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尽管患有晚期癌症,但使用米非司酮单药治疗仍可实现长期高质量生存。

Long-term High-quality Survival with Single-agent Mifepristone Treatment Despite Advanced Cancer.

作者信息

Check Jerome H, Check Diane, Wilson Carrie, Lofberg Patrice

机构信息

Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology & Infertility, Cooper Medical School of Rowan University, Camden, NJ, U.S.A.

Cooper Institute for Reproductive Hormonal Disorders, P.C., Mt. Laurel, NJ, U.S.A.

出版信息

Anticancer Res. 2016 Dec;36(12):6511-6513. doi: 10.21873/anticanres.11251.

Abstract

CASE REPORT

We show long-term high-quality survival following single-agent treatment with a progesterone receptor antagonist in two cases of advanced metastatic cancer. Because no biopsy was performed (patient refused) the exact type of lung cancer was not determined but the majority of oncologists who evaluated the patient thought that the rapid onset and syndrome of inappropriate anti-diuretic hormone was more consistent with small-cell lung cancer. The US Food and Drug Association granted a compassionate-use investigational new drug approval for use of single-agent 200 mg mifepristone orally/day to a moribund woman with never-treated metastatic lung cancer and a male with bilateral renal cell carcinoma who had undergone only a unilateral hemi-nephrectomy. Both had long-term high-quality survival (5 years for the patient with lung cancer with complete remission of all lung lesions, and 12 years for the male patient with kidney cancer). Neither patient had any side-effects from mifepristone therapy.

CONCLUSION

These cases helped influence the US Food and Drug Association in granting an investigator-initiated investigational new drug study on advanced non-small cell lung cancer.

摘要

病例报告

我们展示了两例晚期转移性癌症患者在接受孕激素受体拮抗剂单药治疗后实现长期高质量生存的情况。由于未进行活检(患者拒绝),肺癌的确切类型未确定,但评估该患者的大多数肿瘤学家认为,快速起病和抗利尿激素分泌异常综合征更符合小细胞肺癌。美国食品药品监督管理局批准了一项同情用药研究性新药申请,给予一名从未接受过治疗的晚期转移性肺癌濒死女性患者以及一名仅接受过单侧肾半切除术的双侧肾细胞癌男性患者口服米非司酮,剂量为200毫克/天。两人均实现了长期高质量生存(肺癌患者生存5年,所有肺部病变完全缓解;肾癌男性患者生存12年)。两名患者均未出现米非司酮治疗的任何副作用。

结论

这些病例有助于影响美国食品药品监督管理局批准一项由研究者发起的针对晚期非小细胞肺癌的研究性新药研究。

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