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Elotuzumab has been shown to promote natural killer (<jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>) cell stimulation and antibody\u2010dependent cellular cytotoxicity (<jats:styled-content style=\"fixed-case\">ADCC<\/jats:styled-content>) <jats:italic>in\u00a0vitro<\/jats:italic>. <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>56<jats:sup>dim<\/jats:sup> (<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>56<jats:sup>dim<\/jats:sup>\/<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>16<jats:sup>+<\/jats:sup>\/<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>3<jats:sup>\u2212<\/jats:sup>\/<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>45<jats:sup>+<\/jats:sup>) <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells represent the primary subset responsible for elotuzumab\u2010induced <jats:styled-content style=\"fixed-case\">ADCC<\/jats:styled-content>. In this phase <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>, non\u2010randomized study (<jats:styled-content style=\"fixed-case\">NCT<\/jats:styled-content>01441973), patients with <jats:styled-content style=\"fixed-case\">SMM<\/jats:styled-content> received elotuzumab 20\u00a0mg\/kg intravenously (cycle 1: days 1, 8; monthly thereafter) or 10\u00a0mg\/kg (cycles 1, 2: weekly; every 2\u00a0weeks thereafter). The primary endpoint was the relationship between baseline proportion of bone marrow\u2010derived <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>56<jats:sup>dim<\/jats:sup> <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells and maximal M protein reduction; secondary endpoints included overall response rate (<jats:styled-content style=\"fixed-case\">ORR<\/jats:styled-content>) and progression\u2010free survival (<jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content>). Fifteen patients received 20\u00a0mg\/kg and 16 received 10\u00a0mg\/kg; combined data arepresented. At database lock (<jats:styled-content style=\"fixed-case\">DBL<\/jats:styled-content>, September 2014), no association was found between baseline <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>56<jats:sup>dim<\/jats:sup> <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell proportion and maximal M protein reduction. With minimum 28\u00a0months' follow\u2010up (<jats:styled-content style=\"fixed-case\">DBL<\/jats:styled-content>: January 2016), <jats:styled-content style=\"fixed-case\">ORR<\/jats:styled-content> (90% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>) was 10% (2\u00b77\u201323\u00b72) and 2\u2010year <jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content> rate was 69% (52\u201381%). Upper respiratory tract infections occurred in 18\/31 (58%) patients. Four (13%) patients experienced infusion reactions, all grade 1\u20132. Elotuzumab plus lenalidomide\/dexamethasone is under investigation for <jats:styled-content style=\"fixed-case\">SMM<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/bjh.15384","type":"journal-article","created":{"date-parts":[[2018,5,29]],"date-time":"2018-05-29T10:40:20Z","timestamp":1527590420000},"page":"495-503","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":37,"title":["Elotuzumab monotherapy in patients with smouldering multiple myeloma: a phase 2 study"],"prefix":"10.1111","volume":"182","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2934-6518","authenticated-orcid":false,"given":"Sundar","family":"Jagannath","sequence":"first","affiliation":[{"name":"The Tisch Cancer Institute, Mount Sinai Medical Center New York NY USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7565-2052","authenticated-orcid":false,"given":"Jacob","family":"Laubach","sequence":"additional","affiliation":[{"name":"Harvard Medical School Jerome Lipper Multiple Myeloma Center Dana\u2010Farber Cancer Institute Boston MA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ellice","family":"Wong","sequence":"additional","affiliation":[{"name":"Section\u00a0of Medical Oncology Department of Medicine Yale University New Haven CT USA"},{"name":"Department of Medicine VA Connecticut Healthcare System West Haven CT USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Keith","family":"Stockerl\u2010Goldstein","sequence":"additional","affiliation":[{"name":"Division of Oncology Washington University St Louis MO USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cara","family":"Rosenbaum","sequence":"additional","affiliation":[{"name":"Division of Hematology and Medical Oncology Weill Cornell Medicine Cornell University New York NY USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Madhav","family":"Dhodapkar","sequence":"additional","affiliation":[{"name":"Section\u00a0of Hematology Department of Medicine Yale University New Haven CT USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ying\u2010Ming","family":"Jou","sequence":"additional","affiliation":[{"name":"Bristol\u2010Myers\u00a0Squibb Princeton NJ USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mark","family":"Lynch","sequence":"additional","affiliation":[{"name":"Bristol\u2010Myers\u00a0Squibb Princeton NJ USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Robbins","sequence":"additional","affiliation":[{"name":"Bristol\u2010Myers\u00a0Squibb Princeton NJ USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Suresh","family":"Shelat","sequence":"additional","affiliation":[{"name":"Bristol\u2010Myers\u00a0Squibb Princeton NJ USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenneth C.","family":"Anderson","sequence":"additional","affiliation":[{"name":"Harvard Medical School Jerome Lipper Multiple Myeloma Center Dana\u2010Farber Cancer Institute Boston MA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7426-8865","authenticated-orcid":false,"given":"Paul G.","family":"Richardson","sequence":"additional","affiliation":[{"name":"Harvard Medical School Jerome Lipper Multiple Myeloma Center Dana\u2010Farber Cancer Institute Boston MA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2018,5,29]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1182\/blood.V112.11.108.108","article-title":"Elotuzumab (HuLuc63) activates CD56dim natural killer cells and monocytes resulting in the release of IP\u201010 and MCP\u20101. 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