Concurrent adjuvant radiotherapy and interferon-α2b for resected high risk stage III melanoma -: a retrospective single centre study

被引:20
作者
Gyorki, DE
Ainslie, J
Joon, ML
Henderson, MA
Millward, M
McArthur, GA
机构
[1] Peter MacCallum Canc Ctr, Div Haematol & Med Oncol, Skin & Melanoma Serv, Melbourne, Vic 3002, Australia
[2] Sir Charles Gairdiner Hosp, Nedlands, WA 6009, Australia
关键词
melanoma; stage III; interferon-alpha; 2b; radiotherapy; lymph node metastases;
D O I
10.1097/01.cmr.0000129375.14518.ab
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Interferon-alpha2b (IFNalpha2b) is the only form of systemic adjuvant therapy for stage III melanoma with documented survival benefit. Radiotherapy can also be utilized in the adjuvant setting in patients at high risk of nodal basin recurrence. As IFNalpha2b is associated with substantial toxicity, we sought to determine both the systemic and radiation-related toxicities in patients treated with combined adjuvant IFNalphaE2b and regional adjuvant radiotherapy delivered in the setting of a single institution. Eighteen consecutive patients who commenced adjuvant IFNalpha2b between November 1997 and August 2002 were analysed retrospectively for toxicities associated with the combination of IFNalpha2b and adjuvant radiotherapy (40-50 Gy in 15-25 fractions) to nodal basins delivered during the maintenance phase of IFNalpha2b therapy (median dose during radiotherapy of 6.5 MU/m(2) three times per week). Seven out of 18 patients who received concurrent radiotherapy and IFNalpha2b displayed grade 3 skin reactions. Severe radiation-induced toxicity was seen in three further patients, one who developed radiation pneumonitis, one who developed severe oral mucositis, and one who developed wound dehiscence that took 10 months to resolve. Non-radiation-related toxicity to IFNalpha2b therapy was typical for this dose and schedule. We conclude that concurrent use of adjuvant radiotherapy and IFNalpha2b may enhance radiation-induced toxicity. However, overall we found concurrent radiation and IFNalpha2b could be safely delivered with appropriate clinical monitoring. (C) 2004 Lippincott Williams Wilkins.
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收藏
页码:223 / 230
页数:8
相关论文
共 38 条
[1]
POSTOPERATIVE RADIOTHERAPY FOR CUTANEOUS MELANOMA OF THE HEAD AND NECK REGION [J].
ANG, KK ;
PETERS, LJ ;
WEBER, RS ;
MORRISON, WH ;
FRANKENTHALER, RA ;
GARDEN, AS ;
GOEPFERT, H ;
HA, CS ;
BYERS, RM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1994, 30 (04) :795-798
[2]
ANGIOLI R, 1993, CANCER, V71, P3717, DOI 10.1002/1097-0142(19930601)71:11<3717::AID-CNCR2820711140>3.0.CO
[3]
2-I
[4]
Prognostic factors analysis of 17,600 melanoma patients: Validation of the American Joint Committee on Cancer melanoma staging system [J].
Balch, CM ;
Soong, SJ ;
Gershenwald, JE ;
Thompson, JF ;
Reintgen, DS ;
Cascinelli, N ;
Urist, M ;
McMasters, KM ;
Ross, MI ;
Kirkwood, JM ;
Atkins, MB ;
Thompson, JA ;
Coit, DG ;
Byrd, D ;
Desmond, R ;
Zhang, YT ;
Liu, PY ;
Lyman, GH ;
Morabito, A .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3622-3634
[5]
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
[6]
Buckner JC, 2001, CANCER-AM CANCER SOC, V92, P420, DOI 10.1002/1097-0142(20010715)92:2<420::AID-CNCR1338>3.0.CO
[7]
2-3
[8]
RADIATION-THERAPY FOR NODAL DISEASE IN MALIGNANT-MELANOMA [J].
BURMEISTER, BH ;
SMITHERS, BM ;
POULSEN, M ;
MCLEOD, GR ;
BRYANT, G ;
TRIPCONY, L ;
THORPE, C .
WORLD JOURNAL OF SURGERY, 1995, 19 (03) :369-371
[9]
CALABRO A, 1989, ARCH SURG-CHICAGO, V124, P1051
[10]
*CANC AUSTR, 1999, AUSTR I HLTH WELF AU