Abstract
Background: ML18147 evaluated continued bevacizumab with second-line chemotherapy for patients with metastatic colorectal cancer (mCRC) progressing after the standard first-line bevacizumab-containing therapy. Patients and methods: Evaluating outcomes according to tumor Kirsten rat sarcoma virus oncogene (KRAS) status was an exploratory analysis. KRAS data were collected from local laboratories (using their established methods) and/or from a central laboratory (mutation-specific Scorpion amplification-refractory mutation system). No adjustment was made for multiplicity; analyses were not powered to detect statistically significant differences. Results: Of 820 patients, 616 (75%) had unambiguous KRAS data; 316 (51%) had KRAS wild-type tumors and 300 (49%) had mutant KRAS tumors. The median progression-free survival (PFS) was 6.4 months for bevacizumab plus chemotherapy and 4.5 months for chemotherapy [P < 0.0001; HR = 0.61; 95% confidence interval (CI): 0.49-0.77] for wild-type KRAS and 5.5 and 4.1 months, respectively (P = 0.0027; HR = 0.70; 95% CI: 0.56-0.89) for mutant KRAS. The median overall survival (OS) was 15.4 and 11.1 months, respectively (P = 0.0052; HR = 0.69; 95% CI: 0.53-0.90) for wild-type KRAS and 10.4 versus 10.0 months, respectively (P = 0.4969; HR = 0.92; 95% CI: 0.71-1.18) for mutant KRAS. In both analyses, no treatment interaction by KRAS status was observed (PFS, P = 0.4436; OS, P = 0.1266). Conclusions: Bevacizumab beyond first progression represents an option for patients with mCRC treated with bevacizumab plus standard first-line chemotherapy, independent of KRAS status.
Originalsprache | Englisch |
---|---|
Zeitschrift | Annals of Oncology |
Jahrgang | 24 |
Ausgabenummer | 9 |
Seiten (von - bis) | 2342-2349 |
Seitenumfang | 8 |
ISSN | 0923-7534 |
DOIs | |
Publikationsstatus | Veröffentlicht - 09.2013 |
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in: Annals of Oncology, Jahrgang 24, Nr. 9, 09.2013, S. 2342-2349.
Publikation: Beiträge in Fachzeitschriften › Zeitschriftenaufsätze › Forschung › Begutachtung
TY - JOUR
T1 - Bevacizumab plus chemotherapy continued beyond first progression in patients withmetastatic colorectal cancer previously treated with bevacizumab plus chemotherapy: ML18147 study KRAS subgroup findings
AU - Kubicka Prof., Stefan
AU - Greil, R.
AU - André, T.
AU - Bennouna, J.
AU - Sastre, J.
AU - Van Cutsem, E.
AU - Von Moos, R.
AU - Österlund, P.
AU - Reyes-Rivera, I.
AU - Müller, T.
AU - Makrutzki, M.
AU - Arnold, D.
AU - Andel, J.
AU - Balcke, P.
AU - Benedicic, B.
AU - Eisterer, W.
AU - Fridrik, M.
AU - Jagdt, B.
AU - Keil, F.
AU - Kretschmer, A.
AU - Krippl, P.
AU - Oexle, H.
AU - Pecherstorfer, M.
AU - Samonigg, H.
AU - Schmid, M.
AU - Thaler, J.
AU - Tinchon, C.
AU - Weiss, H.
AU - Arts, J.
AU - De Man, M.
AU - Demolin, G.
AU - Janssens, J.
AU - Polus, M.
AU - Benczikova, B.
AU - Melichar, B.
AU - Prausova, J.
AU - Vitek, P.
AU - Andersen, F. Z.
AU - Jensen, B. B.
AU - Keldsen, N.
AU - Østerlind, K.
AU - Vistisen, K.
AU - Elme, A.
AU - Magi, A.
AU - Ojamaa, K.
AU - Ristamäki, R.
AU - Salminen, T.
AU - Ben Abdelghani, M.
AU - Bouche, O.
AU - Borg, C.
AU - Bouhier-Leporrier, K.
AU - Breysacher, G.
AU - Chone, L.
AU - Clavero Fabri, M. C.
AU - Deplanque, G.
AU - Desseigne, F.
AU - Dourthe, L. M.
AU - Ezenfis, J.
AU - Faroux, R.
AU - François, E.
AU - Garnier, C.
AU - Gaspard, M. H.
AU - Hebbar, M.
AU - Illory, J. F.
AU - Kaminsky, M. C.
AU - Lecomte, T.
AU - Legoux, J. L.
AU - Levache, B.
AU - Lobry, C.
AU - Lotz, J. P.
AU - Mabro, M.
AU - Manet-Lacombe, S.
AU - Manfredi, S.
AU - Matysiak Budnik, T.
AU - Miglianico, L.
AU - Mineur, L.
AU - Moullet, I.
AU - Naman, H.
AU - Nouyrigat, P.
AU - Oziel-Taieb, S.
AU - Perrier, H.
AU - Pezet, D.
AU - Philip, J.
AU - Pottier, V.
AU - Porneuf, M.
AU - Ramdani, M.
AU - Re, D.
AU - Rinaldi, Y.
AU - Spaeth, D.
AU - Taieb, J.
AU - Terrebonne, E.
AU - Texereau, P.
AU - Thirot Bidault, A.
AU - Tournigand, C.
AU - Tubiana-Mathieu, N.
AU - Vantelon, J. M.
AU - Viret, F.
AU - Ychou, M.
AU - Bangerter, M.
AU - Bertram, M. E.
AU - Bohnsteen, B.
AU - Brinkmann, L.
AU - Caca, K.
AU - Constantin, C.
AU - Cordes, H. J.
AU - Dietrich, G.
AU - Eggert, J.
AU - Engel, E.
AU - Fahlke, J.
AU - Fensterer, H.
AU - Florschütz, A.
AU - Folprecht, G.
AU - Forstbauer, H.
AU - Freier, W.
AU - Freund, M.
AU - Frickhofen, N.
AU - Gäbele, E.
AU - Geißler, M.
AU - Gieseler, F.
AU - Göhler, T.
AU - Graeven, U.
AU - Groschek, M.
AU - Grundeis, M.
AU - Hacker, U.
AU - Hagen, V.
AU - Hebart, H. F.
AU - Hegewisch-Becker, S.
AU - Heike, M.
AU - Herrmann, T.
AU - Hildebrandt, B.
AU - Höffkes, H. G.
AU - Hübner, G.
AU - Hübner, J.
AU - Kettner, E.
AU - Kneba, M.
AU - Kohnke, J. W.
AU - Kojouharoff, G.
AU - König, C.
AU - Kretzschmar, A.
AU - Kröning, H.
AU - Kürner, K.
AU - Lammert, F.
AU - Lerchenmüller, C.
AU - Lück, A.
AU - Meiler, J.
AU - Mergenthaler, H. G.
AU - Müller, L.
AU - Müller-Naendrup, C.
AU - Nusch, A.
AU - Papke, J.
AU - Porschen, R.
AU - Rädle, J.
AU - Reddemann, C.
AU - Ridwelski, K.
AU - Riera-Knorrenschild, J.
AU - Rudi, J.
AU - Schmalenberger, A.
AU - Schimanski, C. C.
AU - Schlegel, F.
AU - Schlichting, C.
AU - Schmidt, P.
AU - Schmiegel, W.
AU - Schmitz, S.
AU - Schulze-Bergkamen, H.
AU - Schwaner, I.
AU - Schwarzer, A.
AU - Schwerdtfeger, M.
AU - Selbach, J.
AU - Sieber, M.
AU - Siebler, J.
AU - Staib, P.
AU - Stauch, M.
AU - Steffens, C. C.
AU - Stübs, P.
AU - Tischendorf, J.
AU - Trarbach, T.
AU - Tummes, D.
AU - Valdix, A. R.
AU - Vogel, A.
AU - Von Wichert, G. P.L.
AU - Walther, M.
AU - Welslau, W.
AU - Wilhelm, G.
AU - Wobster, H.
AU - Wolf, T.
AU - Zeigenhagen, N.
AU - Zomorodbaksch, B.
AU - Batman, E.
AU - Bloemendal, H. J.
AU - Kehrer, D. F.S.
AU - Guren, T.
AU - Indrebø, G.
AU - Kersten, C.
AU - Soerbye, H.
AU - Fragoso, M.
AU - Fragoso, R.
AU - Mellidez, J. C.
AU - Sa, A.
AU - Aljobran, A.
AU - Darwish, T.
AU - Alonso-Orduna, V.
AU - Aparicio, J.
AU - Aranda, E.
AU - Bosch, C.
AU - Galan-Brotons, A.
AU - Busquier Hernandez, I.
AU - Camara, J. C.
AU - Campos Cervera, J. M.
AU - Carlos Garcia Giron, C.
AU - Del Prado, P. M.
AU - Donnay, O.
AU - Escudero, P.
AU - Falco, E.
AU - Gallego Plazas, J.
AU - Garcia Alfonso, P.
AU - Gonzalez Flores, E.
AU - Gravalos, C.
AU - Guardeno, R.
AU - Juárez, A.
AU - Lopez Ladron, A.
AU - Losa Gaspa, F.
AU - MaVicent Vergé, J.
AU - Marcuello Gaspar, E.
AU - Massuti Sureda, B.
AU - Molina, J.
AU - Montero, I. C.
AU - Muñoa, A. L.
AU - Naranjo, M. B.
AU - Oruezabal Moreno, M. J.
AU - Pachón Olmos, V.
AU - Pericay, C.
AU - Reina Zoilo, J. J.
AU - Rivera, F.
AU - Ruiz Casado, A.
AU - Safont, M. J.
AU - Salud Salvia, A.
AU - Tobena, M.
AU - Toral, J. C.
AU - Valenti, V.
AU - Valladares Ayerbes, M.
AU - Vieitez, J. M.
AU - Vera, R.
AU - Vieitez, J. M.
AU - Berglund, A.
AU - Fernebro, E.
AU - Hess-Umbricht, V.
AU - Pless, M.
AU - Popescu, R.
AU - Winterhalder, R.
N1 - Funding Information: DA has received consulting fees or honoraria from Roche, Merck, and Amgen and research funding from Roche. TA is a consultant for Roche and Amgen and has received honoraria from Roche, Amgen, and Merck Serono. JB is an advisory board member for and has received honoraria from Roche. SK has received consulting fees/honoraria, travel grants, and payment for lectures including service on speakers bureaus from Roche. MM is an employee of Roche. TM is an employee of Roche Genentech. PÖ has received consulting fees, honoraria, travel grants, or lecturing fees from Roche, Amgen, and Merck, research funding from Roche, and is an advisory board member for Roche, Amgen, Bayer, Sanofi Oncology, and Merck. IR-R is an employee of Roche. JS has received honoraria for consultant or advisory activity from Sanofi-Aventis and Roche. EVC has received research funding from Roche, paid to his institution. RvM is an advisory board member for Roche, Novartis, Merck, Amgen, and Bristol-Myers Squibb and has received an unrestricted research grant from Roche, Amgen, and Merck. RG has no conflict to declare. Funding Information: This study was sponsored by F. Hoffmann-La Roche. Support for third-party writing assistance for this manuscript was provided by F. Hoffmann-La Roche.
PY - 2013/9
Y1 - 2013/9
N2 - Background: ML18147 evaluated continued bevacizumab with second-line chemotherapy for patients with metastatic colorectal cancer (mCRC) progressing after the standard first-line bevacizumab-containing therapy. Patients and methods: Evaluating outcomes according to tumor Kirsten rat sarcoma virus oncogene (KRAS) status was an exploratory analysis. KRAS data were collected from local laboratories (using their established methods) and/or from a central laboratory (mutation-specific Scorpion amplification-refractory mutation system). No adjustment was made for multiplicity; analyses were not powered to detect statistically significant differences. Results: Of 820 patients, 616 (75%) had unambiguous KRAS data; 316 (51%) had KRAS wild-type tumors and 300 (49%) had mutant KRAS tumors. The median progression-free survival (PFS) was 6.4 months for bevacizumab plus chemotherapy and 4.5 months for chemotherapy [P < 0.0001; HR = 0.61; 95% confidence interval (CI): 0.49-0.77] for wild-type KRAS and 5.5 and 4.1 months, respectively (P = 0.0027; HR = 0.70; 95% CI: 0.56-0.89) for mutant KRAS. The median overall survival (OS) was 15.4 and 11.1 months, respectively (P = 0.0052; HR = 0.69; 95% CI: 0.53-0.90) for wild-type KRAS and 10.4 versus 10.0 months, respectively (P = 0.4969; HR = 0.92; 95% CI: 0.71-1.18) for mutant KRAS. In both analyses, no treatment interaction by KRAS status was observed (PFS, P = 0.4436; OS, P = 0.1266). Conclusions: Bevacizumab beyond first progression represents an option for patients with mCRC treated with bevacizumab plus standard first-line chemotherapy, independent of KRAS status.
AB - Background: ML18147 evaluated continued bevacizumab with second-line chemotherapy for patients with metastatic colorectal cancer (mCRC) progressing after the standard first-line bevacizumab-containing therapy. Patients and methods: Evaluating outcomes according to tumor Kirsten rat sarcoma virus oncogene (KRAS) status was an exploratory analysis. KRAS data were collected from local laboratories (using their established methods) and/or from a central laboratory (mutation-specific Scorpion amplification-refractory mutation system). No adjustment was made for multiplicity; analyses were not powered to detect statistically significant differences. Results: Of 820 patients, 616 (75%) had unambiguous KRAS data; 316 (51%) had KRAS wild-type tumors and 300 (49%) had mutant KRAS tumors. The median progression-free survival (PFS) was 6.4 months for bevacizumab plus chemotherapy and 4.5 months for chemotherapy [P < 0.0001; HR = 0.61; 95% confidence interval (CI): 0.49-0.77] for wild-type KRAS and 5.5 and 4.1 months, respectively (P = 0.0027; HR = 0.70; 95% CI: 0.56-0.89) for mutant KRAS. The median overall survival (OS) was 15.4 and 11.1 months, respectively (P = 0.0052; HR = 0.69; 95% CI: 0.53-0.90) for wild-type KRAS and 10.4 versus 10.0 months, respectively (P = 0.4969; HR = 0.92; 95% CI: 0.71-1.18) for mutant KRAS. In both analyses, no treatment interaction by KRAS status was observed (PFS, P = 0.4436; OS, P = 0.1266). Conclusions: Bevacizumab beyond first progression represents an option for patients with mCRC treated with bevacizumab plus standard first-line chemotherapy, independent of KRAS status.
UR - http://www.scopus.com/inward/record.url?scp=84883381780&partnerID=8YFLogxK
U2 - 10.1093/annonc/mdt231
DO - 10.1093/annonc/mdt231
M3 - Journal articles
C2 - 23852309
AN - SCOPUS:84883381780
SN - 0923-7534
VL - 24
SP - 2342
EP - 2349
JO - Annals of Oncology
JF - Annals of Oncology
IS - 9
ER -