Oren Pasvolsky, Curtis Marcoux, Denái R. Milton, Babar Pal, Mark R. Tanner, Qaiser Bashir, Samer Srour, Jaehyun Lee, Neeraj Saini, Paul Lin, Jeremy Ramdial, Yago Nieto, Guilin Tang, Yosra Aljawai, Partow Kebriaei, Melody R. Becnel, Hans C. Lee, Krina K. Patel, Sheeba K. Thomas, Robert Z. Orlowski, Elizabeth J. Shpall, Richard E. Champlin, Muzaffar H. Qazilbash
{"title":"接受前期自体造血干细胞移植的多发性骨髓瘤患者的最佳输注 CD34+ 细胞剂量","authors":"Oren Pasvolsky, Curtis Marcoux, Denái R. Milton, Babar Pal, Mark R. Tanner, Qaiser Bashir, Samer Srour, Jaehyun Lee, Neeraj Saini, Paul Lin, Jeremy Ramdial, Yago Nieto, Guilin Tang, Yosra Aljawai, Partow Kebriaei, Melody R. Becnel, Hans C. Lee, Krina K. Patel, Sheeba K. Thomas, Robert Z. Orlowski, Elizabeth J. Shpall, Richard E. Champlin, Muzaffar H. Qazilbash","doi":"10.1038/s41408-024-01165-w","DOIUrl":null,"url":null,"abstract":"<p>Autologous transplantation remains the standard of care for eligible multiple myeloma (MM) patients, yet optimal CD34<sup>+</sup> cell dose remains unclear. We conducted a retrospective study on MM patients undergoing upfront transplant between 2005 and 2021 and divided them into low (≤2.5 × 10<sup>6</sup> cells/kg) and high (>2.5 × 10<sup>6</sup> cells/kg) CD34<sup>+</sup> dose groups. We included 2479 patients, 95 in the low CD34<sup>+</sup> group and 2384 in the high CD34<sup>+</sup> group. Patients in the low CD34<sup>+</sup> group were older (63.2 vs 61.1 years, <i>p</i> = 0.013), more often had R-ISS III (19% vs 9%, <i>p</i> = 0.014), received plerixafor (60% vs 35%, <i>p</i> < 0.001) and transplanted after 2009 (88% vs 80%, <i>p</i> = 0.047). Time to neutrophil and platelet recovery was longer in the low CD34<sup>+</sup> group. Median PFS and OS were lower in the low CD34<sup>+</sup> group (31.6 vs. 43.6 months, <i>p</i> = 0.011 and 76.4 vs. 108.2 months, <i>p</i> < 0.001, respectively). Evaluation of incrementally higher CD34<sup>+</sup> dose did not show significant improvement in survival at thresholds >2.5 × 10<sup>6</sup> cells/kg. Multivariable analysis affirmed that CD34<sup>+</sup> >2.5 × 10<sup>6</sup> cells/kg was associated with better PFS (HR 0.71, <i>p</i> = 0.008) and OS (0.59, <i>p</i> < 0.001). After propensity score matching, a CD34<sup>+</sup> dose >2.5 × 10<sup>6</sup> cells/kg remained a predictor of better OS (0.42, <i>p</i> < 0.001). In conclusion, CD34<sup>+</sup> dose >2.5 × 10<sup>6</sup> cells/kg was associated with improved survival, without any additional benefit at incrementally higher doses.</p>","PeriodicalId":8989,"journal":{"name":"Blood Cancer Journal","volume":"41 1","pages":""},"PeriodicalIF":12.9000,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimal infused CD34+ cell dose in multiple myeloma patients undergoing upfront autologous hematopoietic stem cell transplantation\",\"authors\":\"Oren Pasvolsky, Curtis Marcoux, Denái R. Milton, Babar Pal, Mark R. Tanner, Qaiser Bashir, Samer Srour, Jaehyun Lee, Neeraj Saini, Paul Lin, Jeremy Ramdial, Yago Nieto, Guilin Tang, Yosra Aljawai, Partow Kebriaei, Melody R. Becnel, Hans C. Lee, Krina K. Patel, Sheeba K. Thomas, Robert Z. Orlowski, Elizabeth J. Shpall, Richard E. Champlin, Muzaffar H. Qazilbash\",\"doi\":\"10.1038/s41408-024-01165-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Autologous transplantation remains the standard of care for eligible multiple myeloma (MM) patients, yet optimal CD34<sup>+</sup> cell dose remains unclear. We conducted a retrospective study on MM patients undergoing upfront transplant between 2005 and 2021 and divided them into low (≤2.5 × 10<sup>6</sup> cells/kg) and high (>2.5 × 10<sup>6</sup> cells/kg) CD34<sup>+</sup> dose groups. We included 2479 patients, 95 in the low CD34<sup>+</sup> group and 2384 in the high CD34<sup>+</sup> group. Patients in the low CD34<sup>+</sup> group were older (63.2 vs 61.1 years, <i>p</i> = 0.013), more often had R-ISS III (19% vs 9%, <i>p</i> = 0.014), received plerixafor (60% vs 35%, <i>p</i> < 0.001) and transplanted after 2009 (88% vs 80%, <i>p</i> = 0.047). Time to neutrophil and platelet recovery was longer in the low CD34<sup>+</sup> group. Median PFS and OS were lower in the low CD34<sup>+</sup> group (31.6 vs. 43.6 months, <i>p</i> = 0.011 and 76.4 vs. 108.2 months, <i>p</i> < 0.001, respectively). Evaluation of incrementally higher CD34<sup>+</sup> dose did not show significant improvement in survival at thresholds >2.5 × 10<sup>6</sup> cells/kg. Multivariable analysis affirmed that CD34<sup>+</sup> >2.5 × 10<sup>6</sup> cells/kg was associated with better PFS (HR 0.71, <i>p</i> = 0.008) and OS (0.59, <i>p</i> < 0.001). After propensity score matching, a CD34<sup>+</sup> dose >2.5 × 10<sup>6</sup> cells/kg remained a predictor of better OS (0.42, <i>p</i> < 0.001). In conclusion, CD34<sup>+</sup> dose >2.5 × 10<sup>6</sup> cells/kg was associated with improved survival, without any additional benefit at incrementally higher doses.</p>\",\"PeriodicalId\":8989,\"journal\":{\"name\":\"Blood Cancer Journal\",\"volume\":\"41 1\",\"pages\":\"\"},\"PeriodicalIF\":12.9000,\"publicationDate\":\"2024-10-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Blood Cancer Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1038/s41408-024-01165-w\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Blood Cancer Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41408-024-01165-w","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEMATOLOGY","Score":null,"Total":0}
Autologous transplantation remains the standard of care for eligible multiple myeloma (MM) patients, yet optimal CD34+ cell dose remains unclear. We conducted a retrospective study on MM patients undergoing upfront transplant between 2005 and 2021 and divided them into low (≤2.5 × 106 cells/kg) and high (>2.5 × 106 cells/kg) CD34+ dose groups. We included 2479 patients, 95 in the low CD34+ group and 2384 in the high CD34+ group. Patients in the low CD34+ group were older (63.2 vs 61.1 years, p = 0.013), more often had R-ISS III (19% vs 9%, p = 0.014), received plerixafor (60% vs 35%, p < 0.001) and transplanted after 2009 (88% vs 80%, p = 0.047). Time to neutrophil and platelet recovery was longer in the low CD34+ group. Median PFS and OS were lower in the low CD34+ group (31.6 vs. 43.6 months, p = 0.011 and 76.4 vs. 108.2 months, p < 0.001, respectively). Evaluation of incrementally higher CD34+ dose did not show significant improvement in survival at thresholds >2.5 × 106 cells/kg. Multivariable analysis affirmed that CD34+ >2.5 × 106 cells/kg was associated with better PFS (HR 0.71, p = 0.008) and OS (0.59, p < 0.001). After propensity score matching, a CD34+ dose >2.5 × 106 cells/kg remained a predictor of better OS (0.42, p < 0.001). In conclusion, CD34+ dose >2.5 × 106 cells/kg was associated with improved survival, without any additional benefit at incrementally higher doses.
期刊介绍:
Blood Cancer Journal is dedicated to publishing high-quality articles related to hematologic malignancies and related disorders. The journal welcomes submissions of original research, reviews, guidelines, and letters that are deemed to have a significant impact in the field. While the journal covers a wide range of topics, it particularly focuses on areas such as:
Preclinical studies of new compounds, especially those that provide mechanistic insights
Clinical trials and observations
Reviews related to new drugs and current management of hematologic malignancies
Novel observations related to new mutations, molecular pathways, and tumor genomics
Blood Cancer Journal offers a forum for expedited publication of novel observations regarding new mutations or altered pathways.