Final analyses of OPTiM: a randomized phase III trial of talimogene laherparepvec versus granulocyte-macrophage colony-stimulating factor in unresectable stage III- IV melanoma

被引:306
作者
Andtbacka, Robert H., I [1 ]
Collichio, Frances [2 ]
Harrington, Kevin J. [3 ]
Middleton, Mark R. [4 ]
Downey, Gerald [5 ]
Ohrling, Katarina [6 ]
Kaufman, Howard L. [7 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[2] Univ N Carolina, Med Ctr, Chapel Hill, NC 27515 USA
[3] Royal Marsden Hosp NIHR Biomed Res Ctr, Inst Canc Res, London SW3 6JB, England
[4] NIHR Biomed Res Ctr, Oxford, England
[5] Amgen Ltd, Global Biostat Sci, Cambridge, England
[6] Amgen Europe GmbH, Med Dev, Zug, Switzerland
[7] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
Efficacy; Final analysis; Melanoma; Overall survival; Talimogene laherparepvec; IPILIMUMAB; PEMBROLIZUMAB; ANTI-PD-1; SAFETY; CHEMOTHERAPY;
D O I
10.1186/s40425-019-0623-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Talimogene laherparepvec is an oncolytic immunotherapy approved in the US, Europe, Australia and Switzerland. We report the final planned analysis of OPTiM, a randomized open-label phase III trial in patients with unresectable stage IIIB-IVM1c melanoma. Methods: Patients were randomized 2:1 to receive intratumoral talimogene laherparepvec or subcutaneous recombinant GM-CSF. In addition to overall survival (OS), durable response rate (DRR), objective response rate (ORR), complete responses (CR), and safety are also reported. All final analyses are considered to be descriptive and treatment responses were assessed by the investigators. Results: Of 436 patients in the intent-to-treat population, 295 were allocated to talimogene laherparepvec and 141 to GM-CSF. Median follow-up in the final OS analysis was 49 months. Median OS was 23.3 months (95% confidence interval [CI], 19.5-29.6) and 18.9 months (95% CI, 16.0-23.7) in the talimogene laherparepvec and GM-CSF arms, respectively (unstratified hazard ratio, 0.79; 95% CI, 0.62-1.00; p = 0.0494 [descriptive]). DRR was 19.0 and 1.4% (unadjusted odds ratio, 16.6; 95% CI, 4.0-69.2; p < 0.0001); ORR was 31.5 and 6.4%. Fifty (16.9%) and 1 (0.7%) patient in the talimogene laherparepvec and GM-CSF arms, respectively, achieved CR. In talimogene laherparepvec-treated patients, median time to CR was 8.6 months; median CR duration was not reached. Among patients with a CR, 88.5% were estimated to survive at a 5-year landmark analysis. Talimogene laherparepvec efficacy was more pronounced in stage IIIB-IVM1a melanoma as already described in the primary analysis. The safety reporting was consistent with the primary OPTiM analysis. Conclusions: In this final planned OPTiM analysis, talimogene laherparepvec continued to result in improved longer-term efficacy versus GM-CSF and remained well tolerated. The final analysis also confirms that talimogene laherparepvec was associated with durable CRs that were associated with prolonged survival.
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页数:11
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