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Old 10-01-2012, 12:58 AM   #1
Lani
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FINALLY!!!!! the HERA 1 yr vs 2 yrs herceptin results (& early 6mos. vs 1yr results)

Public release date: 1-Oct-2012

Contact: ESMO PRESS OFFICE
media@esmo.org
European Society for Medical Oncology

New findings on optimal duration of trastuzumab therapy for women with HER2+ early breast cancer

VIENNA, Austria, 1 October 2012 – New studies that advance understanding of the optimal duration of therapy with the targeted cancer drug trastuzumab were released today at the ESMO 2012 Congress of the European Society for Medical Oncology in Vienna.

"These long awaited results constitute a further milestone in the treatment of patients with early breast cancer over-expressing HER2/neu, corresponding to a population of about 12-15% of all cases of breast cancer," commented Prof Christoph Zielinski, Chairman of the Clinical Division of Oncology, at Medical University Vienna, Austria, who was not involved in the studies.

Landmark results from HERA trial -- extending trastuzumab for 2 years does not significantly improve outcomes versus 1 year

One year of treatment with the targeted drug trastuzumab is as good as two years of treatment, for women with HER2-positive early breast cancer who have already received initial treatment with surgery, chemotherapy and radiotherapy as needed, researchers have found.

The HERA trial, which has been run by the Breast International Group (BIG) since 2001, is an international, multi-center, phase III randomized study involving 5102 women with early HER2-positive breast cancer. After finishing primary therapy with surgery, chemotherapy and radiotherapy as indicated, they were randomly assigned to trastuzumab therapy every 3 weeks for 1 year, 2 years or observation.

As of 12 April 2012, the unadjusted hazard ratio for a woman experiencing disease relapse in the 2-year treatment arm versus the 1-year arm was 0.99 (95% CI and P-value), Prof Richard Gelber of Harvard Medical School and Dana-Farber Cancer Institute, Boston, MA, USA, said. The overall survival rate in the two arms was comparable [HR=1.05 (95% CI 0.86-1.28; P=0.6333)].

"The key message for 2012 is that 1 year of treatment with trastuzumab remains the standard of care for HER2 positive early breast cancer patients," Prof Gelber said.

The researchers found that the durable benefit in disease-free survival and overall survival of 1-year trastuzumab compared to no trastuzumab that had been reported previously remained stable at 8 years of median follow-up.

"This prolonged benefit in disease-free survival and overall survival of 1-year trastuzumab over no trastuzumab is remarkably impressive and reassuring to patients," Prof Gelber said. "These results show that the benefit of adjuvant trastuzumab remains over time and it is not lost after some years. Patients can be reassured that 1 year trastuzumab is a very effective treatment, reducing the risk of disease recurrence and death by one-quarter compared to not using trastuzumab."

"While extending the duration of trastuzumab administration to 2 years did not significantly improve outcome compared with 1 year trastuzumab, ongoing trials are testing whether combining trastuzumab with other anti-HER2 agents (for example pertuzumab or lapatinib) might further benefit patients with HER2-positive early breast cancer," Prof Gelber noted.

Commenting on the data, Prof Zielinski noted: "Progress in the treatment of patients with early breast cancer over-expressing HER2/neu was extremely impressive and particularly successful by the introduction of trastuzumab as adjuvant treatment. This was administered in the first trials for one year and resulted in a highly significant prolongation of progression-free and overall survival. However, the question lingered whether a prolongation of treatment to two years would result in even better data than the ones obtained before."

"The present trial shows that this is not the case, which strongly supports the correctness of adjuvant treatment duration delivered to patients with HER2/neu over-expressing early breast cancer. Moreover, it teaches us about the biology of the disease in that the therapeutic interference with growth factor signaling for a period of one year cannot be improved by a longer duration of such treatment," said Prof Zielinski.

"Thus, we can be assured that patients are being treated in the best possible and most cost-effective way, by weighing benefit versus costs for the healthcare system. The latter aspect is quite important, as the recurrence of disease in a patient leads not only to suffering and death, but also to an immensely increased burden for the society. The current data thus add to the evidence how the latter aspects can be avoided by the delivery of an optimal duration of treatment for a selected patient population."

PHARE trial results comparing 6 to 12 months of trastuzumab in adjuvant early breast cancer

An academic randomized, non-inferiority trial instituted by the French National Cancer Institute (INCa) has compared a shorter trastuzumab exposure of 6 months versus the standard 12 months.

The Phare trial addressed the question of the trastuzumab duration in HER-positive early breast cancer adjuvant treatment. More than 150 cancer care centers all over France participated, recruiting more than 3380 patients representative of the French population. The trial's primary objective was to compare 6 months versus 12 months trastuzumab therapy in terms of disease free-survival according to a non-inferiority schema.

"The trial results are inconclusive for this non-inferiority hypothesis," said Prof Xavier Pivot, of the Université de Franche Comté, France. "Nevertheless, there is a trend in favor of 12 months treatment for the overall population. Analysis of subgroups will be presented in December."

The median follow-up in the trial was 42.5 months and at the time of the analysis 395 disease-free survival events were reported. "According to the design of this trial, which allowed for a non-inferiority hazard ratio margin of 1.15, the 6-month trastuzumab arm (arm B) was not demonstrated to be significantly inferior to 12-month trastuzumab (arm A), since the confidence interval contains the 1.15 non inferiority margin (HR=1.28 (95%CI: 1.04 – 1.56, p=0.29). However despite the inconclusive result in terms of non-inferiority, the HR of 1.28 suggests a trend favoring 12 months," Prof Pivot said.

"Further exploration of the data, especially in selected subgroups is ongoing; further results will be presented in a couple of months. The results probably won't give a black and white answer, and the researchers will probably need to look at subsets of patients to see who benefits from six months of treatment and who should get a full year," Prof Pivot said.
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Old 10-01-2012, 07:19 AM   #2
Debbie L.
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Re: FINALLY!!!!! the HERA 1 yr vs 2 yrs herceptin results (& early 6mos. vs 1yr resul

Thanks, Lani, for keeping us on the cutting edge once again.

The thing that has most interested me about these trials of Herceptin duration is to see whether there are any differences by subtypes, specifically ER- (no endocrine tx) vs. ER+. We often hear that for triple positive cancers, the "dual blockade" of endocrine tx plus Herceptin is crucial, so I've wondered if it would make a difference if the Herceptin lasted as long as the endocrine tx. It appears not (that is a good thing, no one wants to do, or pay for, Herceptin for 5 years). Although I guess we'll have to wait for the details to know that for sure.

The second report (PHARE) did hint at subgroup differences and I'll be eager to see those. Perhaps (can't help speculating) the 6 month duration might be not be quite as good not because of duration specifically but because most ER+women have barely started their endocrine tx when the Herceptin is stopped? Perhaps for ER- cancers, a very short duration (ala FinHer) is enough, whereas a year is best for ER+'s (TOTAL speculation).

Debbie Laxague
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Old 10-01-2012, 01:49 PM   #3
suzan w
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Re: FINALLY!!!!! the HERA 1 yr vs 2 yrs herceptin results (& early 6mos. vs 1yr resul

well, that is music to my ears!!!!!!! la lala la la...singing and dancing!!! Thanks for posting this, Lani!!!
__________________
Suzan W.
age 54 at diagnosis
5/05 suspicious mammogram-left breast
5/05 biopsy-invasive lobular carcinoma with LCIS,8mm tumor,stage 1 grade 2, ER+ PR+ Her2+++
6/14/05 bilateral mastectomy, node neg. all scans neg.
Oncotype DX-high risk
8/05-10/05 4 rounds A/C
10/05 -10/06 1 yr. herceptin
arimidex-5 years
2/14/08 started daily self administered injections..FORTEO for severe osteoporosis
7/28/09 BRCA 1 negative BRCA2 POSITIVE
8/17/09 prophylactic salpingo-oophorectomy
10/15/10 last FORTEOinjection
RECLAST infusion(ostoeporosis)
6/14/10 5 year cancerversary!
8/2010-18%increase in bone density!
no further treatments
Oncologist says, "Go do the Happy Dance"
I say,"What a long strange trip its been"
'One day at a time'
6-14-2015. 10 YEAR CANCERVERSARY!
7-16 to 9-16. Extensive (and expensive) dental work done to save teeth. Damage from osteoporosis and chemo and long term bisphosphonate use
6-14-16. 11 YEAR CANCERVERSARY!!
7-20-16 Prolia injection for severe osteoporosis
2 days later, massive hive outbreak. This led to an eventual dx of Chronic Ideopathic Urticaria, an auto-immune disease from HELL.
6-14-17 12 YEAR CANCERVERSARY!!
still suffering from CIU. 4 hospitilizations in the past year

as of today, 10-31-17 in remission from CIU and still, CANCER FREE!!!
6-14-18 13 YEAR CANCERVERSARY!! NED!!
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