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Sens. Continue To Press Sotomayor On Abortion Rights On Third Day Of Confirmation Hearings
In her third day of confirmation hearings before the Senate Judiciary Committee, Supreme Court nominee Sonia Sotomayor deflected lawmakers" attempts to elicit specific answers on how she would rule on abortion-rights cases and other contentious issues, the Washington Post reports (Goldstein et al., Washington Post, 7/16). As she entered what likely will be the final day of testimony on Thursday, Sotomayor"s confirmation "seemed on track," and Republicans appeared to be "conceding that they had not built the momentum necessary to derail the nomination," according to the New York Times, (Stolberg/Lewis, New York Times, 7/16). Cornyn Questions Abortion-Rights ViewsSen. John Cornyn (R-Texas) asked Sotomayor whether reports that Obama administration officials had sought to elicit her views on abortion were accurate. She responded that she "was asked no question by anyone including the president about my views on any specific legal issue" (Espo/Sherman, AP/Houston Chronicle, 7/15). Cornyn cited comments from George Pavia -- the senior partner at the New York law firm where Sotomayor previously worked -- who stated that he could "guarantee" that she would "be for abortion rights." Sotomayor said, "I have no idea why he"s drawing that conclusion," adding, "If he was talking about the fact that I served on a particular board that promoted equal opportunity for people, the Puerto Rican Legal Defense and Education Fund, then you could talk about that being a liberal instinct, in the sense that I promote equal opportunity in America and the attempts to ensure that." She continued, "But he has not read my jurisprudence for 17 years, I can assure you. He"s a corporate litigator. And my experience with corporate litigators is that they only look at the law when it affects the case before them" (Washington Post, 7/16). Sotomayor added that she "know[s] for a fact that I never spoke to [Pavia] on my views on abortion or my views on any social issue" (Bendavid, "Washington Wire," Wall Street Journal, 7/15). Sotomayor noted that she once ruled to uphold the "global gag rule," also known as the "Mexico City" policy, which barred federal funding of international family planning groups that provide abortion information or services (New York Times, 7/16).Coburn Presses on Hypothetical CasesDuring his questioning, Sen. Tom Coburn (R-Okla.) asked Sotomayor about hypothetical cases related to abortion-rights issues, including if it would be legal if a woman sought an abortion at 38 weeks" gestation if the fetus had spina bifida. Sotomayor said, "I can"t answer that question in the abstract, because I would have to look at what the state of the state"s law was on that question and what the state said with respect to that issue." She continued, "The question is, is the state regulation regulating what a woman does an undue burden? And so I can"t answer your hypothetical, because I can"t look at it as an abstract without knowing what state laws exist on this issue or not. And even if I knew that, I probably couldn"t opine, because I"m sure that situation might well arise before the court" (Holman, "NewsHour with Jim Lehrer," PBS, 7/15). Sotomayor also said that the Supreme Court"s 1992 ruling in Planned Parenthood v. Casey "reaffirmed the core holding of Roe v. Wade that a woman has a constitutional right to terminate her pregnancy in certain cases" (Hirschfeld Davis, AP/Boston Globe, 7/16). She added that the ruling said the court should consider whether any state regulation "has an undue burden on the woman"s constitutional right" (Sherman, AP/Sacramento Bee, 7/15). Coburn also asked whether medical advancements that help premature infants survive might "have any bearing on how we look at" Roe (Savage/Oliphant, Chicago Tribune, 7/16). She said, "I can"t answer that in the abstract," adding, "The question as it would come before me wouldn"t be in the way that you form it as a citizen, it would come to me as a judge" (AP/Houston Chronicle, 7/15).Specter Seeks Clarification on RoeDuring question
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Availability Of Diagnostic Tests Drive Success In Hospitalist-Run Short-Stay Units
The most important factors for a successful stay in hospital short-stay units (SSUs) are the types of diagnostic tests performed and whether or not specialty consultations are needed. When hospitalists staff these units, they can ensure that only patients who need readily accessible services are admitted. These are the findings of a study published today in the Journal of Hospital Medicine.
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Saint Barnabas Medical Center Is Only Hospital In New Jersey To Offer Clinical Trial For The Treatment Of Recurrent Chest Wall Breast Cancer
Some patients who suffer from recurrent cancer at the chest wall now have another option. The Radiation Oncology Department at Saint Barnabas Medical Center is one of a few hospitals nationwide to participate in a study which combines the use of the heat-sensitive chemotherapeutic agent ThermoDox® with microwave hyperthermia, or heat.
Oncology

Biothera Launches Clinical Trial In KRAS-Mutated Colorectal Cancer Patients

Biothera has initiated a Phase II clinical trial in stage IV KRAS-mutated colorectal cancer patients with its investigational drug Imprime PGG® in combination with Erbitux® (cetuximab), the company announced today. Published research demonstrates that colorectal cancers with mutated KRAS genes do not respond to anti-EGFR monoclonal antibodies such as Erbitux®. However, researchers believe that Imprime PGG® uses the body"s own immune system by engaging a type of white blood cell called the neutrophil to fight cancer cells that are coated with antibodies like Erbitux. Such a strategy might be effective against tumors regardless of whether KRAS is mutated or not. Preclinical studies indicate that Imprime PGG® in combination with Erbitux® can reduce tumor growth. "About 35-40 percent of all colorectal cancers have a mutation in the KRAS gene," said Leonard B. Saltz, M.D., medical oncologist and colorectal cancer expert at Memorial Sloan-Kettering Cancer Center, and principal investigator of the trial. "Erbitux and related antibodies are ineffective against these KRAS-mutated cells." While Erbitux® doesn"t kill cancer cells that have mutated KRAS, it can bind to the tumor cells and activate the binding of another protein in the immune system called complement to the tumor cell. When neutrophils primed with Imprime PGG® bind to the "fixed" complement on the tumor cell, the neutrophils attack the cancer cell. Imprime PGG® is being developed as combination treatment for a wide range of cancers, including colorectal and lung cancer. "The beauty of this trial design is that since drugs like Erbitux® alone can"t work in a KRAS-mutated tumor, if we see patients" tumors shrinking, we"ll be pretty confident that it is the presence of the investigational drug that is making that happen," said Saltz. The open-label, 56-patient KRAS-mutated colorectal cancer study is being conducted at three U.S. locations. Patient enrollment begins this week. All subjects will receive Imprime PGG® at 4 mg/kg weekly plus standard doses of Erbitux®. Tumor measurements and determination of tumor responses for this study will be performed according to Response Evaluation Criteria in Solid Tumors (RECIST). "Based on the results of our first clinical trial in second- and third-line metastatic colorectal cancer patients, we are excited at the prospect that Imprime PGG® in combination with monoclonal anti-EGFR therapies might provide hope to patients with KRAS-mutated tumors," said Daniel K. Conners, Biothera chairman and Pharmaceutical Group president. "This KRAS-mutated colorectal trial has the potential to become a pivotal trial and may lead to a fast-track application to the FDA." About Imprime PGG® Imprime PGG® is a novel immunotherapy that works synergistically with anti-tumor monoclonal antibodies to activate a large population of the body"s immune cells (neutrophils) to kill cancer cells. Unlike other drugs that trigger a broad innate immune response, Imprime PGG® selectively activates immune cells without inducing systemic pro-inflammatory cytokines, which reduces potential side effects. As a platform therapeutic in oncology, Imprime PGG® has the potential to improve patient response rates for existing monoclonal antibody therapies in approved indications, create new indications for these drugs and enhance the efficacy of development-stage monoclonal antibody drugs. Biothera, the Immune Health Company


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