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. Author manuscript; available in PMC: 2014 Feb 6.
Published in final edited form as: Cancer Res. 2013 Feb 19;73(8):2412–2417. doi: 10.1158/0008-5472.CAN-12-4561

Table 2.

Survival Benefits From the FDA-Approved Nanomedicines To Date*

Generic Drug Trade name (s) Indication Benefit
Pegylated liposomal doxorubicin Doxil®and Caelyx® HIV-related Kaposi's sarcoma No statistically significant change in overall survival (23 weeks) vs. doxorubicin, bleomycin and vincristine treatment (22.3 weeks) for HIV-related Kaposi's sarcoma
Metastatic ovarian cancer Statistically significant overall survival improvement (108 weeks, P= 0.008) vs. topotecan treatment (71.1 weeks) for platinum-sensitive patients with ovarian cancer
Metastatic breast cancer No statistically significant overall survival change (84 weeks) vs. conventional doxorubicin (88 weeks) for breast cancer patients receiving first-line therapy
Liposomal daunorubicin DaunoXome® HIV-related Kaposi's sarcoma No statistically significant overall survival change (52.7 weeks) vs. doxorubicin, bleomycin, vincristine treatment (48.9 weeks)
Poly (styren-co- maleic acid) conjugated naocarzinostatin SMANCS® Liver cancer, renal cancer Approved 1993 in Japan. Far more effective when the EPR is enhanced by increasing the blood pressure in difficult- to-treat tumors including metastatic liver cancer, cancers of pancreas, gallbladder, etc
Liver cancer: 5 year survival
1 seg.+ > 2 seg
Child A > 90 % ~ >50%
Child B 40% 30%
Five year survival (%) based on the liver function (cirrhosis) by Child classification, and intrahepatic+ metastasis
Albumin-bound paclitaxel Abraxane® Metastatic cancer breast Statistically significant overall survival change (56.4 weeks, P= 0.024) vs. polyethoxylated castor oil-based paclitaxel treatment (46.7 weeks) for patients receiving second-line treatment
*

The polymeric platform methoxy PEG-poly(D,L-lactide) taxol with the trade name Genexol-PM (Sanayang Co., Seoul, Korea) has been approved in Korea for the treatment of metastatic breast cancer.

Adapted from: 14 Jain, R. K. & Stylianopoulos, T., Nat. Rev. Clin. Oncol. (2010) 7, 653; SMANCS data in the table were provided by prof. Hiroshi Maeda.