AbbVie Shares Fall on Low Survival Data for Lung Cancer Drug

  • Patients survived fewer month than typical with chemotherapy
  • Stock declines 4 percent after data released at cancer meeting

AbbVie Inc.’s shares fell Monday after an early trial showed patients taking the company’s experimental lung cancer drug survived fewer months than typical of those on chemotherapy, raising questions as to whether the company was right to buy the medicine in a $5.8 billion deal.

AbbVie’s drug is known as Rova-T. In patients with an aggressive form of lung cancer who expressed more of the protein marker known as DLL3 that’s targeted by the drug, median survival was 5.8 months, according to data presented Sunday at the annual meeting of the American Society for Clinical Oncology in Chicago. With the only approved drug for recurrent disease, a form of chemotherapy called topotecan, median overall survival is about seven months, according to Tony Butler, an analyst at Guggenheim Partners.

Rova-T’s initial survival data could be a disappointment to investors, Barclays analyst Geoff Meacham said in a note to clients. AbbVie’s shares dropped 4 percent to $62.42 at 10:32 a.m. in New York.

AbbVie said on April 28 it would buy Stemcentrx Inc and its Rova-T for $5.8 billion, a price that some analysts said at the time might be too high. The acquisition was completed on June 1.

In the trial, 68 percent of patients’ tumors stopped growing, including 18 percent whose tumors shrank, according to data on 60 people whose cancer had progressed after one or more previous courses of therapy.

In the 26 patients with high levels of DLL3 expression, 89 percent of tumors stopped growing, and 39 percent were reduced in size, according to a statement from Memorial Sloan Kettering Cancer Center, whose researcher Charles Rudin led the study.

“The most exciting thing about this therapeutic is the fact that it’s the first time in small-cell lung cancer that we have a predictive biomarker, one that we can associate with a higher probability of response to the drug,” Rudin said in a telephone interview. He cautioned the results were early, in small numbers of patients.

Four patients who had failed two prior therapies were still alive more than six months after treatment, including two who lived for at least 18 months, according to the statement.

Rova-T is an antibody drug conjugate, a type of treatment where one part latches onto a specific marker on the tumor, delivering a toxic payload once it enters the cell.

“Cancer stem cells initiate cancer and drive recurrence,” said Brian Slingerland, chief executive officer of Stemcentrx. In theory, targeting stem cells could help ensure that malignancies are eradicated and that the cancer won’t come back.

Stemcentrx identified the DLL3 marker, which is found in 80 percent of tumors of small cell lung cancer patients and, critically, isn’t present on normal tissue. The drug’s toxicity is “manageable,” according to the Sloan Kettering statement, with the main side effects being inflammation and fluid accumulation, low platelet count and rash.

The inflammation and fluid accumulation is “an unusual toxicity,” Sloan Kettering’s Rudin said. Still, he said he wasn’t very concerned because the effect was largely reversed by anti-inflammatory agents and corresponded with the highest dosage levels, which won’t be used in future trials.

Slingerland, of Stemcentrx, said on Friday at an AbbVie presentation to investors that patients who already have done a biopsy would not need to redo one to test for DLL3 expression.

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