Comparison of therapeutic efficacy and host toxicity of two different 131 I‐labelled antibodies and their fragments in the GW‐39 colonic cancer xenograft model

The in vivo uptake, therapeutic potential, and host toxicity were evaluated for both the intact IgG and F(ab′) 2 fragment of 2 murine monoclonal antibodies (MAbs) directed against either carcino‐embryonic antigen (CEA), called NP‐4, or colon‐specific antigen‐p (CSAp), called Mu‐9, in the GW‐39 human colorectal carcinoma grown in the hamster cheek pouch. Mu‐9 IgG and F(ab′) 2 were retained longer by the tumor than was the NP‐4 IgG or F(ab′) 2 , respectively. Localization of the two antibodies by micro‐autoradiography revealed two distinct patterns. Mu‐9 was seen densely around whole acini of tumor cells, whereas NP‐4 was found around each individual cell, albeit less densely. The anti‐tumor effects of 131 l‐labelled Mu‐9 and NP‐4 IgG were equal, but the therapeutic effectiveness of Mu‐9 F(ab′) 2 was significantly higher than NP‐4 F(ab′) 2 , as measured by change in tumor size. A dose‐dependent increase in host toxicity, as measured by change in body weight and change in peripheral white blood cells (p‐WBCs), was observed with 0.S to 3.0 mCi doses of 131 l‐lgG regardless of the MAb used. A 10‐22% loss in body weight lasting 3‐7 weeks and a 50‐80% loss in pWBCs lasting 6‐8 weeks were observed in these animals. In contrast, 3 × 2 mCi doses of 131 l‐NP‐4 or Mu‐9 F(ab′) 2 given at 3‐day intervals, a schedule which was equally therapeutic to a single 2‐mCi dose of 131 l‐lgG, resulted in only a 9% loss in body weight and a 50% loss in pWBCs that lasted only I week. This was followed by a complete recovery over the next 2‐3 weeks. These data suggest that multiple doses of F(ab′) 2 can be as tumoricidal as a single dose of an intact MAb IgG, but significantly less toxic to the host.