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Article

Families of Extended Exponentiated Generalized Distributions and Applications of Medical Data Using Burr III Extended Exponentiated Weibull Distribution

1
Department of Statistics, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan
2
Department of Statistics, Stockholm University, SE-106 91 Stockholm, Sweden
3
Department of Computer Science, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan
*
Author to whom correspondence should be addressed.
Mathematics 2023, 11(14), 3090; https://doi.org/10.3390/math11143090
Submission received: 8 June 2023 / Revised: 8 July 2023 / Accepted: 10 July 2023 / Published: 13 July 2023

Abstract

:
In this article, four new families named as Weibull extended exponentiated-X (WEE-X), Lomax extended exponentiated-X (LEE-X), Logistic extended exponentiated-X (LGCEE-X), and Burr III extended exponentiated-X (BIIIEE-X) with their quantile functions are proposed. The expressions for distribution function and density function of BIIIEE-X family are written in terms of linear combinations of the exponentiated densities based to parent model. New models, i.e., Weibul extended exponentiated Weibull (WEEW), Lomax extended exponentiated Weibull (LEEW), Logistic extended exponentiated Weibull (LGCEEW), and Burr III extended exponentiated-Weibull (BIIIEEW) distributions are derived, were plotted for functions of probability density and hazard rate at different levels of parameters. Some mathematical properties of the BIIIEEW model are disclosed. The maximum likelihood method for the BIIIEEW model are described. Numerical applications of the BIIIEEW model to disease of cancer datasets are provided.

1. Introduction

Statistical modeling of lifetime data plays an important role in medical science. To determine reliable results in estimating medical data, it is often required to choose the appropriate statistical distribution of the data. Continuous probability distributions, such as the Weibull, exponential, Rayleigh, lognormal, gamma, logistic, and log-logistic, can be used to model biomedical data (BoMD). However, it is clear that the BoMD deviate from these classical distributions because of the skewness and heavy tails that are present in the data. Due to this, the aforementioned traditional skewed distributions become less suitable for modeling BoMD. Weibull distribution (WD) is not flexible enough to handle data types with a lot of complexity. Practically all clinical issues, including breast, bladder, neck, and other cancers, have unimodel or modified unimodel failure rates. After surgery, risk of bladder, breast, and neck cancer are unimodel. The regular two-parameter WD can simply model monotonically increasing and decreasing failure rate functions (FRFs), making it less relevant for fitting when data show non-monotonic FRFs. These disadvantages have motivated researchers to develop several generalizations of it to obtain more flexible distributions for modeling. Therefore, there is a need to emphasize the importance of enhancing the classical distributions for modeling BoMD. Numerous studies have been conducted to create statistical models that are superior to conventional models in their ability to describe health data.
Based on extended versions of WDs, numerous studies have examined the characteristics of various cancer datasets (CDSs). When data on cancer remission times were applied, the q-Weibull distribution by Jose and Naik (2009) [1] performed better than the regular WD. When it came to modeling colorectal cancer, the generalized WD that was developed by Baghestani et al. (2017) [2] performed well. The performance of the beta- weighted WD described by Idowu and Ikegwu (2013) [3] was validated using bladder cancer datasets (BCDSs). Modeling BCDSs was used to evaluate the empirical proofs of the transmuted exponentiated generalized WD by Yousof et al. (2017) [4], the Marshall- Olkin generalized WD by Elgohari and Yousof (2020) [5], the Marshall–Olkin power generalized WD by Afify et al. (2020) [6], and the Gull alpha power WD by Ijaz et al. (2020) [7]. With these new families, statistical modeling can be more adaptable, especially in practical fields, such as finance, engineering, the environment, and health care. In the statistical literature, one can add one or more parameters to a known distribution to create a family of distributions. The generalized distribution emerges when the parameters are added to the baseline distribution. The generalized distribution can be used effectively in fitting lifetime datasets because it can accommodate monotonic and non-monotonic data characteristics.
The transformed-transformer (T-X) technique was proposed by Alzaatreh et al. (2013) [8] to develop new G-families. Let T [ t 1 , t 2 ] for t 1 ,   t 2 be a random variable (rv) having probability density function (PDF) π ( t ) and cumulative distribution function (CDF) Π ( t ) and let Φ [ G ( x ) ] be a function of CDF G ( x ) of any parent rv X so that Φ [ G ( x ) ] satisfies the conditions below:
Φ [ G ( x ) ] [ t 1 , t 2 ] , lim x Φ [ G ( x ) ] = t 1 and lim x + Φ [ G ( x ) ] = t 2 , Φ [ G ( x ) ] is non - decreases monotone and differentiable .
The CDF of T-X family of distributions (FoDs) is:
F T X ( x ) = t 1 Φ [ G ( x ) ] π ( t ) d t , = Π Φ [ G ( x ) ] .
The PDF associated with Equation (2) is:
f T X ( x ) = π Φ [ G ( x ) ] d d x Φ [ G ( x ) ] .
In Equation (2), the PDF π ( t ) is transformed into CDF F T X ( x ) by function Φ [ G ( x ) ] , which behaves similar to a transformer, and in Equation (3), the distribution f T X ( x ) is transformed from rv T through transformer rv X.
The function Φ [ G ( x ) ] will give a new FODs based on the support of the rv T. By using the following equation:
Φ [ G ( x ) ] = log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] ,
the F T X ( x ) in Equation (2) is a CDF of new FoDs, which is defined as:
F T X ( x ) = 0 log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] π ( t ) d t = Π log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] ,
where Π ( t ) is the CDF of rv T. The corresponding PDF related to Equation (5) is:
f T X ( x ) = θ g ( x ) G θ 1 ( x ) 1 G θ ( x ) 1 + 1 1 log [ 1 G θ ( x ) ] π log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] .
The main objectives for proposing new X-families are:
i.
Developing new X-families related to the function of CDF, i.e., Φ [ G ( x ) ] .
ii.
The developed families based on a generator, i.e., log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] instead of G ( x ) .
iii.
The generator discussed in step ii has the ability to generate better goodness of fit results and parameters estimates that can make it distinguishable and attractive for the researcher.
The article is arranged as follows. Section 2 presents four new proposed T-X distribution families, such as the WEE-X family, LEE-X family, LGCEE-X family, and BIIIEE-X family with their quantile functions. In Section 2.1.1, Section 2.2.1, Section 2.3.1 and Section 2.4.1, submodels WEEW of the WEE-X family, LEEW of the LEE-X family, LGCEE of the LGCEE-X family, and BIIIEEW of the BIIIEE-X family are characterized by PDF and FRF plots. The useful expressions for BIIIEE-X family are derived in Section 3. For the BIIIEEW model, we derive few mathematical properties in Section 4. The estimation of BIIEEWD by the maximum likelihood method is explained analytically in Section 5. Section 6 describes the applications of the proposed model to different datasets of cancer disease. Lastly, the conclusion is drawn in Section 7.

2. Some New T-X Distributions Families with Different T Distributions

Based on the classification of the T-X family, two subfamilies can be identified: the first subfamily has different T distributions, but the same X distribution, while the second subfamily has different X distributions but the same T distribution. This section considers the subfamily of different T distributions with their submodels. Here, we considered Weibull, Lomax, Logistic, and Burr III as T distributions and Weibull as an X distribution.

2.1. Weibull Extended Exponentiated-X (WEE-X) Family

If an rv T Weibull distribution (WD) with γ and α parameters, then Π ( t ) = 1 e γ t α , t 0 . From Equation (5), the CDF of the WEE-X family is:
F W E E X ( x ) = 1 exp γ log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] α ,
The PDF of WD is π ( t ) = γ α t α 1 e γ t α , t > 0 , and hence, from Equation (6), the PDF of the WEE-X family is:
f W E E X ( x ) = γ θ α g ( x ) G θ 1 ( x ) 1 G θ ( x ) 1 + 1 1 log [ 1 G θ ( x ) ] × log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] α 1 exp γ log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] α .
From Equation (7), the quantile function (QF) of WEE-X family can be written as:
Q W E E X ( u ) = G 1 1 exp 1 γ log ( 1 u ) 1 α W exp 1 + 1 γ log ( 1 u ) 1 α 1 θ ; 0 u 1 .
where W ( . ) Lambert W function (LWF). For every complex Z, the LWF is the solution of equation p ( Z ) = Z e Z .

2.1.1. Weibull Extended Exponentiated Weibull Distribution (WEEWD)

By considering CDF G ( x ) = 1 exp x δ β and PDF g ( x ) = β δ x δ β 1 exp x δ β in Equations (7) and (8), we develop a WEE-Weibull (WEEW) submodel having a CDF and PDF as follows:
F W E E W ( x ) = 1 exp γ log 1 1 exp x δ β θ 1 log [ 1 1 exp x δ β θ ] α ,
and
f W E E W ( x ) = γ θ α β x β 1 δ β exp x δ β 1 exp x δ β θ 1 1 1 exp x δ β θ 1 + 1 1 log [ 1 1 exp x δ β θ ] × log 1 1 exp x δ β θ 1 log [ 1 1 exp x δ β θ ] α 1 exp γ log 1 1 exp x δ β θ 1 log [ 1 1 exp x δ β θ ] α .

2.2. Lomax Extended Exponentiated-X (LEE-X) Family

If rv T Lomax distribution (LD) with γ and β parameters, then Π ( t ) = 1 [ 1 + β t ] γ , t 0 . From Equation (5), the CDF of LEE-X family is:
F L E E X ( x ) = 1 1 + β log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] γ ,
The PDF of LD is π ( t ) = γ β [ 1 + β t ] ( γ + 1 ) , t > 0, and hence, from Equation (6), the PDF of LEE-X family is:
f L E E X ( x ) = γ θ β g ( x ) G θ 1 ( x ) 1 G θ ( x ) 1 + 1 1 log [ 1 G θ ( x ) ] 1 + β log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] ( γ + 1 ) .
From Equation (12), the QF of LEE-X family can be written as:
Q L E E X ( u ) = G 1 1 exp 1 ( 1 u ) 1 γ β W exp β 1 + ( 1 u ) 1 γ β 1 θ ; 0 u 1 .

2.2.1. Lomax Extended Exponentiated Weibull Distribution (LEEWD)

By taking G ( x ) = 1 exp x λ α and g ( x ) = α λ x λ α 1 exp x λ α as CDF and PDF in Equations (12) and (13), we obtain a LEE-Weibull (LEEW) submodel with a CDF and PDF as:
F L E E W ( x ) = 1 1 + β log 1 1 exp x λ α θ 1 log [ 1 1 exp x λ α θ ] γ ,
and
f L E E W ( x ) = γ θ β α x α 1 λ α exp x λ α 1 exp x λ α θ 1 1 1 exp x λ α θ 1 1 log [ 1 1 exp x λ α θ ] + 1 × 1 + β log 1 1 exp x λ α θ 1 log [ 1 1 exp x λ α θ ] ( γ + 1 ) .

2.3. Logistic Extended Exponentiated-X (LGCEE-X) Family

If rv T Logistic (LGC) distribtion (LGCD) with δ parameter, then Π ( t ) = ( 1 + e δ t ) 1 , t 0 . From Equation (5), the CDF of LGCEE-X family is:
F L G C E E X ( x ) = 1 + exp δ log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] 1 ,
The PDF of LGCD is π ( t ) = δ e δ x ( 1 + e δ x ) 2 , t > 0 , and hence, from Equation (6), the PDF of LGCEE-X family is:
f L G C E E X ( x ) = δ θ g ( x ) G θ 1 ( x ) 1 G θ ( x ) exp δ log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] × 1 + 1 1 log [ 1 G θ ( x ) ] 1 + exp δ log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] 2 .
From Equation (17), the QF of LGCEE-X family can be written as:
Q L G C E E X ( u ) = G 1 1 1 u u 1 δ W 1 u u 1 δ exp ( 1 ) 1 θ ; 0 u 1 .

2.3.1. Logistic Extended Exponentiated Weibull Distribution (LGCEEWD)

By substituting G ( x ) = 1 exp x α γ and g ( x ) = γ α x α γ 1 exp x α γ in Equations (17) and (18), we derive a submodel LGCEE-Weibull (LGCEEW) having CDF and PDF as:
F L G C E E W ( x ) = 1 + exp δ log 1 1 exp x α γ θ 1 log [ 1 1 exp x α γ θ ] 1 ,
and
f L G C E E W ( x ) = δ θ γ x γ 1 α γ exp x α γ 1 exp x α γ θ 1 1 1 exp x α γ θ exp δ log 1 1 exp x α γ θ 1 log [ 1 1 exp x α γ θ ] × 1 + 1 1 log [ 1 1 exp x α γ θ ] 1 + exp δ log 1 1 exp x α γ θ 1 log [ 1 1 exp x α γ θ ] 2 .

2.4. Burr III Extended Exponentiated-X (BIIIEE-X) Family

If rv T Burr III distribution (BIIID) having c and k parameters, then Π ( t ) = ( 1 + t c ) k , t 0 . From Equation (5), the CDF of the BIIIEE-X family is:
F B I I I E E X ( x ) = 1 + log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] c k ,
The PDF of BIIID is π ( t ) = c k t c 1 ( 1 + t c ) k 1 , t > 0 , and hence, from Equation (6), the PDF of the BIIIEE-X family is:
f B I I I E E X ( x ) = c θ k g ( x ) G θ 1 ( x ) 1 G θ ( x ) 1 + 1 1 log [ 1 G θ ( x ) ] × log 1 G θ ( x ) 1 log [ 1 G θ ( x ) ] c 1 1 + log 1 G θ ( x ) 1 l o g [ 1 G θ ( x ) ] c k 1 .
From Equation (22), the QF of the BIIIEE-X family can be written as:
Q B I I I E E X ( u ) = G 1 1 exp ( u 1 k 1 ) 1 c W exp 1 + ( u 1 k 1 ) 1 c 1 θ ; 0 u 1 .

2.4.1. Burr III Extended Exponentiated Weibull Distribution

If X Weibull rv with CDF G ( x ) = 1 exp x β γ and PDF g ( x ) = γ β x β γ 1 exp x β γ , then using Equations (22) and (23), we generate CDF and PDF of the BIIIEE-Weibull distribution (BIIIEEWD) as:
F B I I I E E W ( x ) = 1 + log 1 1 exp x β γ θ 1 log 1 1 exp x β γ θ c k ,
and
f B I I I E E W ( x ) = c θ k γ x γ 1 β γ exp x β γ 1 exp x β γ θ 1 1 1 exp x β γ θ 2 log 1 1 exp x β γ θ 1 log 1 1 exp x β γ θ × log 1 1 exp x β γ θ 1 log 1 1 exp x β γ θ c 1 1 + log 1 1 exp x β γ θ 1 log 1 1 exp x β γ θ c k 1 .
where, β > 0 is scale and c , k , γ , θ > 0 are shapes parameters.
Plots for the PDFs of WEEWD, LEEWD, LGCEEWD, and BIIIEEWD are displayed in Figure 1, Figure 2, Figure 3 and Figure 4 and plots for failure rate function (FRF) of BIIIEEWD are presented in Figure 5 at various levels of parametes θ , c , k , β , and γ (some of them are fixed, the other differ). These plots indicate that the FRF shapes of the BIIIEEWD are decreasing, increasing, upside-down bathtub, and bathtub.
In the following sections, we explore different aspects of the BIIIEE-X family. The Burr III model (BIIIM) attracts extraordinary consideration because it includes several distributions families and it incorporates the characteristic of various distributions such as logistic and exponential. The BIIIM extensively applied in different areas, such as reliability and survival analysis, study of environment, water resources, forestry, meteorology, economics, and medical field, among others. It is also applied to datasets of wages, income, and wealth. For more details on well-known X-classes, review [9,10].

3. Useful Expansions for the BIIIEE-X Family

Here, we derived useful expressions for CDF and PDF of BIIIEE-X family. The expansion of binomial series (EoBS) is:
1 + Y α = i = 0 ( 1 ) i α + i 1 i Y i ; | Y | < 1 ,
where α is +ve non-integer real numbers. Using Equation (27) in Equation (22) and after simplification, we have:
F B I I I E E X ( x ) = i = 0 ( 1 ) i k + i 1 i log [ 1 G θ ( x ) ] c i 1 log { 1 l o g [ 1 G θ ( x ) ] } log [ 1 G θ ( x ) ] c i
The generalized EoBS is:
1 Y α = j = 0 α 1 + j j Y j ,
where | α | > 0 is real number. Applying Equation (29) in Equation (28), we obtain:
F B I I I E E X ( x ) = i , j = 0 ( 1 ) i k + i 1 i c i 1 + j j log [ 1 G θ ( x ) ] ( c i + j ) log { 1 log [ 1 G θ ( x ) ] } j ,
For any real parameters, a and B ( 0 , 1 ) , we have:
log [ 1 B ] a = B a + a b = 0 p b ( a + b ) B b + a + 1 ,
where p b ( a ) are Stirling poloynomials. For more explanation on Equation (31), see Flajonet and Odlyzko (1990) [11]; Flajonet and Sedgewick (2009) [12]; and Hussain et al. (2022, 2023) [13,14].
Using Equation (31), we obtain the expression below:
F B I I I E E X ( x ) = i , j = 0 ( 1 ) ( c 1 ) i j k + i 1 i c i 1 + j j [ ( 1 ) c i log [ 1 G θ ( x ) ] c i + j b = 0 ( 1 ) c i b 1 p b ( j + b ) l o g [ 1 G θ ( x ) ] c i + b + 1 ]
The power series concept is:
Y α = m 1 = 0 m 2 = m 1 ( 1 ) m 2 + m 1 α m 2 m 2 m 1 Y m 1
Using Equations (31) and (33) in Equation (32), we have:
F B I I I E E X ( x ) = i , j = 0 ( 1 ) ( c 1 ) i j k + i 1 i c i 1 + j j ( 1 ) c i A 1 + j b = 0 ( 1 ) c i b 1 p b ( j + b ) A 2 G m 1 ( x )
where
A 1 = m 1 = 0 m 2 = m 1 ( 1 ) m 2 + m 1 m 2 m 1 θ c i m 2 + c i l 1 = 0 p l 1 ( c i + l 1 ) θ ( l 1 + c i + 1 ) m 2 1
and
A 2 = m 1 = 0 m 2 = m 1 ( 1 ) m 2 + m 1 m 2 m 1 θ ( c i b 1 ) m 2 + ( c i b 1 ) l 1 = 0 p l 1 ( c i b 1 + l 1 ) θ ( l 1 + c i b ) m 2 1
Now, we can write Equation (34) as:
F B I I I E E X ( x ) = A 3 1 1 G m 1 ( x ) 1
where
A 3 = i , j = 0 ( 1 ) i j k + i 1 i c i 1 + j j A 1 + j b = 0 ( 1 ) ( b + 1 ) p b ( j + b ) A 2
Using Equation (29) in Equation (37), we obtain:
F B I I I E E X ( x ) = q = 0 A 3 1 G m 1 ( x ) q
The binomial expansion is:
1 Y α = s = 0 ( 1 ) s α s Y s
Applying Equation (40) in Equation (39), we obtain:
F B I I I E E X ( x ) = s = 0 q = 0 A 3 ( 1 ) s q s G m 1 s ( x )
Again, applying Equation (33) in Equation (41), we produce the following:
F B I I I E E X ( x ) = n 1 = 0 V n 1 G n 1 ( x ) = n 1 = 0 V n 1 H n 1 ( x )
where
V n 1 = s , q , n 2 = 0 A 3 ( 1 ) s + n 2 + n 1 q s m 1 s n 2 n 2 n 1
and H n 1 ( x ) = G n 1 ( x ) for n 1 1 , since H 0 ( x ) = 1 , is the CDF of the exponentiated-G (exp-G) with power parameter n 1 .
We can write the PDF of BIIIEE-X family as:
f B I I I E E X ( x ) = n 1 = 0 V n 1 + 1 ( n 1 + 1 ) g ( x ) G n 1 ( x ) = n 1 = 0 V n 1 + 1 h n 1 + 1 ( x )
where h n 1 + 1 ( x ) = ( n 1 + 1 ) g ( x ) G n 1 ( x ) is the PDF of the exp-G with power parameter n 1 + 1 .

Useful Expansions for the BIIIEEW Distribution

Using Equations (42) and (43), we can write useful expressions for CDF and PDF of BIIIEEWD as below:
F B I I I E E W ( x ) = n 1 = 0 V n 1 1 exp x β γ n 1
and
f B I I I E E W ( x ) = n 1 = 0 V n 1 + 1 ( n 1 + 1 ) γ β x β γ 1 exp x β γ 1 exp x β γ n 1

4. Mathematical Properties of the BIIIEEWD

4.1. Incomplete Moments

Let, in Equation (45), X follow the BIIIEEW density. Then, the nth incomplete moment of BIIIEEWD is:
T n ( x ) = x y n f B I I I E E W ( y ) d y ,
Using Equations (45) and (40) in Equation (46), we produce:
T n ( x ) = n 1 , t 1 = 0 ( 1 ) t 1 V n 1 + 1 ( n 1 + 1 ) γ β γ n 1 t 1 0 x y n + γ 1 exp ( n 1 + 1 ) y β γ d y ,
Put Z = ( n 1 + 1 ) β γ y γ , we have y = β ( n 1 + 1 ) 1 γ Z 1 γ and d y = β γ ( n 1 + 1 ) 1 γ Z 1 γ 1 d Z with new limits Z 1 = 0 and Z 2 = ( n 1 + 1 ) β γ x γ .
Equation (47) reduces to:
T n ( x ) = n 1 , t 1 = 0 ( 1 ) t 1 V n 1 + 1 ( n 1 + 1 ) n 1 t 1 β n ( n 1 + 1 ) n γ + 1 Γ ( n γ + 1 , Z 2 ) .
where Γ ( n γ + 1 , Z 2 ) = 0 Z 2 Z n γ exp ( Z ) d Z is the incomplete gamma function and Z 2 = ( n 1 + 1 ) β γ x γ .
For n = 1 , we obtain the first incomplete moment for the BIIIEEWD as:
T 1 ( x ) = n 1 , t 1 = 0 ( 1 ) t 1 V n 1 + 1 ( n 1 + 1 ) n 1 t 1 β ( n 1 + 1 ) 1 γ + 1 Γ ( 1 γ + 1 , Z 2 ) .

4.2. Moments

The rth raw moment for BIIIEEWD having PDF (45) of an rv X can be obtained by the following integral:
μ r = E ( X r ) = 0 x r f B I I I E E W ( x ) d x ,
Applying Equations (40) and (45) in Equation (50), we obtain:
μ r = n 1 , t 1 = 0 ( 1 ) t 1 ( n 1 + 1 ) V n 1 + 1 n 1 t 1 γ β γ 0 x r + γ 1 exp n 1 + 1 β γ x γ d x ,
Substituting Z = n 1 + 1 β γ x γ , then x = β ( n 1 + 1 ) 1 γ Z 1 γ and d x = β γ ( n 1 + 1 ) 1 γ Z 1 γ 1 d Z . Equation (51) simplifies as:
μ r = n 1 , t 1 = 0 ( 1 ) t 1 ( n 1 + 1 ) V n 1 + 1 n 1 t 1 β r ( n 1 + 1 ) r γ + 1 Γ ( r γ + 1 ) .
where the smooth function, Γ ( r γ + 1 ) = 0 Z r γ exp ( Z ) d Z , is the gamma function for positive non-integers.
Putting r = 1 , 2 in Equation (52), we obtain the first and second raw moments for BIIIEEWD, given as:
μ 1 = n 1 , t 1 = 0 ( 1 ) t 1 ( n 1 + 1 ) V n 1 + 1 n 1 t 1 β ( n 1 + 1 ) 1 γ + 1 Γ ( 1 γ + 1 ) ,
μ 2 = n 1 , t 1 = 0 ( 1 ) t 1 ( n 1 + 1 ) V n 1 + 1 n 1 t 1 β 2 ( n 1 + 1 ) 2 γ + 1 Γ ( 2 γ + 1 ) .
Equation (53) is the mean for BIIIEEWD, and Equation (54) in relation to Equation (55) is the variance for BIIIEEWD:
μ 2 = μ 2 ( μ 2 ) 2

4.3. Mean Residual Life Function (MRLF)

Let a continuous rv X support the lifetime of an substance or a part with CDF defined in Equation (44), and the MRLF is obtained as:
μ ( x ) = 1 1 F B I I I E E W ( x ) μ 1 0 x y f B I I I E E W ( y ) d y x ; x 0 , = 1 1 F B I I I E E W ( x ) μ 1 T 1 ( x ) x .
Using Equations (44), (49) and (53) in Equation (56), we have:
μ ( x ) = 1 1 n 1 = 0 V n 1 1 exp x β γ n 1 n 1 , t 1 = 0 n 1 t 1 β ( 1 ) t 1 V n 1 + 1 ( n 1 + 1 ) 1 γ Γ ( 1 γ + 1 ) Γ ( 1 γ + 1 , Z 2 ) x .

4.4. Mean Inactivity Time Function (MITF)

If an rv X follows BIIIEEWD, then the MITF is expressed as:
M ( x ) = x T 1 ( x ) F B I I I E E W ( x ) ; x > 0 ,
Putting the values of Equations (44) and (49) in Equation (58), we obtain MITF for BIIIEEWD as
M ( x ) = x n 1 , t 1 = 0 ( 1 ) t 1 β V n 1 + 1 ( n 1 + 1 ) 1 γ n 1 t 1 Γ ( 1 γ + 1 , Z 2 ) n 1 = 0 V n 1 1 exp x β γ n 1 .

4.5. Moment Generating Function (MGF)

The MGF of the BIIIEEWD is defined as:
M X ( t ) = E ( e t x ) = 0 e t x f B I I I E E W ( x ) d x = 0 t 2 = 0 t t 2 t 2 ! x t 2 f B I I I E E W ( x ) d x ,
Using Equations (40) and (45) in Equation (60), we obtain:
M X ( t ) = t 1 , t 2 , n 1 = 0 ( 1 ) t 1 γ ( 1 + n 1 ) V 1 + n 1 β γ t t 2 t 2 ! n 1 t 1 0 x γ + t 2 1 exp 1 + n 1 β γ x γ d x ,
Put Z = 1 + n 1 β γ x γ we have x = β ( 1 + n 1 ) 1 γ Z 1 γ and d x = β γ ( 1 + n 1 ) 1 γ Z 1 γ 1 d Z .
After simplification, Equation (61) becomes:
M X ( t ) = t 1 , t 2 , n 1 = 0 ( 1 ) t 1 V 1 + n 1 β t 2 t t 2 ( 1 + n 1 ) t 2 γ t 2 ! n 1 t 1 Γ ( t 2 γ + 1 ) .

4.6. Quantile Function (QnF)

If X B I I I E E W D with CDF Equation (25), then QnF of X, x u , is:
x u = β log 1 1 e 1 + u 1 k 1 c W e 1 + 1 + u 1 k 1 c 1 θ 1 γ .
where u ( 0 , 1 ) , and W ( . ) the LWF.

4.7. Quantile Based Skewness and Kurtosis

Based QnF given in Equation (63), Bowley skewness ( B s k ) using quartiles (Kenney and Keeping, 1962) [15] is as follows:
B s k = Q 0.75 2 Q 0.50 + Q 0.25 Q 0.75 Q 0.25 .
The Moor’s kurtosis ( M k u r ) using octiles (Moors, 1998) [16] is given as:
M k u r = ( Q 0.875 Q 0.625 ) + ( Q 0.375 Q 0.125 ) Q 0.75 Q 0.25 .
For specific values of u = 0.25 , 0.50 , and 0.75 , the first, second, and third quartiles of BIIIEEWD are obtained.

4.8. The Mean Deviation (MD)

The MD of BIIIEEWD for rv X w.r.t. mean ( μ 1 ) and median (M) having CDF and PDF in Equations (44) and (45), respectively, can be expressed as:
Δ 1 ( x ) = x | x μ 1 | f B I I I E E W ( x ) d x = 2 μ 1 F B I I I E E W ( μ 1 ) 2 T 1 ( μ 1 ) ,
and
Δ 2 ( x ) = x | x M | f B I I I E E W ( x ) d x = μ 1 2 T 1 ( M ) .
Here, we use μ 1 from Equation (53), M = x 0.50 from Equation (63), F B I I I E E W ( μ 1 ) from Equation (44), and T 1 ( x ) from Equation (49).

5. Maximum Likelihood Method for BIIIEEWD

The values x 1 , x 2 , , x n are taken from BIIIEEWD having a PDF in Equation (26). The log-likelihood function (LLF), l ( Θ ) , for the vector of parameter Θ = ( c , k , θ , γ , β ) T is as below:
l = l ( c , k , θ , γ , β ) = n log c + n log θ + n log k + n log γ n γ log β + ( γ 1 ) i = 1 n log x i 1 β γ i = 1 n x i γ + ( θ 1 ) i = 1 n log 1 e ( x i β ) γ i = 1 n log 1 1 e ( x i β ) γ θ + i = 1 n log 1 + 1 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ( c + 1 ) × i = 1 n log log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ( k + 1 ) i = 1 n log 1 + l o g 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c .
To obtain the maximum likelihood estimates (MLEs) for a vector of parameter Θ , we maximized the LLF given in Equation (68). The components of the score function w.r.t. c , k , θ , γ , and β  are:
l c = n c + ( k + 1 ) i = 1 n 1 + log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c 1 log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c × log log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] i = 1 n log log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ,
l k = n k i = 1 n log 1 + log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c ,
l θ = n θ + i = 1 n log 1 e ( x i β ) γ + i = 1 n log 1 e ( x i β ) γ 1 e ( x i β ) γ θ 1 i = 1 n [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] 2 1 + [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] 1 log 1 e ( x i β ) γ 1 e ( x i β ) γ θ 1 ( c + 1 ) i = 1 n log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] 1 log 1 e ( x i β ) γ 1 e ( x i β ) γ θ 1 1 + 1 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] + c ( k + 1 ) i = 1 n 1 + log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c 1 log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ( c + 1 ) × log 1 e ( x i β ) γ 1 e ( x i β ) γ θ 1 2 log [ 1 ( 1 e ( x i β ) γ ) θ ] 1 log [ 1 ( 1 e ( x i β ) θ ) θ ] ,
l γ = n γ + i = 1 n log x i β 1 x i β γ + ( θ 1 ) i = 1 n ( x i β ) γ log ( x i β ) e ( x i β ) γ 1 + θ i = 1 n e ( x i β ) γ ( x i β ) γ log ( x i β ) ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ θ i = 1 n ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] 2 log ( x i β ) ( x i β ) γ e ( x i β ) γ 1 + [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] 1 ( c + 1 ) θ i = 1 n ( x i β ) γ log ( x i β ) e ( x i β ) γ × log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] 1 ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ [ 2 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] + c ( k + 1 ) θ × i = 1 n log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ( c + 1 ) 1 + 1 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ × 1 + log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c 1 e ( x i β ) γ ( x i β ) γ log ( x i β ) ,
and
l β = n β n ( γ 1 ) β + γ β γ + 1 i = 1 n x i γ γ ( θ 1 ) β γ + 1 i = 1 n x i γ e ( x i β ) γ 1 θ γ β γ + 1 i = 1 n x i γ e ( x i β ) γ ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ + γ θ β γ + 1 × i = 1 n x i γ e ( x i β ) γ ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ [ 1 + [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] 1 ] 1 [ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ] 2 + ( c + 1 ) γ θ β ( γ + 1 ) i = 1 n e ( x i β ) γ x i γ × ( 1 e ( x i β ) γ ) θ 1 1 ( 1 e ( x i β ) γ ) θ 2 log [ 1 ( 1 e ( x i β ) γ ) θ ] 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] 1 c γ ( k + 1 ) θ × β ( 1 + γ ) i = 1 n 1 + 1 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] ( 1 + c ) × 1 + log 1 ( 1 e ( x i β ) γ ) θ 1 log [ 1 ( 1 e ( x i β ) γ ) θ ] c 1 ( 1 e ( x i β ) γ ) θ 1 x i γ e ( x i β ) γ 1 ( 1 e ( x i β ) γ ) θ .
Setting the following:
l c = 0 ,
l k = 0 ,
l θ = 0 ,
l γ = 0 ,
l β = 0 .
The MLEs Θ ^ of Θ can be obtained analytically by handling the normal Equations (74)–(78), but it is a tedious effort. The MLEs are obtained numerically for the BIIIEEW model to different datasets of cancer disease, as described in the following section.

6. Numerical Applications of BIIIEEWD to Disease of Cancer Datasets

This section provide applicability of the new developed BIIIEEWD by empirical datasets consisting cancer diseases, such as blood, neck and head, acute bone, and bladder cancers. The efficiency of BIIIEEWD is checked and compared with other competing models, including generalized odd beta prime Weibull (GOBPW) (Suleiman et al., 2022) [17], gamma log-logistic Weibull (GmLLW) (Foya et al., 2017) [18], gamma generalized modified Weibull (GmGMoW) (Oluyede et al., 2015) [19], beta modified Weibull (BMoW) (Silva et al., 2010) [20], Kumaraswamy modified Weibull (KmMoW) (Cordeiro et al. 2012) [21], and beta log-logistic Weibull (BeLLW) (Makubate et al., 2018) [22].
The PDF of the competing models are defined below:
  • The GOBPW model:
    f G O B P W ( x ) = β θ γ x β 1 exp [ θ x β ] B ( c , k ) 1 exp [ θ x β ] c γ 1 1 1 exp [ θ x β ] γ 1 k ,
  • The GmLLW model:
    f G m L L W ( x ) = 1 Γ ( k ) c k ( 1 + x γ ) 1 exp ( β x θ ) log { 1 ( 1 + x γ ) 1 exp ( β x θ ) } k 1 × 1 ( 1 + x γ ) 1 exp ( β x θ ) 1 c 1 [ β θ x θ 1 + γ ( 1 + x γ ) 1 x γ 1 ] ,
  • The GmGMoW model:
    f G m G M o W ( x ) = 1 Γ ( c ) exp [ ( k x + θ x γ exp ( β x ) ) ] { k + θ ( γ + β x ) x γ 1 exp ( β x ) } log { 1 exp [ ( θ x γ exp ( β x ) + k x ) ] } c 1 ,
  • The BMoW model:
    f B M o W ( x ) = θ ( γ + β x ) x γ 1 B ( c , k ) exp [ β x k θ x γ exp ( β x ) ] 1 exp [ θ x γ exp ( β x ) ] c 1 ,
  • The KmMoW model:
    f K m M o W ( x ) = c k θ ( β x + γ ) x γ 1 exp [ θ x γ exp ( β x ) + β x ] 1 exp [ θ x γ exp ( β x ) ] c 1 × 1 exp [ θ x γ exp ( β x ) ] + 1 c k 1
  • The BeLLW model:
    f B e L L W ( x ) = 1 B ( c , k ) [ θ β x θ 1 + γ x γ 1 ( 1 + x γ ) 1 ] exp ( β x θ ) ( 1 + x γ ) 1 k × 1 exp ( β x θ ) ( 1 + x γ ) 1 c 1
Here, we use the maximum likelihood (ML) method for parameter estimation of each model and then compare them by the maximum value of log-likelihood ( L ^ ) analyzed at ML estimates together with their standard errors (SEs). Furthermore, some criteria, including the Anderson ( A * ), Cramer von Mises ( W * ), Bayesian information criterion (BIC), and Akaike information criterion (AIC), are considered as conventional goodness-of-fit (GoF) measures. The Kolmogorov–Smirnov (KS) statistic value and its p-value are also calculated for models comparative analysis. We follow the selection rule as follows: the model with the smallest statistics values must be selected as the best one for fitting data. All calculations in study are computed using the AdequacyModel package in R language. R-codes are given in Appendix A. As described, the BIIIEEWD is estimated as being a model to investigate cancer datasets (CDSs), as listed below.

6.1. Blood CDS (BCDS-1)

BCDS-1, which we considered, was previously reported by (Al-Saiary and Bakoban, 2020) [23], from a hospital in Saudia Arabia, which included the ordered life time (in years) of patients suffering blood cancer (leukemia). The data are given in Table 1.

6.2. Head and Neck CDS (HNCDS-2)

HNCDS-2, used by (Ibrahim et al., 2020) [24], represents the survival time for patients suffering from head and neck cancer. The data are shown in Table 2.

6.3. Acute Bone CDS (ABCDS-3)

ABCDS-3 is taken from (Mansour et al., 2020) [25], which gives the survival times (in days) of patients that were diagnosed with acute bone cancer. The dataset is shown in Table 3.

6.4. Bladder CDS (BCDS-4)

BCDS-4 is reported in (Varghese and Jose, 2022) [26], which represents the remission times (in months) of a random sample of bladder cancer patients. The data are shown in Table 4.
The descriptive statistics of CDSs are described in Table 5 and box and TTT plots are displayed in Figure 6, Figure 7, Figure 8 and Figure 9. From Table 5, it could be observed that HNCDS-2 and ABCDS-3 are right-skewed with high coefficients of kurtosis, while BCDS-1 is left-skewed. In Figure 7 and Figure 8, box plots indicate that HNCDS-2 and ABCDS-3 have extreme vales statistical behavior. Thus, these are suitable for distributions of extreme values and skewed models.
Furthermore, the results of ML estimates with corresponding SEs of the proposed BIIIEEWD in contrast of the other competing models for CDSs are provided in Table 6, Table 7, Table 8 and Table 9. The considered GoF measures values for CDSs of all candidate models are displayed in Table 10, Table 11, Table 12 and Table 13. From Table 10, Table 11, Table 12 and Table 13, it could be observed that the BIIIEEWD posses the smallest L ^ , W * , A * , AIC, BIC, and KS values for CDSs. In addition, it has the highest p-value at KS statistics against all fitted competing models. These results suggest that all fitted competing models fit quite well, but the proposed BIIIEEW model provides the best fit. Furthermore, Figure 10, Figure 11, Figure 12 and Figure 13 support these results for CDSs.

7. Conclusions

The field of medical research relies heavily on applications of statistical distributions, where applications have the potential to significantly improve public health, particularly for cancer patients. In this article, therefore, the WEE-X, LEE-X, LGCEE-X, and BIIIEE-X families have been proposed as new families of continuous distributions. Four new models, i.e., WEEW, LEEW, LGCEEW, and BIIIEEW, are derived and explored graphically. In this regard, we characterized the BIIIEE-X family with a five-parameter model, i.e., BIIIEE-Weibull. Various properties of the proposed model have also been derived. Consequently, the proposed model is applied to four distinct cancer data, including bladder, acute bone, neck and head, and blood. GoF measures have been compared with other competing models to see how well the proposed BIIIEEW model performed. Our proposed model have shown superior graphical and numerical results. When it comes to modeling positively skewed lifetime data, particularly cancer research, we hoped that our proposed model would serve as a better alternative to other more conventional distributions.
Using a Bayesian approach, the parameters of the various models derived from these proposed families can be estimated in future work. Besides, other datasets in various regions can be utilized to actually take a look at the adaptability of the determined models. For the bivariate families of distributions, this work can also be extended. Some other flexible distributions should also be considered besides the distribution proposed in this study to fit the data of the real-life case studies.

Author Contributions

Conceptualization, S.H., M.U.H. and R.A.; Methodology, S.H. and M.U.H.; Software, S.H., M.U.H. and M.S.R.; Investigation, S.H., M.S.R. and R.A.; Writing—original draft, S.H., M.U.H. and M.S.R.; Writing—review & editing, R.A.; Supervision, M.U.H. and R.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

The data are fully available in the article and the mentioned references.

Acknowledgments

The authors are thankful to the reviewers for their valuable correction and suggestions.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A. R Code for Application

  • rm(list=ls ())
  • library(AdequacyModel)
  • ### Blood cancer dataset
  • data<-c(0.315, 0.496, 0.616, 1.145, 1.208, 1.263, 1.414, 2.025, 2.036, 2.162, 2.211, 2.370, 2.532, 2.693, 2.805, 2.910, 2.912, 3.192, 3.263, 3.348, 3.348, 3.427, 3.499, 3.534, 3.767, 3.751, 3.858, 3.986, 4.049, 4.244, 4.323, 4.381, 4.392, 4.397, 4.647, 4.753, 4.929, 4.973, 5.074, 5.381)
  • ### The PDF of the BIIIEEW
  • ### Note: In the following R-code, a is used for θ , c is used for c, K is used for k, B is used for β and g is used for γ for derived model BIIIEEW.
  • dBIIIEEW <-function(par,x)
  • {
  • a=par[1];c=par[2];K=par[3];B=par[4];g=par[5]
  • a c K ( ( g / B ) ( ( x / B ) ( g 1 ) ) ( exp ( ( x / B ) g ) ) ) ( ( 1 exp ( ( x / B ) g ) ) ( a 1 ) ) ( 1 / ( 1 ( 1 exp ( ( x / B ) g ) ) a ) ) ( 1 + ( 1 / ( 1 log ( 1 ( 1 exp ( ( x / B ) g ) ) a ) ) ) ) ( ( log ( ( 1 ( ( 1 exp ( ( x / B ) g ) ) a ) ) / ( 1 log ( 1 ( 1 exp ( ( x / B ) g ) ) a ) ) ) ) ( c 1 ) ) ( ( 1 + ( log ( ( 1 ( ( 1 exp ( ( x / B ) g ) ) a ) ) / ( 1 log ( 1 ( 1 exp ( ( x / B ) g ) ) a ) ) ) ) ( c ) ) ( K 1 ) )
  • }
  • ### The CDF of the BIIIEEW
  • pBIIIEEW <- function(par,x)
  • {
  • a=par[1];c=par[2];K=par[3];B=par[4];g=par[5]
  • ( ( 1 + ( log ( ( 1 ( ( 1 exp ( ( x / B ) g ) ) a ) ) / ( 1 log ( 1 ( 1 exp ( ( x / B ) g ) ) a ) ) ) ) ( c ) ) ( K ) )
  • }
  • goodness.fit(pdf= dBIIIEEW, cdf= pBIIIEEW, starts = c(1.1,1.1,1.11,0.21,0.03), data=data, method="BFGS", domain=c(0,Inf),mle=NULL)

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Figure 1. Plots for PDF of WEEWD.
Figure 1. Plots for PDF of WEEWD.
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Figure 2. Plots for PDF of LEEWD.
Figure 2. Plots for PDF of LEEWD.
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Figure 3. Plots for PDF of LGCEEWD.
Figure 3. Plots for PDF of LGCEEWD.
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Figure 4. Plots for PDF of BIIIEEWD.
Figure 4. Plots for PDF of BIIIEEWD.
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Figure 5. Plots for FRF of BIIIEEWD.
Figure 5. Plots for FRF of BIIIEEWD.
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Figure 6. Boxplot (left) and TTT plot (right) for BCDS-1.
Figure 6. Boxplot (left) and TTT plot (right) for BCDS-1.
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Figure 7. Boxplot (left) and TTT plot (right) for HNCDS-2.
Figure 7. Boxplot (left) and TTT plot (right) for HNCDS-2.
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Figure 8. Boxplot (left) and TTT plot (right) for ABCDS-3.
Figure 8. Boxplot (left) and TTT plot (right) for ABCDS-3.
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Figure 9. Boxplot (left) and TTT plot (right) for BCDS-4.
Figure 9. Boxplot (left) and TTT plot (right) for BCDS-4.
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Figure 10. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) Kaplan–Meier (K-M) survival probability of BIIIEEWD for BCDS-1.
Figure 10. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) Kaplan–Meier (K-M) survival probability of BIIIEEWD for BCDS-1.
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Figure 11. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) K-M survival probability of BIIIEEWD for HNCDS-2.
Figure 11. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) K-M survival probability of BIIIEEWD for HNCDS-2.
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Figure 12. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) K-M survival probability of BIIIEEWD for ABCDS-3.
Figure 12. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) K-M survival probability of BIIIEEWD for ABCDS-3.
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Figure 13. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) K-M survival probability of BIIIEEWD for BCDS-4.
Figure 13. Plots of the estimated (a) PDF using a histogram, (b) CDF using empirical CDF, (c) failure rate, (d) K-M survival probability of BIIIEEWD for BCDS-4.
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Table 1. Blood cancer dataset-1.
Table 1. Blood cancer dataset-1.
0.3150.4960.6161.1451.2081.2631.4142.0252.0362.162
2.2112.3702.5322.6932.8052.9102.9123.1923.2633.348
3.3483.4273.4993.5343.7673.7513.8583.9864.0494.244
4.3234.3814.3924.3974.6474.7534.9294.9735.0745.381
Table 2. Head and Neck cancer dataset-2.
Table 2. Head and Neck cancer dataset-2.
12.2023.5623.7425.8731.9837.0041.3547.3855.46
58.3663.4768.4678.2674.4781.4384.0092.0094.00
110.00112.00119.00127.00130.00133.00140.00146.00155.00
159.00173.00179.00194.00195.00209.00249.00281.00319.00
339.00432.00469.00519.00633.00725.00817.001776.00
Table 3. Acute Bone cancer dataset-3.
Table 3. Acute Bone cancer dataset-3.
0.090.761.811.103.720.722.491.000.53
0.6631.610.600.201.611.880.701.360.43
3.161.574.9311.071.631.394.543.1286.01
1.920.924.041.162.260.200.941.823.99
1.462.751.382.761.862.681.760.671.29
1.562.830.711.482.410.660.652.361.29
13.750.673.700.763.630.682.650.952.30
2.570.613.931.561.299.941.671.424.18
1.37
Table 4. Bladder cancer dataset-4.
Table 4. Bladder cancer dataset-4.
0.080.200.400.500.510.810.870.901.051.191.261.35
1.401.461.762.022.022.072.092.232.262.462.542.62
2.642.692.692.752.832.873.023.253.313.363.363.36
3.483.523.573.643.703.823.884.184.234.264.334.33
4.344.404.504.514.654.704.874.985.065.095.175.32
5.325.345.415.415.495.625.715.856.256.546.766.93
6.946.977.097.267.287.327.397.597.627.287.327.39
7.597.627.637.667.877.938.268.378.538.608.658.66
9.029.229.479.7410.0610.3410.6610.7510.8611.2511.6411.79
11.9812.0212.0312.0712.6913.1113.2913.8014.2414.7614.7714.83
15.9616.6217.1217.1417.3618.1019.1319.3620.2821.7322.6923.60
Table 5. Descriptive statistics for CDSs.
Table 5. Descriptive statistics for CDSs.
DataBCDS-1HNCDS-2ABCDS-3BCDS-4
n404473132
Min.0.315012.200.0900.080
Ist Qu.2.199067.210.9203.348
Median3.3480128.501.5705.665
3rd Qu.4.2640219.002.7509.537
Mean3.1407223.483.7557.149
Max.5.38101776.0086.01023.600
Variance1.846593286.41112.33127.673
Skewness−0.41673.38386.7991.072
Kurtosis−0.726213.559648.7770.669
Table 6. ML estimates and SEs of parameters of the BIIIEEW model for BCDS-1.
Table 6. ML estimates and SEs of parameters of the BIIIEEW model for BCDS-1.
Model θ ^ c ^ k ^ β ^ γ ^
BIIIEEW0.7198213.033920.046036.821693.55227
(1.44108)(41.79737)(0.05557)(7.47865)(10.36960)
GOBPW2.846303.219400.788201.454605.64530
(0.17340)(0.21990)(0.10240)(0.11350)(2.47530)
GmLLW4.956403.140701.341302.703407.94530
(1.73540)(0.21210)(0.15050)(0.20350)(3.74620)
GmGMoW3.253902.500303.518301.392605.65720
(0.28450)(0.33780)(0.23160)(0.07450)(0.54930)
BMoW2.645103.069803.011700.872104.87210
(0.17340)(0.41920)(0.26480)(0.06450)(0.53910)
KmMoW2.183503.464601.103201.742904.08320
(0.63190)(0.74040)(0.25300)(0.14390)(1.35410)
BeLLW1.945300.993200.646300.845302.62930
(0.43520)(0.10210)(0.07260)(0.09360)(0.74530)
Table 7. ML estimates and SEs of parameters of the BIIIEEW model for HNCDS-2.
Table 7. ML estimates and SEs of parameters of the BIIIEEW model for HNCDS-2.
Model θ ^ c ^ k ^ β ^ γ ^
BIIIEEW3.3139312.269441.206360.495480.07396
(5.22705)(20.01934)(0.88527)(4.85634)(0.08751)
GOBPW5.256701.6909025.037801.701803.44340
(2.67430)(0.21280)(9.39440)(1.18230)(0.42360)
GmLLW0.256304.846901.040803.456305.22080
(0.13240)(0.15690)(0.11090)(0.53410)(2.97440)
KmMoW1.354601.023400.457804.103602.97430
(0.64540)(0.18270)(0.09910)(1.03430)(0.45830)
GmGMoW8.3452016.357206.724703.2436018.25460
(3.25430)(4.74430)(2.86690)(1.01240)(7.45320)
BeLLW5.7352051.1783029.707104.8322017.63240
(2.11530)(17.43520)(8.84320)(1.87430)(6.53620)
BMoW7.8732037.5243023.477005.5325011.63490
(2.65230)(9.32450)(6.96340)(2.53420)(3.64530)
Table 8. ML estimates and SEs of parameters of the BIIIEEW model for ABCDS-3.
Table 8. ML estimates and SEs of parameters of the BIIIEEW model for ABCDS-3.
Model θ ^ c ^ k ^ β ^ γ ^
BIIIEEW2.847551.467520.570651.636290.89759
(1.04539)(0.24194)(0.22568)(0.00470)( 0.00604)
GOBPW1.741301.869001.616300.073101.98330
(0.41310)(0.18540)(0.17250)(0.00410)(0.20230)
GmGMoW0.097300.519601.038203.345700.56530
(0.03670)(0.12150)(0.08590)(1.95850)(0.32010)
KmMoW1.070401.117401.128002.706902.72850
(0.21560)(0.16440)(0.20770)(0.87170)(1.19810)
GmLLW0.382201.434200.718303.224700.37880
(0.02530)(0.12690)(0.11490)(0.60070)(0.05830)
BeLLW0.456702.111702.220807.532102.46790
(0.83540)(0.39510)(0.24430)(1.45670)(0.55430)
BMoW2.674903.7552010.525703.3548011.67360
(1.53670)(1.23190)(0.87110)(0.35470)(3.57690)
Table 9. ML estimates and SEs of parameters of the BIIIEEW model for BCDS-4.
Table 9. ML estimates and SEs of parameters of the BIIIEEW model for BCDS-4.
Model θ ^ c ^ k ^ β ^ γ ^
BIIIEEW0.175211.865010.7009717.381245.75015
(0.05814)(0.21181)(0.29749)(0.04119)(0.04196)
GOBPW3.017401.369007.810801.874805.92240
(2.77700)(0.09330)(0.52260)(0.25370)(1.57770)
GmLLW2.647301.633700.228501.600308.38840
(0.40250)(0.18420)(0.03010)(2.2953)(3.65110)
GmGMoW3.199301.970105.573501.424302.10570
(0.70510)(0.14390)(0.42470)(0.54220)(0.23630)
BMoW3.753106.514602.878100.935604.37650
(0.34210)(0.43480)(0.21070)(0.21320)(0.63420)
KmMoW5.384507.148205.240502.411502.10470
(1.27530)(0.45610)(0.32250)(1.19250)(0.38850)
BeLLW1.212205.416002.755701.356405.38260
(0.10930)(0.39990)(0.30860)(0.04320)(0.68030)
Table 10. GoF measures for the BIIIEEW model for BCDS-1.
Table 10. GoF measures for the BIIIEEW model for BCDS-1.
Model L ^ W * A * AICBICKSp-Value
BIIIEEW65.1020.021950.14759140.204148.6480.066100.9948
GOBPW68.5100.048000.42240147.020155.4640.083000.9158
GmLLW69.5900.063700.44720149.180157.6240.090200.8651
GmGMoW70.1500.116600.85640150.300158.7440.118400.7316
BMoW73.3900.176601.54490156.780165.2240.144100.5967
KmMoW76.5400.251801.55700163.080171.5240.158200.3480
BeLLW79.0200.398302.33600168.040176.4840.177100.1478
Table 11. GoF measures for the BIIIEEW model for HNCDS-2.
Table 11. GoF measures for the BIIIEEW model for HNCDS-2.
Model L ^ W * A * AICBICKSp-Value
BIIIEEW277.7030.013170.10698565.407574.3280.045820.9999
GOBPW277.7900.013700.11640565.580574.5010.049600.8438
GmLLW277.4600.021800.14030564.920573.8410.068400.7231
KmMoW282.0100.184400.98610574.020582.9410.147200.6381
GmGMoW289.3900.393802.69420588.780597.7010.188200.3081
BeLLW302.9100.446403.08110615.820624.7410.218000.1721
BMoW313.6800.957405.04830637.360646.2810.269100.0240
Table 12. GoF measures for the BIIIEEW model for ABCDS-3.
Table 12. GoF measures for the BIIIEEW model for ABCDS-3.
Model L ^ W * A * AICBICKSp-Value
BIIIEEW138.5270.048480.37429287.054298.5070.073520.8249
GOBPW139.9800.052400.46870289.960301.4120.067300.5127
GmGMoW144.2600.164901.16500298.520309.9720.094300.4821
KmMoW147.9000.291901.84080305.800317.2520.141100.2386
GmLLW153.2900.530203.58210316.580328.0320.158900.1359
BeLLW221.3601.617603.75730452.720464.1720.286900.0731
BMoW275.4103.742708.34280560.820572.2720.388100.0176
Table 13. GoF measures for the BIIIEEW model for BCDS-4.
Table 13. GoF measures for the BIIIEEW model for BCDS-4.
Model L ^ W * A * AICBICKSp-Value
BIIIEEW382.0210.030020.17785774.042788.4560.040140.9835
GOBPW382.5300.033700.20870775.060789.4740.044300.7146
GmLLW383.3100.036800.24550776.620791.0340.050900.6732
GmGMoW391.0600.076400.89330792.120806.5340.067700.3401
BMoW404.1200.264002.45860818.240832.6540.096500.2721
KmMoW405.9400.565503.45940821.880836.2940.127800.1397
BeLLW418.3400.598104.32780846.680861.0940.151700.1259
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Hussain, S.; Ul Hassan, M.; Rashid, M.S.; Ahmed, R. Families of Extended Exponentiated Generalized Distributions and Applications of Medical Data Using Burr III Extended Exponentiated Weibull Distribution. Mathematics 2023, 11, 3090. https://doi.org/10.3390/math11143090

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Hussain S, Ul Hassan M, Rashid MS, Ahmed R. Families of Extended Exponentiated Generalized Distributions and Applications of Medical Data Using Burr III Extended Exponentiated Weibull Distribution. Mathematics. 2023; 11(14):3090. https://doi.org/10.3390/math11143090

Chicago/Turabian Style

Hussain, Sajid, Mahmood Ul Hassan, Muhammad Sajid Rashid, and Rashid Ahmed. 2023. "Families of Extended Exponentiated Generalized Distributions and Applications of Medical Data Using Burr III Extended Exponentiated Weibull Distribution" Mathematics 11, no. 14: 3090. https://doi.org/10.3390/math11143090

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