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Are Natural Deodorants Better for You? - The New York Times

Much of the marketing suggests that they’re safer than more traditional underarm products, but that hype is not based on science.

New-york
United-states
Stanford
California
Maine
San-diego
San-francisco
American
Nina-botto
Jennifer-chen
Julia-calderone
Harold-burstein

Pandemic leads doctors to rethink unnecessary treatment

Pandemic leads doctors to rethink unnecessary treatment

Pandemic leads doctors to rethink unnecessary treatment Covid-19 is opening the door for researchers to address a problem that has vexed the medical community for decades: the overtreatment and unnecessary treatment of patients. On one hand, the pandemic caused major health setbacks for non-covid patients who were forced to, or chose to, avoid tests and treatments for various illnesses. On the other hand, in cases in which no harm was done by delays or cancellations, medical experts can now reevaluate whether those procedures are truly necessary. But never before, said researcher Allison Oakes, has there been such a large database to compare patients who received a particular test or treatment with those who did not.

Boston
Massachusetts
United-states
William-connell-school
Dana-farber-cancer-institute
Harold-burstein
Allison-oakes
Krista-petruzziello
Heather-lyu
Susan-gennaro
Jill-wruble
Emily-henderson

Covid-19 forces physician to rethink treatments that are overdone or unnecessary

Covid-19 forces physician to rethink treatments that are overdone or unnecessary
washingtonpost.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from washingtonpost.com Daily Mail and Mail on Sunday newspapers.

Boston
Massachusetts
United-states
William-connell-school
Dana-farber-cancer-institute
Harold-burstein
Allison-oakes
Krista-petruzziello
Heather-lyu
Susan-gennaro
Jill-wruble
Research-consortium-for-health-care-value-assessment

Panel Tells FDA to Keep Atezolizumab Approval in TNBC

email article An advisory panel recommended the FDA not revoke the accelerated approval for atezolizumab (Tecentriq) in combination with nab-paclitaxel (Abraxane) for treating metastatic, PD-L1-positive triple-negative breast cancer (TNBC). In a 7-2 vote, the Oncologic Drugs Advisory Committee (ODAC) affirmed the accelerated approval, with members clearly conflicted over the decision. This was a difficult decision in a very difficult disease to treat, said Harold Burstein, MD, PhD, of the Dana-Farber Cancer Institute in Boston, who voted yes on the proposition. I have spent decades caring for these patients, and we all wish we had fundamentally better options. FDA initially granted atezolizumab, a PD-L1 immune checkpoint inhibitor, accelerated approval in 2019 in combination with nab-paclitaxel for patients with untreated metastatic or locally advanced unresectable TNBC whose tumors express PD-L1, based on findings from the IMpassion130 trial, which showed a significant

Dana-farber-cancer-institute
Massachusetts
United-states
Cleveland
Ohio
Boston
Houston
Texas
Maryland
Bethesda
Baylor-college-of-medicine
Philip-hoffman

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