Rosenberg S A, Yang J C, Schwartzentruber D J, Hwu P, Marincola F M, Topalian S L, Seipp C A, Einhorn J H, White D E, Steinberg S M
Surgery Branch and Department of Biostatistics and Data Management Section, Division of Clinical Sciences, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
J Clin Oncol. 1999 Mar;17(3):968-75. doi: 10.1200/JCO.1999.17.3.968.
The combination of chemotherapy with immunotherapeutic agents such as interleukin-2 and interferon alfa-2b has been reported to provide improved treatment results in patients with metastatic melanoma, compared with the use of chemotherapy alone. We have performed a prospective randomized trial in patients with metastatic melanoma, comparing treatment with chemotherapy to treatment with chemoimmunotherapy.
One hundred two patients with metastatic melanoma were prospectively randomized to receive chemotherapy composed of tamoxifen, cisplatin, and dacarbazine or this same chemotherapy followed by interferon alfa-2b and interleukin-2. Objective responses, survival, and toxicity in the two groups were evaluated at a median potential follow-up of 42 months.
In 52 patients randomized to receive chemotherapy, there were 14 objective responses (27%), including four complete responses. In 50 patients randomized to receive chemoimmunotherapy, there were 22 objective responses (44%) (P2 = .071), including three complete responses. In both treatment groups, the duration of partial responses was often short, and there was a trend toward a survival advantage for patients receiving chemotherapy alone (P2 = .052; median survival of 15.8 months compared with 10.7 months). Treatment-related toxicities were greater in patients receiving chemoimmunotherapy.
With the treatment regimens used in this study, the addition of immunotherapy to combination chemotherapy increased toxicity but did not increase survival. The use of combination chemoimmunotherapy regimens is not recommended in the absence of well-designed, prospective, randomized protocols showing the benefit of this treatment strategy.
据报道,与单纯使用化疗相比,化疗联合白细胞介素-2和干扰素α-2b等免疫治疗药物可改善转移性黑色素瘤患者的治疗效果。我们对转移性黑色素瘤患者进行了一项前瞻性随机试验,比较化疗与化疗免疫疗法的治疗效果。
102例转移性黑色素瘤患者被前瞻性随机分组,分别接受由他莫昔芬、顺铂和达卡巴嗪组成的化疗,或在同样的化疗后接受干扰素α-2b和白细胞介素-2治疗。在中位潜在随访42个月时评估两组的客观缓解率、生存率和毒性。
在随机接受化疗的52例患者中,有14例客观缓解(27%),包括4例完全缓解。在随机接受化疗免疫疗法的50例患者中,有22例客观缓解(44%)(P2 = 0.071),包括3例完全缓解。在两个治疗组中,部分缓解的持续时间通常较短,且单独接受化疗的患者有生存优势的趋势(P2 = 0.052;中位生存期为15.8个月,而化疗免疫疗法组为10.7个月)。接受化疗免疫疗法的患者与治疗相关的毒性更大。
采用本研究中的治疗方案,在联合化疗中添加免疫疗法会增加毒性,但不会提高生存率。在没有精心设计的、前瞻性的、随机的方案证明这种治疗策略有益的情况下,不建议使用联合化疗免疫疗法方案。