CPC A61K 31/517 (2013.01) [A61K 31/282 (2013.01); A61K 31/337 (2013.01); A61K 31/4745 (2013.01); A61K 31/502 (2013.01); A61K 31/519 (2013.01); A61K 31/704 (2013.01); A61K 31/7048 (2013.01); A61K 31/7068 (2013.01); A61K 33/243 (2019.01); A61K 39/3955 (2013.01); A61K 47/643 (2017.08); A61K 47/6929 (2017.08); A61P 35/00 (2018.01); A61K 2039/545 (2013.01)] | 25 Claims |
1. A method of treating cancer in a patient in need thereof comprising administering to the patient a compound of formula I
![]() or a pharmaceutically acceptable salt or ester thereof, wherein:
the cancer has the characteristic of being a type prone to being or becoming refractory or resistant to platinum drug based therapy,
the compound or pharmaceutically acceptable salt or ester thereof is administered to the patient at a dose of from 6 mg/m2 to 14 mg/m2 of compound or pharmaceutically acceptable salt or ester thereof per patient body surface area per administration, and
each of the administrations is in a 28-day cycle at 14-day intervals.
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