].
BUZAID, AC ;
GRIMM, EA ;
ALIOSMAN, F ;
RING, S ;
ETON, O ;
PAPADOPOULOS, NE ;
BEDIKIAN, A ;
PLAGER, C ;
LEGHA, SS ;
BENJAMIN, R .
MELANOMA RESEARCH, 1994, 4 (05) :327-330
[10]   Biochemotherapy for advanced melanoma [J].
Buzaid, AC .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2002, 44 (01) :103-108