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. 2021 Dec 21;7:157. doi: 10.1038/s41523-021-00367-w

Table 1.

Characteristics of eligible studies.

Study Latest update Type of trial (registry number) Enrollment period Age range (year) Chemo-regimen-Control arm-Platinum arm TNBC NO.-Control-Platinum Carboplatin dosage TNM stage Stage of therapy Median follow-up HR (95% CI)
DFS OS
CALGB 40603 2015 RCT(NCT00861705) 2009.5−2012.8 18–70 −P/PB*12w-4ddAC−P/PBCb*12w-4ddAC −212−221 AUC 6, d1, q3w Stage II/III Neoadjuvant 39m 0.84 (0.58−1.22) 1.15 (0.74–1.79)
Khalid 2015 RCT(NS) 2008.1−2014.12 17–65 −3CEF-3T−3CEF-3TCb-1yCM −80−78 AUC 5, d1, q3w Stage II/III;T > 1 cm/LN+ Adjuvant 52m 0.61 (0.39–0.96) 0.56 (0.32–0.98)
Zhang 2016 RCT(NS) 2006.5−2012.12 24–73 −4-6EP−4-6PCb −44−47 AUC 5, d1, q3w Stage II/III Neoadjuvant 55m 0.56 (0.25–1.27) 0.70 (0.22–2.26)
GeparSixto 2018 RCT(NCT01426880) 2011.8−2012.12 48 −PM*18w+Beva−PMCb*18w+Beva −157−158 AUC 1.5/2, d1, qw Stage II/III Neoadjuvant 47.3m 0.56 (0.34–0.93) 0.60 (0.32–1.12)
PATTERN 2020 RCT(NCT01216111) 2011.6−2016.4 18–70 −3CEF-3T-6PCb −322−325 AUC 2, d1, 8, 15, q28d N1-3, or T1c-4aN0, M0 Adjuvant 62m 0.65 (0.44–0.96) 0.71 (0.42–1.22)
Du 2020 RCT(NS) 2009.7−2015.10 48 −4EC-4T-6TCb −154−154 AUC 5, d1, q3w N1-3, or T1c-4aN0, M0 Adjuvant 66.9m 1.11 (0.65–1.89) 1.27 (0.49–3.32)
Iwase 2020 RCT(UMIN000003355) 2010.3−2011.9 47 (30–70) −3T-3CEF-3TCb-3CEF −38−37 AUC 5, d1, q3w Stage II/III A Neoadjuvant 6.6y 0.22 (0.06–0.82) 0.12 (0.01–0.96)

Definition of TNBC: in CALGB 40603: (ER/PR < 10%+, HER2−); in other eligible studies: (ER/PR−, HER2−).

When age range was not shown, the median age is filled in.

Abbreviations: RCT randomized controlled trials, TNBC triple-negative breast cancer, P/T paclitaxel/docetaxel, E epirubicin, C cyclophosphamide/CTX, F 5-fuorouracil, A anthracycline, Cb carboplatin, 1yCM oral metronomic chemotherapy of (CTX + MTX) for 1 year, PM paclitaxel+nonpegylated liposomal doxorubicin (NPLD, MyocetVR), B/Beva bevacizumab. No. number.