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Clinical Trial
. 2018 Mar 1;4(3):302-308.
doi: 10.1001/jamaoncol.2017.4612.

Comparing Neoadjuvant Nab-paclitaxel vs Paclitaxel Both Followed by Anthracycline Regimens in Women With ERBB2/HER2-Negative Breast Cancer-The Evaluating Treatment With Neoadjuvant Abraxane (ETNA) Trial: A Randomized Phase 3 Clinical Trial

Luca Gianni  1 , Mauro Mansutti  2 , Antonio Anton  3 , Lourdes Calvo  4 , Giancarlo Bisagni  5 , Begoña Bermejo  6 , Vladimir Semiglazov  7 , Marc Thill  8 , Jose Ignacio Chacon  9 , Arlene Chan  10 , Serafin Morales  11 , Isabel Alvarez  12 , Arrate Plazaola  13 , Milvia Zambetti  1 , Andrew D Redfern  14 , Christian Dittrich  15 , Rebecca Alexandra Dent  16 , Domenico Magazzù  17 , Raffaella De Fato  17 , Pinuccia Valagussa  17 , Ignacio Tusquets  18
Affiliations
Clinical Trial

Comparing Neoadjuvant Nab-paclitaxel vs Paclitaxel Both Followed by Anthracycline Regimens in Women With ERBB2/HER2-Negative Breast Cancer-The Evaluating Treatment With Neoadjuvant Abraxane (ETNA) Trial: A Randomized Phase 3 Clinical Trial

Luca Gianni et al. JAMA Oncol. .

Abstract

Importance: Studies of neoadjuvant chemotherapy regimens using anthracyclines followed by taxanes have reported a doubling of pathological complete remission (pCR) rates compared with anthracycline-based regimens alone. A reverse sequence did not reduce activity. Nab-paclitaxel is an albumin-bound nanoparticle of paclitaxel that allows for safe infusion without premedication, and its use led to a significantly higher rate of pCR in the GeparSepto trial.

Objective: To determine whether nab-paclitaxel improves the outcomes of early and locally advanced human epidermal growth factor receptor 2 (ERBB2/HER2)-negative breast cancer compared with paclitaxel when delivered in a neoadjuvant setting.

Design, setting, and participants: In this multicenter, open-label study, in collaboration with Grupo Español de Investigación en Cáncer de Mama (GEICAM) and Breast Cancer Research Center-Western Australia (BCRC-WA), patients with newly diagnosed and centrally confirmed ERBB2/HER2-negative breast cancer were recruited. Participants were randomly allocated to paclitaxel, 90 mg/m2 (349 patients), or nab-paclitaxel, 125 mg/m2 (346 patients). The 2 drugs were given on weeks 1, 2, and 3 followed by 1 week of rest for 4 cycles before 4 cycles of an anthracycline regimen per investigator choice.

Main outcomes and measures: The primary end point was the rate of pCR, defined as absence of invasive cells in the breast and axillary nodes (ie, ypT0/is ypN0) at the time of surgery. A secondary end point was to assess tolerability and safety of the 2 regimens.

Results: From May 2013 to March 2015, 814 patients were registered to the study; 695 patients met central confirmation eligibility and were randomly allocated to receive either paclitaxel (349), or nab-paclitaxel (346) (median age, 50 years; range, 25-79 years). The intention-to-treat analysis of the primary end point pCR revealed that the improved pCR rate after nab-paclitaxel (22.5%) was not statistically significant compared with paclitaxel (18.6%; odds ratio [OR], 0.77; 95% CI, 0.52-1.13; P = .19). Overall, 38 of 335 patients (11.3%) 11.3% of patients had at least 1 serious adverse event in the paclitaxel arm and 54 of 337 patient (16.0%) in the nab-paclitaxel arm. Peripheral neuropathy of grade 3 or higher occurred in 6 of 335 patients (1.8%) and in 15 of 337 (4.5%), respectively.

Conclusions and relevance: The improved rate of pCR after nab-paclitaxel was not statistically significant. The multivariate analysis revealed that tumor subtype (triple-negative vs luminal B-like) was the most significant factor (OR, 4.85; 95% CI, 3.28-7.18) influencing treatment outcome.

Trial registration: clinicaltrials.gov Identifier: NCT01822314.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Gianni has been an advisory board member and consultant for Roche, Pfizer, Boehringer Ingelheim, AstraZeneca, Celgene, BioScience, Synthon, Genomic Health, Merck Sharp & Dohme, Synaffix, Eli Lilly, Odonate Therapeutics, Sandoz, Onkaido, Oncolytics Biotech, ADC Therapeutics, Seattle Genetics, and Tahio outside the submitted work. Dr Mansutti has received personal fees from Novartis, Roche, Celgene, and Eisai outside the submitted work. Dr Thill has received personal fees and nonfinancial support from Celgene, Roche, Novartis, AstraZeneca, Amgen, and Pfizer outside the submitted work. Dr Dittrich has received personal fees from Novartis, AstraZeneca, Eli Lilly, Merck Serono, Roche, and Sanofi; grants from Merck, Amgen, Pierre Fabre, Eisai, Bayer, AstraZeneca, Boehringer Ingelheim, Pfizer, Roche, Novartis, and Sanofi; and nonfinancial support from Bayer, Takeda, Sanofi, and Merck outside the submitted work. Dr Dent has received grants and personal fees from AstraZeneca, personal fee from Roche, Pfizer, Merck, Eisai, and Novartis outside the submitted work. Ms Valagussa has been an advisory board member for Celgene. No other disclosures are reported.

Figures

Figure 1.
Figure 1.. CONSORT Diagram of the Evaluating Treatment With Neoadjuvant Abraxane (ETNA) Study
HR indicates hormone receptor; ITT, intention-to-treat; pCR, pathologic complete response.
Figure 2.
Figure 2.. Subgroup Analysis of Pathological Complete Response Rate
OR indicates odds ratio.
See this image and copyright information in PMC

Comment in

References

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