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Emerging Immunotherapies for Non-Hodgkin Lymphomas: The Tortoise Approaches the Finish Line

Oliver W. Press, MD, PhD
[+] Article and Author Information

Grant Support: By grants CA55596 and CA76287 from the National Institutes of Health.

Requests for Single Reprints: Oliver W. Press, MD, PhD, Division of Oncology, EE-122, Department of Medicine, University of Washington Medical Center, Box 356043, Seattle, WA 98195-6043; e-mail, press@u.washington.edu.

Requests To Purchase Bulk Reprints (minimum, 100 copies): the Reprints Coordinator; phone, 215-351-2657; e-mail, reprints@mail.acponline.org.


Ann Intern Med. 2000;132(11):916-918. doi:10.7326/0003-4819-132-11-200006060-00012
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Disseminated malignancies continue to pose vexing problems for both patients and health care providers. Although localized malignant lesions can often be extirpated with surgery or radiation therapy, most metastatic neoplasms are difficult to cure despite systemic chemotherapy. Furthermore, the alopecia, nausea, myelosuppression, neurotoxicity, and nephrotoxicity that often accompany conventional chemotherapy are potent deterrents for many patients. Consequently, investigators and patients with cancer have long sought alternative therapies that might be effective while avoiding the dreaded side effects of chemotherapy. Immunologic interventions have been particularly appealing because they use “natural” components of the immune system to selectively eradicate malignant cells while leaving normal cells unharmed. Immunotherapeutic attempts have included “active” approaches, such as development of tumor vaccines, and “passive” or “adoptive” immunotherapy, in which components of the immune system (antibodies, interferons, interleukins, activated T lymphocytes) are produced exogenously before they are administered to patients with cancer. Of these strategies, monoclonal antibodies have achieved the most recent success and publicity.

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