Anti-CD30 diabody-drug conjugates with potent antitumor activity

作者：Kim Kristine M^*; McDonagh Charlotte F; Westendorf Lori; Brown Lindsay L; Sussman Django; Feist Tiffany; Lyon Robert; Alley Stephen C; Okeley Nicole M; Zhang Xinqun; Thompson Melissa C; Stone Ivan; Gerber Hans Peter; Carter Paul J

来源：Molecular Cancer Therapeutics, 2008, 7(8): 2486-2497.

DOI：10.1158/1535-7163.MCT-08-0388

Anti-CD30 diabodies were engineered with two cysteine mutations for site-specific drug conjugation in each chain of these homodimeric antibody fragments. Diabodies were conjugated with similar to 4 equivalents of the anti-tubulin drugs, monomethyl auristatin E or F, via a protease-cleavable dipeptide linker, to create the conjugates, diabody-vcE4 and diabody-vcF4, respectively. Diabody conjugation had only minor (<3-fold) effects on antigen binding. Diabody-vcF4 was potently cytotoxic against the antigen-positive cell lines, Karpas-299 (34 pmol/L IC(50)) and L540cy (22 pmol/L IC(50)), and was 8- and 21-fold more active than diabody-vcE4 against these cell lines, respectively. Clearance of diabody-vcF4 (99-134 mL/d/kg) was 5-fold slower than for the nonconjugated diabody in naive severe combined immunodeficient mice. Diabody-vcF4 had potent and dose-dependent antitumor activity against established Karpas-299 xenografts and gave durable complete responses at well-tolerated doses. Biodistribution experiments with diabody-[(3)H]-vcF4 (0.72-7.2 mg/kg) in tumorbearing mice showed a dose-dependent increase in total auristatin accumulation in tumors (<= 520 nmol/L) and decrease in relative auristatin accumulation (<= 8.1 %ID/g), with peak localization at 4 to 24 h after dosing. Diabody-vcF4 had similar to 4-fold lower cytotoxic activity than the corresponding IgG 1 -vcF4 conjugate in vitro. A similar potency difference was observed in vivo despite 25- to 34-fold faster clearance of diabody-vcF4 than IgG1-vcF4. This may reflect that dose-escalated diabody-vcF4 can surpass lgG1-vcF4 in auristatin delivery to tumors, albeit with higher auristatin exposure to some organs including kidney and liver. Diabody-drug conjugates can have potent antitumor activity at well-tolerated doses and warrant further optimization for cancer therapy.

• 出版日期2008-8