Markman Maurie, Zanotti Kristine, Peterson Gertrude, Kulp Barbara, Webster Kenneth, Belinson Jerome
Department of Hematology/Medical Oncology (R-35), the Cleveland Clinic Foundation, 9500 Euclid Ave, Cleveland, OH 44195, USA.
J Clin Oncol. 2003 Dec 15;21(24):4611-4. doi: 10.1200/JCO.2003.05.539.
Carboplatin-associated hypersensitivity is increasingly recognized as a potentially serious toxicity when this agent is administered for more than six total cycles.
Our group has used a predictive skin test in women with gynecologic cancers who have previously received more than six cumulative cycles of platinum-based chemotherapy. Thirty minutes before all subsequent carboplatin courses, a 0.02-mL aliquot from the solution prepared for treatment is injected intradermally. A positive test is considered to be a > or = 5-mm wheal, with a surrounding flare.
From October 1998 through March 2003, 126 patients received a total of 717 carboplatin skin tests (median per patient, four tests; range, one to 54 tests). Of the 668 negative tests (93% of the total performed), 10 were associated with evidence of carboplatin hypersensitivity (1.5% false-negative rate; 95% CI, 0.6% to 2.4%), none of which were severe (eg, dyspnea, hypotension, cardiac/respiratory compromise). Of the 41 positive tests, the decision was made to not deliver the drug to 32 patients, although seven women ultimately underwent a future attempt at re-treatment with a platinum agent using a desensitization program. In seven episodes where patients received the carboplatin despite the finding of a positive test, six were associated with the development of symptoms of anaphylaxis (none severe).
A negative carboplatin skin test seems to predict with reasonable reliability for the absence of a severe hypersensitivity reaction with the subsequent drug infusion. The implications of a positive test remain less certain, but limited experience with continued treatment suggests this approach must be undertaken with considerable caution.
当卡铂给药总疗程超过六个周期时,与之相关的超敏反应日益被认为是一种潜在的严重毒性反应。
我们的研究小组对先前接受过六个以上累积周期铂类化疗的妇科癌症女性患者进行了预测性皮肤试验。在随后所有卡铂疗程前30分钟,将为治疗准备的溶液中0.02 mL的等分试样进行皮内注射。阳性试验定义为风团直径≥5 mm,并伴有周围红晕。
从1998年10月至2003年3月,126例患者共接受了717次卡铂皮肤试验(每位患者中位数为4次试验;范围为1至54次试验)。在668次阴性试验(占总试验次数的93%)中,有10次与卡铂超敏反应证据相关(假阴性率为1.5%;95%置信区间为0.6%至2.4%),其中无一例严重(如呼吸困难、低血压、心脏/呼吸功能不全)。在41次阳性试验中,决定不给32例患者用药,尽管有7名女性最终使用脱敏方案对铂类药物进行了再次治疗尝试。在7例尽管皮肤试验呈阳性但仍接受卡铂治疗的病例中,有6例出现了过敏反应症状(均不严重)。
卡铂皮肤试验阴性似乎能较为可靠地预测后续药物输注时不会发生严重超敏反应。阳性试验的意义仍不太明确,但继续治疗的有限经验表明,采用这种方法必须相当谨慎。