- Background:
- A significant amount of ductal carcinoma in situ (DCIS):
- Is ER-negative and / or overexpresses HER2
- DCIS is more likely to overexpress HER2:
- Than invasive cancer, and it is possible that trastuzumab (T) is more likely to be effective in DCIS:
- Because it intervenes earlier in the carcinogenic pathway
- Than invasive cancer, and it is possible that trastuzumab (T) is more likely to be effective in DCIS:
- HER2 overexpression:
- Occurs in 45% of estrogen receptor-negative DCIS
- 20% of ER-positive DCIS
- Preclinical data suggest that trastuzumab (T):
- Enhances the effect of radiation in DCIS that overexpresses HER2
- Based on these findings:
- The NSABP protocol B-43 aims to evaluate:
- The effect of trastuzumab in HER2-positive DCIS
- Patients with HER2-positive DCIS treated with breast-conserving surgery were randomized to breast irradiation versus breast irradiation plus two doses of trastuzumab:
- Starting on day one of breast irradiation and repeated three weeks later
- The primary endpoint:
- Is the development of any breast cancer
- The NSABP protocol B-43 aims to evaluate:
- A significant amount of ductal carcinoma in situ (DCIS):
- Methods:
- After lumpectomy (Lx) for pure DCIS:
- Each patients (pts) DCIS lesion:
- Is centrally tested for HER2 using ASCO / CAP guidelines
- Each patients (pts) DCIS lesion:
- HER2+ pts are randomly assigned to:
- Receive two doses of T:
- Three weeks apart during whole breast radiation (WBI) or to WBI alone
- Receive two doses of T:
- After lumpectomy (Lx) for pure DCIS:
- Eligibility:
- Women ≥ 18 yrs
- Margin-clear Lx for pure DCIS
- ECOG status 0 / 1
- Clinically or pathologically node negative
- ER and/or PR status must be known before random assignment
- Primary aims are to determine:
- If T decreases:
- Ipsilateral breast cancer (IBC) recurrence
- Ipsilateral skin cancer recurrence, or
- Ipsilateral DCIS
- If T decreases:
- Secondary aims are to determine:
- The benefit of T in:
- Preventing regional or distant recurrence
- Contralateral invasive breast cancer or DCIS
- The benefit of T in:
- B-43 will determine if:
- DFS, recurrence-free interval, and / or overall survival:
- Can be improved with the use of T
- DFS, recurrence-free interval, and / or overall survival:
- 2000 pts will be accrued over 7.9 yrs:
- With a definitive analysis of primary endpoints performed at 163 IBC events:
- 7.5 – 8 yrs after protocol initiation with an 80% power to detect a hazard reduction of 36%:
- From 1.73 IBC events per 100 pt-yrs to 1.11 events per 100 pt-yrs
- 7.5 – 8 yrs after protocol initiation with an 80% power to detect a hazard reduction of 36%:
- With a definitive analysis of primary endpoints performed at 163 IBC events:
- The 36% observed reduction in the hazard of IIBCR-SCR-DCIS on the T arm is based on a projection of 40% hazard reduction if the compliance were perfect, with a 10% noncompliance rate
- As of January 1, 2013:
- 1,127 pts have been randomized into the study
- Support: PHS NCI-U10-CA-69651, -12027, and -P30-CA-14599 from the US NCI, and Genentech, Inc. Clinical trial information: NCT00769379
- Results:
- NSABP B-43 opened 11/9/08
- As of 7/31/2013:
- 5,861 patients have had specimens received centrally
- 5,645 of those had analyzable blocks
- 1,969 (34.9 %) were HER2 positive
- A total of 1,428 patients have been accrued:
- 1,137 (79.6 %) of whom have follow-up information
- The average follow-up time for the 1,137 patients:
- Is 23.3 months
- No grade 4 or 5 toxicity has been observed
- In NSABP B-43 the HER2-positive rate for pure DCIS among patients undergoing breast-preserving surgery:
- Is 34.9 %:
- Lower than the previously reported rate
- Is 34.9 %:
- No trastuzumab-related safety signals have been observed
- Interest in this trial has been robust