Letter to the Editor

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Blood Res 2022; 57(1):

Published online March 31, 2022

https://doi.org/10.5045/br.2022.2021183

© The Korean Society of Hematology

Daratumumab monotherapy in relapsed and refractory multiple myeloma patients with severely compromised forced expiratory volume in one second

Jin-Hyo Kim, Sung-Soo Park, Jae-Ho Yoon, Sung-Eun Lee, Hee-Je Kim, Chang-Ki Min

Department of Hematology, Seoul St. Mary’s Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

Correspondence to : Sung-Soo Park
Department of Hematology, Seoul St. Mary’s Hematology Hospital, College of Medicine, The Catholic University of Korea, 222 Banpodaero, Seocho-gu, Seoul 06591, Korea
E-mail: sspark@catholic.ac.kr

Received: October 2, 2021; Revised: December 5, 2021; Accepted: December 29, 2021

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

TO THE EDITOR: Daratumumab monotherapy is approved to treat patients with relapsed or refractory multiple myeloma (RRMM) who have previously received three or more treatments, including a proteasome inhibitor and an immunomodulator or presenting with double refractoriness to proteasome inhibitors and immunomodulators [1]. Although daratumumab monotherapy has been introduced in real-world practice based on the results of phase 1 (GEN501) [2] and phase 2 clinical trials (SIRIUS) [3], the results of these clinical trials were limited to individuals with no severe comorbidities according to the trials’ design. For example, patients with respiratory impairment indicated by forced expiratory volume in one second (FEV1) of <50% were excluded from the GEN501 and SIRIUS trials. Accordingly, the safety of daratumumab monotherapy would be limited in these patients. Furthermore, the CD38, which is the target of daratumumab, is not only over-expressed on the multiple myeloma cells [4] but also widely presented on airway smooth muscle cells [5]. Due to general reports that altered CD38 expression on airway smooth muscle cells could contribute to airway hyperresponsiveness [6], the respiratory infusion-related reactions (IRRs), such as bronchospasms or dyspnea, are considered to require particular attention following infusion of daratumumab [2, 3]. Therefore, the administration of daratumumab to patients with FEV1s of <50% could present a difficult challenge. Nevertheless, a clinician could be forced to select a novel agent such as daratumumab for patients who do not fit the selection criteria of clinical trials if there are limited chemotherapeutic options for heavily treated patients with RRMM in real-world clinical practice. Thus, it is important to validate the real-world safety of daratumumab monotherapy for patients with severe comorbidities that make them unfit for clinical trials.

Herein, we report the cases of 3 patients who experienced manageable pulmonary manifestations after the administration of daratumumab monotherapy [7], despite decreased FEV1s of <50% at baseline. This study was approved by the Institutional Review Board of The Catholic University of Korea (KC21RASI0664) and was conducted in accordance with the Declaration of Helsinki.

Table 1 summarizes the baseline clinical characteristics of the 3 cases. At the baseline pulmonary function test assessment, the FEV1 was 43%, 40%, and 44% in case 1, case 2, and case 3, respectively. All patients received daratumumab monotherapy at a dose of 16 mg/kg, and the treatment plan was weekly for the first 8 weeks (cycles 1 and 2), then every 2 weeks from 9 to 24 weeks (cycles 3–6), then every four weeks thereafter (cycles 7 and higher). To prevent IRRs, the patients received 100 mg of intravenous methylprednisolone at the first and second daratumumab infusions. Other supportive care and preventive medications were administered as described in our previous reports [8]. The clinical outcomes of the 3 patients are summarized in Table 2. All adverse events were explored based on the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 [9].

Table 1 Patient baseline characteristics.

Case 1Case 2Case 3
Age/sex61/F71/F40/M
Type of disease at diagnosisIgGIgGLight chain disease
Light chain type at diagnosisKappaLambdaKappa
International staging system at diagnosisIIIIIIII
White blood cell count at baseline, ×109/L7.242.495.12
Absolute neutrophil count at baseline, ×109/L5.061.344.45
Absolute lymphocyte count at baseline, ×109/L1.150.800.31
Hemoglobin at baseline, g/dL12.18.69.1
Platelet count at baseline, ×106/L1115422
Albumin at baseline, g/dL3.62.94.1
b2-microglobulin at baseline, mg/mL3.762.135N/A
Serum creatinine at baseline, mg/dL1.521.250.46
Lactate dehydrogenase at baseline, IU/L (reference, 250–450 IU/L)429739633
Forced expiratory volume at one second at baseline, %434044
Presence of plasmacytoma at baselineYesNoYes
Interval from diagnosis to treatment of daratumumab, months904780
Serum M protein at baseline, g/dL0.993.250
Serum kappa/lambda at baseline, mg/day122.5/14.58.14/368.511.41/<0.76
Presence high-risk cytogenetics at diagnosis
del(17p)NegativeNegativeNegative
t(14;16)NegativeNegativeNegative
t(4;14)NegativeNegativeNegative
Other cytogenetic abnormality at diagnosis
Amp(1q21)NegativePositiveNegative
t(11;14)NegativeNegativeNegative
del(13q)NegativePositiveNegative

Abbreviation: N/A, not available.



Table 2 Outcomes of daratumumab monotherapy.

Case 1Case 2Case 3
N of prior treatments lines before daratumumab435
Interval from diagnosis to treatment of daratumumab, months904780
Administered cycles of daratumumab (total time of infusion)1 cycle (2 times)5 cycles (13 times)1 cycle (4 times)
Best response of daratumumab monotherapyRefractoryMinimal responseRefractory
Survival statusDeath at 2 monthsDeath at 19 monthsDeath at 1 month
Adverse events, infusion-related reaction
Dyspnea, grade2--
CRP elevation, grade3--
Cause of deathProgression of diseaseProgression of diseaseProgression of disease


Case 1

A 61-year-old female, who was diagnosed with multiple myeloma type IgG-kappa 8 years earlier, had relapsed following first-line treatment with autologous stem cell transplantation after vincristine, doxorubicin, and dexamethasone; second-line treatment consisting of eight cycles of bortezomib and dexamethasone; third-line therapy with lenalidomide plus dexamethasone (RD), and fourth-line treatment with pomalidomide, cyclophosphamide, and dexamethasone (PCD). She also presented with relapsed and refractory response status following 13 cycles of PCD.

Before daratumumab monotherapy, the baseline assessment showed a monoclonal protein level of 0.99 g/dL and serum-free light chain differences of 108.00 mg/L with a predominance of kappa chains. The laboratory and radiological tests did not indicate specific implications related to multiple myeloma. Although an IRR grade 2 dyspnea developed on the first day of daratumumab infusion, this event was spontaneously resolved by supportive care with corticosteroids and antihistamine. She also experienced a grade 3 adverse event of elevated C-reactive protein levels. Therefore, we decided to postpone the second infusion of daratumumab to a week later than planned. In the second daratumumab infusion, there was no significant IRR. Her course of RRMM was refractory despite two cycles of daratumumab monotherapy, and she died of disease progression (Fig. 1A).

Fig. 1. Treatment course and adverse events of case 1 (A), case 2 (B), and case 3 (C).

Case 2

A 71-year-old female with multiple myeloma type IgG lambda was diagnosed 3 years earlier and had relapsed. The patient was initially treated with nine cycles of bortezomib, melphalan, and prednisone, which resulted in relapsed and refractory responses. The patient was subsequently treated with 20 cycles of RD, and a partial response was achieved, but the RD course was terminated due to grade 3 neutropenia. Third-line treatment with eight cycles of PCD was administered, and a minimal response was observed, but the patient relapsed. The fourth-line treatment was daratumumab monotherapy.

The monoclonal protein assessment and serum-free light chain differences were 3.25 g/dL and 360.37 mg/L, respectively. Baseline magnetic resonance imaging indicated an L1 compression fracture related to RRMM manifestation. After daratumumab monotherapy, there was no IRR. The best response to daratumumab monotherapy was minimal, with a monoclonal protein value of 2.07 g/dL. However, the disease progressed after five cycles. Despite administering a next-line treatment with thalidomide, cyclophosphamide, and dexamethasone, the patient died due to disease progression (Fig. 1B).

Case 3

A 40-year-old male had kappa light chain multiple myeloma diagnosed 7 years earlier. The patient was treated with two cycles of bortezomib, melphalan, and prednisone, followed by autologous stem cell transplantation and tandem allogeneic stem cell transplantation as the first-line treatment. Eight cycles of bortezomib and dexamethasone were administered for the first relapse. He was treated with six RD cycles for the second relapse, which resulted in the partial response, but showed a relapse and refectory response with multifocal bone lytic lesions. Despite the fourth-line treatment with five cycles of pomalidomide and dexamethasone, the patient became refractory, and the multifocal bone lesions progressed. The Fifth-line treatment with carfilzomib-dexamethasone was initiated but was also limited to a refractory response with multifocal extramedullary plasmacytomas (Fig. 1C). The sixth-line treatment was with daratumumab monotherapy.

Baseline computed tomography showed multiple plasmacytomas at the left orbit and periauricular regions, upper back, left apical axilla, abdominal wall, and left thigh (Fig. 1C). Baseline monoclonal protein was negative in electrophoresis, and there was no significant difference (1.41 mg/L) between the quantity of serum-free light chains. During daratumumab monotherapy, there was no IRR, but the patient died due to disease progression.

Real-world experience with daratumumab monotherapy has continuously been reported since its approval as a treatment for RRMM [10-13]. The studies highlighted that daratumumab monotherapy was safely administered to patients, including those who did not fit the clinical trials selection criteria. Our previous study reported the favorable efficacy and infusion-related safety of 64 RRMM patients who would be unfit to participate in the GEN501 or SIRIUS due to comorbidities including an Eastern Cooperative Oncology Group Performance Status of ≥3, meningeal involvement, anemia of <75 g/L, neutropenia of <1.0×109/L, thrombocytopenia <75×109/L, and renal insufficiency with a glomerular filtration rate of <20 mL/min/1.73 m2. No reported IRRs interrupted the daratumumab schedule, and all IRRs were manageable with supportive care [8].

To the best of our knowledge, this study reports the first daratumumab monotherapy safety profile in patients with decreased lung function demonstrated by an FEV1 <50%. Although 1 in 3 patients experienced a respiratory IRR, it was manageable with supportive care. The best response of the RRMM patients was limited to less than a minimal response. However, regarding the safety perspective, daratumumab monotherapy might be considered for RRMM patients with FEV1 <50%. Moreover, recent suggestions to introduce montelukast as pre-medication for daratumumab [14, 15] could be a part of preventive measures on respiratory IRR for patients with low FEV1. This study’s case series and recent suggestion for preventive montelukast could contribute to establishing a better cohort study reflecting more reliable real-world outcomes of daratumumab monotherapy.

The present study had several limitations. First, this study had a limited number of cases, making the results difficult This study to generalize. Moreover, the treatment efficacy in all patients was disappointing. Therefore, a larger cohort study needs to clarify the efficacy in RRMM patients with pulmonary dysfunction. Finally, the safety of daratumumab monotherapy is not guaranteed in an individual with more severe pulmonary dysfunction since the FEV1 of the patients varied from 40% to 50%.

Conclusively, daratumumab monotherapy should not be considered an absolute contraindication for RRMM patients with 40–50% FEV1 when chemotherapeutic options are limited.

J.H.K. analyzed the data and wrote the paper. J.H.Y. and S.E.L. contributed to the acquisition of the data. H.J.K. and C.K.M contributed to the conception of the study. S.S.P. designed the study. The drafted manuscript was reviewed by all authors. The authors acknowledge all members at the Catholic Hematology Hospital, particularly the house staff, for their excellent care of the patients.

No potential conflicts of interest relevant to this article were reported.

  1. McKeage K. Daratumumab: first global approval. Drugs 2016;76:275-81.
    Pubmed CrossRef
  2. Lokhorst HM, Plesner T, Laubach JP, et al. Targeting CD38 with daratumumab monotherapy in multiple myeloma. N Engl J Med 2015;373:1207-19.
    Pubmed CrossRef
  3. Lonial S, Weiss BM, Usmani SZ, et al. Daratumumab monotherapy in patients with treatment-refractory multiple myeloma (SIRIUS): an open-label, randomised, phase 2 trial. Lancet 2016;387:1551-60.
    Pubmed CrossRef
  4. Lin P, Owens R, Tricot G, Wilson CS. Flow cytometric immunophenotypic analysis of 306 cases of multiple myeloma. Am J Clin Pathol 2004;121:482-8.
    Pubmed CrossRef
  5. White TA, Johnson S, Walseth TF, et al. Subcellular localization of cyclic ADP-ribosyl cyclase and cyclic ADP-ribose hydrolase activities in porcine airway smooth muscle. Biochim Biophys Acta 2000;1498:64-71.
    Pubmed CrossRef
  6. Guedes AG, Deshpande DA, Dileepan M, et al. CD38 and airway hyper-responsiveness: studies on human airway smooth muscle cells and mouse models. Can J Physiol Pharmacol 2015;93:145-53.
    Pubmed KoreaMed CrossRef
  7. Durer C, Durer S, Lee S, et al. Treatment of relapsed multiple myeloma: evidence-based recommendations. Blood Rev 2020;39:100616.
    Pubmed CrossRef
  8. Park SS, Byun JM, Yoon SS, et al. Daratumumab monotherapy for relapsed/refractory multiple myeloma, focussed on clinical trial-unfit patients and subsequent therapy. Br J Haematol 2021;193:101-12.
    Pubmed CrossRef
  9. Common terminology criteria for adverse events (CTCAE). Version 5.0. Bethesda, MD: National Cancer Institute, 2017.
  10. Byun JM, Yoon SS, Shin DY, et al. Real world treatment outcomes of multiple myeloma in Korea. Blood (ASH Annual Meeting Abstracts) 2016;128(Suppl):2367.
    CrossRef
  11. Park SS, Eom HS, Kim JS, et al. Brief report: clinical experiences after emergency use of daratumumab monotherapy for relapsed or refractory multiple myeloma in real practice. Jpn J Clin Oncol 2019;49:92-5.
    Pubmed CrossRef
  12. Byun JM, Yoon SS, Koh Y, et al. Daratumumab monotherapy in heavily pretreated Asian patients with relapsed and refractory multiple myeloma: a real-world experience. Anticancer Res 2019;39:5165-70.
    Pubmed CrossRef
  13. Kuzume A, Tabata R, Terao T, et al. Safety and efficacy of daratumumab in patients with multiple myeloma and severe renal failure. Br J Haematol 2021;193:e33-6.
    Pubmed CrossRef
  14. Nooka AK, Gleason C, Sargeant MO, et al. Managing infusion reactions to new monoclonal antibodies in multiple myeloma: daratumumab and elotuzumab. J Oncol Pract 2018;14:414-22.
    Pubmed CrossRef
  15. Moore DC, Arnall JR, Thompson DL, et al. Evaluation of montelukast for the prevention of infusion-related reactions with daratumumab. Clin Lymphoma Myeloma Leuk 2020;20:e777-81.
    Pubmed CrossRef

Article

Letter to the Editor

Blood Res 2022; 57(1): 76-80

Published online March 31, 2022 https://doi.org/10.5045/br.2022.2021183

Copyright © The Korean Society of Hematology.

Daratumumab monotherapy in relapsed and refractory multiple myeloma patients with severely compromised forced expiratory volume in one second

Jin-Hyo Kim, Sung-Soo Park, Jae-Ho Yoon, Sung-Eun Lee, Hee-Je Kim, Chang-Ki Min

Department of Hematology, Seoul St. Mary’s Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

Correspondence to:Sung-Soo Park
Department of Hematology, Seoul St. Mary’s Hematology Hospital, College of Medicine, The Catholic University of Korea, 222 Banpodaero, Seocho-gu, Seoul 06591, Korea
E-mail: sspark@catholic.ac.kr

Received: October 2, 2021; Revised: December 5, 2021; Accepted: December 29, 2021

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Body

TO THE EDITOR: Daratumumab monotherapy is approved to treat patients with relapsed or refractory multiple myeloma (RRMM) who have previously received three or more treatments, including a proteasome inhibitor and an immunomodulator or presenting with double refractoriness to proteasome inhibitors and immunomodulators [1]. Although daratumumab monotherapy has been introduced in real-world practice based on the results of phase 1 (GEN501) [2] and phase 2 clinical trials (SIRIUS) [3], the results of these clinical trials were limited to individuals with no severe comorbidities according to the trials’ design. For example, patients with respiratory impairment indicated by forced expiratory volume in one second (FEV1) of <50% were excluded from the GEN501 and SIRIUS trials. Accordingly, the safety of daratumumab monotherapy would be limited in these patients. Furthermore, the CD38, which is the target of daratumumab, is not only over-expressed on the multiple myeloma cells [4] but also widely presented on airway smooth muscle cells [5]. Due to general reports that altered CD38 expression on airway smooth muscle cells could contribute to airway hyperresponsiveness [6], the respiratory infusion-related reactions (IRRs), such as bronchospasms or dyspnea, are considered to require particular attention following infusion of daratumumab [2, 3]. Therefore, the administration of daratumumab to patients with FEV1s of <50% could present a difficult challenge. Nevertheless, a clinician could be forced to select a novel agent such as daratumumab for patients who do not fit the selection criteria of clinical trials if there are limited chemotherapeutic options for heavily treated patients with RRMM in real-world clinical practice. Thus, it is important to validate the real-world safety of daratumumab monotherapy for patients with severe comorbidities that make them unfit for clinical trials.

Herein, we report the cases of 3 patients who experienced manageable pulmonary manifestations after the administration of daratumumab monotherapy [7], despite decreased FEV1s of <50% at baseline. This study was approved by the Institutional Review Board of The Catholic University of Korea (KC21RASI0664) and was conducted in accordance with the Declaration of Helsinki.

CASE

Table 1 summarizes the baseline clinical characteristics of the 3 cases. At the baseline pulmonary function test assessment, the FEV1 was 43%, 40%, and 44% in case 1, case 2, and case 3, respectively. All patients received daratumumab monotherapy at a dose of 16 mg/kg, and the treatment plan was weekly for the first 8 weeks (cycles 1 and 2), then every 2 weeks from 9 to 24 weeks (cycles 3–6), then every four weeks thereafter (cycles 7 and higher). To prevent IRRs, the patients received 100 mg of intravenous methylprednisolone at the first and second daratumumab infusions. Other supportive care and preventive medications were administered as described in our previous reports [8]. The clinical outcomes of the 3 patients are summarized in Table 2. All adverse events were explored based on the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 [9].

Table 1 . Patient baseline characteristics..

Case 1Case 2Case 3
Age/sex61/F71/F40/M
Type of disease at diagnosisIgGIgGLight chain disease
Light chain type at diagnosisKappaLambdaKappa
International staging system at diagnosisIIIIIIII
White blood cell count at baseline, ×109/L7.242.495.12
Absolute neutrophil count at baseline, ×109/L5.061.344.45
Absolute lymphocyte count at baseline, ×109/L1.150.800.31
Hemoglobin at baseline, g/dL12.18.69.1
Platelet count at baseline, ×106/L1115422
Albumin at baseline, g/dL3.62.94.1
b2-microglobulin at baseline, mg/mL3.762.135N/A
Serum creatinine at baseline, mg/dL1.521.250.46
Lactate dehydrogenase at baseline, IU/L (reference, 250–450 IU/L)429739633
Forced expiratory volume at one second at baseline, %434044
Presence of plasmacytoma at baselineYesNoYes
Interval from diagnosis to treatment of daratumumab, months904780
Serum M protein at baseline, g/dL0.993.250
Serum kappa/lambda at baseline, mg/day122.5/14.58.14/368.511.41/<0.76
Presence high-risk cytogenetics at diagnosis
del(17p)NegativeNegativeNegative
t(14;16)NegativeNegativeNegative
t(4;14)NegativeNegativeNegative
Other cytogenetic abnormality at diagnosis
Amp(1q21)NegativePositiveNegative
t(11;14)NegativeNegativeNegative
del(13q)NegativePositiveNegative

Abbreviation: N/A, not available..



Table 2 . Outcomes of daratumumab monotherapy..

Case 1Case 2Case 3
N of prior treatments lines before daratumumab435
Interval from diagnosis to treatment of daratumumab, months904780
Administered cycles of daratumumab (total time of infusion)1 cycle (2 times)5 cycles (13 times)1 cycle (4 times)
Best response of daratumumab monotherapyRefractoryMinimal responseRefractory
Survival statusDeath at 2 monthsDeath at 19 monthsDeath at 1 month
Adverse events, infusion-related reaction
Dyspnea, grade2--
CRP elevation, grade3--
Cause of deathProgression of diseaseProgression of diseaseProgression of disease


Case 1

A 61-year-old female, who was diagnosed with multiple myeloma type IgG-kappa 8 years earlier, had relapsed following first-line treatment with autologous stem cell transplantation after vincristine, doxorubicin, and dexamethasone; second-line treatment consisting of eight cycles of bortezomib and dexamethasone; third-line therapy with lenalidomide plus dexamethasone (RD), and fourth-line treatment with pomalidomide, cyclophosphamide, and dexamethasone (PCD). She also presented with relapsed and refractory response status following 13 cycles of PCD.

Before daratumumab monotherapy, the baseline assessment showed a monoclonal protein level of 0.99 g/dL and serum-free light chain differences of 108.00 mg/L with a predominance of kappa chains. The laboratory and radiological tests did not indicate specific implications related to multiple myeloma. Although an IRR grade 2 dyspnea developed on the first day of daratumumab infusion, this event was spontaneously resolved by supportive care with corticosteroids and antihistamine. She also experienced a grade 3 adverse event of elevated C-reactive protein levels. Therefore, we decided to postpone the second infusion of daratumumab to a week later than planned. In the second daratumumab infusion, there was no significant IRR. Her course of RRMM was refractory despite two cycles of daratumumab monotherapy, and she died of disease progression (Fig. 1A).

Figure 1. Treatment course and adverse events of case 1 (A), case 2 (B), and case 3 (C).

Case 2

A 71-year-old female with multiple myeloma type IgG lambda was diagnosed 3 years earlier and had relapsed. The patient was initially treated with nine cycles of bortezomib, melphalan, and prednisone, which resulted in relapsed and refractory responses. The patient was subsequently treated with 20 cycles of RD, and a partial response was achieved, but the RD course was terminated due to grade 3 neutropenia. Third-line treatment with eight cycles of PCD was administered, and a minimal response was observed, but the patient relapsed. The fourth-line treatment was daratumumab monotherapy.

The monoclonal protein assessment and serum-free light chain differences were 3.25 g/dL and 360.37 mg/L, respectively. Baseline magnetic resonance imaging indicated an L1 compression fracture related to RRMM manifestation. After daratumumab monotherapy, there was no IRR. The best response to daratumumab monotherapy was minimal, with a monoclonal protein value of 2.07 g/dL. However, the disease progressed after five cycles. Despite administering a next-line treatment with thalidomide, cyclophosphamide, and dexamethasone, the patient died due to disease progression (Fig. 1B).

Case 3

A 40-year-old male had kappa light chain multiple myeloma diagnosed 7 years earlier. The patient was treated with two cycles of bortezomib, melphalan, and prednisone, followed by autologous stem cell transplantation and tandem allogeneic stem cell transplantation as the first-line treatment. Eight cycles of bortezomib and dexamethasone were administered for the first relapse. He was treated with six RD cycles for the second relapse, which resulted in the partial response, but showed a relapse and refectory response with multifocal bone lytic lesions. Despite the fourth-line treatment with five cycles of pomalidomide and dexamethasone, the patient became refractory, and the multifocal bone lesions progressed. The Fifth-line treatment with carfilzomib-dexamethasone was initiated but was also limited to a refractory response with multifocal extramedullary plasmacytomas (Fig. 1C). The sixth-line treatment was with daratumumab monotherapy.

Baseline computed tomography showed multiple plasmacytomas at the left orbit and periauricular regions, upper back, left apical axilla, abdominal wall, and left thigh (Fig. 1C). Baseline monoclonal protein was negative in electrophoresis, and there was no significant difference (1.41 mg/L) between the quantity of serum-free light chains. During daratumumab monotherapy, there was no IRR, but the patient died due to disease progression.

DISCUSSION

Real-world experience with daratumumab monotherapy has continuously been reported since its approval as a treatment for RRMM [10-13]. The studies highlighted that daratumumab monotherapy was safely administered to patients, including those who did not fit the clinical trials selection criteria. Our previous study reported the favorable efficacy and infusion-related safety of 64 RRMM patients who would be unfit to participate in the GEN501 or SIRIUS due to comorbidities including an Eastern Cooperative Oncology Group Performance Status of ≥3, meningeal involvement, anemia of <75 g/L, neutropenia of <1.0×109/L, thrombocytopenia <75×109/L, and renal insufficiency with a glomerular filtration rate of <20 mL/min/1.73 m2. No reported IRRs interrupted the daratumumab schedule, and all IRRs were manageable with supportive care [8].

To the best of our knowledge, this study reports the first daratumumab monotherapy safety profile in patients with decreased lung function demonstrated by an FEV1 <50%. Although 1 in 3 patients experienced a respiratory IRR, it was manageable with supportive care. The best response of the RRMM patients was limited to less than a minimal response. However, regarding the safety perspective, daratumumab monotherapy might be considered for RRMM patients with FEV1 <50%. Moreover, recent suggestions to introduce montelukast as pre-medication for daratumumab [14, 15] could be a part of preventive measures on respiratory IRR for patients with low FEV1. This study’s case series and recent suggestion for preventive montelukast could contribute to establishing a better cohort study reflecting more reliable real-world outcomes of daratumumab monotherapy.

The present study had several limitations. First, this study had a limited number of cases, making the results difficult This study to generalize. Moreover, the treatment efficacy in all patients was disappointing. Therefore, a larger cohort study needs to clarify the efficacy in RRMM patients with pulmonary dysfunction. Finally, the safety of daratumumab monotherapy is not guaranteed in an individual with more severe pulmonary dysfunction since the FEV1 of the patients varied from 40% to 50%.

Conclusively, daratumumab monotherapy should not be considered an absolute contraindication for RRMM patients with 40–50% FEV1 when chemotherapeutic options are limited.

Acknowledgments

J.H.K. analyzed the data and wrote the paper. J.H.Y. and S.E.L. contributed to the acquisition of the data. H.J.K. and C.K.M contributed to the conception of the study. S.S.P. designed the study. The drafted manuscript was reviewed by all authors. The authors acknowledge all members at the Catholic Hematology Hospital, particularly the house staff, for their excellent care of the patients.

Authors’ Disclosures of Potential Conflicts of Interest

No potential conflicts of interest relevant to this article were reported.

Fig 1.

Figure 1.Treatment course and adverse events of case 1 (A), case 2 (B), and case 3 (C).
Blood Research 2022; 57: 76-80https://doi.org/10.5045/br.2022.2021183

Table 1 . Patient baseline characteristics..

Case 1Case 2Case 3
Age/sex61/F71/F40/M
Type of disease at diagnosisIgGIgGLight chain disease
Light chain type at diagnosisKappaLambdaKappa
International staging system at diagnosisIIIIIIII
White blood cell count at baseline, ×109/L7.242.495.12
Absolute neutrophil count at baseline, ×109/L5.061.344.45
Absolute lymphocyte count at baseline, ×109/L1.150.800.31
Hemoglobin at baseline, g/dL12.18.69.1
Platelet count at baseline, ×106/L1115422
Albumin at baseline, g/dL3.62.94.1
b2-microglobulin at baseline, mg/mL3.762.135N/A
Serum creatinine at baseline, mg/dL1.521.250.46
Lactate dehydrogenase at baseline, IU/L (reference, 250–450 IU/L)429739633
Forced expiratory volume at one second at baseline, %434044
Presence of plasmacytoma at baselineYesNoYes
Interval from diagnosis to treatment of daratumumab, months904780
Serum M protein at baseline, g/dL0.993.250
Serum kappa/lambda at baseline, mg/day122.5/14.58.14/368.511.41/<0.76
Presence high-risk cytogenetics at diagnosis
del(17p)NegativeNegativeNegative
t(14;16)NegativeNegativeNegative
t(4;14)NegativeNegativeNegative
Other cytogenetic abnormality at diagnosis
Amp(1q21)NegativePositiveNegative
t(11;14)NegativeNegativeNegative
del(13q)NegativePositiveNegative

Abbreviation: N/A, not available..


Table 2 . Outcomes of daratumumab monotherapy..

Case 1Case 2Case 3
N of prior treatments lines before daratumumab435
Interval from diagnosis to treatment of daratumumab, months904780
Administered cycles of daratumumab (total time of infusion)1 cycle (2 times)5 cycles (13 times)1 cycle (4 times)
Best response of daratumumab monotherapyRefractoryMinimal responseRefractory
Survival statusDeath at 2 monthsDeath at 19 monthsDeath at 1 month
Adverse events, infusion-related reaction
Dyspnea, grade2--
CRP elevation, grade3--
Cause of deathProgression of diseaseProgression of diseaseProgression of disease

References

  1. McKeage K. Daratumumab: first global approval. Drugs 2016;76:275-81.
    Pubmed CrossRef
  2. Lokhorst HM, Plesner T, Laubach JP, et al. Targeting CD38 with daratumumab monotherapy in multiple myeloma. N Engl J Med 2015;373:1207-19.
    Pubmed CrossRef
  3. Lonial S, Weiss BM, Usmani SZ, et al. Daratumumab monotherapy in patients with treatment-refractory multiple myeloma (SIRIUS): an open-label, randomised, phase 2 trial. Lancet 2016;387:1551-60.
    Pubmed CrossRef
  4. Lin P, Owens R, Tricot G, Wilson CS. Flow cytometric immunophenotypic analysis of 306 cases of multiple myeloma. Am J Clin Pathol 2004;121:482-8.
    Pubmed CrossRef
  5. White TA, Johnson S, Walseth TF, et al. Subcellular localization of cyclic ADP-ribosyl cyclase and cyclic ADP-ribose hydrolase activities in porcine airway smooth muscle. Biochim Biophys Acta 2000;1498:64-71.
    Pubmed CrossRef
  6. Guedes AG, Deshpande DA, Dileepan M, et al. CD38 and airway hyper-responsiveness: studies on human airway smooth muscle cells and mouse models. Can J Physiol Pharmacol 2015;93:145-53.
    Pubmed KoreaMed CrossRef
  7. Durer C, Durer S, Lee S, et al. Treatment of relapsed multiple myeloma: evidence-based recommendations. Blood Rev 2020;39:100616.
    Pubmed CrossRef
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Blood Res
Volume 59 2024

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