TY - JOUR
T1 - Improved survival of multiple myeloma patients treated with autologous transplantation in the modern era of new medicine
AU - the working group of the Japan Society for Transplantation, Cellular Therapy
AU - Shimazu, Yutaka
AU - Mizuno, Shohei
AU - Fuchida, Shin ichi
AU - Suzuki, Kazuhito
AU - Tsukada, Nobuhiro
AU - Hanagaishi, Akira
AU - Itagaki, Mitsuhiro
AU - Kataoka, Keisuke
AU - Kako, Shinichi
AU - Sakaida, Emiko
AU - Yoshioka, Satoshi
AU - Iida, Shinsuke
AU - Doki, Noriko
AU - Oyake, Tatsuo
AU - Ichinohe, Tatsuo
AU - Kanda, Yoshinobu
AU - Astuta, Yoshiko
AU - Takamatsu, Hiroyuki
N1 - Funding Information:
This study was undertaken with the support of the MM working group in JSTCT. This work was supported in part by the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from the Japan Agency for Medical Research and Development (Grant 18ek0510023h0002).
Publisher Copyright:
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2021/12
Y1 - 2021/12
N2 - New drugs for multiple myeloma (MM) have dramatically improved patients’ overall survival (OS). Autologous stem cell transplantation (ASCT) remains the mainstay for transplant-eligible MM patients. To investigate whether the post-ASCT prognosis of MM patients has been improved by new drugs, we undertook a retrospective observational analysis using the Transplant Registry Unified Management Program database in Japan. We analyzed 7323 patients (4135 men and 3188 women; median age, 59 years; range 16-77 years) who underwent upfront ASCT between January 2007 and December 2018. We categorized them by when they underwent ASCT according to the drugs’ introduction in Japan: group 1 (2007-2010), group 2 (2011-2016), and group 3 (2017-2018). We compared the groups’ post-ASCT OS. The 2-year OS rates (95% confidence interval [CI]) of groups 1, 2, and 3 were 85.8% (84.1%-87.4%), 89.1% (88.0%-90.1%), and 92.3% (90.0%-94.2%) (P <.0001) and the 5-year OS (95% CI) rates were 64.9% (62.4%-67.3%), 71.6% (69.7%-73.3%), and not applicable, respectively (P <.0001). A multivariate analysis showed that the post-ASCT OS was superior with these factors: age less than 65 years, performance status 0/1, low International Staging System (ISS) stage, receiving SCT for 180 days or less post-diagnosis, better treatment response pre-ASCT, later year of ASCT, and receiving SCT twice. A subgroup analysis showed poor prognoses for the patients with unfavorable karyotype and poor treatment response post-ASCT. The post-ASCT OS has thus improved over time (group 1 < 2 < 3) with the introduction of new drugs for MM. As the prognosis of high-risk-karyotype patients with ISS stage III remains poor, their treatment requires improvement.
AB - New drugs for multiple myeloma (MM) have dramatically improved patients’ overall survival (OS). Autologous stem cell transplantation (ASCT) remains the mainstay for transplant-eligible MM patients. To investigate whether the post-ASCT prognosis of MM patients has been improved by new drugs, we undertook a retrospective observational analysis using the Transplant Registry Unified Management Program database in Japan. We analyzed 7323 patients (4135 men and 3188 women; median age, 59 years; range 16-77 years) who underwent upfront ASCT between January 2007 and December 2018. We categorized them by when they underwent ASCT according to the drugs’ introduction in Japan: group 1 (2007-2010), group 2 (2011-2016), and group 3 (2017-2018). We compared the groups’ post-ASCT OS. The 2-year OS rates (95% confidence interval [CI]) of groups 1, 2, and 3 were 85.8% (84.1%-87.4%), 89.1% (88.0%-90.1%), and 92.3% (90.0%-94.2%) (P <.0001) and the 5-year OS (95% CI) rates were 64.9% (62.4%-67.3%), 71.6% (69.7%-73.3%), and not applicable, respectively (P <.0001). A multivariate analysis showed that the post-ASCT OS was superior with these factors: age less than 65 years, performance status 0/1, low International Staging System (ISS) stage, receiving SCT for 180 days or less post-diagnosis, better treatment response pre-ASCT, later year of ASCT, and receiving SCT twice. A subgroup analysis showed poor prognoses for the patients with unfavorable karyotype and poor treatment response post-ASCT. The post-ASCT OS has thus improved over time (group 1 < 2 < 3) with the introduction of new drugs for MM. As the prognosis of high-risk-karyotype patients with ISS stage III remains poor, their treatment requires improvement.
KW - autologous stem cell transplantation
KW - multiple myeloma
KW - new medicine
KW - overall survival
KW - prognosis
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UR - http://www.scopus.com/inward/citedby.url?scp=85118237458&partnerID=8YFLogxK
U2 - 10.1111/cas.15163
DO - 10.1111/cas.15163
M3 - Article
C2 - 34644446
AN - SCOPUS:85118237458
SN - 1347-9032
VL - 112
SP - 5034
EP - 5045
JO - Cancer science
JF - Cancer science
IS - 12
ER -