Endpoints News
Eli Lilly and Insilico sign an AI drug discovery deal Read in browser
Endpoints News
Thank you for reading, dupa dupackia!
basic
UPGRADE
Mon T W Th F
30 March, 2026
TOP R&D TRENDS IN 2026:
Every year, John Carroll sizes up the top 15 global pharma pipelines — then brings the findings live with the R&D chiefs shaping them. What's in, what's out, and what's next for 2026? Register now.
presented by Exact Sciences
Health Eco­nom­ic Out­comes of the On­co­type DX Breast Re­cur­rence Test at a Pop­u­la­tion Health Lev­el
top stories
1. Blackstone raises $6.3B life sciences fund in record fundraising haul
2. Eli Lilly and Insilico sign an AI drug discovery deal, paying $115M upfront
3. Viridian’s autoimmune eye disease shot passes Phase 3, but can it compete with Amgen?
4. Braveheart Bio posts promising China data in heart disease where Bristol Myers, Cytokinetics have drugs
5. 'A bit of a surprise': Kardigan's repeat dosing of blood pressure drug has no benefit over single shot
6.
news briefing
Takeda cuts 600+ US jobs; United's stock rises on Tyvaso data
7. Kailera plans IPO to raise money for its China-licensed obesity pipeline
8. Sanofi reports underwhelming Phase 3 OX40 data in eczema, second case of Kaposi’s sarcoma
9. Biogen declares Phase 2 lupus success for anti-BDCA2 antibody
10. Merck leans toward lower Winrevair dose for pivotal trial in rare form of heart failure
11. Exclusive: Tanabe’s Phase 3 win for drug targeting rare diseases that cause pain upon light exposure
more stories
 
Drew Armstrong
.

We’re coming out of a big weekend for news from cardiology and dermatology conferences and already starting off with a bang, as Blackstone closes a $6.3 billion fundraise, Insilico and Lilly ink a preclinical deal, and Viridian’s stock tanks despite strong topline results in a Phase 3 trial.

.
Drew Armstrong
Executive Editor, Endpoints News
@ArmstrongDrew
sponsored post
Health Eco­nom­ic Out­comes of the On­co­type DX Breast Re­cur­rence Test at a Pop­u­la­tion Health Lev­el
by Brian Baranick

How the On­co­type DX® test’s pre­dic­tive util­i­ty pro­pelled pre­ci­sion on­col­o­gy 

In 2003, Kather­ine Y., a 53-year-old po­di­a­trist, found a lump in her breast dur­ing a self-ex­am. The fog of a can­cer di­ag­no­sis fol­lowed: back-to-back ap­point­ments, scans and pathol­o­gy re­ports, a new, can­cer-cen­tric vo­cab­u­lary to learn. Kather­ine un­der­went a dou­ble mas­tec­to­my to re­move the can­cer, then faced her hard­est de­ci­sion yet: Should she have chemother­a­py to re­duce the chance of can­cer re­turn­ing some­where else in her body?

Stan­dard tu­mor as­sess­ments sug­gest­ed chemother­a­py would be nec­es­sary, and Kather­ine heard the fa­mil­iar log­ic: treat broad­ly, treat ag­gres­sive­ly, re­duce risk. But she al­so un­der­stood how chemother­a­py could neg­a­tive­ly im­pact her qual­i­ty of life. What she need­ed was clar­i­ty.

In Jan­u­ary 2004, Kather­ine be­came the first com­mer­cial pa­tient to re­ceive the On­co­type DX Breast Re­cur­rence Score® test. She had a Re­cur­rence Score® re­sult of 18 — a low score in­di­cat­ing she like­ly would not ben­e­fit from chemother­a­py. That num­ber wasn’t just da­ta — it was a turn­ing point for Kather­ine and for the more than 2 mil­lion pa­tients that have used the On­co­type DX test since then.

The im­me­di­ate ben­e­fit was per­son­al and pro­found: Kather­ine avoid­ed months of tox­ic treat­ment and the long tail of pos­si­ble side ef­fects. Twen­ty-two years lat­er, Kather­ine re­mains can­cer-free*. To­day, she and her hus­band, Mel — both re­tired — spend their time ski­ing, bik­ing, and hik­ing in the Sier­ras with their dog, Crit­ter.

“I feel so blessed I had the op­por­tu­ni­ty to be the first to take this test, forego chemother­a­py, and learn my po­ten­tial for dis­tant re­cur­rence. Very im­por­tant­ly, I want­ed to help oth­er women learn about this test so they could have a say in their own, tai­lored can­cer treat­ment,” Kather­ine, who is now an On­co­type DX Pa­tient Am­bas­sador, re­cent­ly shared.

Kather­ine’s sto­ry il­lus­trates the hu­man side of pre­ci­sion on­col­o­gy: per­son­al­ized treat­ment plans, few­er side ef­fects, pre­served qual­i­ty of life, and — most im­por­tant­ly — peace of mind. When you mul­ti­ply the ef­fect of a bet­ter de­ci­sion across mil­lions of pa­tients, the sto­ry be­comes more than clin­i­cal — it high­lights the eco­nom­ic val­ue of the test.

The Health Eco­nom­ics Be­hind Bet­ter Care

Af­ter more than two decades of clin­i­cal ev­i­dence and re­al-world use in more than 100 coun­tries, more than two mil­lion breast can­cer pa­tients1 and their care teams have used the On­co­type DX test to help guide their de­ci­sion-mak­ing. The On­co­type DX Breast Re­cur­rence Score test de­liv­ers per­son­al­ized ge­nom­ic re­sults to help guide treat­ment de­ci­sions for pa­tients with ear­ly-stage HR+, HER2- breast can­cer. Twen­ty-two years af­ter launch, the On­co­type DX Breast Re­cur­rence Score test is the on­ly ge­nom­ic test proven to pre­dict chemother­a­py ben­e­fit from ran­dom­ized con­trolled stud­ies2, guid­ing per­son­al­ized treat­ment de­ci­sions with the high­est lev­el of ev­i­dence.

Prog­nos­tic and pre­dic­tive tests serve very dif­fer­ent pur­pos­es; prog­nos­tic tests pro­vide in­sight in­to how can­cer may be­have over time — such as the like­li­hood of re­cur­rence — but they do not pro­vide in­for­ma­tion about treat­ment ben­e­fits. Pre­dic­tive bio­mark­ers, on the oth­er hand, help de­ter­mine whether a pa­tient is like­ly to ben­e­fit from a spe­cif­ic ther­a­py, in­for­ma­tion that can di­rect­ly guide treat­ment choice and sup­port more in­di­vid­u­al­ized care.3

When a test can pre­dict chemother­a­py ben­e­fit and safe­ly re­duce its use, there are both clin­i­cal and fi­nan­cial ben­e­fits. By iden­ti­fy­ing who is — and is not — like­ly to ben­e­fit, the test has en­abled clin­i­cians and pa­tients to de-es­ca­late treat­ment con­fi­dent­ly.  An es­ti­mat­ed 1.6 mil­lion4 of the 2 mil­lion pa­tients test­ed world­wide may have been spared from po­ten­tial­ly un­nec­es­sary chemother­a­py, avoid­ing the acute and long-term tox­i­c­i­ties of treat­ment.

Chemother­a­py is ex­pen­sive, but its true cost ex­tends be­yond treat­ment ac­qui­si­tion. There are in­fu­sion vis­its, sup­port­ive med­ica­tions, man­age­ment of side ef­fects, as well as emer­gency vis­its and ad­mis­sions for com­pli­ca­tions. There are al­so in­di­rect bur­dens: di­min­ished qual­i­ty of life, time away from work, care­giv­er strain, trav­el costs, and pro­duc­tiv­i­ty loss­es.

Us­ing a pub­lished eco­nom­ic mod­el, it is es­ti­mat­ed that use of the On­co­type DX test to in­form ad­ju­vant treat­ment de­ci­sions among HR+, HER2- pa­tients re­sult­ed in av­er­age life­time sav­ings of ap­prox­i­mate­ly $10,000 per pa­tient in the U.S. health­care sys­tem. Us­ing the pub­lished eco­nom­ic mod­el, based on cur­rent treat­ment pat­terns, it is es­ti­mat­ed that use of the On­co­type DX test to in­form ad­ju­vant treat­ment de­ci­sions among HR+, HER2- pa­tients (com­pared to clin­i­cal-patho­log­i­cal fac­tors alone) could have saved more than $14 bil­lion to the U.S. health­care sys­tem since the in­tro­duc­tion of the test.

A re­cent large, re­al-world analy­sis5 of pa­tients with ear­ly-stage HR+, HER2- breast can­cer demon­strat­ed that chemother­a­py uti­liza­tion in­creas­es ap­pro­pri­ate­ly with high­er Re­cur­rence Score re­sults in the U.S., con­sis­tent with guide­line-based care. The On­co­type DX test strength­ens de­ci­sion con­sis­ten­cy among providers, un­der­scor­ing its val­ue not on­ly in guid­ing in­di­vid­ual care but al­so in har­mo­niz­ing ex­pert judg­ment in rou­tine prac­tice, in­clud­ing across all racial and eth­nic groups. The On­co­type DX Breast Re­cur­rence Score test’s per­for­mance has been con­sis­tent­ly val­i­dat­ed across di­verse pop­u­la­tions, and this analy­sis found that chemother­a­py use was gen­er­al­ly con­sis­tent across racial and eth­nic groups6, sug­gest­ing eq­ui­table ap­pli­ca­tion of Re­cur­rence Score re­sult-guid­ed treat­ment rec­om­men­da­tions.

Glob­al Health Eco­nom­ic and Out­comes Im­pact

The On­co­type DX test has been avail­able in­ter­na­tion­al­ly since 2010, so the glob­al health eco­nom­ics im­pact of this test is im­mea­sur­able. But com­pelling da­ta points ex­ist; a re­cent study pre­sent­ed at the San An­to­nio Breast Can­cer Sym­po­sium (SABCS) in 2025 found that the On­co­type DX test sig­nif­i­cant­ly in­flu­enced ad­ju­vant treat­ment de­ci­sions, pri­mar­i­ly lead­ing to chemother­a­py de-es­ca­la­tion and strength­en­ing de­ci­sion con­sis­ten­cy among Swiss breast can­cer spe­cial­ists7. An­oth­er analy­sis pre­sent­ed at the same con­gress es­ti­mat­ed that On­co­type DX test­ing in node-pos­i­tive pa­tients across five on­col­o­gy cen­ters in Ire­land over an 11-year pe­ri­od led to sav­ings of more than €60 mil­lion to the Irish health­care sys­tem8. This was cal­cu­lat­ed by specif­i­cal­ly iden­ti­fy­ing pa­tients who did not un­der­go chemother­a­py, thus avoid­ing di­rect med­ical costs and broad­er so­ci­etal bur­dens.

For more than two decades, clin­i­cians and pa­tients have re­lied on the On­co­type DX test to move be­yond one-size-fits-all care and use pre­dic­tive in­sights to make more con­fi­dent, in­di­vid­u­al­ized de­ci­sions. With that con­fi­dence comes some­thing pa­tients and their physi­cians val­ue deeply: the abil­i­ty to pur­sue the right treat­ment plan for them. The en­dur­ing qual­i­ty of the On­co­type DX test has en­abled those de­ci­sions and brought clar­i­ty when it was need­ed the most.

Click here to continue reading
Nick Galakatos, global head of Blackstone Life Sciences (Blackstone via website)
1
by Kyle LaHucik

The life sci­ences in­dus­try's largest-ever pri­vate in­vest­ment fund has ar­rived, and it comes from the world's biggest al­ter­na­tive as­set man­ag­er.

On Mon­day, Black­stone an­nounced it had raised $6.3 bil­lion for its lat­est life sci­ences in­vest­ment fund, Black­stone Life Sci­ences VI. The huge fundraise is equal to more than half the val­ue of new in­vest­ment funds raised in all of 2025, ac­cord­ing to a year-end re­port from bankers at William Blair.

Nick Galakatos, glob­al head of Black­stone Life Sci­ences, said the fundrais­ing ef­forts had ben­e­fit­ed from some of the un­cer­tain­ty in mar­kets, in Wash­ing­ton, and around the globe, de­scrib­ing it as a "com­pli­cat­ed mar­ket on many fronts."